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Genetic variation in C-reactive protein in ethnic Chinese population in Taiwan

机译:台湾华裔人口C反应蛋白的遗传变异

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Background: High-sensitivity C-reactive protein (hs-CRP) is a sensitive inflammatory marker suggested for cardiovascular risk stratification. This study aimed to assess the potential genetic determinants for serum hs-CRP levels in a cohort with well-controlled nondiabetic hypertension. Materials and methods: Ethnic Chinese nondiabetic hypertensive patients were enrolled in Taiwan. They received comprehensive evaluation including history taking, physical check-up, blood pressure (BP) measurement, 24-h ambulatory BP monitoring and blood sampling. Serum hs-CRP levels were determined. CRP genotyping was performed in two stages. In the first stage, 4 single-nucleotide polymorphisms (SNPs) of CRP including rs1572970, rs2794520, rs3093077 and rs2808630 were investigated in the 400 participants. In the second stage, only SNPs significant in the first stage were selected for complete genotyping in the whole population. Results: Total 915 consecutive patients (40·9 ± 7·3 years, 68·3% male) completed the study. Two of the 4 SNPs including rs1572970 and rs3093077 were correlated to hs-CRP levels in the whole population. Stepwise multiple linear regression indicated that age (P = 0·001), body mass index (P < 0·001), waist-hip ratio (P = 0·032), smoking habits (P = 0·001), night-time systolic BP (P = 0·040), total cholesterol (P = 0·005) and CRP rs3093077 polymorphism (P < 0·001) were independently associated with serum hs-CRP levels. Overall, genetic correlates explained 2·4%, BMI explained 11·9% and all other clinical correlates explained 4·8% of interindividual variability in serum hs-CRP level. Conclusion: C-reactive protein genotype contributed limitedly to serum hs-CRP levels in subjects with well-controlled hypertension, suggesting the impacts of clinical rather than genetic determinants to serum hs-CRP levels for cardiovascular risk stratification in this intermediate-risk Taiwanese cohort.
机译:背景:高敏C反应蛋白(hs-CRP)是一种敏感的炎症标志物,提示可用于心血管疾病危险分层。这项研究旨在评估在控制良好的非糖尿病性高血压人群中血清hs-CRP水平的潜在遗传决定因素。资料与方法:台湾非华裔非糖尿病高血压患者入组。他们接受了综合评估,包括历史记录,身体检查,血压(BP)测量,24小时动态血压监测和血液采样。测定血清hs-CRP水平。 CRP基因分型分两个阶段进行。在第一阶段,在400名参与者中研究了4种CRP的单核苷酸多态性(SNP),包括rs1572970,rs2794520,rs3093077和rs2808630。在第二阶段,仅选择在第一阶段重要的SNP进行整个人群的完整基因分型。结果:总共915名患者(40·9±7·3岁,男性68·3%)完成了研究。 rs1572970和rs3093077这4个SNP中的两个与整个人群中的hs-CRP水平相关。逐步多元线性回归表明年龄(P = 0·001),体重指数(P <0·001),腰臀比(P = 0·032),吸烟习惯(P = 0·001),夜间收缩压时间(P = 0·040),总胆固醇(P = 0·005)和CRP rs3093077多态性(P <0·001)与血清hs-CRP水平独立相关。总体而言,遗传相关因素解释了2·4%,BMI解释了11·9%,所有其他临床相关因素解释了血清hs-CRP水平个体间差异的4·8%。结论:C反应蛋白基因型在控制良好的高血压患者中对血清hs-CRP水平的贡献有限,这表明在这一中度风险台湾人群中,临床而非基因决定因素对血清hs-CRP水平对心血管风险分层的影响。

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