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因子V莱顿突变、亚甲基四氢叶酸还原酶及血管紧张素转换酶(插入/缺失)基因突变在成年高血压患者中的联合作用:一项来自土耳其锡瓦斯和恰纳卡莱的基于人群的研究

Combined effect of Factor V Leiden, MTHFR, and angiotensin-converting enzyme (insertion/deletion) gene mutations in hypertensive adult individuals: a population-based study from Sivas and Canakkale, Turkey.

作者信息

Demirel Yeltekin, Dogan Sezai, Uludag Ahmet, Silan Coskun, Atik Sinem, Silan Fatma, Ozdemir Ozturk

机构信息

Department of Family Medicine, Cumhuriyet University, Sivas, Turkey.

出版信息

Genet Test Mol Biomarkers. 2011 Nov;15(11):785-91. doi: 10.1089/gtmb.2011.0044. Epub 2011 Jun 23.

Abstract

BACKGROUND

Hypertension is one of the leading causes of mortality and morbidity in the world, which is influenced by environmental and genetic factors. The methylenetetrahydrofolate reductase (MTHFR) and angiotensin-converting enzymes (ACE) are possible candidate genes that may influence both body fatness and blood pressure (BP). The purpose of this study was to examine the carriage of gene combinations of the ACE (insertion/deletion [I/D]), MTHFR 677T and 1298C, and lipid profiles in patients with essential hypertension (EH) in Turkey.

METHODS

A total of 150 adult individuals (50 hypertensive, 50 first-degree relatives, and 50 healthy controls) from Sivas/Turkey with the same age and gender were assessed for body composition, lipid profiles, resting BP, and gene profiles. Additionally, 149 individuals (99 hypertensive, 50 controls) from Canakkale/Turkey had been investigated for ACE I/D polymorphism. Peripheral blood samples were genotyped using strip assay reverse-hybridization multiplex polymerase chain reaction tests for target genes.

RESULTS

Heterozygous mutation in FV Leiden was found to be higher in the hypertensive and first-degree relatives when compared with the control group (p<0.05). Homozygous DD alleles of the ACE gene were also higher than the ACE I/D and control groups (p<0.05). The high rates of cholesterol and low-density lipoprotein and low rates of high-density lipoprotein were found in patients with EH when compared with the control.

CONCLUSION

Results show that ACE with DD alleles and mutated alleles of FV Leiden and MTHFR genes were significantly different between genotypes and have a combined effect on EH in Turkish population. Further studies are needed to investigate the genetics of obesity, EH, and BP phenotypes in the current adult population.

摘要

背景

高血压是全球死亡和发病的主要原因之一,受环境和遗传因素影响。亚甲基四氢叶酸还原酶(MTHFR)和血管紧张素转换酶(ACE)是可能影响身体脂肪和血压(BP)的候选基因。本研究的目的是检测土耳其原发性高血压(EH)患者中ACE(插入/缺失[I/D])、MTHFR 677T和1298C基因组合的携带情况以及血脂谱。

方法

对来自土耳其锡瓦斯的150名年龄和性别相同的成年个体(50名高血压患者、50名一级亲属和50名健康对照)进行身体成分、血脂谱、静息血压和基因谱评估。此外,对来自土耳其恰纳卡莱的149名个体(99名高血压患者、50名对照)进行了ACE I/D多态性研究。使用针对目标基因的条带分析反向杂交多重聚合酶链反应试验对外周血样本进行基因分型。

结果

与对照组相比,高血压患者和一级亲属中FV Leiden杂合突变率更高(p<0.05)。ACE基因的纯合DD等位基因也高于ACE I/D组和对照组(p<0.05)。与对照组相比,EH患者中胆固醇和低密度脂蛋白水平高,高密度脂蛋白水平低。

结论

结果表明,在土耳其人群中,携带DD等位基因的ACE以及FV Leiden和MTHFR基因的突变等位基因在基因型之间存在显著差异,并且对EH有联合作用。需要进一步研究调查当前成年人群中肥胖、EH和BP表型的遗传学。

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