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GWAS Study

Genetic association and Mendelian randomization for hypothyroidism highlight immune molecular mechanisms.

Mathieu S, Briend M, Abner E et al.

36093044 PubMed ID
GWAS Study Type
689720 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MS
Mathieu S
BM
Briend M
AE
Abner E
CC
Couture C
LZ
Li Z
BY
Bossé Y
TS
Thériault S
ET
Esko T
AB
Arsenault BJ
MP
Mathieu P
Chapter II

Abstract

Summary of the research findings

We carried out a genome-wide association analysis including 51,194 cases of hypothyroidism and 443,383 controls. In total, 139 risk loci were associated to hypothyroidism with genes involved in lymphocyte function. Candidate genes associated with hypothyroidism were identified by using molecular quantitative trait loci, colocalization, and enhancer-promoter chromatin looping. Mendelian randomization (MR) identified 42 blood expressed genes and circulating proteins as candidate causal molecules in hypothyroidism. Drug-gene interaction analysis provided evidence that immune checkpoint and tyrosine kinase inhibitors used in cancer therapy increase the risk of hypothyroidism. Hence, integrative mapping and MR support that expression of genes and proteins enriched in lymphocyte function are associated with the risk of hypothyroidism and provide genetic evidence for drug-induced hypothyroidism and identify actionable potential drug targets.

51,194 European ancestry cases, 443,383 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

689720
Total Participants
GWAS
Study Type
Yes
Replicated
17,002 cases, 178,141 controls
Replication Participants
European
Ancestry
Finland, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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