Evidence map›Paper›PMID 37423269›Full record

ArticleAnnals of epidemiology2023

A flexible matching strategy for matched nested case-control studies.

Andrew Ratanatharathorn, Stephen J Mooney, Benjamin A Rybicki, Andrew G Rundle

Abstract read
In one paragraph

Article in Annals of epidemiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
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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.

Andrew RatanatharathornDepartment of Epidemiology, Columbia University Mailman School of Public Health, New York, NY.
Stephen J MooneyDepartment of Epidemiology, School of Public Health, University of Washington, Seattle.
Benjamin A RybickiDepartment of Public Health Services, Henry Ford Health System, Detroit, MI.
Andrew G RundleDepartment of Epidemiology, Columbia University Mailman School of Public Health, New York, NY. Electronic address: Agr3@cumc.columbia.edu.

Funding

GENE-ENVIRONMENT INTERACTION IN PROSTATE CANCERR01ES011126 · NIEHS · HENRY FORD HEALTH SYSTEM · PI RYBICKI, BENJAMIN A. · 2000 to 2017
$8.0M
Pediatric Injury Research Training ProgramT32HD057822 · NICHD · UNIVERSITY OF WASHINGTON · PI CAROLYN A MC CARTY, Ali Rowhani-Rahbar · 2010 to 2026
$4.0M
Novel Protein Risk Markers for Lung CancerR21CA195110 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PERERA, FREDERICA P · 2016 to 2017
$406k
NCI NIH HHS R21 CA195110NICHD NIH HHS T32 HD057822NIEHS NIH HHS R01 ES011126
6 · The paper itself

Abstract

purposeIndividual matching in case-control studies improves statistical efficiency over random selection of controls but can lead to selection bias if cases are excluded due to the lack of appropriate controls or residual confounding with less strict matching criteria. We introduce flex matching, an algorithm using multiple rounds of control selection with successively relaxed matching criteria to select controls for cases.

methodsWe simulated exposure-disease relationships in multiple cohort data sets with a range of confounding scenarios and conducted 16,800,000 nested case-control studies, comparing random selection of controls, strict matching, and flex matching. We computed average bias and statistical efficiency in estimates of exposure-disease relationships under each matching strategy.

resultsOn average, flex matching produced the least biased estimates of exposure-disease associations with the smallest standard errors. Strict matching algorithms that excluded cases for whom matched controls could not be identified produced biased estimates with larger standard errors. Estimates from studies with random assignment of controls were relatively unbiased, but the standard errors were larger than from studies using flex matching.

conclusionsFlex matching should be considered for case-control designs, especially for biomarker studies where matching on technical artifacts is necessary and maximizing efficiency is a priority.

Indexed as

AlgorithmsBiasCase-Control StudiesComputer SimulationConfounding Factors, EpidemiologicHumansResearch DesignSelection BiasBiasConfoundingEfficiencyMatchingNested case-control studies

Identifiers

PMID37423269
PMCPMC10538416

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Registered trials

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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.