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Naturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion.


ABSTRACT:

Objectives

We aimed to determine whether the common variation at the chromogranin A (CHGA) locus increases susceptibility to hypertension.

Background

CHGA regulates catecholamine storage and release. Previously we systematically identified genetic variants across CHGA.

Methods

We carried out dense genotyping across the CHGA locus in >1,000 individuals with the most extreme blood pressures (BPs) in the population, as well as twin pairs with autonomic phenotypes. We also characterized the function of a trait-associated 3'-untranslated region (3'-UTR) variant with transfected CHGA 3'-UTR/luciferase reporter plasmids.

Results

CHGA was overexpressed in patients with hypertension, especially hypertensive men, and CHGA predicted catecholamines. In individuals with extreme BPs, CHGA genetic variants predicted BP, especially in men, with a peak association occurring in the 3'-UTR at C+87T, accounting for up to approximately 12/ approximately 9 mm Hg. The C+87T genotype predicted CHGA secretion in vivo, with the +87T allele (associated with lower BP) also diminishing plasma CHGA by approximately 10%. The C+87T 3'-UTR variant also predicted the BP response to environmental (cold) stress; the same allele (+87T) that diminished basal BP in the population also decreased the systolic BP response to stress by approximately 12 mm Hg, and the response was smaller in women (by approximately 6 mm Hg). In a chromaffin cell-transfected CHGA 3'-UTR/luciferase reporter plasmid, the +87T allele associated with lower BP also decreased reporter expression by approximately 30%. In cultured chromaffin cells, reducing endogenous CHGA expression by small interfering ribonucleic acid caused approximately two-thirds depletion of catecholamine storage vesicles.

Conclusions

Common variant C+87T in the CHGA 3'-UTR is a functional polymorphism causally associated with hypertension especially in men of the population, and we propose steps ("intermediate phenotypes") whereby in a sex-dependent fashion this genetic variant influences the ultimate disease trait. These observations suggest new molecular strategies to probe the pathophysiology, risk, and rational treatment of hypertension.

SUBMITTER: Chen Y 

PROVIDER: S-EPMC2659417 | biostudies-literature | 2008 Oct

REPOSITORIES: biostudies-literature

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Publications

Naturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion.

Chen Yuqing Y   Rao Fangwen F   Rodriguez-Flores Juan L JL   Mahata Manjula M   Fung Maple M MM   Stridsberg Mats M   Vaingankar Sucheta M SM   Wen Gen G   Salem Rany M RM   Das Madhusudan M   Cockburn Myles G MG   Schork Nicholas J NJ   Ziegler Michael G MG   Hamilton Bruce A BA   Mahata Sushil K SK   Taupenot Laurent L   O'Connor Daniel T DT  

Journal of the American College of Cardiology 20081001 18


<h4>Objectives</h4>We aimed to determine whether the common variation at the chromogranin A (CHGA) locus increases susceptibility to hypertension.<h4>Background</h4>CHGA regulates catecholamine storage and release. Previously we systematically identified genetic variants across CHGA.<h4>Methods</h4>We carried out dense genotyping across the CHGA locus in >1,000 individuals with the most extreme blood pressures (BPs) in the population, as well as twin pairs with autonomic phenotypes. We also char  ...[more]

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