Evidence for association of the E23K variant of KCNJ11 gene with type 2 diabetes in Tunisian population: population-based study and meta-analysis
- PMID: 25165692
- PMCID: PMC4140131
- DOI: 10.1155/2014/265274
Evidence for association of the E23K variant of KCNJ11 gene with type 2 diabetes in Tunisian population: population-based study and meta-analysis
Abstract
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 this variant. We aimed to replicate and validate the association between the E23K variant and Type 2 diabetes in Tunisian and Arab populations.
Methods: We have performed a case-control association study including 250 Tunisian patients with Type 2 diabetes and 267 controls. Allelic association has also been evaluated by 2 meta-analyses including all population-based studies among Tunisians and Arabs (2 and 5 populations, resp.).
Results: A significant association between the E23K variant and Type 2 diabetes was found (OR = 1.6, 95% CI = 1.14-2.27, and P = 0.007). Furthermore, our meta-analysis has confirmed the significant role of the E23K variant in susceptibility of Type 2 diabetes in Tunisian and Arab populations (OR = 1.29, 95% CI = 1.15-1.46, and P < 10(-3) and OR = 1.33, 95% CI = 1.13-1.56, and P = 0.001, resp.).
Conclusion: Both case-control and meta-analyses results revealed the significant association between the E23K variant of KCNJ11 and Type 2 diabetes among Tunisians and Arabs.
Figures
References
-
- Gerich JE. The genetic basis of type 2 diabetes mellitus: impaired insulin secretion versus impaired insulin sensitivity. Endocrine Reviews. 1998;19(4):491–503. - PubMed
-
- Bouguerra R, Alberti H, Salem LB, et al. The global diabetes pandemic: the Tunisian experience. European Journal of Clinical Nutrition. 2007;61(2):160–165. - PubMed
-
- Papoz L, Achour N, Henry-Amar M, Ben Khalifa F, Eschwege E, Ben Ayed H. Cross-sectional study of growth between 3 and 20 years in the population of Tunis. Revue d’Epidemiologie et de Sante Publique. 1983;31(1):1–10. - PubMed
-
- James C, Kapoor RR, Ismail D, Hussain K. The genetic basis of congenital hyperinsulinism. Journal of Medical Genetics. 2009;46(5):289–299. - PubMed
-
- Sagen JV, Ræder H, Hathout E, et al. Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy. Diabetes. 2004;53(10):2713–2718. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
