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GWAS Study

Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults.

Pozarickij A, Gan W, Lin K et al.

39048560 PubMed ID
GWAS Study Type
100453 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PA
Pozarickij A
GW
Gan W
LK
Lin K
CR
Clarke R
FZ
Fairhurst-Hunter Z
KM
Koido M
KM
Kanai M
OY
Okada Y
KY
Kamatani Y
BD
Bennett D
DH
Du H
CY
Chen Y
YL
Yang L
AD
Avery D
GY
Guo Y
YM
Yu M
YC
Yu C
SV
Schmidt Valle D
LJ
Lv J
CJ
Chen J
PR
Peto R
CR
Collins R
LL
Li L
CZ
Chen Z
MI
Millwood IY
WR
Walters RG
Chapter II

Abstract

Summary of the research findings

Elevated blood pressure (BP) is major risk factor for cardiovascular diseases (CVD). Genome-wide association studies (GWAS) conducted predominantly in populations of European ancestry have identified >2,000 BP-associated loci, but other ancestries have been less well-studied. We conducted GWAS of systolic, diastolic, pulse, and mean arterial BP in 100,453 Chinese adults. We identified 128 non-overlapping loci associated with one or more BP traits, including 74 newly-reported associations. Despite strong genetic correlations between populations, we identified appreciably higher heritability and larger variant effect sizes in Chinese compared with European or Japanese ancestry populations. Using instruments derived from these GWAS, multivariable Mendelian randomisation demonstrated that BP traits contribute differently to the causal associations of BP with CVD. In particular, only pulse pressure was independently causally associated with carotid plaque. These findings reinforce the need for studies in diverse populations to understand the genetic determinants of BP traits and their roles in disease risk.

100,453 Chinese Han ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

100453
Total Participants
GWAS
Study Type
No
Replicated
East Asian
Ancestry
China
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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