Skip to contents

table_regression() produces a coefficient summary table from one or several fitted regression models. The output is publication-ready by default and follows APA Manual 7 (American Psychological Association 2020, Tables 7.13–7.15) formatting conventions: paired estimate-and-CI columns, APA p-values without leading zero, factor levels grouped under their parent variable, fit statistics at the foot of the table, and a self-documenting note line that names the variance estimator and any methodological choice that affected the rendered values.

The function is fit-first: you pass already-fitted models, not raw data and a formula. The same object exports cleanly to a long broom-canonical frame (broom::tidy()) and to a one-row-per-model glance summary (broom::glance()).

This vignette teaches the shared mechanics on lm() and glm() fits. The Generalised linear models section covers the glm-specific argument semantics; the Mixed-effects models section introduces the Random effects rows that mixed-effects fits add below the fixed effects (lmer, glmer, glmmTMB, lme). Each further model family has a dedicated vignette that applies these mechanics to its own estimands: vignette("table-regression-mixed") for mixed-effects models, vignette("table-regression-gee") for population-averaged (GEE) models, vignette("table-regression-counts") for Poisson, negative-binomial, and two-part models, vignette("table-regression-ordinal") for ordinal models (polr, clm), vignette("table-regression-multinomial") for multinomial models (multinom, mlogit), vignette("table-regression-survival") for survival models (coxph, survreg), and vignette("table-regression-bayesian") for Bayesian fits (rstanarm, brms). The mechanics covered here — confidence levels, multi-model and nested layouts, p-value adjustment, coefficient filtering, output formats, and the broom methods — apply across every supported class; variance-estimator availability varies by family, and the complete map — every supported class with its estimands, variance estimators and fit statistics, including the families without a dedicated article (quantile regression, fixest, betareg, …) — is vignette("table-regression-supported-models"). One decision cuts across all of them — how to code, test, and present categorical predictors — and has its own vignette: vignette("categorical-predictors").

Basic usage

Pass a fitted lm() object. The default rendering returns a single-model table with B, SE, 95% CI, and p columns and a fit-statistics footer (n, , Adj.R²):

fit <- lm(wellbeing_score ~ age + sex + smoking, data = sochealth)
table_regression(fit)
#> Linear regression: wellbeing_score
#> 
#>  Variable            B      SE       95% CI        p   
#> ─────────────────┼──────────────────────────────────────
#>  (Intercept)        65.20  1.66  [61.95, 68.45]  <.001 
#>  age                 0.05  0.03  [-0.01,  0.11]   .130 
#>  sex:                                                  
#>    Female (ref.)      –     –          –          –    
#>    Male              3.86  0.91  [ 2.08,  5.63]  <.001 
#>  smoking:                                              
#>    No (ref.)          –     –          –          –    
#>    Yes              -1.72  1.11  [-3.89,  0.45]   .121 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1175                                 
#>  R²                  0.02                              
#>  Adj.R²              0.02                              
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).

Reading the table:

  • Each predictor occupies one row; factor predictors are grouped under their parent variable name with one row per level. The reference level carries the (ref.) annotation and an en dash across the statistic columns, so the substantive comparison is visible in a single glance (NEJM / BMJ clinical convention).
  • The 95% CI column reports a symmetric Wald interval at the level set by ci_level (default 0.95). The CI header tracks the chosen level — switching to ci_level = 0.99 re-labels the column accordingly.
  • The footer line names the variance estimator in plain English so the reader can find the inferential regime without leaving the table. The estimator switches with vcov (covered in Robust variance below).
  • Read substantively, one sentence per coefficient, from the exact numbers shown: Male — B = 3.86, 95% CI [2.08, 5.63], p < .001 — holding age and smoking constant, men score on average 3.9 points higher than women on the 0–100 WHO-5 wellbeing index. age — B = 0.05, 95% CI [-0.01, 0.11], p = .130 — the interval spans effects from slightly negative to about a tenth of a point per year, so the data do not establish an adjusted age gradient.

Standardised coefficients

Standardised coefficients (β) make predictors with different natural scales comparable: a one-standard-deviation increase in X predicts a β-standard-deviation change in Y. APA Manual 7 §7.13 recommends reporting both B and β so the unstandardised effect (natural units, interpretable) stays alongside the standardised effect (comparable across predictors).

standardized selects the method. Four apply to linear models — a fifth, glm-specific "pseudo", is covered in the Generalised linear models section — and the choice is consequential and well-documented (Cohen, Cohen, West, and Aiken 2003 §3.4; Gelman 2008). The methods differ most visibly in how they treat factor dummies:

  • "refit" — refit the model on the z-scored outcome and z-scored numeric predictors; factors stay factors, so their dummies keep the 0/1 scale (the Cohen et al. 2003 convention, matching the effectsize package). A dummy’s β is its group contrast in SD(Y) units.
  • "posthoc" — the same estimand as "refit", obtained by algebraic rescaling of the original fit: β = B × SD(X) / SD(Y) for numeric predictors, β = B / SD(Y) for factor dummies (which stay on 0/1). Numerically identical to "refit" for purely linear-additive Gaussian models; preferred when refitting is expensive or when lm() was wrapped in a pipeline that resists re-execution.
  • "basic" — algebraic, but every design column is scaled by its column SD, factor dummies included: β = B × SD(column) / SD(Y). This is the Beta definition of SPSS REGRESSION and Stata regress, beta (spicy’s oracle tests pin it against PSPP): reach for it when you need numbers that reproduce those packages, at the price of a dummy β that depends on the level’s base rate through SD(dummy).
  • "smart" — Gelman’s (2008) input scaling: numeric predictors divided by 2 × SD(X); binary predictors and factor dummies kept on their 0/1 scale. The resulting β is the change in Y, in SD(Y) units, for a two-standard-deviation change in X (from mean − SD to mean + SD), which puts a continuous predictor’s ±1 SD swing on the same footing as a binary’s 0 → 1 step. Where the paper leaves Y raw, spicy divides by SD(Y) so β stays comparable across the four methods.

When standardized != "none", the "beta" token is auto-injected into show_columns immediately after "b":

fit <- lm(wellbeing_score ~ age + sex + smoking, data = sochealth)
table_regression(fit, standardized = "refit")
#> Linear regression: wellbeing_score
#> 
#>  Variable            B       β     SE       95% CI        p   
#> ─────────────────┼─────────────────────────────────────────────
#>  (Intercept)        65.20  -0.10  1.66  [61.95, 68.45]  <.001 
#>  age                 0.05   0.04  0.03  [-0.01,  0.11]   .130 
#>  sex:                                                         
#>    Female (ref.)      –      –     –          –          –    
#>    Male              3.86   0.25  0.91  [ 2.08,  5.63]  <.001 
#>  smoking:                                                     
#>    No (ref.)          –      –     –          –          –    
#>    Yes              -1.72  -0.11  1.11  [-3.89,  0.45]   .121 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1175                                        
#>  R²                  0.02                                     
#>  Adj.R²              0.02                                     
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).
#> β = standardised coefficient ("refit": outcome and numeric predictors z-scored, factor dummies on 0/1).

On the standardised scale the predictors become directly comparable: being male predicts a 0.25-SD higher wellbeing score, the largest standardised effect in the model, while a one-SD increase in age predicts a change of only 0.04 SD. The raw B column could not support that ranking — 3.86 versus 0.05 compares a factor contrast with a per-year slope, two different units.

Caveat: standardised coefficients with interactions or transformed terms. When the model contains a product term, an I(), poly(), log(), or splines::ns() wrapper, the standardised coefficient of the non-additive term has no closed-form “one-SD change in X” reading (Aiken and West 1991; Cohen et al. 2003 §7.7). The function emits a classed spicy_caveat warning at runtime and prints a method-specific caveat line in the table footer, so the limitation is exposed at the point of use without blocking the table.

Per-coefficient effect sizes

For each predictor, you can request a partial effect-size column. Three measures are available — Cohen’s (partial_f2), Pearson’s partial η² (partial_eta2), and the Olejnik–Algina bias-corrected partial ω² (partial_omega2). Each carries a confidence interval derived from noncentral-F inversion (Smithson 2003; Steiger 2004), exposed as a separate <token>_ci column. The shortcuts "all_f2", "all_eta2", and "all_omega2" each expand to the point estimate together with its CI column.

sochealth$education is stored as an ordered factor, which R codes with polynomial contrasts (.L = linear, .Q = quadratic) — trend components across the ordered levels, not per-level effects against a reference. For a coefficient table read level-against-reference, convert it to a plain factor; we reuse this copy throughout the vignette:

sh <- sochealth |>
  dplyr::mutate(education = factor(education, ordered = FALSE))

fit <- lm(wellbeing_score ~ age + sex + smoking + education,
          data = sh)
table_regression(
  fit,
  show_columns = c("b", "p", "all_eta2", "all_omega2")
)
#> Linear regression: wellbeing_score
#> 
#>  Variable                     B       p     η²    η² 95% CI     ω²  
#> ──────────────────────────┼──────────────────────────────────────────
#>  (Intercept)                 53.96  <.001                           
#>  age                          0.03   .344  0.00  [0.00, 0.00]  0.00 
#>  sex:                                                               
#>    Female (ref.)               –     –                              
#>    Male                       3.57  <.001  0.02  [0.00, 0.03]  0.02 
#>  smoking:                                                           
#>    No (ref.)                   –     –                              
#>    Yes                        0.68   .496  0.00  [0.00, 0.00]  0.00 
#>  education:                                                         
#>    Lower secondary (ref.)      –     –                              
#>    Upper secondary           11.89  <.001  0.21  [0.17, 0.25]  0.21 
#>    Tertiary                  19.71  <.001  0.21  [0.17, 0.25]  0.21 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                                     
#>  R²                           0.22                                  
#>  Adj.R²                       0.22                                  
#> 
#>  Variable                   ω² 95% CI   
#> ──────────────────────────┼──────────────
#>  (Intercept)                            
#>  age                       [0.00, 0.00] 
#>  sex:                                   
#>    Female (ref.)                        
#>    Male                    [0.00, 0.03] 
#>  smoking:                               
#>    No (ref.)                            
#>    Yes                     [0.00, 0.00] 
#>  education:                             
#>    Lower secondary (ref.)               
#>    Upper secondary         [0.17, 0.25] 
#>    Tertiary                [0.17, 0.25] 
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).
#> η² = partial eta-squared; ω² = bias-corrected partial omega-squared.

