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GWAS Study

GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements.

Dixon PH, Levine AP, Cebola I et al.

35977952 PubMed ID
GWAS Study Type
154780 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DP
Dixon PH
LA
Levine AP
CI
Cebola I
CM
Chan MMY
AA
Amin AS
AA
Aich A
MM
Mozere M
MH
Maude H
MA
Mitchell AL
ZJ
Zhang J
CJ
Chambers J
SA
Syngelaki A
DJ
Donnelly J
CS
Cooley S
GM
Geary M
NK
Nicolaides K
TM
Thorsell M
HW
Hague WM
EM
Estiu MC
MH
Marschall HU
GD
Gale DP
WC
Williamson C
Chapter II

Abstract

Summary of the research findings

Intrahepatic cholestasis of pregnancy (ICP) is a pregnancy-specific liver disorder affecting 0.5-2% of pregnancies. The majority of cases present in the third trimester with pruritus, elevated serum bile acids and abnormal serum liver tests. ICP is associated with an increased risk of adverse outcomes, including spontaneous preterm birth and stillbirth. Whilst rare mutations affecting hepatobiliary transporters contribute to the aetiology of ICP, the role of common genetic variation in ICP has not been systematically characterised to date. Here, we perform genome-wide association studies (GWAS) and meta-analyses for ICP across three studies including 1138 cases and 153,642 controls. Eleven loci achieve genome-wide significance and have been further investigated and fine-mapped using functional genomics approaches. Our results pinpoint common sequence variation in liver-enriched genes and liver-specific cis-regulatory elements as contributing mechanisms to ICP susceptibility.

1,138 European ancestry cases, 153,642 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

154780
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Finland, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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