Rodríguez-Esparragón Francisco J, Rodríguez-Pérez José C, Macías-Reyes Antonio, Alamo-Santana Fayna
Research Unit, Hospital de Gran Canaria Dr Negrín, Universidad de Las Palmas de Gran Canaria, Las Palmas de Gran Canaria, Spain.
J Hypertens. 2003 Sep;21(9):1649-55. doi: 10.1097/01.hjh.0000084719.53355.20.
Peroxisome proliferator-activated receptor-gamma2 (PPARgamma2) belongs to the family of the nuclear hormone receptors and has been recently implicated in vascular biology. PPARgamma2(Pro12Ala) gene polymorphism is associated with obesity, body mass index and diabetes mellitus. The endothelial nitric oxide synthase (eNOS) (4a/b) gene polymorphism contributes to coronary heart disease and hypertension risk. We tested whether both polymorphic variants were associated with hypertension risk, and their inter-relationship with plasma homocysteine.
A case-control study was conducted selecting 235 subjects with arterial hypertension and 223 normotensive matched controls.
Genotyping for the PPARgamma2(Pro12Ala) and the eNOS(4a/b) were performed by mutagenically separated polymerase chain reaction and by polymerase chain reaction. Glucose, lipid profile, plasma creatinine, homocysteine and microalbuminuria were measured. RESULTS We found a significant contribution of the PPARgamma2(Pro12Ala) and eNOS(4a/b) gene polymorphisms to hypertensive risk in our population (odds ratio, 1.9 and 1.6, respectively), confirmed by multiple logistic regression analysis. Those subjects with normal plasma homocysteine values had an increased hypertensive risk with an odds ratio of 2.6 for the PP genotype of the PPARgamma2 gene and an odds ratio of 1.8 for the a allele of the eNOS gene.
Both analyzed polymorphisms were associated in a synergistic manner with hypertension. This effect manifested only in those subjects with normal homocysteine plasma values. Our findings suggest complex genotype-environmental interactions on hypertensive risk.
过氧化物酶体增殖物激活受体γ2(PPARγ2)属于核激素受体家族,最近被认为与血管生物学有关。PPARγ2(Pro12Ala)基因多态性与肥胖、体重指数和糖尿病有关。内皮型一氧化氮合酶(eNOS)(4a/b)基因多态性会增加冠心病和高血压风险。我们测试了这两种多态性变体是否与高血压风险相关,以及它们与血浆同型半胱氨酸的相互关系。
进行一项病例对照研究,选取235名动脉高血压患者和223名血压正常的匹配对照。
通过诱变分离聚合酶链反应和聚合酶链反应对PPARγ2(Pro12Ala)和eNOS(4a/b)进行基因分型。测量血糖、血脂、血浆肌酐、同型半胱氨酸和微量白蛋白尿。结果:我们发现PPARγ2(Pro12Ala)和eNOS(4a/b)基因多态性对我们研究人群的高血压风险有显著影响(优势比分别为1.9和1.6),多元逻辑回归分析证实了这一点。血浆同型半胱氨酸值正常的受试者患高血压的风险增加,PPARγ2基因PP基因型的优势比为2.6,eNOS基因a等位基因的优势比为1.8。
两种分析的多态性与高血压呈协同关联。这种效应仅在同型半胱氨酸血浆值正常的受试者中表现出来。我们的研究结果表明高血压风险存在复杂的基因型-环境相互作用。