Methodology notes:

  • The partial F-test is a Type-II test (marginality-respecting, contrast-invariant; Fox 2016; Fox and Weisberg 2019): the focal term is tested by comparing the two nested models that both exclude every higher-order term containing it — A in y ~ A * B is SS(A | B), with A:B left out of both sides — over the full model’s mean squared error. This matches car::Anova(type = 2). For additive models it reduces to the classic “each term after all the others” partial F, and the result does not depend on the factor coding (treatment, sum, Helmert, polynomial). Readers coming from SPSS UNIANOVA or SAS PROC GLM, whose default is Type III, should note the difference is a deliberate convention choice, not an oversight; the two conventions coincide for models without interactions.
  • The ω² point estimate is bias-corrected via the Olejnik and Algina (2003) formula ((F − 1) × df1) / (F × df1 + N − df1), yielding a less-biased small-sample estimator than partial η².
  • The CI bounds come from inverting the noncentrality parameter of the F-distribution at the lower and upper confidence levels (Steiger 2004 §4), anchored at the bias-corrected F implied by ω² rather than at the observed F. Population partial η² and partial ω² are the same quantity — ω² is simply the less-biased small-sample estimator — so both columns share that single interval, and it always brackets the bias-corrected point estimate, even when the lower bound clips at zero (common for near-null terms). Expect small differences from the effectsize package on both columns: it inverts the observed F for its η² bounds and its own implied F for ω².
  • For factor predictors with k levels, the partial F-test is the joint (k − 1) df Wald test, so the same effect-size value is broadcast across all non-reference dummy rows; the reference row leaves the effect-size cells blank.

Average marginal effects (AME)

The B coefficient is the model’s structural effect — the change in the linear predictor for a one-unit change in x, holding the other predictors constant. The average marginal effect (AME) is the observable effect on the response. For a numeric predictor it is the average partial derivative dE[Y|X] / dx over the sample; for a factor level it is the average discrete change — the difference in predicted response between that level and the reference, averaged over the sample (Long and Freese 2014 §6.2 distinguish the two). For a purely linear-additive lm() both coincide with B. For models with interactions or transformed terms, and for any glm() with a non-identity link, the AME is the quantity the substantive reader actually needs. The average in the name is load-bearing: the effect is computed for every observation and then averaged over the sample, not evaluated once at the covariate means — the marginal effect at the mean (MEM), a point at which no actual observation may sit. The two generally differ in nonlinear models; Long and Freese (2014, §6.2.3) discuss the choice in detail.

Add "ame" to show_columns for the point estimate. Companion tokens display the SE, CI, and p-value: "ame_se", "ame_ci", "ame_p". The shortcut "all_ame" expands to the full set.

fit <- lm(wellbeing_score ~ age + sex + smoking, data = sochealth)
table_regression(
  fit,
  show_columns = c("b", "se", "p", "ame", "ame_ci", "ame_p")
)
#> Linear regression: wellbeing_score
#> 
#>  Variable            B      SE     p     AME      95% CI        p   
#> ─────────────────┼───────────────────────────────────────────────────
#>  (Intercept)        65.20  1.66  <.001                              
#>  age                 0.05  0.03   .130   0.05  [-0.01, 0.11]   .130 
#>  sex:                                                               
#>    Female (ref.)      –     –     –       –          –         –    
#>    Male              3.86  0.91  <.001   3.86  [ 2.08, 5.63]  <.001 
#>  smoking:                                                           
#>    No (ref.)          –     –     –       –          –         –    
#>    Yes              -1.72  1.11   .121  -1.72  [-3.89, 0.45]   .121 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1175                                              
#>  R²                  0.02                                           
#>  Adj.R²              0.02                                           
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).
#> AME = average marginal effect.

Reading conventions:

  • "p" always refers to the B (or β) coefficient, never to the AME. Use "ame_p" for the AME-specific p-value.
  • Placing "ame" after "p" keeps the attribution of each p-value unambiguous — the B-block (B / SE / p) is closed before the AME-block opens.
  • For non-linear models the AME is reported on the response scale, not the link scale. The Generalised linear models section below works out a logistic-regression example.

Inference is delegated to marginaleffects::avg_slopes() and respects the chosen variance estimator. Under cluster-robust variance (covered in Robust variance), the AME inference shares the coefficient’s t-distribution and Satterthwaite-corrected degrees of freedom via clubSandwich::linear_contrast(), so B and AME are reported on the same inferential footing in the same table. marginaleffects is a Suggests dependency with two distinct failure modes: requesting AME columns without the package installed is a hard, classed error (spicy_missing_pkg, with the install hint), while a computation failure inside avg_slopes() on an installed system warns (spicy_fallback) and dashes the AME cells, leaving the rest of the table intact.

Multiple models side by side

Pass a list of lm() fits. The default column layout places each model in its own panel under a centered spanner label showing the model name; sub-columns (B / SE / p) are repeated under the spanner. When dependent variables differ across models and the user did not supply labels (model_labels = or named list), the bare DV name is lifted into the spanner automatically:

m_wellbeing <- lm(wellbeing_score ~ age + sex + smoking,
                   data = sochealth)
m_bmi       <- lm(bmi             ~ age + sex + smoking,
                   data = sochealth)
table_regression(list(m_wellbeing, m_bmi))
#> Linear regression comparison
#> 
#>                      wellbeing_score             bmi          
#>                    ────────────────────  ──────────────────── 
#>  Variable            B      SE     p       B      SE     p   
#> ─────────────────┼────────────────────────────────────────────
#>  (Intercept)        65.20  1.66  <.001    23.98  0.40  <.001 
#>  age                 0.05  0.03   .130     0.04  0.01  <.001 
#>  sex:                                                        
#>    Female (ref.)      –     –     –         –     –     –    
#>    Male              3.86  0.91  <.001     0.51  0.22   .018 
#>  smoking:                                                    
#>    No (ref.)          –     –     –         –     –     –    
#>    Yes              -1.72  1.11   .121    -0.06  0.26   .822 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1175                  1163                 
#>  R²                  0.02                  0.02              
#>  Adj.R²              0.02                  0.02              
#> 
#> Note. Linear regression models.
#> Std. errors: classical (OLS).

When all models share the same DV, the DV appears in the title. Use a named list — e.g. list(Crude = m1, Adjusted = m2) — to set the spanner labels explicitly; pass model_labels = c(...) to override the names from the list.

Univariable screening

Epidemiological reporting often starts one step before the side-by-side table: a univariable screen — one simple regression per candidate predictor — set against the multivariable model, the classic “Table 2” of clinical and epidemiological journals (the layout of gtsummary::tbl_uvregression() and the EpiRHandbook workflow). table_regression_uv() builds that entire layout in one call: pass the data, the outcome, and the candidate predictors — reusing sh, the unordered-education copy of sochealth introduced in Per-coefficient effect sizes:

table_regression_uv(sh, outcome = smoking,
                    predictors = c(sex, age, education),
                    family = binomial(), exponentiate = TRUE)
#> Univariable and multivariable logistic regression: smoking
#> 
#>                                       Univariable            Multiv… 
#>                             ───────────────────────────────  ─────── 
#>  Variable                   N     OR      95% CI       p      OR    
#> ──────────────────────────┼──────────────────────────────────────────
#>  sex:                                                               
#>    Female (ref.)              –   –         –         –         –   
#>    Male                    1175  0.95  [0.72, 1.26]   .713     0.96 
#>  age                       1175  1.01  [1.00, 1.01]   .292     1.01 
#>  education:                                                         
#>    Lower secondary (ref.)     –   –         –         –         –   
#>    Upper secondary         1175  0.62  [0.44, 0.87]   .005     0.62 
#>    Tertiary                      0.41  [0.28, 0.60]  <.001     0.40 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                                                          1175    
#>  R² (McFadden)                                                 0.02 
#>  R² (Nagelkerke)                                               0.03 
#>  AIC                                                        1200.9  
#> 
#>                                Multivariable    
#>                             ─────────────────── 
#>  Variable                     95% CI       p   
#> ──────────────────────────┼─────────────────────
#>  sex:                                          
#>    Female (ref.)                –         –    
#>    Male                    [0.73, 1.28]   .800 
#>  age                       [1.00, 1.02]   .214 
#>  education:                                    
#>    Lower secondary (ref.)       –         –    
#>    Upper secondary         [0.44, 0.87]   .005 
#>    Tertiary                [0.27, 0.59]  <.001 
#> 
#> Note. Logistic regression models.
#> Std. errors: classical (Fisher information).
#> OR = odds ratio.
#> Coefficients exponentiated and displayed as OR; CI bounds exponentiated.

Reading it: each Univariable row is its own simple logistic regression — the N column is per predictor, because listwise deletion can differ across candidates — while the Multivariable column group is the single joint model on the same candidates (multivariable = FALSE drops it, complete_cases = TRUE aligns every fit on the common complete cases). Comparing the two columns per row is the point of the layout: an association that survives adjustment reads differently from one that collapses. The multivariable n appears once, as a fit statistic — it belongs to the joint model, not to any predictor. A p_adjust argument treats the screen as one family of tests. For a time-to-event screen the same call takes method = "coxph" with a Surv() outcome — see vignette("table-regression-survival").

