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Research Reports

An analysis of the relationship between ABCC8 and KCNJ11 gene polymorphisms and diabetic retinopathy in Turkish population

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Pages 126-132 | Received 16 May 2023, Accepted 06 Feb 2024, Published online: 27 Feb 2024

References

  • Liu NJ, Wu HH, Li YL, Yang Z, Tao XM, Du YP, Wang XC, Lu B, Zhang ZY, Hu RM, et al. An analysis of the association between a polymorphism of KCNJ11 and diabetic retinopathy in a Chinese han population. Eur J Med Res. 2015;20(1):3. doi:10.1186/s40001-014-0075-3.
  • Fong DS, Aiello LP, FL F 3rd, Klein R. Diabetic retinopathy. Diabetes Care. 2004;27(10):2540–53. doi:10.2337/diacare.27.10.2540.
  • Shah CA. Diabetic retinopathy: a comprehensive review. Indian J Med Sci. 2008;62(12):500–19. doi:10.4103/0019-5359.48562.
  • Zhang W, Liu H, Al-Shabrawey M, Caldwell RW, Caldwell RB. Inflammation and diabetic retinal microvascular complications. J Cardiovasc Dis Res. 2011 Apr;2(2):96–103. doi:10.4103/0975-3583.83035.
  • Mounirou BAM, Adam ND, Yakoura AKH, Aminou MSM, Liu YT, Tan LY. Diabetic retinopathy: an overview of treatments. Indian J Endocrinol Metab. 2022;26(2):111–118. doi:10.4103/ijem.ijem_480_21.
  • Hampton BM, Schwartz SG, MA B Jr, HW F Jr. Update on genetics and diabetic retinopathy. Clin Ophthalmol. 2015;9:2175–93. doi:10.2147/OPTH.S94508.
  • Alidoust L, Ajamian F, Abbaspour S, Sharafshah A, Keshavarz P. The E23K Polymorphism of KCNJ11 and diabetic retinopathy in northern Iran. Br J Biomed Sci. 2022;79:10245. doi:10.3389/bjbs.2021.10245.
  • Haghvirdizadeh P, Mohamed Z, Abdullah NA, Haghvirdizadeh P, Haerian MS, Haerian BS. KCNJ11: genetic polymorphisms and risk of diabetes mellitus. J Diabetes Res. 2015;2015:908152. doi:10.1155/2015/908152.
  • Tran NQ, Truong SD, Ma PT, Hoang CK, Le BH, Dinh TTN, Van Tran L, Tran TV, LHG L, KT L, et al. Association of KCNJ11 and ABCC8 single-nucleotide polymorphisms with type 2 diabetes mellitus in a kinh Vietnamese population. Medicine (Baltimore). 2022;101(46):e31653. doi:10.1097/MD.0000000000031653.
  • Wang DD, Chen X, Yang Y, Liu CX. Association of Kir6.2 gene rs5219 variation with type 2 diabetes: a meta-analysis of 21,464 individuals. Prim Care Diabetes. 2018;12(4):345–353. doi:10.1016/j.pcd.2018.03.004.
  • Qin LJ, Lv Y, Huang QY. Meta-analysis of association of common variants in the KCNJ11-ABCC8 region with type 2 diabetes. Genet Mol Res. 2013;12(3):2990–3002. doi:10.4238/2013.August.20.1.
  • Makhzoom O, Kabalan Y, Al-Quobaili F. Association of KCNJ11 rs5219 gene polymorphism with type 2 diabetes mellitus in a population of Syria: a case-control study. BMC Med Genet. 2019;20(1):107. doi:10.1186/s12881-019-0846-3.
  • Li YY. The KCNJ11 E23K gene polymorphism and type 2 diabetes mellitus in the Chinese Han population: a meta-analysis of 6,109 subjects. Mol Biol Rep. 2013;40(1):141–6. doi:10.1007/s11033-012-2042-9.
  • Lu J, Luo Y, Wang J, Hu C, Zhang R, Wang C, Jia W. Association of type 2 diabetes susceptibility loci with peripheral nerve function in a Chinese population with diabetes. J Diabetes Investig. 2017;8(1):115–120. doi:10.1111/jdi.12546.
  • Mota-Zamorano S, González LM, Robles NR, Valdivielso JM, Arévalo-Lorido JC, López-Gómez J, Gervasini G. Polymorphisms in glucose homeostasis genes are associated with cardiovascular and renal parameters in patients with diabetic nephropathy. Ann Med. 2022;54(1):3039–51. doi:10.1080/07853890.2022.2138531.
  • Zhou X, Chen C, Yin D, Zhao F, Bao Z, Zhao Y, Wang X, Li W, Wang T, Jin Y, et al. A variation in the ABCC8 gene is associated with type 2 diabetes mellitus and repaglinide efficacy in Chinese type 2 diabetes mellitus patients. Intern Med. 2019;58(16):2341–2347. doi:10.2169/internalmedicine.2133-18.
