Evidence map›Paper›PMID 38869698›Full record

ArticleBehavior genetics2024

Using Alternative Definitions of Controls to Increase Statistical Power in GWAS.

Sarah E Benstock, Katherine Weaver, John M Hettema, Brad Verhulst

Abstract read
In one paragraph

Article in Behavior genetics, 2024. 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.

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2 · The registry

The trial behind it

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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

5 · Who and what money

Authors and funding

4 authors.

Sarah E BenstockDepartment of Psychiatry and Behavioral Sciences, Texas A&M University School of Medicine, College Station, TX, USA.
Katherine WeaverDepartment of Psychiatry and Behavioral Sciences, Texas A&M University School of Medicine, College Station, TX, USA.
John M HettemaDepartment of Psychiatry and Behavioral Sciences, Texas A&M University School of Medicine, College Station, TX, USA.
Brad VerhulstDepartment of Psychiatry and Behavioral Sciences, Texas A&M University School of Medicine, College Station, TX, USA. verhulst@tamu.edu.

Funding

Genome-wide association studies of anxiety spectrum phenotypes: Furthering the PGC Anxiety Disorders Working GroupR01MH113665 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI JOHN M HETTEMA · 2017 to 2026
$2.6M
NIMH NIH HHS R01 MH113665Office of Extramural Research, National Institutes of Health R01MH113665
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) are often underpowered due to small effect sizes of common single nucleotide polymorphisms (SNPs) on phenotypes and extreme multiple testing thresholds. The most common approach for increasing statistical power is to increase sample size. We propose an alternative strategy of redefining case-control outcomes into ordinal case-subthreshold-asymptomatic variables. While maintaining the clinical case threshold, we subdivide controls into two groups: individuals who are symptomatic but do not meet the clinical criteria for diagnosis (subthreshold) and individuals who are effectively asymptomatic. We conducted a simulation study to examine the impact of effect size, minor allele frequency, population prevalence, and the prevalence of the subthreshold group on statistical power to detect genetic associations in three scenarios: a standard case-control, an ordinal, and a case-asymptomatic control analysis. Our results suggest the ordinal model consistently provides the greatest statistical power while the case-control model the least. Power in the case-asymptomatic control model reflects the case-control or ordinal model depending on the population prevalence and size of the subthreshold category. We then analyzed a major depression phenotype from the UK Biobank to corroborate our simulation results. Overall, the ordinal model improves statistical power in GWAS consistent with increasing the sample size by approximately 10%.

Indexed as

Computer SimulationGenome-Wide Association StudyPolymorphism, Single NucleotideCase-Control StudiesGene FrequencyHumansModels, GeneticModels, StatisticalPhenotypeSample SizeGWASMDDSimulationStatistical Power

Identifiers

PMID38869698
PMCPMC11661655

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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.