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黎巴嫩患者样本中血管紧张素转换酶插入/缺失基因多态性与高血压之间的关联。

Association between angiotensin-converting enzyme insertion/deletion genetic polymorphism and hypertension in a sample of Lebanese patients.

作者信息

Akra-Ismail Maya, Makki Rajaa Fakhoury, Chmaisse Hania Nakkash, Kazma Alia, Zgheib Nathalie Khoueiry

机构信息

Facultie of Biochemistry, Beirut Arab University, Beirut, Lebanon.

出版信息

Genet Test Mol Biomarkers. 2010 Dec;14(6):787-92. doi: 10.1089/gtmb.2010.0096. Epub 2010 Oct 12.

DOI:10.1089/gtmb.2010.0096
PMID:20939740
Abstract

BACKGROUND/AIM: several studies have looked at the potential link between angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism and the risk of hypertension and have shown that the DD polymorphism may be associated with a higher prevalence of hypertension. Our objective was to assess for possible association between ACE variants and hypertension in a sample of Lebanese patients.

METHODS

one hundred ninety-two Lebanese subjects were included. DNA was isolated and amplified by polymerase chain reaction. The products were identified by gel electrophoresis according to their size.

RESULTS

one hundred fifteen (59.9%) patients were hypertensive and 77 (40.1%) were nonhypertensive with the following genotype frequencies: 43.4% DD, 45.2% ID, and 11.4% II compared with 35.2% DD, 51.9% ID, and 12.9% II, respectively. Age was found to be the most significant risk factor for hypertension. This was more prominent when accounting for ACE genotype; for instance, the DD genotype with age had a significantly higher odds ratio (OR = 11.852; p = 0.001) than the ID genotype with age (OR = 4.599; p = 0.006), II genotype with age (OR = 1.866; p = 0.519), and age alone (OR = 5.558; p = 0.006).

CONCLUSION

our results show that the ACE I/D polymorphism is common in Lebanon, and the combinations of ACE D allele and age is associated with an increased risk of hypertension.

摘要

背景/目的:多项研究探讨了血管紧张素转换酶(ACE)插入/缺失(I/D)多态性与高血压风险之间的潜在联系,结果表明DD多态性可能与高血压的较高患病率相关。我们的目的是评估黎巴嫩患者样本中ACE基因变异与高血压之间可能存在的关联。

方法

纳入192名黎巴嫩受试者。通过聚合酶链反应分离并扩增DNA。根据产物大小通过凝胶电泳进行鉴定。

结果

115名(59.9%)患者患有高血压,77名(40.1%)为非高血压患者,其基因型频率如下:DD为43.4%,ID为45.2%,II为11.4%;相比之下,非高血压患者中DD为35.2%,ID为51.9%,II为12.9%。年龄被发现是高血压最显著的危险因素。在考虑ACE基因型时这一点更为突出;例如,DD基因型与年龄相关的优势比(OR = 11.852;p = 0.001)显著高于ID基因型与年龄相关的优势比(OR = 4.599;p = 0.006)、II基因型与年龄相关的优势比(OR = 1.866;p = 0.519)以及单独年龄相关的优势比(OR = 5.558;p = 0.006)。

结论

我们的结果表明,ACE I/D多态性在黎巴嫩很常见,ACE D等位基因与年龄的组合与高血压风险增加相关。

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