Zhao Qi, Su Shao-yong, Chen Shu-feng, Li Biao, Gu Dong-feng
Division of Population Genetics and Prevention, Cardiovascular Institute and Fuwai Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100037, China.
Chin Med J (Engl). 2006 Jul 5;119(13):1065-71.
Nitric oxide (NO) synthesized by endothelial nitric oxide synthase (eNOS) plays an important role in both the regulation of endothelial function and the control of blood pressure. Up to now, there has been conflicting data regarding the association between three clinically relevant polymorphisms (T-786C, intron4b/a and G894T) of the eNOS gene and essential hypertension.
To examine the contribution of the three eNOS gene polymorphisms to the development of hypertension in the northern Han Chinese, a case-control study including 503 hypertensive cases and 490 age-, gender-, and area-matched controls recruited from the International Collaborative Study of Cardiovascular Disease in Asia (InterASIA) was conducted. Genotyping was performed by polymerase chain reaction (PCR) or PCR-restriction fragment length polymorphism (RFLP).
The T-786C and intron4b/a polymorphisms were observed in significant linkage disequilibrium (D' = 0.87, P < 0.001). The minor allele frequencies of these three polymorphisms in healthy controls were much lower than those of Caucasians (9.3% vs 39.6% - 42.0%, 8.9% vs 15.0% - 16.0% and 10.9% vs 34.5% - 34.9% for -786C, intron4a and 894T, respectively). Genotype distributions and allele frequencies of the three polymorphisms did not differ between cases and controls (all P > 0.05). In addition, none of the eight estimated haplotypes significantly increased or decreased the risk of hypertension before or after adjustment for several known risk factors.
The study results suggest that the three eNOS gene polymorphisms are unlikely to be major genetic susceptibility factors for essential hypertension in the northern Han Chinese population.
由内皮型一氧化氮合酶(eNOS)合成的一氧化氮(NO)在调节内皮功能和控制血压方面均发挥重要作用。迄今为止,关于eNOS基因的三种临床相关多态性(T-786C、内含子4b/a和G894T)与原发性高血压之间的关联,存在相互矛盾的数据。
为了研究这三种eNOS基因多态性对中国北方汉族人群高血压发生的影响,我们进行了一项病例对照研究,纳入了从亚洲心血管疾病国际合作研究(InterASIA)中招募的503例高血压患者和490例年龄、性别及地区匹配的对照。采用聚合酶链反应(PCR)或PCR-限制性片段长度多态性(RFLP)进行基因分型。
观察到T-786C和内含子4b/a多态性处于显著的连锁不平衡状态(D' = 0.87,P < 0.001)。这三种多态性在健康对照中的次要等位基因频率远低于白种人(-786C、内含子4a和894T分别为9.3%对39.6% - 42.0%、8.9%对15.0% - 16.0%以及10.9%对34.5% - 34.9%)。病例组和对照组之间这三种多态性的基因型分布和等位基因频率无差异(所有P > 0.05)。此外,在对几个已知危险因素进行调整前后,八种估计单倍型中没有一种显著增加或降低高血压风险。
研究结果表明,这三种eNOS基因多态性不太可能是中国北方汉族人群原发性高血压的主要遗传易感性因素。