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Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry

Authors :
Xiaohui Li
James D. Stewart
Rikje Ruiter
Yongmei Liu
Joop Jukema
Donna K. Arnett
Leslie A. Lange
Daniel S. Evans
Jerome I. Rotter
Solomon K. Musani
Susan R. Heckbert
Christy L. Avery
L. de las Fuentes
D. C. Rao
C E de Keyser
Steve Cummings
L. A. Cupples
Kerri L. Wiggins
Y-Di Chen
David J. Stott
Vilmundur Gudnason
Ulrich Broeckel
Yun J. Sung
T.B. Harris
B. H. Stricker
J. C. Bis
M. A. Ikram
Kent D. Taylor
Traci M. Bartz
Fangui Sun
Nona Sotoodehnia
Nicholas L. Smith
Colleen M. Sitlani
L. J. Launer
Eric A. Whitsel
Alexander P. Reiner
A.G. Uitterlinden
Karen Schwander
Xuejiang Guo
Adolfo Correa
Hanfei Xu
Albert V. Smith
Til Stürmer
James S. Floyd
James G. Wilson
Ramachandran S. Vasan
Evan L. Busch
Bruce M. Psaty
Stella Trompet
Ian Ford
Epidemiology
Source :
Pharmacogenomics Journal, 20(3), 482-493. Nature Publishing Group, The pharmacogenomics journal, The pharmacogenomics journal, vol 20, iss 3, Pharmacogenomics Journal, 20(3), 482-493. NATURE PUBLISHING GROUP
Publication Year :
2020

Abstract

Hypertension (HTN) is a significant risk factor for cardiovascular morbidity and mortality. Metabolic abnormalities, including adverse cholesterol and triglycerides (TG) profiles, are frequent comorbid findings with HTN and contribute to cardiovascular disease. Diuretics, which are used to treat HTN and heart failure, have been associated with worsening of fasting lipid concentrations. Genome-wide meta-analyses with 39,710 European-ancestry (EA) individuals and 9925 African-ancestry (AA) individuals were performed to identify genetic variants that modify the effect of loop or thiazide diuretic use on blood lipid concentrations. Both longitudinal and cross sectional data were used to compute cohort-specific interaction results, which were then combined through meta-analysis in each ancestry. These ancestry-specific results were further combined through trans-ancestry meta-analysis. Analysis of EA data identified two genome-wide significant (p

Details

Language :
English
ISSN :
1470269X
Database :
OpenAIRE
Journal :
Pharmacogenomics Journal, 20(3), 482-493. Nature Publishing Group, The pharmacogenomics journal, The pharmacogenomics journal, vol 20, iss 3, Pharmacogenomics Journal, 20(3), 482-493. NATURE PUBLISHING GROUP
Accession number :
edsair.doi.dedup.....f149bd21077f1f4f66b609ac099934ee