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GWAS Study

Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.

Salvi E, Wang Z, Rizzi F et al.

27802415 PubMed ID
GWAS Study Type
2169 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SE
Salvi E
WZ
Wang Z
RF
Rizzi F
GY
Gong Y
MC
McDonough CW
PS
Padmanabhan S
HT
Hiltunen TP
LC
Lanzani C
ZR
Zaninello R
CM
Chittani M
BK
Bailey KR
SA
Sarin AP
BM
Barcella M
MO
Melander O
CA
Chapman AB
MP
Manunta P
KK
Kontula KK
GN
Glorioso N
CD
Cusi D
DA
Dominiczak AF
JJ
Johnson JA
BC
Barlassina C
BE
Boerwinkle E
CR
Cooper-DeHoff RM
TS
Turner ST
Chapter II

Abstract

Summary of the research findings

This study aimed to identify novel loci influencing the antihypertensive response to hydrochlorothiazide monotherapy. A genome-wide meta-analysis of blood pressure (BP) response to hydrochlorothiazide was performed in 1739 white hypertensives from 6 clinical trials within the International Consortium for Antihypertensive Pharmacogenomics Studies, making it the largest study to date of its kind. No signals reached genome-wide significance (P<5×10-8), and the suggestive regions (P<10-5) were cross-validated in 2 black cohorts treated with hydrochlorothiazide. In addition, a gene-based analysis was performed on candidate genes with previous evidence of involvement in diuretic response, in BP regulation, or in hypertension susceptibility. Using the genome-wide meta-analysis approach, with validation in blacks, we identified 2 suggestive regulatory regions linked to gap junction protein α1 gene (GJA1) and forkhead box A1 gene (FOXA1), relevant for cardiovascular and kidney function. With the gene-based approach, we identified hydroxy-delta-5-steroid dehydrogenase, 3 β- and steroid δ-isomerase 1 gene (HSD3B1) as significantly associated with BP response (P<2.28×10-4 ). HSD3B1 encodes the 3β-hydroxysteroid dehydrogenase enzyme and plays a crucial role in the biosynthesis of aldosterone and endogenous ouabain. By amassing all of the available pharmacogenomic studies of BP response to hydrochlorothiazide, and using 2 different analytic approaches, we identified 3 novel loci influencing BP response to hydrochlorothiazide. The gene-based analysis, never before applied to pharmacogenomics of antihypertensive drugs to our knowledge, provided a powerful strategy to identify a locus of interest, which was not identified in the genome-wide meta-analysis because of high allelic heterogeneity. These data pave the way for future investigations on new pathways and drug targets to enhance the current understanding of personalized antihypertensive treatment.

1,739 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

2169
Total Participants
GWAS
Study Type
Yes
Replicated
430 African American individuals
Replication Participants
European, African American or Afro-Caribbean
Ancestry
Finland, Sweden, U.S., Norway
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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