Replication of KCNJ11 (p.E23K) and ABCC8 (p.S1369A) Association in Russian Diabetes Mellitus 2 Type Cohort and Meta-Analysis
- PMID: 25955821
- PMCID: PMC4425644
- DOI: 10.1371/journal.pone.0124662
Replication of KCNJ11 (p.E23K) and ABCC8 (p.S1369A) Association in Russian Diabetes Mellitus 2 Type Cohort and Meta-Analysis
Abstract
The genes ABCC8 and KCNJ11 have received intense focus in type 2 diabetes mellitus (T2DM) research over the past two decades. It has been hypothesized that the p.E23K (KCNJ11) mutation in the 11p15.1 region may play an important role in the development of T2DM. In 2009, Hamming et al. found that the p.1369A (ABCC8) variant may be a causal factor in the disease; therefore, in this study we performed a meta-analysis to evaluate the association between these single nucleotide polymorphisms (SNPs), including our original data on the Siberian population (1384 T2DM and 414 controls). We found rs5219 and rs757110 were not associated with T2DM in this population, and that there was linkage disequilibrium in Siberians (D'=0.766, r(2)= 0.5633). In addition, the haplotype rs757110[T]-rs5219[C] (p.23K/p.S1369) was associated with T2DM (OR = 1.52, 95% CI: 1.04-2.24). We included 44 original studies published by June 2014 in a meta-analysis of the p.E23K association with T2DM. The total OR was 1.14 (95% CI: 1.11-1.17) for p.E23K for a total sample size of 137,298. For p.S1369A, a meta-analysis was conducted on a total of 10 studies with a total sample size of 14,136 and pooled OR of 1.14 [95% CI (1.08-1.19); p = 2 x 10-6]. Our calculations identified causal genetic variation within the ABCC8/KCNJ11 region for T2DM with an OR of approximately 1.15 in Caucasians and Asians. Moreover, the OR value was not dependent on the frequency of p.E23K or p.S1369A in the populations.
Conflict of interest statement
Figures
Similar articles
-
Meta-analysis of association of common variants in the KCNJ11-ABCC8 region with type 2 diabetes.Genet Mol Res. 2013 Aug 20;12(3):2990-3002. doi: 10.4238/2013.August.20.1. Genet Mol Res. 2013. PMID: 24065655
-
Association of KCNJ11 and ABCC8 single-nucleotide polymorphisms with type 2 diabetes mellitus in a Kinh Vietnamese population.Medicine (Baltimore). 2022 Nov 18;101(46):e31653. doi: 10.1097/MD.0000000000031653. Medicine (Baltimore). 2022. PMID: 36401380 Free PMC article.
-
Coexpression of the type 2 diabetes susceptibility gene variants KCNJ11 E23K and ABCC8 S1369A alter the ATP and sulfonylurea sensitivities of the ATP-sensitive K(+) channel.Diabetes. 2009 Oct;58(10):2419-24. doi: 10.2337/db09-0143. Epub 2009 Jul 8. Diabetes. 2009. PMID: 19587354 Free PMC article.
-
ATP-dependent potassium channels and type 2 diabetes mellitus.Clin Biochem. 2015 May;48(7-8):476-82. doi: 10.1016/j.clinbiochem.2014.12.026. Epub 2015 Jan 10. Clin Biochem. 2015. PMID: 25583094 Review.
-
Association of Kir6.2 gene rs5219 variation with type 2 diabetes: A meta-analysis of 21,464 individuals.Prim Care Diabetes. 2018 Aug;12(4):345-353. doi: 10.1016/j.pcd.2018.03.004. Epub 2018 Apr 22. Prim Care Diabetes. 2018. PMID: 29685723 Review.
Cited by
-
Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case-control study and meta-analysis.Sci Rep. 2022 Dec 1;12(1):20709. doi: 10.1038/s41598-022-24931-x. Sci Rep. 2022. PMID: 36456687 Free PMC article.
-
Polymorphisms in glucose homeostasis genes are associated with cardiovascular and renal parameters in patients with diabetic nephropathy.Ann Med. 2022 Dec;54(1):3039-3051. doi: 10.1080/07853890.2022.2138531. Ann Med. 2022. PMID: 36314849 Free PMC article.
-
Associations of ATP-Sensitive Potassium Channel's Gene Polymorphisms With Type 2 Diabetes and Related Cardiovascular Phenotypes.Front Cardiovasc Med. 2022 Mar 23;9:816847. doi: 10.3389/fcvm.2022.816847. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 35402560 Free PMC article.
-
Drug Discovery of Plausible Lead Natural Compounds That Target the Insulin Signaling Pathway: Bioinformatics Approaches.Evid Based Complement Alternat Med. 2022 Mar 20;2022:2832889. doi: 10.1155/2022/2832889. eCollection 2022. Evid Based Complement Alternat Med. 2022. PMID: 35356248 Free PMC article. Review.
-
Identifying the association between single nucleotide polymorphisms in KCNQ1, ARAP1, and KCNJ11 and type 2 diabetes mellitus in a Chinese population.Int J Med Sci. 2020 Aug 29;17(15):2379-2386. doi: 10.7150/ijms.48072. eCollection 2020. Int J Med Sci. 2020. PMID: 32922204 Free PMC article.
References
-
- Health at a Glance: Europe: 2012. OECD Publishing; 2012. 10.1787/9789264183896-en Available: http://www.oecd-ilibrary.org/social-issues-migration-health/health-at-a-.... - DOI
-
- Ashfield R, Ashcroft SJ. Cloning of the promoters for the beta-cell ATP-sensitive K-channel subunits Kir6.2 and SUR1. Diabetes. 1998; 47: 1274–1280. - PubMed
-
- Clement JP, Kunjilwar K, Gonzalez G, Schwanstecher M, Panten U, Aguilar-Bryan L, et al. Association and stoichiometry of K(ATP) channel subunits. Neuron. 1997; 18: 827–838. - PubMed
-
- Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, et al. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science. 1995; 268: 426–429. - PubMed
-
- Thomas P, Ye Y, Lightner E. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet. 1996; 5: 1809–1812. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous
