Annals of the Academy of Medicine, Singapore
July 23, 2026 · via Europe PMC
Interpreting multivariable regression coefficients in observational clinical research: The Table 2 fallacy.
Tay JRH, Bashir NZ, Cooray U.
AI summary — for doctors, generated from the abstract only
This methodological commentary warns clinicians and researchers against the 'Table 2 fallacy'—misinterpreting adjustment variable coefficients in multivariable regression models as independent causal risk factors when the analysis was only designed to estimate the effect of one specific exposure.
What was studied
A methodological commentary using a directed acyclic graph and a worked example to illustrate why coefficients for adjustment variables (age, sex, comorbidities, etc.) in a regression model built to estimate one exposure's effect should not be interpreted as independent, clinically actionable risk estimates, and why similar errors occur with interaction term interpretation.
Key findings
- Not applicable: this is a conceptual/methodological commentary rather than an original empirical study with quantitative results.
- The authors recommend specifying a target estimand and exposure, choosing adjustment variables based on assumed causal structure, interpreting only the exposure coefficient, and fitting separate models for additional questions.
Clinical relevance
This may be relevant to clinicians and researchers interpreting published regression tables, cautioning that a statistically significant adjustment-variable coefficient does not necessarily represent a modifiable, clinically actionable risk factor unless the study was specifically designed to estimate that effect.
Who should care
Limitations
As a methodological commentary rather than an empirical study, it does not provide new patient data; its guidance applies broadly across observational research rather than to a specific clinical question.
Clinicians reading regression tables should be cautious: coefficients for adjustment variables are often misread as independent risk factors when the study was not designed to estimate their effects.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
Multivariable regression tables are common in observational clinical research, but their coefficients are often over-interpreted. A model built to estimate the effect of 1 exposure may also report coefficients for age, sex, comorbidities, behaviours, and other adjustment variables. These additional rows are frequently read as independent risk factors, even when the analysis was not designed to estimate their effects. This is the Table 2 fallacy. The problem is not the use of adjustment, but the interpretation of adjustment terms as if each were a separate causal estimate. In this commentary, we use a directed acyclic graph and a single worked example to show why the coefficient for the exposure of interest can answer the intended clinical question, while coefficients for adjustment variables may not represent clinically actionable effects. We also show how similar errors arise when interaction terms are interpreted as causal. Authors should specify the target estimand (the causal effect the analysis is designed to estimate) and exposure, choose adjustment variables from the assumed causal structure, interpret only the exposure coefficient, and fit a separate model for each further question. We set out red flags, recurring pitfalls, and questions to ask of any risk-factor table. A regression table is not a menu of modifiable risks. An association is clinically actionable only when the study was designed to support that interpretation.
DOI
10.47102/annals-acadmedsg.2026420
PMID
42531045
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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