Hierarchical / nested regression

Set nested = TRUE to add in-table change-statistic rows (APA Table 7.13 / Stata esttab / SPSS Model Summary convention). Each adjacent pair (M2 vs M1, M3 vs M2, …) contributes one column of change stats below R² / Adj.R²; the first model column gets en-dashes (no previous model to compare to).

Hierarchical regression requires every model in the sequence to share the same analytic sample: identical nobs and an identical response variable. R’s listwise deletion otherwise produces different n per model as soon as a predictor introduced by M2 or M3 has missing values that M1 did not see — a silent bias on the change statistics. We restrict to complete cases on the union of predictors up front:

sochealth_cc <- sochealth |>
  dplyr::select(wellbeing_score, age, sex, smoking, bmi, region) |>
  na.omit()
m1 <- lm(wellbeing_score ~ age + sex,                 data = sochealth_cc)
m2 <- lm(wellbeing_score ~ age + sex + smoking,       data = sochealth_cc)
m3 <- lm(wellbeing_score ~ age + sex + smoking + bmi, data = sochealth_cc)
table_regression(list(m1, m2, m3), nested = TRUE)
#> Hierarchical linear regression: wellbeing_score
#> 
#>                          Model 1                Model 2            Model 3     
#>                    ────────────────────  ─────────────────────  ────────────── 
#>  Variable            B      SE     p       B       SE     p       B       SE  
#> ─────────────────┼─────────────────────────────────────────────────────────────
#>  (Intercept)        64.70  1.66  <.001    65.00   1.67  <.001    80.57   3.37 
#>  age                 0.05  0.03   .118     0.05   0.03   .109     0.07   0.03 
#>  sex:                                                                         
#>    Female (ref.)      –     –     –         –      –     –         –      –   
#>    Male              3.89  0.91  <.001     3.88   0.91  <.001     4.21   0.90 
#>  smoking:                                                                     
#>    No (ref.)                                –      –     –         –      –   
#>    Yes                                    -1.68   1.11   .132    -1.71   1.10 
#>  bmi                                                             -0.65   0.12 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1163                  1163                   1163           
#>  R²                  0.02                  0.02                   0.04        
#>  Adj.R²              0.02                  0.02                   0.04        
#>  ΔR²                  –                   +0.00                  +0.02        
#>  F-change             –                   +2.28                 +28.13        
#>  p (change)           –                     .132                  <.001       
#> 
#>                    Mode… 
#>                    ───── 
#>  Variable           p   
#> ─────────────────┼───────
#>  (Intercept)      <.001 
#>  age               .019 
#>  sex:                   
#>    Female (ref.) 
#>    Male           <.001 
#>  smoking:               
#>    No (ref.)     
#>    Yes             .119 
#>  bmi              <.001 
#> 
#> Note. Linear regression models.
#> Std. errors: classical (OLS).

Reading the change rows: adding smoking in Model 2 does not improve fit over the age + sex baseline (ΔR² = +0.00, F-change = 2.28, p = .132) — with a single added term, this test is equivalent to the test on the smoking coefficient itself (p = .132 in the Model 2 column). Adding bmi in Model 3 does (ΔR² = +0.02, F-change = 28.13, p < .001). The hierarchical sequence therefore supports retaining bmi and provides no incremental evidence for smoking.

Default change tokens auto-injected: c("r2_change", "f_change", "p_change") for lm (APA hierarchical-regression standard), c("lrt_change", "p_change") for glm (Hosmer & Lemeshow §3.5), c("aic_change", "bic_change", "lrt_change", "p_change") for mixed-effects fits (lmer / glmer / glmmTMB / nlme::lme — Pinheiro & Bates 2000 §2.4.1). Customise via show_fit_stats; the order of tokens controls the order of the rows. Other change tokens are available: "adj_r2_change", "f2_change", "deviance_change", "aic_change" / "aicc_change" / "bic_change". Variance-explained change tokens (Δr², Δf²) are undefined for mixed-effects pairs and their rows are dropped from the table — the F-test framework that grounds them doesn’t apply.

Validation is strict: identical nobs and identical response across all models, otherwise a spicy_invalid_input error explains the listwise-deletion trap and suggests refitting on the common subset.

Robust variance

The default vcov = "classical" reports the OLS standard error, valid under homoskedastic, independent errors. Two robust alternatives are first-class arguments; bootstrap and jackknife variants are also available via vcov = "bootstrap" / "jackknife".

Heteroskedasticity-consistent (HC)

When error variance plausibly depends on the predictors (a ubiquitous concern in cross-sectional social-science data), set vcov = "HC*" for sandwich-style standard errors via sandwich::vcovHC(). The valid types are HC0 through HC5; HC3 is the small-sample-friendly default (Long and Ervin 2000):

fit <- lm(wellbeing_score ~ age + sex + smoking, data = sochealth)
table_regression(fit, vcov = "HC3")
#> Linear regression: wellbeing_score
#> 
#>  Variable            B      SE       95% CI        p   
#> ─────────────────┼──────────────────────────────────────
#>  (Intercept)        65.20  1.61  [62.05, 68.35]  <.001 
#>  age                 0.05  0.03  [-0.01,  0.11]   .127 
#>  sex:                                                  
#>    Female (ref.)      –     –          –          –    
#>    Male              3.86  0.91  [ 2.07,  5.64]  <.001 
#>  smoking:                                              
#>    No (ref.)          –     –          –          –    
#>    Yes              -1.72  1.11  [-3.91,  0.47]   .123 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1175                                 
#>  R²                  0.02                              
#>  Adj.R²              0.02                              
#> 
#> Note. Linear regression.
#> Std. errors: heteroskedasticity-robust (HC3).

The footer reads “Std. errors: heteroskedasticity-robust (HC3)”; the column header for the confidence interval automatically tracks ci_level.

Cluster-robust (CR)

For clustered observations (repeated measures on the same person, students within schools, observations within regions), vcov = "CR*" requests cluster-robust variance via clubSandwich::vcovCR(), with the cluster identifier supplied through cluster. Three forms are accepted:

  • Formulacluster = ~region. The variables are looked up in model.frame(fit) first, then in the model’s original data argument. Recommended: independent of the dataset’s name, composable for multi-way clustering (cluster = ~region:year).
  • Stringcluster = "region". Single column name resolved the same way. Convenient but cannot express interactions.
  • Vectorcluster = df$region. Atomic vector of length nobs(fit). Use this when the cluster key is derived on the fly (cluster = interaction(df$region, df$year)) or pulled from a different dataset with matching row order.

Bare unquoted names (cluster = region) are not accepted — they would require non-standard evaluation that breaks under programmatic use (function wrapping, loops, dynamic column choice).

fit <- lm(wellbeing_score ~ age + sex + smoking, data = sochealth_cc)
table_regression(
  fit,
  vcov = "CR2",
  cluster = ~region,
  show_columns = c("b", "se", "ci", "p", "ame", "ame_p")
)
#> Linear regression: wellbeing_score
#> 
#>  Variable            B      SE       95% CI        p     AME     p   
#> ─────────────────┼────────────────────────────────────────────────────
#>  (Intercept)        65.00  1.74  [60.49, 69.51]  <.001               
#>  age                 0.05  0.04  [-0.05,  0.15]   .247   0.05   .247 
#>  sex:                                                                
#>    Female (ref.)      –     –          –          –       –     –    
#>    Male              3.88  0.85  [ 1.68,  6.07]   .006   3.88   .006 
#>  smoking:                                                            
#>    No (ref.)          –     –          –          –       –     –    
#>    Yes              -1.68  1.55  [-5.72,  2.37]   .331  -1.68   .331 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1163                                               
#>  R²                  0.02                                            
#>  Adj.R²              0.02                                            
#> 
#> Note. Linear regression.
#> Std. errors: cluster-robust (CR2), clusters by region.
#> AME = average marginal effect.
#> AME inference: t-test with Satterthwaite df.

CR2 (the Bell-McCaffrey adjustment) is the recommended default under few clusters (Pustejovsky and Tipton 2018; Imbens and Kolesár 2016). Coefficient inference uses clubSandwich::coef_test() with Satterthwaite-corrected degrees of freedom. When AME columns are requested, the same Satterthwaite framework is applied to the AME contrast via clubSandwich::linear_contrast(), so B and AME share the same t-distribution with the same df — visible in the footer.

Multiple-comparison adjustment

p_adjust applies a family-wise or false-discovery-rate adjustment to the p-values via stats::p.adjust(). The family is the model’s full coefficient set (intercept and reference rows excluded); B and AME are adjusted as independent families within the same call. Available methods are the same as in stats::p.adjust(): "none" (default), "holm", "hochberg", "hommel", "bonferroni", "BH" / "fdr", "BY".

fit <- lm(wellbeing_score ~ age + sex + smoking + education,
          data = sh)
table_regression(fit, p_adjust = "bonferroni")
#> Linear regression: wellbeing_score
#> 
#>  Variable                     B      SE       95% CI        p   
#> ──────────────────────────┼──────────────────────────────────────
#>  (Intercept)                 53.96  1.66  [50.70, 57.22]  <.001 
#>  age                          0.03  0.03  [-0.03,  0.08]  1.000 
#>  sex:                                                           
#>    Female (ref.)               –     –          –          –    
#>    Male                       3.57  0.81  [ 1.99,  5.15]  <.001 
#>  smoking:                                                       
#>    No (ref.)                   –     –          –          –    
#>    Yes                        0.68  0.99  [-1.27,  2.63]  1.000 
#>  education:                                                     
#>    Lower secondary (ref.)      –     –          –          –    
#>    Upper secondary           11.89  1.05  [ 9.82, 13.96]  <.001 
#>    Tertiary                  19.71  1.12  [17.51, 21.91]  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                                 
#>  R²                           0.22                              
#>  Adj.R²                       0.22                              
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).
#> P-values adjusted via stats::p.adjust(method = "bonferroni"); m = 5 coefficient(s) per model.

