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

Author:

Arfa Imen1,Abid Abdelmajid2,Nouira Sonia3,Elloumi-Zghal Houda1,Malouche Dhafer4,Mannai Imen5,Zorgati Mohamed Majdi1,Ben Alaya Nissaf6,Rebai Ahmed7,Zouari Béchir8,Ben Ammar Slim1,Ben Rayana Mohamed Chiheb2,Hmida Slama9,Blousa-Chabchoub Samira2,Abdelhak Sonia1

Affiliation:

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

2. National Institute of Nutrition, Tunis, Tunisia

3. Molecular Investigation of Genetic Orphan Diseases Research Unit, Institut Pasteur de Tunis. Tunis, Tunisia, sonia.abdelhak @pasteur.rns.tn

4. Engineering school of statistic and information analysis (LEGI-EPT-ESSAIT), University of 7th November at Carthage Tunis, Tunisia

5. Molecular Investigation of Genetic Orphan Diseases Research Unit, Institut Pasteur de Tunis. Tunis, Tunisia, Engineering school of statistic and information analysis (LEGI-EPT-ESSAIT), University of 7th November at Carthage Tunis, Tunisia

6. Laboratory of Epidemiology. Institut Pasteur de Tunis, Tunis, Tunisia

7. Center of Biotechnology Sfax, Tunisia

8. Department of Epidemiology and Statistics, School University of Medicine, Tunis, Tunisia

9. National Center of Blood Transfusion Tunis, Tunisia

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) polymorphis within the ACE gene is likely not associated with diabetic nephropathy nor with type 2 diabetes in the Tunisian studied population.

Publisher

Hindawi Limited

Subject

Endocrinology,Internal Medicine

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