Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group. (23rd September 2019)

• Record Type: Journal Article
• Authors: Irvin, Marguerite R; Sitlani, Colleen M; Floyd, James S; Psaty, Bruce M; Bis, Joshua C; Wiggins, Kerri L; Whitsel, Eric A; Sturmer, Til; Stewart, James; Raffield, Laura; Sun, Fangui; Liu, Ching-Ti; Xu, Hanfei; Cupples, Adrienne L; Tanner, Rikki M; Rossing, Peter; Smith, Albert; Zilhão, Nuno R; Launer, Lenore J; Noordam, Raymond; Rotter, Jerome I; Yao, Jie; Li, Xiaohui; Guo, Xiuqing; Limdi, Nita; Sundaresan, Aishwarya; Lange, Leslie; Correa, Adolfo; Stott, David J; Ford, Ian; Jukema, J Wouter; Gudnason, Vilmundur; Mook-Kanamori, Dennis O; Trompet, Stella; Palmas, Walter; Warren, Helen R; Hellwege, Jacklyn N; Giri, Ayush; O'donnell, Christopher; Hung, Adriana M; Edwards, Todd L; Ahluwalia, Tarunveer S; Arnett, Donna K; Avery, Christy L;
• Is Part Of: American journal of hypertension. Volume 32:Number 12(2019)
• Page Start: 1146
• Page End: 1153
• Publication Date: 2019-09-23
• Subjects: blood pressure -- hypertension -- genome-wide association study -- severe hypertension -- treatment-resistant hypertension; Hypertension -- Periodicals; 616.132005
• DOI: 10.1093/ajh/hpz150
• Languages: English
• ISSNs: 0895-7061

Abstract

Abstract: BACKGROUND: Only a handful of genetic discovery efforts in apparent treatment-resistant hypertension (aTRH) have been described. METHODS: We conducted a case–control genome-wide association study of aTRH among persons treated for hypertension, using data from 10 cohorts of European ancestry (EA) and 5 cohorts of African ancestry (AA). Cases were treated with 3 different antihypertensive medication classes and had blood pressure (BP) above goal (systolic BP ≥ 140 mm Hg and/or diastolic BP ≥ 90 mm Hg) or 4 or more medication classes regardless of BP control ( n EA = 931, n AA = 228). Both a normotensive control group and a treatment-responsive control group were considered in separate analyses. Normotensive controls were untreated ( n EA = 14, 210, n AA = 2, 480) and had systolic BP/diastolic BP < 140/90 mm Hg. Treatment-responsive controls ( n EA = 5, 266, n AA = 1, 817) had BP at goal (<140/90 mm Hg), while treated with one antihypertensive medication class. Individual cohorts used logistic regression with adjustment for age, sex, study site, and principal components for ancestry to examine the association of single-nucleotide polymorphisms with case–control status. Inverse variance-weighted fixed-effects meta-analyses were carried out using METAL. RESULTS: The known hypertension locus, CASZ1, was a top finding among EAs ( P = 1.1 × 10 −8 ) and in the race-combined analysis ( P = 1.5 × 10 −9 ) using the normotensive control group (rs12046278, odds ratio = 0.71 (95% confidence interval: 0.6–0.8)). Single-nucleotide polymorphisms in this locus were robustly replicated in the Million Veterans Program (MVP) study in consideration of a treatment-responsive control group. There were no statistically significant findings for the discovery analyses including treatment-responsive controls. CONCLUSION: This genomic discovery effort for aTRH identified CASZ1 as an aTRH risk locus.