The footer documents the chosen method and the family size; the SE column is unchanged. p_adjust is orthogonal to vcov: combining a robust SE with a family-wise correction is fully supported, e.g. vcov = "HC3", p_adjust = "holm". The adjustment is applied before keep / drop filtering, so the family stays the model’s full coefficient set and the displayed adjusted p-values reflect the right denominator regardless of which subset is shown.

A methodological note. Adjusting the p-values of every coefficient of a single regression model is not the standard convention in social-science or clinical reporting (Rothman 1990; Gelman, Hill, and Yajima 2012; Greenland 2017; Harrell 2015 §5.4; APA Manual 7 §6.46). Each coefficient tests a scientifically distinct hypothesis on a distinct predictor, which is not the situation that family-wise procedures were designed for. The default "none" reflects this consensus.

Adjustment is nonetheless legitimate in three contexts:

  1. Mass screening with many candidate predictors and no prior hypothesis — typically "BH" (Benjamini–Hochberg, false discovery rate).
  2. Pre-registered multi-endpoint confirmatory designs — typically "holm" (Holm’s step-down, strong family-wise error rate control).
  3. When a reviewer, an editor, or a statistical analysis plan explicitly requests it — apply the requested method and document it in the footer.

The argument follows the same transparency over rejection rule as standardized: the method is available, the choice among methods is the analyst’s, and the footer makes that choice visible to the reader.

Filtering displayed coefficients

keep and drop accept regular expressions matched against coefficient names (as returned by stats::coef()). They are mutually exclusive — use keep to retain only the focal predictors, or drop to hide a few control variables. Multiple patterns combine with logical OR.

fit <- lm(wellbeing_score ~ age + sex + smoking + bmi + education,
          data = sh)
table_regression(fit, keep = c("^smoking", "^bmi$"))
#> Linear regression: wellbeing_score
#> 
#>  Variable        B      SE       95% CI        p   
#> ─────────────┼──────────────────────────────────────
#>  (Intercept)    51.41  3.52  [44.50, 58.32]  <.001 
#>  smoking:                                          
#>    No (ref.)      –     –          –          –    
#>    Yes           0.79  1.00  [-1.17,  2.75]   .428 
#>  bmi             0.10  0.12  [-0.14,  0.33]   .418 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n            1163                                 
#>  R²              0.23                              
#>  Adj.R²          0.22                              
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).
table_regression(fit, drop = "^education")
#> Linear regression: wellbeing_score
#> 
#>  Variable            B      SE       95% CI        p   
#> ─────────────────┼──────────────────────────────────────
#>  (Intercept)        51.41  3.52  [44.50, 58.32]  <.001 
#>  age                 0.02  0.03  [-0.03,  0.08]   .407 
#>  sex:                                                  
#>    Female (ref.)      –     –          –          –    
#>    Male              3.50  0.81  [ 1.91,  5.10]  <.001 
#>  smoking:                                              
#>    No (ref.)          –     –          –          –    
#>    Yes               0.79  1.00  [-1.17,  2.75]   .428 
#>  bmi                 0.10  0.12  [-0.14,  0.33]   .418 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1163                                 
#>  R²                  0.23                              
#>  Adj.R²              0.22                              
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).

Together with p_adjust, this is the article-ready workflow: adjust on the full model, display only the rows the reader cares about — table_regression(fit, p_adjust = "BH", keep = "^treatment").

Significance stars

Stars are off by default. APA 7 §6.46 explicitly discourages asterisks-only reporting in favour of exact p-values, and ASA’s post-2019 guidance (Wasserstein, Schirm, and Lazar 2019) reinforces the same point. Set stars = TRUE for the APA preset (*** p < .001, ** p < .01, * p < .05) or pass a named numeric vector for custom thresholds:

fit <- lm(wellbeing_score ~ age + sex + smoking, data = sochealth)
table_regression(fit, stars = TRUE)
#> Linear regression: wellbeing_score
#> 
#>  Variable             B        SE       95% CI        p   
#> ─────────────────┼─────────────────────────────────────────
#>  (Intercept)        65.20***  1.66  [61.95, 68.45]  <.001 
#>  age                 0.05     0.03  [-0.01,  0.11]   .130 
#>  sex:                                                     
#>    Female (ref.)      –        –          –          –    
#>    Male              3.86***  0.91  [ 2.08,  5.63]  <.001 
#>  smoking:                                                 
#>    No (ref.)          –        –          –          –    
#>    Yes              -1.72     1.11  [-3.89,  0.45]   .121 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                1175                                    
#>  R²                  0.02                                 
#>  Adj.R²              0.02                                 
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).
#> *** p < .001, ** p < .01, * p < .05.

Stars suffix the B column (or β when standardisation is requested); the threshold mapping is auto-documented in the footer. The p column itself remains unstarred so the numeric value stays readable.

Display options

labels accepts a named character vector keyed by either formula term labels ("sex") or coefficient names ("sexMale"), so individual contrast rows can be relabelled. intercept_position switches the intercept to the bottom (Stata convention). reference_style = "annotation" lifts the reference level into the factor header ("sex: [ref: Female]") and drops the explicit reference row, for compact tables. decimal_mark = "," switches to European decimal notation and automatically changes the CI separator to ";" to avoid ambiguity:

fit <- lm(wellbeing_score ~ age + sex + education, data = sh)
table_regression(
  fit,
  labels = c(
    age            = "Age (years)",
    sex            = "Sex",
    education      = "Education"
  ),
  reference_style = "annotation",
  intercept_position = "last",
  decimal_mark = ","
)
#> Linear regression: wellbeing_score
#> 
#>  Variable                              B      SE       95% CI        p   
#> ───────────────────────────────────┼──────────────────────────────────────
#>  Age (years)                           0,03  0,03  [-0,03;  0,08]   ,343 
#>  Sex: [ref: Female]                                                      
#>    Male                                3,65  0,80  [ 2,09;  5,22]  <,001 
#>  Education: [ref: Lower secondary]                                       
#>    Upper secondary                    11,85  1,04  [ 9,81; 13,89]  <,001 
#>    Tertiary                           19,52  1,10  [17,36; 21,67]  <,001 
#>  (Intercept)                          54,18  1,63  [50,99; 57,37]  <,001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                                  1200                                 
#>  R²                                    0,22                              
#>  Adj.R²                                0,22                              
#> 
#> Note. Linear regression.
#> Std. errors: classical (OLS).

Generalised linear models (glm)

table_regression() accepts any glm() fit. Inference defaults to the z-asymptotic Wald regime — the convention summary.glm() applies to fixed-dispersion families (binomial, Poisson), shared by Stata’s logit, or and SPSS LOGISTIC REGRESSION. One caveat for cross-checking: for families with an estimated dispersion (gaussian, Gamma, inverse.gaussian, and the quasi- families), summary.glm() switches to t statistics on the residual degrees of freedom, so its p-values run larger than the table’s z-based ones in small samples — there the table follows Stata’s glm default rather than summary.glm(). The table title becomes family-aware (“Logistic regression”, “Poisson regression”, “Probit regression”, …) and the default fit-statistics block swaps in nobs, pseudo_r2_mcfadden, pseudo_r2_nagelkerke, and AIC instead of and Adj.R².

We illustrate with a logistic regression of smoking on sex, age, and education from sochealth, reusing sh — the copy of sochealth with education as a plain (unordered) factor, introduced in Per-coefficient effect sizes — so contrasts are dummy-coded, one row per level. The model mixes a binary factor (sex), a numeric predictor (age), and a 3-level factor (education) — enough to exercise every glm-specific feature below.

fit <- glm(smoking ~ sex + age + education, data = sh,
           family = binomial)
table_regression(fit)
#> Logistic regression: smoking
#> 
#>  Variable                     B      SE       95% CI        p   
#> ──────────────────────────┼──────────────────────────────────────
#>  (Intercept)                 -1.11  0.29  [-1.67, -0.55]  <.001 
#>  sex:                                                           
#>    Female (ref.)               –     –          –          –    
#>    Male                      -0.04  0.14  [-0.32,  0.25]   .800 
#>  age                          0.01  0.00  [-0.00,  0.02]   .214 
#>  education:                                                     
#>    Lower secondary (ref.)      –     –          –          –    
#>    Upper secondary           -0.48  0.17  [-0.82, -0.14]   .005 
#>    Tertiary                  -0.91  0.20  [-1.29, -0.52]  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                                 
#>  R² (McFadden)                0.02                              
#>  R² (Nagelkerke)              0.03                              
#>  AIC                       1200.9                               
#> 
#> Note. Logistic regression.
#> Std. errors: classical (Fisher information).

Read the fit block with care. McFadden and Nagelkerke R² are likelihood-based analogues of R², not proportions of explained variance — their values are not comparable to an OLS R², and different measures disagree by construction on the same fit (here 0.02 for McFadden versus 0.03 for Nagelkerke). Long and Freese (2014, §3.3) find these scalar measures of limited utility except as a rough index for comparing competing models on the same data, and prefer the information criteria — hence AIC in the default block. When reporting one, name the specific measure, as the row labels here do; a generic “pseudo-R²” is ambiguous across software. Tjur’s (2009) coefficient of discrimination, an alternative on the probability scale for binary outcomes, is available as the opt-in token pseudo_r2_tjur via show_fit_stats.

