Evidence map›Paper›PMID 32565216›Full record

ArticleJournal of clinical epidemiology2020

How subgroup analyses can miss the trees for the forest plots: A simulation study.

Michael Webster-Clark, John A Baron, Michele Jonsson Funk, Daniel Westreich

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical epidemiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Article
  3. Tutorial on directed acyclic graphs.Journal of clinical epidemiology · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Michael Webster-ClarkDepartment of Epidemiology, UNC-Chapel Hill, Chapel Hill, NC 27599. Electronic address: mawc@live.unc.edu.
John A BaronDepartment of Medicine, UNC-Chapel Hill, Chapel Hill, NC 27599.
Michele Jonsson FunkDepartment of Epidemiology, UNC-Chapel Hill, Chapel Hill, NC 27599.
Daniel WestreichDepartment of Epidemiology, UNC-Chapel Hill, Chapel Hill, NC 27599.
University of North Carolina at Chapel Hill · USUniversity of North Carolina Health Care · US

Funding

Methods for Estimating Sex Differences in Safety and Effectiveness of DrugsR01HL118255 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JONSSON FUNK, MICHELE LAURA · 2014 to 2017
$1.7M
NHLBI NIH HHS R01 HL118255
6 · The paper itself

Abstract

objectivesSubgroup analyses of clinical trial data can be an important tool for understanding when treatment effects differ across populations. That said, even effect estimates from prespecified subgroups in well-conducted trials may not apply to corresponding subgroups in the source population. While this divergence may simply reflect statistical imprecision, there has been less discussion of systematic or structural sources of misleading subgroup estimates. STUDY DESIGN AND

settingWe use directed acyclic graphs to show how selection bias caused by associations between effect measure modifiers and trial selection, whether explicit (e.g., eligibility criteria) or implicit (e.g., self-selection based on race), can result in subgroup estimates that do not correspond to subgroup effects in the source population. To demonstrate this point, we provide a hypothetical example illustrating the sorts of erroneous conclusions that can result, as well as their potential consequences. We also provide a tool for readers to explore additional cases.

conclusionTreating subgroups within a trial essentially as random samples of the corresponding subgroups in the wider population can be misleading, even when analyses are conducted rigorously and all findings are internally valid. Researchers should carefully examine associations between (and consider adjusting for) variables when attempting to identify heterogeneous treatment effects.

Indexed as

BiometryClinical Trials as TopicComputer SimulationData Interpretation, StatisticalFemaleHumansMaleModels, StatisticalModels, TheoreticalMyocardial InfarctionReproducibility of ResultsResearch DesignSample SizeSelection Biascausal graphsexternal validityselection biasSubgroups

Identifiers

PMID32565216
PMCPMC7529905
OpenAlexW3036284897

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.