Polymorphism of Uncoupling Protein 2 (UCP2) Gene in Obes People with the Family History of Type 2 Diabetes Mellitus

Authors

  • Tri Setyawati Department of Biochemistry, Faculty of Medicine, Universitas Tadulako, Palu 94119, Indonesia
  • Ryka Marina Walanda Department of Biochemistry, Faculty of Medicine, Universitas Tadulako, Palu 94119, Indonesia
  • Ahmad Hamim Sadewa Department of Biochemistry, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Farmako Yogyakarta 55281, Indonesia
  • Sunarti Department of Biochemistry, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Farmako Yogyakarta 55281, Indonesia

DOI:

https://doi.org/10.48048/tis.2022.2707

Keywords:

Obesity, Type 2 diabetes mellitus, Polymorphism -866G/A UCP2 gene, Genotype, Insulin resistance

Abstract

History with type 2 diabetes mellitus (T2DM) is manifested by the presence of insulin resistance and β-cell dysfunction which prerequisites for T2DM development involving unbalanced energy intake and expenditure. Uncoupling gene protein 2 is the main regulator of energy balance. This study aims to determine the UCP2 -866G/A genetic variation in obese individuals with a family history of T2DM and without a family history of T2DM. The study was a case control design in which the case subjects (n = 60) were obese individuals with a family history of T2DM and control subjects (n = 60) without a family history of T2DM. Polymorphism was analyzed with PCR-RFLP. The value of HOMA-IR and HOMA-β was calculated by the HOMA formula. Data was analyzed by Independent Sample t-test, Mann Whitney U-test, Chi-Square test and Kruskal-Wallis test with a significance level of p < 0.05. The frequency of genotype and alleles in obese individuals with a family history of T2DM and without a history of T2DM did not differ significantly, GA+AA (56.7 %) and A (32.5 %) allele was higher in individuals with a family history of T2DM. The GG+AA genotype in the male group with a family history of T2DM could significantly increase the risk of UCP2 gene polymorphism in T2DM by 2.23 times (CI 95 % 0.64 - 8.14) whereas in the female group there was no risk of T2DM. HOMA-IR and HOMA-β value in both family background did not differ significantly. The value of HOMA-β in the female gender group had significant relationship between obese individuals with a family history of T2DM (p = 0.04). Conclusion: The result suggests obese individuals with a family history of T2DM have a higher risk of getting GA+AA genotypes and A allele than individuals without a family history of T2DM.

HIGHLIGHTS

  • Energy intake that exceeds energy expenditure will cause body fat mass to increase when a state of positive energy balance occurs
  • The genetic component for obesity is associated with relative risks between family relationships and body composition relationships
  • The obese individuals with a family history of T2DM have a higher risk of GA + AA genotype and A allele than individuals without a family history of T2DM


GRAPHICAL ABSTRACT

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

S Rousset, MC Alves-Guerra, J Mozo, B Miroux, AM Cassard-Doulcier, F Bouillaud and D Ricquier. The biology of mitochondrial uncoupling proteins. Diabetes 2004; 53, S130-S135.

K Kesehatan. Pokok-pokok hasil Riskesdas 2013. Badan Litbang Kesehatan, Jakarta, Indonesia, 2014.

F Eyzaguirre and V Mericq. Insulin resistance markers in children. Horm. Res. Paediat. 2009; 71, 65-74.

F Abbasi, BW Brown, C Lamendola, T McLaughlin and GM Reaven. Relationship between obesity, insulin resistance, and coronary heart disease risk. J. Am. Coll. Cardiol. 2002; 40, 937-43.

Y Song, JE Manson, L Tinker, BV Howard, LH Kuller, L Nathan, N Rifai and S Liu. Insulin sensitivity and insulin secretion determined by homeostasis model assessment and risk of diabetes in a multiethnic cohort of women: The women’s health initiative observational study. Diabetes Care 2007; 30, 1747-52.

S Oktavianthi, H Trimarsanto, CA Febinia, K Suastika, MR Saraswati, P Dwipayana, W Arindrarto, H Sudoyo and SG Malik. Uncoupling protein 2 gene polymorphisms are associated with obesity. Cardiovasc. Diabetol. 2012; 11, 41.

