Evidence map›Paper›PMID 28402496›Full record

ArticleInternational journal of epidemiology2017

Mortality selection in a genetic sample and implications for association studies.

Benjamin W Domingue, Daniel W Belsky, Amal Harrati, Dalton Conley, David R Weir, Jason D Boardman

Abstract read
In one paragraph

Article in International journal of epidemiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 2 pooled it
–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

54 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
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  6. Article
  7. Educational Influences on Late-Life Health: Genetic Propensity and Attained Education.The journals of gerontology. Series B, Psychological sciences and social sciences · 2024
    Article
  8. Article
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  10. The Mode Effect of Web-Based Surveying on the 2018 U.S. Health and Retirement Study Measure of Cognitive Functioning.The journals of gerontology. Series B, Psychological sciences and social sciences · 2023
    Article
  11. Article
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  14. In utero exposure to the Great Depression is reflected in late-life epigenetic aging signatures.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

6 authors.

Benjamin W DomingueGraduate School of Education, Stanford University, 520 Galvez Mall, Stanford, CA 94305, USA.
Daniel W BelskyDepartment of Medicine, Duke University School of Medicine; Duke University Population Research Institute, Duke University, 2020 W. Main St., Durham NC, 27705.
Amal HarratiSchool of Medicine, Stanford University, 1070 Arastradero Rd Palo Alto, CA 94304.
Dalton ConleyOffice of Population Research, Department of Sociology, Princeton University, 153 Wallace Hall Princeton, NJ 08544.
David R WeirPopulation Studies Center, Survey Research Center, University of Michigan, 426 Thompson St, Ann Arbor, MI 48104.
Jason D BoardmanInstitute of Behavioral Science, Department of Sociology, University of Colorado Boulder, 483 UCB Boulder, CO 80309-0483.

Funding

HRS Yrs29-34: Y33 SSA CoFundingU01AG009740 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jessica Faul, KENNETH M LANGA · 1990 to 2026
$555.8M
Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Sarah B. Peskoe · 2006 to 2026
$24.6M
Risk factors for Alzheimer's Disease and Related Dementia: Evidence from a Large Occupational CohortR01AG026291 · NIA · YALE UNIVERSITY · PI CANTLEY, LINDA, EISEN, ELLEN AURA · 2006 to 2021
$12.9M
STALLARD Admin Supp: Predicting Future Care Needs and Costs for Individual Medicare Enrollees with Incident Suspected Alzheimer's DiseaseP30AG034424 · NIA · DUKE UNIVERSITY · PI SCOTT M. LYNCH · 2009 to 2026
$12.2M
Is mental disorder a preventable cause of age-related disease? The Dunedin Study.R01AG032282 · NIA · DUKE UNIVERSITY · PI CASPI, AVSHALOM, MOFFITT, TERRIE E · 2009 to 2025
$9.5M
Creating a National Resource for Genetic Research in Behavioral & Health SciencesRC2AG036495 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WEIR, DAVID R. · 2009 to 2010
$7.4M
Expanding a National Resource for Genetic Research in Behavioral & Health ScienceRC4AG039029 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WEIR, DAVID R. · 2010 to 2010
$6.0M
University of Colorado Population CenterP2CHD066613 · NICHD · UNIVERSITY OF COLORADO · PI JANE A MENKEN · 2015 to 2026
$3.7M
Scientific and Technical Computing CoreP2CHD047879 · NICHD · PRINCETON UNIVERSITY · PI MASSEY, DOUGLAS S · 2014 to 2018
$2.0M
Antibody persistence after conjugate meningococcal group A vaccination in MaliDP5OD009162 · OD · UNIVERSITY OF WASHINGTON · PI BASTA, NICOLE ELAINE · 2011 to 2015
$1.9M
The Social and Genetic Epidemiology of Health Behaviors: An Integrated ApproachR21HD078031 · NICHD · UNIVERSITY OF COLORADO · PI BOARDMAN, JASON D, DOMINGUE, BENJAMIN · 2013 to 2014
$300k
NIA NIH HHS P30 AG028716NIA NIH HHS R01 AG026291NIA NIH HHS R01 AG032282NIA NIH HHS RC2 AG036495NIA NIH HHS RC4 AG039029NIA NIH HHS U01 AG009740NICHD NIH HHS P2C HD047879NICHD NIH HHS P2C HD066613NICHD NIH HHS R21 HD078031
6 · The paper itself

Abstract

Background: Mortality selection occurs when a non-random subset of a population of interest has died before data collection and is unobserved in the data. Mortality selection is of general concern in the social and health sciences, but has received little attention in genetic epidemiology. We tested the hypothesis that mortality selection may bias genetic association estimates, using data from the US-based Health and Retirement Study (HRS). Methods: We tested mortality selection into the HRS genetic database by comparing HRS respondents who survive until genetic data collection in 2006 with those who do not. We next modelled mortality selection on demographic, health and social characteristics to calculate mortality selection probability weights. We analysed polygenic score associations with several traits before and after applying inverse-probability weighting to account for mortality selection. We tested simple associations and time-varying genetic associations (i.e. gene-by-cohort interactions). Results: We observed mortality selection into the HRS genetic database on demographic, health and social characteristics. Correction for mortality selection using inverse probability weighting methods did not change simple association estimates. However, using these methods did change estimates of gene-by-cohort interaction effects. Correction for mortality selection changed gene-by-cohort interaction estimates in the opposite direction from increased mortality selection based on analysis of HRS respondents surviving through 2012. Conclusions: Mortality selection may bias estimates of gene-by-cohort interaction effects. Analyses of HRS data can adjust for mortality selection associated with observables by including probability weights. Mortality selection is a potential confounder of genetic association studies, but the magnitude of confounding varies by trait.

Indexed as

BiasModels, TheoreticalMortalityAgedAged, 80 and overAge DistributionFemaleGenotypeHumansKaplan-Meier EstimateMaleMiddle AgedMolecular EpidemiologySex DistributionUnited Statesgenetic epidemiologygenotypeMortality

Identifiers

PMID28402496
PMCPMC5837559

What OpenQuestion holds

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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.