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GWAS Study

Genome-wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores.

Zhu X, Zhu L, Wang H et al.

34989438 PubMed ID
GWAS Study Type
1076492 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZX
Zhu X
ZL
Zhu L
WH
Wang H
CR
Cooper RS
CA
Chakravarti A
Chapter II

Abstract

Summary of the research findings

Systolic and diastolic blood pressure (S/DBP) are highly correlated modifiable risk factors for cardiovascular disease (CVD). We report here a bidirectional Mendelian Randomization (MR) and horizontal pleiotropy analysis of S/DBP summary statistics from the UK Biobank (UKB)-International Consortium for Blood Pressure (ICBP) (UKB-ICBP) BP genome-wide association study and construct a composite genetic risk score (GRS) by including pleiotropic variants. The composite GRS captures greater (1.11-3.26 fold) heritability for BP traits and increases (1.09- and 2.01-fold) Nagelkerke's R2 for hypertension and CVD. We replicated 118 novel BP horizontal pleiotropic variants including 18 novel BP loci using summary statistics from the Million Veteran Program (MVP) study. An additional 219 novel BP signals and 40 novel loci were identified after a meta-analysis of the UKB-ICBP and MVP summary statistics but without further independent replication. Our study provides further insight into BP regulation and provides a novel way to construct a GRS by including pleiotropic variants for other complex diseases.

757,601 European ancestry individuals, 318,891 European ancestry, African American or Afro-Caribbean, Native American ancestry, Asian ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

1076492
Total Participants
GWAS
Study Type
No
Replicated
European, European, African American or Afro-Caribbean, Native American, Asian unspecified
Ancestry
U.K., U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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