MV Jali, S Kambar, SM Jali and S Gowda. Familial early onset of type-2 diabetes mellitus and its complications. N. Am. J. Med. Sci. 2009; 1, 377-80.

BMD Souza, M Michels, DA Sortica, AP Bouças, J Rheinheimer, MP Buffon, AC Bauer, LH Canani and D Crispim. Polymorphisms of the UCP2 gene are associated with glomerular filtration rate in type 2 diabetic patients and with decreased UCP2 gene expression in human kidney. PLos One 2015; 10, e0132938.

M D’ Adamo, L Perego, M Cardellini, MA Marini, S Frontoni, F Andreozzi, A Sciacqua, D Lauro, P Sbraccia, M Federico, M Paganelli, AE Pontiroli, R Lauro, F Perticone, F Folli and G Sesti. The -866A/A genotype in the promoter of the human uncoupling protein 2 gene is associated with insulin resistance and increased risk of type 2 diabetes. Diabetes 2004; 53, 1905-10.

CB Chan, MC Saleh, V Koshkin and MB Wheeler. Uncoupling protein 2 and islet function. Diabetes 2004; 53, S136-S142.

C Erlanson-Albertsson. The role of uncoupling proteins in the regulation of metabolism. Acta Physiol. Scand. 2003; 178, 405-12.

CY Zhang, G Baffy, P Perret, S Krauss, O Peroni, D Grujic, T Hagen, AJ Vidal-Puig, O Boss, YB Kim, XX Zheng, MB Wheeler, GI Shulman, CB Chan and BB Lowell. Uncoupling protein-2 negatively regulates insulin secretion and is a major link between obesity, beta cell dysfunction, and type 2 diabetes. Cell 2001; 105, 745-55.

M Sasahara, M Nishi, H Kawashima, K Ueda, S Sakagashira, H Furuta, E Matsumoto, T Hanabusa, H Sasaki and K Nanjo. Uncoupling protein 2 promoter polymorphism -866G/A affects its expression in -cells and modulates clinical profiles of Japanese type 2 diabetic patients. Diabetes 2004; 53, 482-5.

G Sesti, M Cardellini, MA Marini, S Frontoni, M D’Adamo, SD Guerra, D Lauro, PD Nicolais, P Sbraccia, SD Prato, S Gambardella, M Federici, P Marchetti and R Lauro. A common polymorphism in the promoter of UCP2 contributes to the variation in insulin secretion in glucose-tolerant subjects. Diabetes 2003; 52, 1280-3.

R Irum, G Qureshi, A Dilawar, R Khurshid and S Khawar. Beta cell function: A useful measure of insulin resistance in adolescent with polycystic ovarian disease. Ann. King Edward Med. Univ. 2016; 22, 202-6.

The InterAct Consortium. The link between family history and risk of type 2 diabetes is not explained by anthropometric, lifestyle or genetic risk factors: The EPIC-InterAct study. Diabetologia 2013; 56, 60-9.

S Hurrle and WH Hsu. The etiology of oxidative stress in insulin resistance. Biomed. J. 2017; 40, 257-62.

M Zhou, S He, F Ping, W Li, L Zhu, X Cui, L Feng, X Zhao, H Zhang, Y Li and Q Sun. Uncoupling protein 2 and peroxisome proliferator-activated receptor γ gene polymorphisms in association with diabetes susceptibility in Chinese Han population with variant glucose tolerance. Int. J. Endocrinol. 2018; 2018, 4636783.

D Zhang, A Chen and Y Gu. Ruptured secondary abdominal pregnancy after primary laparoscopic treatment for tubal pregnancy: A case report. Medicine 2017; 96, e9254.

Downloads

Published

2022-02-15

How to Cite

Setyawati, T. ., Walanda, R. M. ., Sadewa, A. H. ., & Sunarti, S. (2022). Polymorphism of Uncoupling Protein 2 (UCP2) Gene in Obes People with the Family History of Type 2 Diabetes Mellitus. Trends in Sciences, 19(5), 2707. https://doi.org/10.48048/tis.2022.2707