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GWAS Study

Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.

Rämö JT, Kiiskinen T, Seist R et al.

36653343 PubMed ID
GWAS Study Type
864702 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

RJ
Rämö JT
KT
Kiiskinen T
SR
Seist R
KK
Krebs K
KM
Kanai M
KJ
Karjalainen J
KM
Kurki M
HE
Hämäläinen E
HP
Häppölä P
HA
Havulinna AS
HH
Hautakangas H
MR
Mägi R
PP
Palta P
ET
Esko T
MA
Metspalu A
PM
Pirinen M
KK
Karczewski KJ
RS
Ripatti S
ML
Milani L
SK
Stankovic KM
MA
Mäkitie A
DM
Daly MJ
PA
Palotie A
Chapter II

Abstract

Summary of the research findings

Otosclerosis is one of the most common causes of conductive hearing loss, affecting 0.3% of the population. It typically presents in adulthood and half of the patients have a positive family history. The pathophysiology of otosclerosis is poorly understood. A previous genome-wide association study (GWAS) identified a single association locus in an intronic region of RELN. Here, we report a meta-analysis of GWAS studies of otosclerosis in three population-based biobanks comprising 3504 cases and 861,198 controls. We identify 23 novel risk loci (p < 5 × 10-8) and report an association in RELN and three previously reported candidate gene or linkage regions (TGFB1, MEPE, and OTSC7). We demonstrate developmental stage-dependent immunostaining patterns of MEPE and RUNX2 in mouse otic capsules. In most association loci, the nearest protein-coding genes are implicated in bone remodelling, mineralization or severe skeletal disorders. We highlight multiple genes involved in transforming growth factor beta signalling for follow-up studies.

3,504 European ancestry cases, 861,198 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

864702
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Finland, U.K., Estonia
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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