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尼日利亚南部两个城市居民中血管紧张素转换酶基因插入/缺失多态性与高血压风险

Insertion/deletion polymorphism of the angiotensin-converting enzyme gene and the risk of hypertension among residents of two cities, South-South Nigeria.

作者信息

Kooffreh Mary Esien, Anumudu Chiaka Ijeoma, Kumar P Lava

机构信息

Department of Genetics and Biotechnology, University of Calabar, Calabar, Cross River, Nigeria.

Department of Zoology, University of Ibadan, Ibadan, Oyo, Nigeria.

出版信息

Adv Biomed Res. 2014 May 28;3:118. doi: 10.4103/2277-9175.133184. eCollection 2014.

Abstract

BACKGROUND

Hypertension is a public health challenge due to its high prevalence, and is a major risk factor for cardiovascular diseases. This study was designed to determine the frequency of the I/D polymorphism of the angiotensin-converting enzyme gene and its association with hypertension in a sample population of Calabar and Uyo, South-South Nigeria.

MATERIALS AND METHODS

A population-based case control design consisting of total of 1224 participants, 612 each of patients and controls, were randomly recruited from hypertension clinics and the general population. The I/D polymorphism was investigated using polymerase chain reaction. Multiple regression and odds ratio (OR) was applied to test whether the ID genotypes were predictors of hypertension.

RESULTS

The I/D genotype frequencies were 73(12%), 262(43%) and 277(45%); 74(12%), 303(50%) and 235(38%) for the II, ID, DD genotype in patient and control groups, respectively. A higher frequency of the ID genotype was observed in controls of which 208(61%) were females. By multiple regression analysis, age was a predictor for SBP in patients, r = 0.596, and DBP in controls, r = 0.555. Gender, Body mass index, I/D genotypes were not significant predictors for hypertension but the I/D polymorpism was associated with an increased risk for hypertension with an OR of 1.15 95%CI (0.924-1.456).

CONCLUSION

The I/D polymorphism of the angiotensin-converting enzyme gene was a risk factor for hypertension in the sample population of Calabar and Uyo. This research will form baseline information for subsequent molecular studies in this population.

摘要

背景

高血压因其高患病率成为一项公共卫生挑战,且是心血管疾病的主要风险因素。本研究旨在确定尼日利亚南南地区卡拉巴尔和乌约样本人群中血管紧张素转换酶基因I/D多态性的频率及其与高血压的关联。

材料与方法

采用基于人群的病例对照设计,共招募1224名参与者,其中患者和对照各612名,分别从高血压诊所和普通人群中随机选取。使用聚合酶链反应研究I/D多态性。应用多元回归和比值比(OR)来检验ID基因型是否为高血压的预测指标。

结果

患者组和对照组中,II、ID、DD基因型的I/D基因型频率分别为73(12%)、262(43%)和277(45%);74(12%)、303(50%)和235(38%)。在对照组中观察到ID基因型频率更高,其中208名(61%)为女性。通过多元回归分析,年龄是患者收缩压的预测指标,r = 0.596,是对照组舒张压的预测指标,r = 0.555。性别、体重指数、I/D基因型不是高血压的显著预测指标,但I/D多态性与高血压风险增加相关,OR为1.15,95%CI(0.924 - 1.456)。

结论

血管紧张素转换酶基因的I/D多态性是卡拉巴尔和乌约样本人群中高血压的一个风险因素。本研究将为该人群后续的分子研究提供基线信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfca/4063107/322edf405f79/ABR-3-118-g001.jpg

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