Literature DB >> 28199472

Resequencing Study Identifies Rare Renin-Angiotensin-Aldosterone System Variants Associated With Blood Pressure Salt-Sensitivity: The GenSalt Study.

Tanika N Kelly1, Changwei Li2, James E Hixson3, Dongfeng Gu4, Dabeeru C Rao5, Jianfeng Huang4, Treva K Rice5, Jichun Chen4, Jie Cao4, Jianxin Li4, Christopher E Anderson1, Jiang He1,6.   

Abstract

BACKGROUND: The role of rare variants in blood pressure (BP) salt-sensitivity is unknown. We conducted a resequencing study of the renin-angiotensin-aldosterone system (RAAS) to identify rare variants associated with BP salt-sensitivity among participants of the Genetic Epidemiology Network of Salt-Sensitivity (GenSalt) study.
METHODS: The GenSalt study was conducted among 1,906 participants who underwent a 7-day low-sodium (51.3 mmol sodium/day) followed by a 7-day high-sodium feeding study (307.8 mmol sodium/day). The 300 most salt-sensitive and 300 most salt-resistant GenSalt participants were selected for the resequencing study. Seven RAAS genes were resequenced using capillary-based sequencing methods. Rare variants were tested for association with BP salt-sensitivity using traditional burden tests. Single-marker analyses were employed to test associations of low-frequency and common variants.
RESULTS: Aggregate rare variant analysis revealed an association of the RAAS pathway with BP salt-sensitivity. Carriers of rare RAAS variants had a 1.55-fold [95% confidence interval (CI): 1.15, 2.10] higher odds of salt-sensitivity compared to noncarriers (P = 0.004), a finding which was significant after Bonferroni correction. A nominal association of the APLN gene with salt-sensitivity was also identified, with rare APLN variants conferring a 2.22-fold (95% CI: 1.05, 6.58) higher odds of salt-sensitivity (P = 0.03). Single-marker analyses did not identify variant-BP salt-sensitivity associations after Bonferroni adjustment. A nominal association of a low-frequency, missense RENBP variant was identified. Each minor allele of rs78377269 conferred a 2.21-fold (95% CI: 1.10, 4.42) increased odds of salt-sensitivity (P = 0.03).
CONCLUSIONS: This study presents of the first evidence of a contribution of rare RAAS variants to BP salt-sensitivity. Clinical Trial RegistryTrial Number: NCT00721721. © American Journal of Hypertension, Ltd 2017. All rights reserved. For Permissions, please email: journals.permissions@oup.com

Entities:  

Keywords:  blood pressure; dietary sodium; genetics; hypertension; rare variants; resequencing; salt sensitivity.

Mesh:

Substances:

Year:  2017        PMID: 28199472      PMCID: PMC5861585          DOI: 10.1093/ajh/hpx004

Source DB:  PubMed          Journal:  Am J Hypertens        ISSN: 0895-7061            Impact factor:   2.689


  35 in total

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4.  Gender difference in blood pressure responses to dietary sodium intervention in the GenSalt study.

Authors:  Jiang He; Dongfeng Gu; Jing Chen; Cashell E Jaquish; Dabeeru C Rao; James E Hixson; Ji-chun Chen; Xiufang Duan; Jian-feng Huang; Chung-Shiuan Chen; Tanika N Kelly; Lydia A Bazzano; Paul K Whelton
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