Response-scale display: exponentiate = TRUE

Set exponentiate = TRUE to switch the B column to the ratio scale and relabel its header according to the family and link: OR for binomial(logit), IRR for poisson(log), HR for binomial(cloglog), RR for binomial(log), MR for Gamma(log), and the generic exp(B) for other log-link families (a genuine ratio of means). Links whose exponential is not a ratio — probit, cauchit, inverse (the Gamma() default), among others — are refused with a clear error rather than silently mislabelled; report response-scale effects for those models via the AME column instead. The standard error follows the delta-method approximation SE_OR = OR × SE_log-odds (the Stata logit, or convention). The test statistic and the p-value stay on the link scale, where B = 0 and OR = 1 are the same hypothesis and the Wald approximation is most accurate, so they match the unexponentiated table verbatim. (Wald tests are not invariant to reparameterisation — a z rebuilt from SE_OR would give a different statistic and p-value, which is why the link-scale test is kept; Long & Freese 2014 §3.2.2.):

table_regression(fit, exponentiate = TRUE)
#> Logistic regression: smoking
#> 
#>  Variable                    OR      SE      95% CI       p   
#> ──────────────────────────┼────────────────────────────────────
#>  (Intercept)                  0.33  0.09  [0.19, 0.58]  <.001 
#>  sex:                                                         
#>    Female (ref.)               –     –         –         –    
#>    Male                       0.96  0.14  [0.73, 1.28]   .800 
#>  age                          1.01  0.00  [1.00, 1.02]   .214 
#>  education:                                                   
#>    Lower secondary (ref.)      –     –         –         –    
#>    Upper secondary            0.62  0.11  [0.44, 0.87]   .005 
#>    Tertiary                   0.40  0.08  [0.27, 0.59]  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                               
#>  R² (McFadden)                0.02                            
#>  R² (Nagelkerke)              0.03                            
#>  AIC                       1200.9                             
#> 
#> Note. Logistic regression.
#> Std. errors: classical (Fisher information).
#> OR = odds ratio.
#> Coefficients exponentiated and displayed as OR; SE on the OR scale (delta method); CI bounds exponentiated (asymmetric).

Read exponentiated rows with the factor-change template (Long and Freese 2014 §6.1.1): for Tertiary, OR = 0.40, 95% CI [0.27, 0.59] — holding sex and age constant, the odds of smoking for a tertiary-educated respondent are 0.40 times the odds for one with lower secondary education, a 60% decrease in the odds (percentage change = 100 × (OR − 1)). An odds ratio is a ratio of odds, not of probabilities: with a smoking prevalence around 21% it sits farther from 1 than the corresponding risk ratio, so reading it as “a 60% lower probability of smoking” overstates the effect. The Average marginal effects section below reports the probability-scale counterpart for the same contrast (−0.15, that is, 15 percentage points).

Event counts per level

Clinical and epidemiological tables conventionally carry the raw events / N next to each odds ratio (STROBE checklist item 15; the NEJM house style). The opt-in "n_events" column token renders exactly that — per factor level, with the full-sample count on numeric predictors and the intercept row:

table_regression(fit, show_columns = c("n_events", "b", "ci", "p"))
#> Logistic regression: smoking
#> 
#>  Variable                    Events/N       B        95% CI        p   
#> ──────────────────────────┼─────────────────────────────────────────────
#>  (Intercept)                    249/1175  -1.11  [-1.67, -0.55]  <.001 
#>  sex:                                                                  
#>    Female (ref.)                 131/606    –          –          –    
#>    Male                          118/569  -0.04  [-0.32,  0.25]   .800 
#>  age                            249/1175   0.01  [-0.00,  0.02]   .214 
#>  education:                                                            
#>    Lower secondary (ref.)         78/257    –          –          –    
#>    Upper secondary               112/527  -0.48  [-0.82, -0.14]   .005 
#>    Tertiary                       59/391  -0.91  [-1.29, -0.52]  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                               1175                                  
#>  R² (McFadden)                      0.02                               
#>  R² (Nagelkerke)                    0.03                               
#>  AIC                             1200.9                                
#> 
#> Note. Logistic regression.
#> Std. errors: classical (Fisher information).

The token is off by default and deliberately narrow: it is defined for binomial models with an ungrouped 0/1 response and for right-censored Cox models (events per factor level; Cox tables also carry N events as a default fit statistic — see vignette("table-regression-survival")). Requesting it anywhere else is a hard, classed error rather than a silently empty column.

Term-level partial chi-square

partial_chi2 is the glm analog of partial_f2: for each model term, the partial likelihood-ratio chi-square from the same Type-II nested comparison — both models exclude any higher-order term containing the tested one, so the test respects marginality and is contrast-invariant (Fox and Weisberg 2019; equal to drop1(test = "LRT") for additive models; on the LRT itself see Long & Freese 2014 §3.2.2, §3.2.4). Rendered as value (df) so factor terms (k − 1 df) and numeric terms (1 df) read at a glance:

fit2 <- glm(smoking ~ age + education, data = sh, family = binomial)
table_regression(fit2, show_columns = c("b", "partial_chi2", "p"))
#> Logistic regression: smoking
#> 
#>  Variable                     B        χ²        p   
#> ──────────────────────────┼───────────────────────────
#>  (Intercept)                 -1.13             <.001 
#>  age                          0.01   1.55 (1)   .213 
#>  education:                                          
#>    Lower secondary (ref.)      –                –    
#>    Upper secondary           -0.48  21.70 (2)   .005 
#>    Tertiary                  -0.91  21.70 (2)  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                      
#>  R² (McFadden)                0.02                   
#>  R² (Nagelkerke)              0.03                   
#>  AIC                       1198.9                    
#> 
#> Note. Logistic regression.
#> Std. errors: classical (Fisher information).
#> χ² = partial likelihood-ratio chi-squared.

The p column and the χ² column answer different questions. Each per-level p-value compares one education level with the reference, so it changes when the reference level changes; the joint test — 21.70 on 2 df, p < .001 — asks whether education as a whole improves the model, and is invariant to the reference choice. When a factor’s levels straddle significance, the joint test is the one to report. Wald and likelihood-ratio tests of the same joint hypothesis are asymptotically equivalent but differ in finite samples; many statisticians prefer the likelihood-ratio form when both are available (Long & Freese 2014 §3.2.2), which is what partial_chi2 computes.

The same token extends to mixed-effects models (lmer, glmer, glmmTMB, nlme::lme), where the term-level test is the Wald chi-square built from the same marginality-respecting Type-II hypothesis, matching car::Anova(type = 2). This is a deliberate departure from SAS PROC MIXED and lmerTest, which report Type-III tests by default; the two conventions coincide for models without interactions.

Standardised coefficients: refit and pseudo

For glm, standardized = "refit" z-scores numeric predictors only and refits the model — the response stays on its observed scale because the link function is fixed. This is the “x-standardization” convention (Long and Freese 2014 §4.7.2). The other algebraic methods ("posthoc", "basic", "smart") apply X-only scaling using the same algebra as in the lm case.

standardized = "pseudo" (glm only) is the latent-scale variant of Menard’s (2004, 2011) fully standardised coefficient: Y* is the latent variable on the link scale, with SD(Y*) = sqrt(var(linear-predictor) + var_link) and var_link = π²/3 for logit, 1 for probit, π²/6 for cloglog. Numeric predictors scale by SD(X) / SD(Y*); factor dummies stay on their 0/1 scale and divide by SD(Y*) only — the same dummy convention as the other methods, which is why the factor rows in the table below are not B × SD(X) / SD(Y*). Defined for binomial families; non-binomial returns NA with a spicy_caveat:

table_regression(fit, standardized = "pseudo")
#> Logistic regression: smoking
#> 
#>  Variable                     B       β     SE       95% CI        p   
#> ──────────────────────────┼─────────────────────────────────────────────
#>  (Intercept)                 -1.11    –    0.29  [-1.67, -0.55]  <.001 
#>  sex:                                                                  
#>    Female (ref.)               –      –     –          –          –    
#>    Male                      -0.04  -0.02  0.14  [-0.32,  0.25]   .800 
#>  age                          0.01   0.05  0.00  [-0.00,  0.02]   .214 
#>  education:                                                            
#>    Lower secondary (ref.)      –      –     –          –          –    
#>    Upper secondary           -0.48  -0.26  0.17  [-0.82, -0.14]   .005 
#>    Tertiary                  -0.91  -0.49  0.20  [-1.29, -0.52]  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                                        
#>  R² (McFadden)                0.02                                     
#>  R² (Nagelkerke)              0.03                                     
#>  AIC                       1200.9                                      
#> 
#> Note. Logistic regression.
#> Std. errors: classical (Fisher information).
#> β = standardised coefficient ("pseudo": latent-scale SD(X)/SD(Y*) for numeric predictors, 1/SD(Y*) for factor dummies).

Average marginal effects: probability units, not log-odds

For glm, AME is averaged over the observed sample — the partial derivative for numeric predictors, the discrete change for factor levels — on the response scale, not the link scale. For logistic regression this means the displayed AME is in probability units, not log-odds: an AME of -0.15 for education = Tertiary reads “on average, holding sex and age constant, a respondent with tertiary education is 15 percentage points less likely to be a current smoker than one with lower secondary education”. This is almost always the quantity a substantive reader wants from a logistic regression, and it is the reason AME is increasingly recommended over odds ratios for communicating logistic effects (Mood 2010; Long and Freese 2014 §6.2.3).

table_regression(fit, show_columns = c("b", "p", "ame", "ame_ci", "ame_p"))
#> Logistic regression: smoking
#> 
#>  Variable                     B       p     AME       95% CI        p   
#> ──────────────────────────┼──────────────────────────────────────────────
#>  (Intercept)                 -1.11  <.001                               
#>  sex:                                                                   
#>    Female (ref.)               –     –       –          –          –    
#>    Male                      -0.04   .800  -0.01  [-0.05,  0.04]   .800 
#>  age                          0.01   .214   0.00  [-0.00,  0.00]   .214 
#>  education:                                                             
#>    Lower secondary (ref.)      –     –       –          –          –    
#>    Upper secondary           -0.48   .005  -0.09  [-0.16, -0.02]   .007 
#>    Tertiary                  -0.91  <.001  -0.15  [-0.22, -0.09]  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                                         
#>  R² (McFadden)                0.02                                      
#>  R² (Nagelkerke)              0.03                                      
#>  AIC                       1200.9                                       
#> 
#> Note. Logistic regression.
#> Std. errors: classical (Fisher information).
#> AME = average marginal effect.

