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首页> 外文期刊>Human Biology: Official Publication of the Human Biology Council >Angiotensin converting enzyme gene polymorphism (insertion/deletion) and hypertension in adult Asian Indians: a population-based study from Calcutta, India.
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Angiotensin converting enzyme gene polymorphism (insertion/deletion) and hypertension in adult Asian Indians: a population-based study from Calcutta, India.

机译:亚洲成年印度人的血管紧张素转换酶基因多态性(插入/缺失)和高血压:来自印度加尔各答的一项基于人群的研究。

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摘要

The angiotensin converting enzyme (ACE) gene insertion/deletion polymorphism has been identified as a potential genetic risk factor for essential hypertension. The purpose of the present study is to investigate the association of the insertion/deletion polymorphism of the ACE gene with essential hypertension in adult Asian Indians. Three hundred fifty (184 males and 166 females) adult (30 years and older) Asian Indians of Calcutta and its suburbs participated in this population-based cross-sectional study. Anthropometric measures, lipids profiles, blood glucose, and blood pressure measures were collected from participants. ACE insertion/deletion polymorphism was determined by agarose gel electrophoresis and D/D typing was further reconfirmed using insertion-allele-specific amplification. Essential hypertension was defined as a systolic blood pressure (SBP) greater than 160 mm Hg and/or a diastolic blood pressure (DBP) greater than 90 mm Hg or use of any antihypertensive treatment by participants. Significantly higher SBP, DBP, and mean arterial pressure were recorded in D/D subjects compared to I/I and I/D subjects. We also observed that the odds of being hypertensive were 7.483 (95% CI = 1.746, 30.192) in D/D individuals compared to those carrying one or no D alleles. This finding suggests that ACE insertion/deletion polymorphism is associated with essential hypertension in Asian Indians. Moreover, individuals who are homozygous for the D allele of the ACE gene are more likely to have essential hypertension.
机译:血管紧张素转换酶(ACE)基因的插入/缺失多态性已被确定为原发性高血压的潜在遗传危险因素。本研究的目的是调查成人亚洲印第安人中ACE基因的插入/缺失多态性与原发性高血压的关系。加尔各答及其郊区的三百五十名(184名男性和166名女性)成人(30岁及以上)亚洲印第安人参加了这项基于人口的横断面研究。从参与者那里收集人体测量指标,脂质分布,血糖和血压指标。 ACE插入/缺失多态性通过琼脂糖凝胶电泳确定,并使用插入等位基因特异性扩增进一步确认D / D分型。原发性高血压定义为收缩压(SBP)大于160毫米汞柱和/或舒张压(DBP)大于90毫米汞柱或参与者使用任何降压治疗。与I / I和I / D受试者相比,D / D受试者的SBP,DBP和平均动脉压明显更高。我们还观察到,与携带一个或没有D个等位基因的人相比,D / D个体中高血压的几率是7.483(95%CI = 1.746,30.192)。这一发现表明,ACE插入/缺失多态性与亚洲印第安人的原发性高血压有关。而且,ACE基因的D等位基因纯合的个体更有可能患有原发性高血压。

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