内皮素-1基因多态性与类风湿关节炎患者高血压相关

Vasileios F Panoulas, Karen M J Douglas, Jacqueline P Smith, Patrick Taffé, Antonios Stavropoulos-Kalinoglou, Tracey E Toms, Moses S Elisaf, Peter Nightingale, George D Kitas
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引用次数: 55

摘要

类风湿性关节炎(RA)与过多的心血管(CV)发病率和死亡率相关。高血压是类风湿性关节炎中非常普遍的一种疾病,它与内皮素-1 (ET-1)基因位点(EDN1)有关,在一些人群中,如非洲-加勒比人、肥胖者和低肾素状态者,但在一般人群中并非如此。高水平的血浆ET-1在RA中被观察到。本研究评估了EDN1基因位点和血清ET-1水平与RA患者高血压的潜在关联。收集397例特征明确的RA患者的基因组DNA和血清样本;在401个没有RA的当地普通人群对照中也可获得DNA。为了探索EDN1的整体相关性,我们选择了两个合适的单核苷酸多态性(SNPs) rs1800541和rss5370,并进行了单倍型分析。采用实时聚合酶链反应(PCR)和熔融曲线分析对两个snp进行鉴定。遗传分析与高血压作为二分类特征和血压指数作为连续变量相关。同时评估RA患者的血清内皮素水平。RA与对照组之间无基因型或单倍型差异。在RA中,分别对每个SNP进行logistic回归分析显示,与GG纯合子相比,rs5370 TT纯合子患高血压的调整后几率增加了三倍(OR = 2.89, 95%CI: 1.02 ~ 8.19)。在对多个潜在混杂因素进行校正后,单倍型分析显示,rs1800541- rss5370 T-T单倍型与高血压存在加性效应(OR = 2.96, 95%CI: 1.28 ~ 6.86;p = 0.011),收缩压(SBP) (β = 6.75 +/- 2.57 mm Hg;p = 0.009),脉压(PP) (beta = 4.37 +/- 2.12 mm Hg;P = .040)。高血压类风湿性关节炎患者中ET-1水平升高的患病率增加,而T-T单倍型携带者中也观察到类似的趋势。携带rs1800541- rss5370 T-T EDN1单倍型的RA患者似乎更有可能患有高血压,同时收缩压和血压升高。这些发现,如果在未来的研究中得到重复,可以用作高血压升高的RA患者的筛查工具,从而增加心血管风险。
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Polymorphisms of the endothelin-1 gene associate with hypertension in patients with rheumatoid arthritis.

Rheumatoid arthritis (RA) associates with excess cardiovascular (CV) morbidity and mortality. Hypertension, a highly prevalent entity in RA, has been associated with the endothelin-1 (ET-1) gene locus (EDN1) in some groups, such as Afro-Caribbean, the obese, and in low-renin states, but not in the general population as a whole. High levels of plasma ET-1 have been observed in RA. This study evaluated the potential association of EDN1 gene locus and serum ET-1 levels with hypertension in patients with RA. Genomic DNA and serum samples were collected from 397 well-characterized RA patients; DNA was also available from 401 local general population controls without RA. To explore the overall relevance of EDN1, two suitable single-nucleotide polymorphisms (SNPs), rs1800541 and rs5370, were selected and haplotype analysis was performed. Both SNPs were identified using real-time polymerase chain reaction (PCR) and melting curve analysis. Genetic analysis was related to hypertension as dichotomous trait and to blood pressure indices as continuous variables. Serum endothelin levels were also assessed in the RA patients. No genotype or haplotype differences were observed between RA and control subjects. Within RA, logistic regression analysis of each SNP separately revealed a threefold increase in the adjusted odds of being hypertensive of rs5370 TT homozygotes compared to GG homozygotes (OR = 2.89, 95%CI: 1.02 to 8.19). After adjustment for multiple potential confounders, haplotype analysis revealed an additive effect of the rs1800541-rs5370 T-T haplotype on hypertension (OR = 2.96, 95%CI: 1.28 to 6.86; p = .011), systolic blood pressure (SBP) (beta = 6.75 +/- 2.57 mm Hg; p = .009), and pulse pressure (PP) (beta = 4.37 +/- 2.12 mm Hg; p = .040). There was an increased prevalence of raised ET-1 levels amongst hypertensive RA patients, whereas a similar trend was observed for T-T haplotype carriers. RA patients who carry the rs1800541-rs5370 T-T EDN1 haplotype appear more likely to be hypertensive with an increased SBP and PP. These findings, if replicated in future studies, could be used as a screening tool for RA patients at increased hypertension, and thus cardiovascular, risk.

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