Point estimate and inference are delegated to marginaleffects::avg_slopes(). Under cluster-robust variance, the Satterthwaite-df handling described in the Robust variance section applies to glm AME as well.

Profile-likelihood CIs: ci_method = "profile"

The default is ci_method = "wald" (symmetric estimate ± z × SE, matching summary.glm). For glm you can also request ci_method = "profile", which calls MASS::confint.glm() to compute the profile-likelihood CI — asymmetric, obtained by inverting the likelihood-ratio statistic rather than the quadratic Wald approximation, and the preferred choice under sparse data or near-boundary estimates (Venables & Ripley MASS §7.2). The estimate, SE, statistic, and p-value all remain Wald; "profile" only refines the CI bounds:

table_regression(fit, ci_method = "profile")
#> Logistic regression: smoking
#> 
#>  Variable                     B      SE       95% CI        p   
#> ──────────────────────────┼──────────────────────────────────────
#>  (Intercept)                 -1.11  0.29  [-1.68, -0.55]  <.001 
#>  sex:                                                           
#>    Female (ref.)               –     –          –          –    
#>    Male                      -0.04  0.14  [-0.32,  0.25]   .800 
#>  age                          0.01  0.00  [-0.00,  0.02]   .214 
#>  education:                                                     
#>    Lower secondary (ref.)      –     –          –          –    
#>    Upper secondary           -0.48  0.17  [-0.82, -0.14]   .005 
#>    Tertiary                  -0.91  0.20  [-1.29, -0.52]  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                                 
#>  R² (McFadden)                0.02                              
#>  R² (Nagelkerke)              0.03                              
#>  AIC                       1200.9                               
#> 
#> Note. Logistic regression.
#> Std. errors: classical (Fisher information).
#> 95% CIs: profile likelihood.

One consequence worth naming when combining with exponentiate = TRUE: the CI bounds are the exponentiated profile bounds (asymmetric), while the SE column is the delta-method SE on the ratio scale — the interval can no longer be reconstructed as estimate ± z × SE. Both choices are disclosed in the footer, which is why the table names them rather than leaving the mismatch for a careful reader to discover.

Hierarchical glm (LRT)

nested = TRUE on a list of nested glm fits appends Δχ² and p (change) rows to the fit-statistics block — default change tokens c("lrt_change", "p_change"), as in Hierarchical / nested regression above — the APA-conventional layout for hierarchical logistic regression (Hosmer & Lemeshow §3.5; Long & Freese 2014 §3.2.4). The chi-square statistic comes from anova(test = "LRT"). The variance-explained change tokens (r2_change, f_change) are not defined for glm — requesting them in show_fit_stats raises a spicy_invalid_input error that points to the pseudo-R² family and to lrt_change + p_change instead:

m1 <- glm(smoking ~ sex,                   data = sh, family = binomial)
m2 <- glm(smoking ~ sex + age,             data = sh, family = binomial)
m3 <- glm(smoking ~ sex + age + education, data = sh, family = binomial)
table_regression(list(m1, m2, m3), nested = TRUE)
#> Hierarchical logistic regression: smoking
#> 
#>                                   Model 1                Model 2        
#>                             ────────────────────  ───────────────────── 
#>  Variable                     B      SE     p       B       SE     p   
#> ──────────────────────────┼─────────────────────────────────────────────
#>  (Intercept)                 -1.29  0.10  <.001    -1.54   0.26  <.001 
#>  sex:                                                                  
#>    Female (ref.)               –     –     –         –      –     –    
#>    Male                      -0.05  0.14   .713    -0.05   0.14   .722 
#>  age                                                0.01   0.00   .294 
#>  education:                                                            
#>    Lower secondary (ref.)                                              
#>    Upper secondary                                                     
#>    Tertiary                                                            
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                  1175                  
#>  R² (McFadden)                0.00                  0.00               
#>  R² (Nagelkerke)              0.00                  0.00               
#>  AIC                       1217.6                1218.5                
#>  Δχ²                           –                   +1.10               
#>  p (change)                    –                     .294              
#> 
#>                                    Model 3        
#>                             ───────────────────── 
#>  Variable                     B       SE     p   
#> ──────────────────────────┼───────────────────────
#>  (Intercept)                 -1.11   0.29  <.001 
#>  sex:                                            
#>    Female (ref.)               –      –     –    
#>    Male                      -0.04   0.14   .800 
#>  age                          0.01   0.00   .214 
#>  education:                                      
#>    Lower secondary (ref.)      –      –     –    
#>    Upper secondary           -0.48   0.17   .005 
#>    Tertiary                  -0.91   0.20  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                         1175                  
#>  R² (McFadden)                0.02               
#>  R² (Nagelkerke)              0.03               
#>  AIC                       1200.9                
#>  Δχ²                        +21.64               
#>  p (change)                   <.001              
#> 
#> Note. Logistic regression models.
#> Std. errors: classical (Fisher information).

Gaussian glm caveat

A glm() with family = gaussian and link = "identity" is mathematically equivalent to lm() but lacks the variance- explained effect-size family (partial_f2 / η² / ω²) and the Satterthwaite-corrected AME path. Following the transparency over rejection rule, spicy accepts the fit and emits a spicy_caveat suggesting a refit with lm().

Mixed-effects models

table_regression() supports four mixed-effects engines: lme4::lmer() and lme4::glmer(), glmmTMB::glmmTMB(), and nlme::lme(). The fixed-effects section of the table follows the same conventions as lm / glm. Below it, a subordinate Random effects block reports the variance components as rows — one per random standard deviation (σ), correlation (ρ), and the residual — each with its estimate, SE, and CI in the shared coefficient columns. The number of groups — one N (<grouping factor>) row per grouping factor, here N (Subject) — and the Nakagawa marginal / conditional R² (Nakagawa & Schielzeth 2013) join the fit-statistic rows, so they align per model in a comparison table:

library(lme4)
fit <- lmer(Reaction ~ Days + (Days | Subject), data = sleepstudy)
table_regression(fit)
#> Linear mixed-effects regression: Reaction
#> 
#>  Variable                            B      SE        95% CI         p   
#> ─────────────────────────────────┼────────────────────────────────────────
#>  (Intercept)                       251.41  6.82  [238.03, 264.78]  <.001 
#>  Days                               10.47  1.55  [  7.44,  13.50]  <.001 
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  Random effects:                                                         
#>    σ Subject (Intercept)            24.74  5.84  [  6.79,  34.32]   –    
#>    σ Subject Days                    5.92  1.25  [  2.47,   8.00]   –    
#>    ρ Subject ((Intercept), Days)     0.07  0.33  [ -0.57,   0.70]   –    
#>    σ (Residual)                     25.59  1.51  [ 22.44,  28.39]   –    
#> ╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌┼╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌╌
#>  n                                 180                                   
#>  N (Subject)                        18                                   
#>  R² (marginal)                       0.28                                
#>  R² (conditional)                    0.80                                
#>  AIC                              1755.6                                 
#>  BIC                              1774.8                                 
#> 
#> Note. Linear mixed-effects regression.
#> Std. errors: Wald (model-based).
#> p-values: Wald-z, large-sample approximation. Load `lmerTest` for Satterthwaite t-tests.
#> Random effects (REML): LR test vs linear regression, χ̄²(3) = 150.04, p < .001.

No ICC row appears here: a random-slope fit has no single intra-class correlation, so the row is dropped automatically (the intercept-only case shows it).

Two deliberate conventions:

  • The variance-component rows carry no p-value. The null hypothesis σ = 0 sits on the boundary of the parameter space, where a Wald test is invalid (Self & Liang 1987); no reporting guideline requests a per-component p, and the R ecosystem (lme4, nlme, parameters, broom.mixed), Stata, and MLwiN all omit it. The correct significance signal for the random part is the footer’s likelihood-ratio test against the no-random-effects model, whose p-value applies a boundary correction. With a single variance component the halving p = 0.5 × P(χ²₁ > LR) is the exact Self & Liang (1987) 50:50 mixture — the chibar2(01) line Stata’s mixed prints. With more random parameters, as here (two variances and a correlation), the exact reference is a multi-component mixture (Stram & Lee 1994); spicy reports the pragmatic halved χ²_q, less conservative than the plain χ²_q that Stata prints for joint tests with a caveat that it is conservative.
  • The footer also carries the estimator label — (REML) for restricted maximum likelihood (the lmer / lme default) or (ML) for full ML (glmer, glmmTMB default, and lmer(..., REML = FALSE)). The label is informational: it tells the reader which likelihood the variance estimates are anchored to, without implying that REML and ML estimates are interchangeable for inference.

