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突尼斯杰尔巴岛两个族群中血管紧张素转换酶基因插入/缺失多态性与2型糖尿病的关联

Association of the insertion/deletion polymorphism of the angiotensin-converting enzyme gene with type 2 diabetes in two ethnic groups of Jerba Island in Tunisia.

作者信息

Baroudi Thouraya, Bouhaha Rym, Moran-Moguel Chrystine, Sanchez-Corona Jose, Ben Maiz Hedi, Kammoun Abid Hafaoua, Benammar-Elgaaied Amel

机构信息

Laboratory of Genetics, Immunology and Human Pathology, Faculty of Sciences of Tunis, El Manar II University, 2092 Tunis, Tunisia.

出版信息

J Renin Angiotensin Aldosterone Syst. 2009 Mar;10(1):35-40. doi: 10.1177/1470320309102314.

Abstract

INTRODUCTION

The aim of the current study was to evaluate the role of angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism on the prediction of type 2 diabetes in two ethnic populations from Jerba Island,Tunisia.

METHODS

In this study, we analysed the genotypic and the allelic distributions of the ACE I/D polymorphism and conducted a case/control association study between healthy normoglycaemic controls and diabetic patients in the two studied groups.ACE gene polymorphism was analysed by polymerase chain reaction in 272 individuals consisting of 172 diabetic subjects and 100 controls.

RESULTS

The genotype frequencies for DD, ID and II were 75.50%, 19.60% and 4.89% inArabs and 76.66%, 16.66% and 6.67% in Berbers, respectively, in the case group, and 42.85%, 35.71% and 21.43% inArabs and 57.50%, 22.50% and 20.00% in Berbers, respectively, in the control group.The DD frequency was significantly higher in the case group than in the control group (p<0.001), suggesting that the DD genotype is associated with an increased susceptibility to type 2 diabetes in our study populations.

CONCLUSIONS

The current investigation provides new evidence regarding the role of the ACE I/D polymorphism in the pathogenesis of type 2 diabetes in Jerbian populations. Furthermore, it underlines the importance of ethnicity, which should be considered in all studies aiming to test the genetic effects on the susceptibility to type 2 diabetes.

摘要

引言

本研究的目的是评估血管紧张素转换酶(ACE)插入/缺失(I/D)多态性在预测突尼斯杰尔巴岛两个种族人群2型糖尿病方面的作用。

方法

在本研究中,我们分析了ACE I/D多态性的基因型和等位基因分布,并在两个研究组的健康血糖正常对照组和糖尿病患者之间进行了病例/对照关联研究。通过聚合酶链反应对272名个体进行ACE基因多态性分析,其中包括172名糖尿病患者和100名对照。

结果

病例组中,阿拉伯人的DD、ID和II基因型频率分别为75.50%、19.60%和4.89%,柏柏尔人的分别为76.66%、16.66%和6.67%;对照组中,阿拉伯人的分别为42.85%、35.71%和21.43%,柏柏尔人的分别为57.50%、22.50%和20.00%。病例组的DD频率显著高于对照组(p<0.001),表明在我们的研究人群中,DD基因型与2型糖尿病易感性增加有关。

结论

本研究为ACE I/D多态性在杰尔巴岛人群2型糖尿病发病机制中的作用提供了新证据。此外,强调了种族的重要性,在所有旨在测试基因对2型糖尿病易感性影响的研究中都应予以考虑。

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