Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension.

Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension.
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DOI:
10.2217/pgs.09.101
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发表时间:
2009-11
期刊:
影响因子:
2.1
通讯作者:
McCarty CA
McCarty CA
中科院分区:
医学4区
文献类型:
--
作者:
Wilke RA;Simpson RU;Mukesh BN;Bhupathi SV;Dart RA;Ghebranious NR;McCarty CA

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我们检验了维生素D依赖性信号传导的遗传变异与高血压患者充血性心力衰竭相关的假设。从CYP 27 B1、CYP 24 A1、VDR、REN和ACE五个候选基因中筛选出功能多态性。使用马什菲尔德诊所个性化医学研究项目,我们对205名高血压和充血性心力衰竭患者、206名单纯高血压患者和206名对照者(按年龄和性别匹配频率)进行基因分型。在高血压背景下,CYP 27 B1中的SNP与充血性心力衰竭相关(优势比:C等位基因纯合子受试者为2.14; 95% CI:1.05-4.39)。维生素D生物合成的遗传变异与心力衰竭风险增加有关。
We tested the hypothesis that genetic variation in vitamin D-dependent signaling is associated with congestive heart failure in human subjects with hypertension. Functional polymorphisms were selected from five candidate genes: CYP27B1, CYP24A1, VDR, REN and ACE. Using the Marshfield Clinic Personalized Medicine Research Project, we genotyped 205 subjects with hypertension and congestive heart failure, 206 subjects with hypertension alone and 206 controls (frequency matched by age and gender). In the context of hypertension, a SNP in CYP27B1 was associated with congestive heart failure (odds ratio: 2.14 for subjects homozygous for the C allele; 95% CI: 1.05–4.39). Genetic variation in vitamin D biosynthesis is associated with increased risk of heart failure.
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