The display and inference controls are arguments, not conventions: show_re = FALSE hides the block, re_scale = "variance" switches the rows from σ to σ², re_columns restricts which quantities the variance rows show, re_ci = "profile" replaces the Wald CIs on variance components with boundary-respecting profile-likelihood CIs (Wald is the default because profiling is far slower), and re_test = "lrt" or "rlrt" adds an opt-in per-component test (“do we need this random slope?”) with the boundary correction applied. The footer names the fixed-effect inference method per engine — Satterthwaite t when lmerTest is loaded, Wald-z for glmer / glmmTMB and plain lmer, containment-df t for nlme::lme. The AME tokens of show_columns (see Average marginal effects above) work identically for mixed-effects fits — always on the response scale, with Wald-z inference.

nested = TRUE works on mixed-effects fits with the change tokens listed in Hierarchical / nested regression; note that its plain-χ² reference is appropriate for steps that add fixed effects, while random-structure steps belong to re_test, whose reference respects the boundary.

For the model-building sequence, the REML/ML estimator choice, the Nakagawa R² and ICC mechanics, per-class inference paths, singular fits, testing random components, and the glmmTMB / nlme::lme specifics — including a worked glmer AME example — see vignette("table-regression-mixed", package = "spicy").

Output formats

The default print method draws an ASCII table to the console. The same content is available as a plain data.frame (output = "data.frame"), a long broom-style data.frame (output = "long"), or as a rich-format table for gt, tinytable, flextable, excel, word, or clipboard:

out <- table_regression(
  lm(wellbeing_score ~ age + sex + smoking, data = sochealth),
  output = "data.frame"
)
str(out)
#> 'data.frame':    11 obs. of  5 variables:
#>  $ Variable: chr  "(Intercept)" "age" "sex:" "  Female (ref.)" ...
#>  $ B       : chr  "  65.20" "   0.05" "       " "    –  " ...
#>  $ SE      : chr  "1.66" "0.03" "    " " –  " ...
#>  $ 95% CI  : chr  "[61.95, 68.45]" "[-0.01,  0.11]" "              " "      –       " ...
#>  $ p       : chr  "<.001" " .130" "     " " –   " ...
#>  - attr(*, "title")= chr "Linear regression: wellbeing_score"
#>  - attr(*, "note")= chr "Note. Linear regression.\nStd. errors: classical (OLS)."
#>  - attr(*, "col_spec")=List of 4
#>   ..$ :List of 7
#>   .. ..$ col_name     : chr "B"
#>   .. ..$ display_label: chr "B"
#>   .. ..$ token        : chr "b"
#>   .. ..$ model_id     : chr "M1"
#>   .. ..$ estimate_type: chr "B"
#>   .. ..$ fields       : chr "estimate"
#>   .. ..$ outcome_level: chr NA
#>   ..$ :List of 7
#>   .. ..$ col_name     : chr "SE"
#>   .. ..$ display_label: chr "SE"
#>   .. ..$ token        : chr "se"
#>   .. ..$ model_id     : chr "M1"
#>   .. ..$ estimate_type: chr "B"
#>   .. ..$ fields       : chr "se"
#>   .. ..$ outcome_level: chr NA
#>   ..$ :List of 7
#>   .. ..$ col_name     : chr "95% CI"
#>   .. ..$ display_label: chr "95% CI"
#>   .. ..$ token        : chr "ci"
#>   .. ..$ model_id     : chr "M1"
#>   .. ..$ estimate_type: chr "B"
#>   .. ..$ fields       : chr [1:2] "ci_low" "ci_high"
#>   .. ..$ outcome_level: chr NA
#>   ..$ :List of 7
#>   .. ..$ col_name     : chr "p"
#>   .. ..$ display_label: chr "p"
#>   .. ..$ token        : chr "p"
#>   .. ..$ model_id     : chr "M1"
#>   .. ..$ estimate_type: chr "B"
#>   .. ..$ fields       : chr "p_value"
#>   .. ..$ outcome_level: chr NA
#>  - attr(*, "group_sep_rows")= int 9
#>  - attr(*, "section_sep_rows")= int(0) 
#>  - attr(*, "align")= chr "decimal"
#>  - attr(*, "decimal_mark")= chr "."
#>  - attr(*, "structured")=List of 12
#>   ..$ body                   :'data.frame':  11 obs. of  6 variables:
#>   .. ..$ Variable  : chr [1:11] "(Intercept)" "age" "sex:" "  Female (ref.)" ...
#>   .. ..$ B         : num [1:11] 65.2009 0.0465 NA NA 3.8558 ...
#>   .. ..$ SE        : num [1:11] 1.6567 0.0307 NA NA 0.9053 ...
#>   .. ..$ 95% CI: LL: num [1:11] 61.9504 -0.0137 NA NA 2.0796 ...
#>   .. ..$ 95% CI: UL: num [1:11] 68.451 0.107 NA NA 5.632 ...
#>   .. ..$ p         : num [1:11] 1.59e-216 1.30e-01 NA NA 2.22e-05 ...
#>   ..$ reference_rows         : int [1:2] 4 7
#>   ..$ reference_models_by_row:List of 2
#>   .. ..$ 4: chr "M1"
#>   .. ..$ 7: chr "M1"
#>   ..$ outcome_labels_by_col  : chr(0) 
#>   ..$ factor_header_rows     : int [1:2] 3 6
#>   ..$ fit_stat_rows          : int [1:3] 9 10 11
#>   ..$ level_rows             : int [1:4] 4 5 7 8
#>   ..$ outcome_row            : int(0) 
#>   ..$ col_meta               :List of 5
#>   .. ..$ B         :List of 13
#>   .. .. ..$ token             : chr "b"
#>   .. .. ..$ model_id          : chr "M1"
#>   .. .. ..$ source_field      : chr "estimate"
#>   .. .. ..$ precision         : int 2
#>   .. .. ..$ p_style           : NULL
#>   .. .. ..$ threshold         : NULL
#>   .. .. ..$ signif            : NULL
#>   .. .. ..$ ci_role           : NULL
#>   .. .. ..$ ci_pair           : NULL
#>   .. .. ..$ ci_label          : NULL
#>   .. .. ..$ is_df             : logi FALSE
#>   .. .. ..$ display_label     : chr "B"
#>   .. .. ..$ fit_stat_overrides:List of 3
#>   .. .. .. ..$ :List of 5
#>   .. .. .. .. ..$ fit_stat : chr "nobs"
#>   .. .. .. .. ..$ precision: int 0
#>   .. .. .. .. ..$ p_style  : NULL
#>   .. .. .. .. ..$ threshold: NULL
#>   .. .. .. .. ..$ row      : int 9
#>   .. .. .. ..$ :List of 5
#>   .. .. .. .. ..$ fit_stat : chr "r2"
#>   .. .. .. .. ..$ precision: int 2
#>   .. .. .. .. ..$ p_style  : NULL
#>   .. .. .. .. ..$ threshold: NULL
#>   .. .. .. .. ..$ row      : int 10
#>   .. .. .. ..$ :List of 5
#>   .. .. .. .. ..$ fit_stat : chr "adj_r2"
#>   .. .. .. .. ..$ precision: int 2
#>   .. .. .. .. ..$ p_style  : NULL
#>   .. .. .. .. ..$ threshold: NULL
#>   .. .. .. .. ..$ row      : int 11
#>   .. ..$ SE        :List of 12
#>   .. .. ..$ token        : chr "se"
#>   .. .. ..$ model_id     : chr "M1"
#>   .. .. ..$ source_field : chr "se"
#>   .. .. ..$ precision    : int 2
#>   .. .. ..$ p_style      : NULL
#>   .. .. ..$ threshold    : NULL
#>   .. .. ..$ signif       : NULL
#>   .. .. ..$ ci_role      : NULL
#>   .. .. ..$ ci_pair      : NULL
#>   .. .. ..$ ci_label     : NULL
#>   .. .. ..$ is_df        : logi FALSE
#>   .. .. ..$ display_label: chr "SE"
#>   .. ..$ 95% CI: LL:List of 12
#>   .. .. ..$ token        : chr "ci"
#>   .. .. ..$ model_id     : chr "M1"
#>   .. .. ..$ source_field : chr "ci_low"
#>   .. .. ..$ precision    : int 2
#>   .. .. ..$ p_style      : NULL
#>   .. .. ..$ threshold    : NULL
#>   .. .. ..$ signif       : NULL
#>   .. .. ..$ ci_role      : chr "LL"
#>   .. .. ..$ ci_pair      : chr "95% CI: UL"
#>   .. .. ..$ ci_label     : chr "95% CI"
#>   .. .. ..$ is_df        : logi FALSE
#>   .. .. ..$ display_label: chr "95% CI"
#>   .. ..$ 95% CI: UL:List of 12
#>   .. .. ..$ token        : chr "ci"
#>   .. .. ..$ model_id     : chr "M1"
#>   .. .. ..$ source_field : chr "ci_high"
#>   .. .. ..$ precision    : int 2
#>   .. .. ..$ p_style      : NULL
#>   .. .. ..$ threshold    : NULL
#>   .. .. ..$ signif       : NULL
#>   .. .. ..$ ci_role      : chr "UL"
#>   .. .. ..$ ci_pair      : chr "95% CI: LL"
#>   .. .. ..$ ci_label     : chr "95% CI"
#>   .. .. ..$ is_df        : logi FALSE
#>   .. .. ..$ display_label: chr "95% CI"
#>   .. ..$ p         :List of 12
#>   .. .. ..$ token        : chr "p"
#>   .. .. ..$ model_id     : chr "M1"
#>   .. .. ..$ source_field : chr "p_value"
#>   .. .. ..$ precision    : int 3
#>   .. .. ..$ p_style      : chr "apa"
#>   .. .. ..$ threshold    : num 0.001
#>   .. .. ..$ signif       : NULL
#>   .. .. ..$ ci_role      : NULL
#>   .. .. ..$ ci_pair      : NULL
#>   .. .. ..$ ci_label     : NULL
#>   .. .. ..$ is_df        : logi FALSE
#>   .. .. ..$ display_label: chr "p"
#>   ..$ spanners               : NULL
#>   ..$ ci_pairs               :List of 1
#>   .. ..$ :List of 2
#>   .. .. ..$ label: chr "95% CI"
#>   .. .. ..$ cols : int [1:2] 4 5
#>   ..$ format_spec            :List of 9
#>   .. ..$ decimal_mark      : chr "."
#>   .. ..$ digits            : int 2
#>   .. ..$ p_digits          : int 3
#>   .. ..$ effect_size_digits: int 2
#>   .. ..$ fit_digits        : int 2
#>   .. ..$ ic_digits         : int 1
#>   .. ..$ p_style           : chr "apa"
#>   .. ..$ p_threshold       : num 0.001
#>   .. ..$ ci_level          : num 0.95
#>  - attr(*, "padding")= int 0
#>  - attr(*, "fit_stats_layout")= chr "first_col"
#>  - attr(*, "model_ids")= chr "M1"
#>  - attr(*, "outcome")= chr "wellbeing_score"
out <- table_regression(
  lm(wellbeing_score ~ age + sex + smoking, data = sochealth),
  output = "long"
)
out[, c("model_id", "term", "estimate_type", "estimate",
        "std.error", "p.value")]
#> # A tibble: 6 × 6
#>   model_id term        estimate_type estimate std.error    p.value
#>   <chr>    <chr>       <chr>            <dbl>     <dbl>      <dbl>
#> 1 M1       (Intercept) B              65.2       1.66    1.59e-216
#> 2 M1       age         B               0.0465    0.0307  1.30e-  1
#> 3 M1       sexFemale   B              NA        NA      NA        
#> 4 M1       sexMale     B               3.86      0.905   2.22e-  5
#> 5 M1       smokingNo   B              NA        NA      NA        
#> 6 M1       smokingYes  B              -1.72      1.11    1.21e-  1
pkgdown_dark_gt(
  table_regression(
    lm(wellbeing_score ~ age + sex + smoking, data = sochealth),
    output = "gt"
  )
)

