Evidence map›Paper›PMID 22714934›Full record

ArticleGenetic epidemiology2012

Stratification-score matching improves correction for confounding by population stratification in case-control association studies.

Michael P Epstein, Richard Duncan, K Alaine Broadaway, Min He, Andrew S Allen, Glen A Satten

Abstract read
In one paragraph

Article in Genetic epidemiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Contributions of Rare Gene Variants to Familial and Sporadic FSGS.Journal of the American Society of Nephrology : JASN · 2019
    Article
  7. Article
  8. Article
  9. Observational
  10. Article
  11. Article
  12. A genome-wide association study identifies major loci affecting the immune response against infectious bronchitis virus in chicken.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2014
    Article
  13. Article
  14. 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

6 authors at 3 institutions in 1 country.

Michael P EpsteinDepartment of Human Genetics, Emory University, 615 Michael Street, Atlanta, GA 30322, USA. mpepste@emory.edu
Richard Duncan
K Alaine Broadaway
Min He
Andrew S Allen
Glen A Satten
Emory University · USDuke University · USCenters for Disease Control and Prevention · US

Funding

Novel Statistical Methods for Human Gene MappingR01HG003618 · NHGRI · EMORY UNIVERSITY · PI EPSTEIN, MICHAEL PHILIP · 2006 to 2010
$1.5M
Robust Methods for the Efficient Analysis and Integration of DNA Sequence DataR01MH084680 · NIMH · DUKE UNIVERSITY · PI ALLEN, ANDREW S · 2008 to 2010
$912k
Advanced Haplotype Analyses in Coronary Artery DiseaseK25HL077663 · NHLBI · DUKE UNIVERSITY · PI ALLEN, ANDREW S · 2004 to 2008
$711k
NHGRI NIH HHS HG003618NHGRI NIH HHS R01 HG003618NHLBI NIH HHS HL077663NHLBI NIH HHS K25 HL077663NIMH NIH HHS R01 MH084680
6 · The paper itself

Abstract

Proper control of confounding due to population stratification is crucial for valid analysis of case-control association studies. Fine matching of cases and controls based on genetic ancestry is an increasingly popular strategy to correct for such confounding, both in genome-wide association studies (GWASs) as well as studies that employ next-generation sequencing, where matching can be used when selecting a subset of participants from a GWAS for rare-variant analysis. Existing matching methods match on measures of genetic ancestry that combine multiple components of ancestry into a scalar quantity. However, we show that including nonconfounding ancestry components in a matching criterion can lead to inaccurate matches, and hence to an improper control of confounding. To resolve this issue, we propose a novel method that assigns cases and controls to matched strata based on the stratification score (Epstein et al. [2007] Am J Hum Genet 80:921-930), which is the probability of disease given genomic variables. Matching on the stratification score leads to more accurate matches because case participants are matched to control participants who have a similar risk of disease given ancestry information. We illustrate our matching method using the African-American arm of the GAIN GWAS of schizophrenia. In this study, we observe that confounding due to stratification can be resolved by our matching approach but not by other existing matching procedures. We also use simulated data to show our novel matching approach can provide a more appropriate correction for population stratification than existing matching approaches.

Indexed as

Case-Control StudiesGenome-Wide Association StudyModels, GeneticBlack or African AmericanHumansSchizophreniaSoftware

Identifiers

PMID22714934
PMCPMC3671578
OpenAlexW2157010141

What Socratic 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 Socratic graph.