Literature DB >> 24460047

Lack of genetic susceptibility of KCNJ11 E23K polymorphism with risk of type 2 diabetes in an Iranian population.

Parvaneh Keshavarz1, Razie Habibipour, Malaeke Ghasemi, Ehsan Kazemnezhad, Maryam Alizadeh, Mohammad Hasan Hedayati Omami.   

Abstract

AIMS: The KCNJ11 gene has a strong effect on glucose-stimulated insulin secretion. Common polymorphism KCNJ11 E23K has been reported to be associated with type 2 diabetes in various European-descent populations. However, there were inconsistent results in previous studies in Asian populations, and no study has been carried out in the Iranian population. We examined the contribution of KCNJ11 E23K variant in the susceptibility to type 2 diabetes in the Iranian population.
METHODS: We undertook a population-based association study between type 2 diabetes and E23K mutation using 400 people with type 2 diabetes and 420 controls. Genotyping was performed using TaqMan technology on an ABI7300 system.
RESULTS: No significant difference was observed in either genotype distribution (p = 0.71) or allele frequency (p = 0.88) between individuals with and without type 2 diabetes. After adjusting for the confounding effects of age, gender and body mass index (BMI), no significant effect of genotypes on type 2 diabetes was found regarding any genetic models tested (recessive, dominant or co-dominant models). Following subgroup analysis of individuals with and without diabetes based on BMI, a nominal significant association was observed between type 2 diabetes in the presence of obesity and E23K genotype in the recessive model (p = 0.03).
CONCLUSION: The KCNJ11 E23K polymorphism is not associated with genetic susceptibility to type 2 diabetes in the Iranian population; however, it may play a role in disease progression in the presence of obesity.

Entities:  

Keywords:  Association study; E23K; Iranian population; KCNJ11; type two diabetes

Mesh:

Substances:

Year:  2014        PMID: 24460047     DOI: 10.3109/07435800.2013.860607

Source DB:  PubMed          Journal:  Endocr Res        ISSN: 0743-5800            Impact factor:   1.720


  5 in total

1.  The E23K Polymorphism of KCNJ11 and Diabetic Retinopathy in Northern Iran.

Authors:  L Alidoust; F Ajamian; S Abbaspour; A Sharafshah; P Keshavarz
Journal:  Br J Biomed Sci       Date:  2022-04-22       Impact factor: 2.432

2.  Single locus and haplotype association of ENPP1 gene variants with the development of retinopathy among type 2 diabetic patients.

Authors:  Sahar Gohari-Lasaki; Alireza Sharafshah; Saima Abbaspour; Parvaneh Keshavarz
Journal:  Int Ophthalmol       Date:  2020-01-04       Impact factor: 2.031

Review 3.  Role of GNB3, NET, KCNJ11, TCF7L2 and GRL genes single nucleotide polymorphism in the risk prediction of type 2 diabetes mellitus.

Authors:  Saliha Rizvi; Syed Tasleem Raza; Qamar Rahman; Farzana Mahdi
Journal:  3 Biotech       Date:  2016-12-02       Impact factor: 2.406

4.  Association of KCNJ11 rs5219 gene polymorphism with type 2 diabetes mellitus in a population of Syria: a case-control study.

Authors:  Osama Makhzoom; Younes Kabalan; Faizeh Al-Quobaili
Journal:  BMC Med Genet       Date:  2019-06-13       Impact factor: 2.103

Review 5.  KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus.

Authors:  Polin Haghvirdizadeh; Zahurin Mohamed; Nor Azizan Abdullah; Pantea Haghvirdizadeh; Monir Sadat Haerian; Batoul Sadat Haerian
Journal:  J Diabetes Res       Date:  2015-09-13       Impact factor: 4.011

  5 in total

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