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GWAS Study

Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.

Fransen E, Bonneux S, Corneveaux JJ et al.

24939585 PubMed ID
GWAS Study Type
1489 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

FE
Fransen E
BS
Bonneux S
CJ
Corneveaux JJ
SI
Schrauwen I
DB
Di Berardino F
WC
White CH
OJ
Ohmen JD
VD
Van de Heyning P
AU
Ambrosetti U
HM
Huentelman MJ
VC
Van Camp G
FR
Friedman RA
Chapter II

Abstract

Summary of the research findings

We performed a genome-wide association study (GWAS) to identify the genes responsible for age-related hearing impairment (ARHI), the most common form of hearing impairment in the elderly. Analysis of common variants, with and without adjustment for stratification and environmental covariates, rare variants and interactions, as well as gene-set enrichment analysis, showed no variants with genome-wide significance. No evidence for replication of any previously reported genes was found. A study of the genetic architecture indicates for the first time that ARHI is highly polygenic in nature, with probably no major genes involved. The phenotype depends on the aggregated effect of a large number of SNPs, of which the individual effects are undetectable in a modestly powered GWAS. We estimated that 22% of the variance in our data set can be explained by the collective effect of all genotyped SNPs. A score analysis showed a modest enrichment in causative SNPs among the SNPs with a P-value below 0.01.

1,489 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

1489
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Belgium
Recruitment Country
Chapter IV

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