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突尼斯2型糖尿病患者血管紧张素转换酶基因(I/D)多态性与糖尿病肾病之间无关联。

Lack of association between the angiotensin-converting enzyme gene (I/D) polymorphism and diabetic nephropathy in Tunisian type 2 diabetic patients.

作者信息

Arfa Imen, Abid Abdelmajid, Nouira Sonia, Elloumi-Zghal Houda, Malouche Dhafer, Mannai Imen, Zorgati Mohamed Majdi, Ben Alaya Nissaf, Rebai Ahmed, Zouari Béchir, Ben Ammar Slim, Ben Rayana Mohamed Chiheb, Hmida Slama, Blousa-Chabchoub Samira, Abdelhak Sonia

机构信息

Molecular Investigation of Genetic Orphan Diseases Research Unit, Institut Pasteur de Tunis. Tunis, Tunisia.

出版信息

J Renin Angiotensin Aldosterone Syst. 2008 Mar;9(1):32-6. doi: 10.3317/jraas.2008.002.

Abstract

OBJECTIVE

The aim of the present study was to investigate whether the angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism is associated with diabetic nephropathy and type 2 diabetes in the Tunisian population.

DESIGN

A case-control study was conducted among 141 unrelated type 2 diabetic patients with (90 patients) or without nephropathy (51 patients) and 103 non-diabetic controls with normal fasting blood glucose. Genotyping was performed using a nested polymerase chain reaction amplification in order to identify correctly heterozygous individuals.

RESULTS

The distribution of DD, ID and II genotypes did not significantly differ between type 2 diabetic patients with or without nephropathy (DD: 44%; ID: 46%; II: 10% vs. DD: 41%; ID: 47 %; II: 12%, respectively). There was also no significant statistical difference between the genotype distribution and allele frequencies of the (I/D) polymorphism in all type 2 diabetic subjects compared to non-diabetic controls with normal fasting blood glucose (DD: 43%; ID: 46%; II: 11% vs. DD: 37%; ID: 48%; II: 15%, respectively).

CONCLUSIONS

In the present preliminary study, the (I/D) polymorphism within the ACE gene is likely not associated with diabetic nephropathy nor with type 2 diabetes in the Tunisian studied population.

摘要

目的

本研究旨在调查血管紧张素转换酶(ACE)插入/缺失(I/D)多态性是否与突尼斯人群中的糖尿病肾病及2型糖尿病相关。

设计

对141例无亲缘关系的2型糖尿病患者(其中90例患有肾病,51例未患肾病)以及103例空腹血糖正常的非糖尿病对照者进行了病例对照研究。采用巢式聚合酶链反应扩增进行基因分型,以准确识别杂合个体。

结果

患肾病和未患肾病的2型糖尿病患者之间,DD、ID和II基因型的分布无显著差异(DD分别为44%和41%;ID分别为46%和47%;II分别为10%和12%)。与空腹血糖正常的非糖尿病对照者相比,所有2型糖尿病患者中(I/D)多态性的基因型分布和等位基因频率也无显著统计学差异(DD分别为43%和37%;ID分别为46%和48%;II分别为11%和15%)。

结论

在本初步研究中,ACE基因内的(I/D)多态性可能与突尼斯研究人群中的糖尿病肾病及2型糖尿病均无关。

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