Linear regression: wellbeing_score
Variable
B
SE
95% CI
p
LL UL
(Intercept)   65.20 1.66 61.95 68.45 <.001
age    0.05 0.03 -0.01  0.11  .130
sex:
Female (ref.)    –    –     –     –    –    
Male    3.86 0.91  2.08  5.63 <.001
smoking:
No (ref.)    –    –     –     –    –    
Yes   -1.72 1.11 -3.89  0.45  .121
n 1175   
   0.02
Adj.R²    0.02
Note. Linear regression. Std. errors: classical (OLS).

broom integration

broom::tidy() returns a long tibble with one row per (model_id, term, estimate_type) and broom-canonical column names (estimate, std.error, conf.low, conf.high, statistic, p.value). broom::glance() returns one row per (model_id, outcome) with model-level statistics; df.residual is preserved as a numeric so cluster-robust Satterthwaite df flows through verbatim:

fit <- lm(wellbeing_score ~ age + sex + smoking, data = sochealth)
out <- table_regression(fit, standardized = "refit")

broom::tidy(out)
#> # A tibble: 8 × 16
#>   model_id outcome outcome_level term  estimate_type estimate std.error conf.low
#>   <chr>    <chr>   <chr>         <chr> <chr>            <dbl>     <dbl>    <dbl>
#> 1 M1       wellbe… NA            (Int… B              65.2       1.66    62.0   
#> 2 M1       wellbe… NA            (Int… beta           -0.0961    0.0431  -0.181 
#> 3 M1       wellbe… NA            age   B               0.0465    0.0307  -0.0137
#> 4 M1       wellbe… NA            age   beta            0.0439    0.0290  -0.0130
#> 5 M1       wellbe… NA            sexM… B               3.86      0.905    2.08  
#> 6 M1       wellbe… NA            sexM… beta            0.247     0.0579   0.133 
#> 7 M1       wellbe… NA            smok… B              -1.72      1.11    -3.89  
#> 8 M1       wellbe… NA            smok… beta           -0.110     0.0708  -0.249 
#> # ℹ 8 more variables: conf.high <dbl>, statistic <dbl>, df <dbl>,
#> #   p.value <dbl>, test_type <chr>, is_intercept <lgl>, factor_term <chr>,
#> #   factor_level <chr>
broom::glance(out)
#> # A tibble: 1 × 15
#>   model_id outcome       nobs weighted_nobs r.squared adj.r.squared omega2 sigma
#>   <chr>    <chr>        <int>         <dbl>     <dbl>         <dbl>  <dbl> <dbl>
#> 1 M1       wellbeing_s…  1175            NA    0.0190        0.0165 0.0165  15.5
#> # ℹ 7 more variables: rmse <dbl>, f2 <dbl>, AIC <dbl>, AICc <dbl>, BIC <dbl>,
#> #   deviance <dbl>, df.residual <dbl>

The long format is the right entry point when the table is one step in a larger pipeline — saving to disk for the manuscript appendix, faceting by subgroup, or feeding a downstream post-estimation analysis. The tidy() output keeps the estimate_type column so the same data frame can hold rows for B, β, AME, and per-coefficient effect-size estimates without ambiguity.

See also

Model-family vignettes build on the mechanics shown here:

Descriptive and reporting companions:

References

Aiken, L. S., and West, S. G. (1991). Multiple Regression: Testing and Interpreting Interactions. Sage.

American Psychological Association (2020). Publication Manual of the American Psychological Association (7th ed.). Section 6.46.

Cohen, J., Cohen, P., West, S. G., and Aiken, L. S. (2003). Applied Multiple Regression / Correlation Analysis for the Behavioral Sciences (3rd ed.). Lawrence Erlbaum.

Fox, J. (2016). Applied Regression Analysis and Generalized Linear Models (3rd ed.). Sage.

Fox, J., and Weisberg, S. (2019). An R Companion to Applied Regression (3rd ed.). Sage.

Gelman, A. (2008). Scaling regression inputs by dividing by two standard deviations. Statistics in Medicine, 27(15), 2865–2873.

Gelman, A., Hill, J., and Yajima, M. (2012). Why we (usually) don’t have to worry about multiple comparisons. Journal of Research on Educational Effectiveness, 5(2), 189–211.

Greenland, S. (2017). For and against methodologies: Some perspectives on recent causal and statistical inference debates. European Journal of Epidemiology, 32(1), 3–20.

Harrell, F. E. (2015). Regression Modeling Strategies (2nd ed.). Springer. Section 5.4 on multiplicity.

Hosmer, D. W., Lemeshow, S., and Sturdivant, R. X. (2013). Applied Logistic Regression (3rd ed.). Wiley.

Imbens, G. W., and Kolesár, M. (2016). Robust standard errors in small samples: Some practical advice. Review of Economics and Statistics, 98(4), 701–712.

Long, J. S., and Ervin, L. H. (2000). Using heteroscedasticity consistent standard errors in the linear regression model. The American Statistician, 54(3), 217–224.

Long, J. S., and Freese, J. (2014). Regression Models for Categorical Dependent Variables Using Stata (3rd ed.). Stata Press.

McFadden, D. (1974). Conditional logit analysis of qualitative choice behavior. In P. Zarembka (Ed.), Frontiers in Econometrics (pp. 105–142). Academic Press.

Menard, S. (2004). Six approaches to calculating standardized logistic regression coefficients. The American Statistician, 58(3), 218–223.

Menard, S. (2011). Standards for standardized logistic regression coefficients. Social Forces, 89(4), 1409–1428.

Mood, C. (2010). Logistic regression: Why we cannot do what we think we can do, and what we can do about it. European Sociological Review, 26(1), 67–82.

Nagelkerke, N. J. D. (1991). A note on a general definition of the coefficient of determination. Biometrika, 78(3), 691–692.

Nakagawa, S., and Schielzeth, H. (2013). A general and simple method for obtaining R² from generalized linear mixed-effects models. Methods in Ecology and Evolution, 4(2), 133–142.

Olejnik, S., and Algina, J. (2003). Generalized eta and omega squared statistics: Measures of effect size for some common research designs. Psychological Methods, 8(4), 434–447.

Pinheiro, J. C., and Bates, D. M. (2000). Mixed-Effects Models in S and S-PLUS. Springer.

Pustejovsky, J. E., and Tipton, E. (2018). Small-sample methods for cluster-robust variance estimation and hypothesis testing in fixed effects models. Journal of Business & Economic Statistics, 36(4), 672–683.

Rothman, K. J. (1990). No adjustments are needed for multiple comparisons. Epidemiology, 1(1), 43–46.

Self, S. G., and Liang, K.-Y. (1987). Asymptotic properties of maximum likelihood estimators and likelihood ratio tests under non-standard conditions. Journal of the American Statistical Association, 82(398), 605–610.

Smithson, M. (2003). Confidence Intervals. Sage.

Steiger, J. H. (2004). Beyond the F test: Effect size confidence intervals and tests of close fit in the analysis of variance and contrast analysis. Psychological Methods, 9(2), 164–182.

Stram, D. O., and Lee, J. W. (1994). Variance components testing in the longitudinal mixed effects model. Biometrics, 50(4), 1171–1177.

Tjur, T. (2009). Coefficients of determination in logistic regression models — A new proposal: The coefficient of discrimination. The American Statistician, 63(4), 366–372.

Venables, W. N., and Ripley, B. D. (2002). Modern Applied Statistics with S (4th ed.). Springer. Section 7.2 on profile likelihood.

Wasserstein, R. L., Schirm, A. L., and Lazar, N. A. (2019). Moving to a world beyond “p < 0.05”. The American Statistician, 73(sup1), 1–19.