Evidence map›Paper›PMID 27241694›Full record

ArticleStatistics in medicine2016

Robust analysis of secondary phenotypes in case-control genetic association studies.

Chuanhua Xing, Janice M McCarthy, Josée Dupuis, L Adrienne Cupples, James B Meigs, Xihong Lin, Andrew S Allen

Abstract read
In one paragraph

Article in Statistics in medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. 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

7 authors.

Chuanhua XingDepartment of Biostatistics, Boston University School of Public Health, Boston, 02118, MA, U.S.A.
Janice M McCarthyDepartment of Biostatistics and Bioinformatics, Duke University, Durham, 27710, NC, U.S.A.
Josée DupuisDepartment of Biostatistics, Boston University School of Public Health, Boston, 02118, MA, U.S.A.ORCID 0000-0003-2871-3603
L Adrienne CupplesDepartment of Biostatistics, Boston University School of Public Health, Boston, 02118, MA, U.S.A.
James B MeigsGeneral Medicine Division, Massachusetts General Hospital, Boston, 02114, MA, U.S.A.
Xihong LinDepartment of Biostatistics, Harvard University, Cambridge, 01238, MA, U.S.A.
Andrew S AllenDepartment of Biostatistics and Bioinformatics, Duke University, Durham, 27710, NC, U.S.A.

Funding

Statistical Methods for Analysis of Massive Genetic and Genomic Data in Cancer ResearchR35CA197449 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI XIHONG LIN · 2015 to 2026
$10.9M
Common Genetic Variation and Quantitative Diabetes TraitsR01DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2008 to 2014
$5.0M
Rare Sequence Variation and Diabetes Quantitative TraitsU01DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2015 to 2019
$3.6M
Epidemiology of Precursors to Type 2 DiabetesK24DK080140 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2007 to 2016
$1.9M
Robust Methods for the Efficient Analysis and Integration of DNA Sequence DataR01MH084680 · NIMH · DUKE UNIVERSITY · PI ALLEN, ANDREW S · 2008 to 2010
$912k
NCI NIH HHS R35 CA197449NIDDK NIH HHS K24 DK080140NIDDK NIH HHS R01 DK078616NIDDK NIH HHS U01 DK078616NIMH NIH HHS R01 MH084680
6 · The paper itself

Abstract

The case-control study is a common design for assessing the association between genetic exposures and a disease phenotype. Though association with a given (case-control) phenotype is always of primary interest, there is often considerable interest in assessing relationships between genetic exposures and other (secondary) phenotypes. However, the case-control sample represents a biased sample from the general population. As a result, if this sampling framework is not correctly taken into account, analyses estimating the effect of exposures on secondary phenotypes can be biased leading to incorrect inference. In this paper, we address this problem and propose a general approach for estimating and testing the population effect of a genetic variant on a secondary phenotype. Our approach is based on inverse probability weighted estimating equations, where the weights depend on genotype and the secondary phenotype. We show that, though slightly less efficient than a full likelihood-based analysis when the likelihood is correctly specified, it is substantially more robust to model misspecification, and can out-perform likelihood-based analysis, both in terms of validity and power, when the model is misspecified. We illustrate our approach with an application to a case-control study extracted from the Framingham Heart Study. Copyright © 2016 John Wiley & Sons, Ltd.

Indexed as

Genome-Wide Association StudyPhenotypeCase-Control StudiesGenetic Association StudiesHumansLikelihood FunctionsModels, GeneticPolymorphism, Single Nucleotidecase-controlestimating equationgenetic association studyinverse-probability-weightedsecondary phenotype

Identifiers

PMID27241694
PMCPMC5870885

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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.