Hou Xu-Wei, Wang Li-Fang, Wang Ningfu, Pang Detang, Hui Bo, Zhou Yu-Ling, He Xiuying
Department of Cardiology, Hangzhou First Municipal Hospital & Hangzhou Hospital, Nanjing Medical University, Hangzhou, China.
Clin Chim Acta. 2008 Feb;388(1-2):200-3. doi: 10.1016/j.cca.2007.11.016. Epub 2007 Nov 29.
Oxidized LDL receptor gene 1 (OLR-1) polymorphism is reportedly associated with several cardiovascular conditions. However, its relationship with essential hypertension remains unknown. The aim of this study is to explore the association of OLR-1 polymorphism at position 501 in the open reading frame (G501C), with the susceptibility of essential hypertension.
2-hundred eighty Chinese essential hypertensive and 284 control subjects were enrolled and genetic study was performed. The clinical data, i.e., sex, age, blood pressure, body mass index, smoking history, lipid profile and serum C-reactive protein concentration in both hypertensives and controls were obtained.
A significant difference in OLR-1 genotype distributions was noted between the hypertensives and the controls (GG: 67.9% vs. 70.8%; GC: 20.0% vs. 23.6%; CC: 12.1% vs. 5.6%, P=0.021). For G and C allele frequencies, the difference between these 2 groups was significant as well (G: 67.5% vs. 23.5%, C: 82.6% vs. 17.4%, P=0.011). Logistic regression analysis revealed that the CC genotype is an independent risk factor for hypertension (OR=3.036, 95% CI: 1.572-6.174, P=0.016). Furthermore, when the serum C-reactive protein concentration in the hypertensive group was studied according to OLR-1 genotypes, the serum CRP concentration in CC homozygous carriers were found significantly higher than that in GC and GG carriers (1.53+/-0.32, 1.31+/-0.32 and 2.94+/-1.29 respectively, P=0.002).
The CC genotype of OLR-1 G501C polymorphism is associated with susceptibility and serum C-reactive protein concentration in Chinese essential hypertensive population.
据报道,氧化型低密度脂蛋白受体基因1(OLR-1)多态性与多种心血管疾病有关。然而,其与原发性高血压的关系尚不清楚。本研究旨在探讨开放阅读框中第501位(G501C)的OLR-1多态性与原发性高血压易感性的关联。
招募了280名中国原发性高血压患者和284名对照受试者,并进行了基因研究。获取了高血压患者和对照者的临床数据,即性别、年龄、血压、体重指数、吸烟史、血脂谱和血清C反应蛋白浓度。
高血压患者和对照者之间的OLR-1基因型分布存在显著差异(GG:67.9%对70.8%;GC:20.0%对23.6%;CC:12.1%对5.6%,P=0.021)。对于G和C等位基因频率,这两组之间的差异也很显著(G:67.5%对23.5%,C:82.6%对17.4%,P=0.011)。逻辑回归分析显示,CC基因型是高血压的独立危险因素(OR=3.036,95%可信区间:1.572-6.174,P=0.016)。此外,根据OLR-1基因型研究高血压组的血清C反应蛋白浓度时,发现CC纯合子携带者的血清CRP浓度显著高于GC和GG携带者(分别为1.53±0.32、1.31±0.32和2.94±1.29,P=0.002)。
OLR-1 G501C多态性的CC基因型与中国原发性高血压人群的易感性和血清C反应蛋白浓度有关。