  • Venkatesan R, Bodhini D, Narayani N, Mohan V. Association study of the ABCC8 gene variants with type 2 diabetes in south Indians. Indian J Hum Genet. 2014;20(1):37–42. doi:10.4103/0971-6866.132752.
  • Solé X, Guinó E, Valls J, Iniesta R, Moreno V. Snpstats: a web tool for the analysis of association studies. Bioinformatics. 2006;22(15):1928–9. doi:10.1093/bioinformatics/btl268.
  • Gauderman WJ, Mukherjee B, Aschard H, Hsu L, Lewinger JP, Patel CJ, Witte JS, Amos C, Tai CG, Conti D, et al. Update on the state of the science for analytical methods for gene-environment interactions. Am J Epidemiol. 2017;186(7):762–770. doi:10.1093/aje/kwx228.
  • Haghvirdizadeh P, Sadat Haerian M, Haghvirdizadeh P, Sadat Haerian B. ABCC8 genetic variants and risk of diabetes mellitus. Gene. 2014;545(2):198–204. doi:10.1016/j.gene.2014.04.040.
  • Moazzam-Jazi M, Najd-Hassan-Bonab L, Masjoudi S, Tohidi M, Hedayati M, Azizi F, Daneshpour MS. Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case-control study and meta-analysis. Sci Rep. 2022;12(1):20709. doi:10.1038/s41598-022-24931-x.
  • Rastegari A, Rabbani M, Sadeghi HM, Imani EF, Hasanzadeh A, Moazen F. Association of KCNJ11 (E23K) gene polymorphism with susceptibility to type 2 diabetes in Iranian patients. Adv Biomed Res. 2015 Jan;4:1. doi:10.4103/2277-9175.148256.
  • Ko JM, Yang S, Kim SY, Lee HS, Hwang JS, Hwang IT. E23K polymorphism of the KCNJ11 gene in Korean children with type 1 diabetes. World J Pediatr. 2012;8(2):169–72. doi:10.1007/s12519-012-0355-3.
  • Shi WW, Yang Y, Shi Y, Jiang C. K(ATP) channel action in vascular tone regulation: from genetics to diseases. Sheng Li Xue Bao. 2012;64(1):1–13.
  • Şahintürk S, İ̇şbil N. Sıçanlarda Vasküler Tonusun Düzenlenmesinde Potasyum Kanallarının Rolünün İncelenmesi. Uludağ Üniversitesi Tıp Fakültesi Dergisi. 2022;48(3):327–34. doi:10.32708/uutfd.1160369.
  • Rodríguez-Rivera NS, Cuautle-Rodríguez P, Castillo-Nájera F, Molina-Guarneros JA. Identification of genetic variants in pharmacogenetic genes associated with type 2 diabetes in a Mexican-Mestizo population. Biomed Rep. 2017;7(1):21–8. doi:10.3892/br.2017.921. Epub 2017 Jun 2.
  • Zhao C, Wang W, Xu D, Li H, Li M, Wang F. Insulin and risk of diabetic retinopathy in patients with type 2 diabetes mellitus: data from a meta-analysis of seven cohort studies. Diagn Pathol. 2014;9:130. doi:10.1186/1746-1596-9-130.
  • Jingi AM, Tankeu AT, Ateba NA, Noubiap JJ. Mechanism of worsening diabetic retinopathy with rapid lowering of blood glucose: the synergistic hypothesis. BMC Endocr Disord. 2017;17(1):63. doi:10.1186/s12902-017-0213-3.
  • Hansen T, Echwald SM, Hansen L, Møller AM, Almind K, Clausen JO, Urhammer SA, Inoue H, Ferrer J, Bryan J, et al. Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor gene. Diabetes. 1998;47(4):598–605. doi:10.2337/diabetes.47.4.598.
  • Weisnagel SJ, Rankinen T, Nadeau A, Rao DC, Chagnon YC, Pérusse L, Bouchard C. Decreased fasting and oral glucose stimulated C-peptide in nondiabetic subjects with sequence variants in the sulfonylurea receptor 1 gene. Diabetes. 2001;50(3):697–702. doi:10.2337/diabetes.50.3.697.
  • Nielsen DM, Ehm MG, Weir BS. Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus. Am J Hum Genet. 1998 Nov;63(5):1531–40. doi:10.1086/302114.
  • Gonen MS, Arikoglu H, Erkoc Kaya D, Ozdemir H, Ipekci SH, Arslan A, Kayis SA, Gogebakan B. Effects of single nucleotide polymorphisms in K(ATP) channel genes on type 2 diabetes in a Turkish population. Arch Med Res. 2012;43(4):317–23. doi:10.1016/j.arcmed.2012.06.001.

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