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

Archive ouverte

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

Edité par CCSD ; SAGE Publications (UK and US) -

International audience. 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.

Suggestions

Du même auteur

Familial aggregation and excess maternal transmission of type 2 diabetes in Tunisia.

Archive ouverte | Arfa, Imen | CCSD

International audience. AIM: To evaluate the degree of familial aggregation of type 2 diabetes mellitus in Tunisia and to investigate transmission patterns of the disease and their relationships with patients' clini...

Evidence for Association of the E23K Variant of KCNJ11 Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis.

Archive ouverte | Lasram, Khaled | CCSD

International audience. Aims. Genetic association studies have reported the E23K variant of KCNJ11 gene to be associated with Type 2 diabetes. In Arab populations, only four studies have investigated the role of thi...

Consanguinity, endogamy, and genetic disorders in Tunisia.

Archive ouverte | Ben Halim, Nizar | CCSD

International audience. Consanguinity refers to marriages between individuals who share at least one common ancestor. In clinical genetics, a consanguineous marriage is defined as a union between two individuals who...

Chargement des enrichissements...