Preview

Diabetes mellitus

Advanced search

Pathogenetic significance of single nucleotide polymorphisms in the gastric inhibitory polypeptide receptor gene for the development of carbohydrate metabolism disorders in obesity

https://doi.org/10.14341/DM7927

Abstract

Aim. To investigate the association of the GIPR gene polymorphisms rs2302382 and rs8111428 with increased risk of type 2 diabetes mellitus and abdominal obesity.

Materials and methods. The study involved 163 patients with abdominal obesity (BMI, 39.5 ± 8.3 kg/m2; age, 44.7 ± 8.9 years; men, 61; women, 102), 72 with type 2 diabetes mellitus (BMI, 43.70 ± 9.32 kg/m2; age, 46.5 ± 10.1 years; men, 29; women, 43) and 91 patients without carbohydrate metabolism disorders (BMI, 36.13 ± 6.72 kg/m2; age, 43.93 ± 8.35 years; men, 32; women 59). The control group comprised 109 relatively healthy volunteers (BMI, 22.6 ± 2.7 kg/m2; age, 39.5 ± 7.6 years; men, 66; women, 43). Genotypes were analysed by real-time PCR and serum insulin and C-peptide levels were evaluated by ELISA.

Results. The AA genotype in the rs2302382 polymorphism of GIPR was associated with an increased risk for type 2 diabetes mellitus in abdominal obesity and the CA genotype was associated with a reduced risk. In individuals with abdominal obesity and type 2 diabetes mellitus carrying the CA genotype in rs2302382 polymorphism of GIPR, serum insulin and C-peptide levels were elevated to 56.27 mU/L (55.49–58.41 mU/L) and 2.04 ng/ml (1.37–2.85 ng/ml), respectively (p < 0.05). In obese patients with the same genotype and without type 2 diabetes, serum insulin levels and C-peptide levels were 22.73 mU/L (19.07–25.76 mU/L) and 0.73 ng/ml (0.53–1.03 ng/ml), respectively (p < 0.05). The GIPR rs8111428 polymorphism was not associated with increased risk of type 2 diabetes mellitus in obesity for any of the groups examined.

Conclusion. Serum insulin and C-peptide levels were increased in patients with abdominal obesity who were carriers of the CA genotype in the rs2302382 polymorphism of GIPR, which is associated with a decreased risk of type 2 diabetes mellitus in obesity compared with the CC genotype.

About the Authors

Daria S. Skuratovskaia
Immanuel Kant Baltic Federal University
Russian Federation
biologist  laboratory immunology and cell
biotechnolog

Competing Interests:

The authors declare that they have no competing interests



Maria A. Vasilenko
Immanuel Kant Baltic Federal University
Russian Federation

junior research assistant laboratory immunology and cell
biotechnolog


Competing Interests:

The authors declare that they have no competing interests



Nikolai S. Fattakhov
Immanuel Kant Baltic Federal University
Russian Federation
PhD-student Laboratory of Immunology and Cell Biotechnologie
Competing Interests:

The authors declare that they have no competing interests



Elena V. Kirienkova
Immanuel Kant Baltic Federal University
Russian Federation

MD, PhD Laboratory of Immunology and Cell Biotechnology


Competing Interests:

The authors declare that they have no competing interests



Natalia I. Mironyuk
Kaliningrad Regional Hospital
Russian Federation

MD, endocrinologist Kaliningrad Regional Hospital


Competing Interests:

The authors declare that they have no competing interests



Pavel A. Zatolokin
Kaliningrad Regional Hospital, Immanuel Kant Baltic Federal University
Russian Federation
MD, Head of Department of Reconstructive and Endoscopic
Surgery

Competing Interests:

The authors declare that they have no competing interests



Larisa S. Litvinova
Immanuel Kant Baltic Federal University
Russian Federation

MD, PhD, Head of Laboratory immunology and cell
biotechnology


Competing Interests: The authors declare that they have no competing interest


References

1. World Health Organization - [cited 2016 May 8]. Available from: http://www.who.int/mediacentre/factsheets/fs312/ru.

2. Polychronakos C, Alriyami M. Diabetes in the post-GWAS era. Nat Genet. 2015;47(12):1373-1374. doi: 10.1038/ng.3453

3. Wu T, Rayner CK, Horowitz M. Incretins. Handb Exp Pharmacol. 2016;233:137-171. doi: 10.1007/164_2015_9

4. Baggio LL, Drucker DJ. Biology of incretins: GLP-1 and GIP. Gastroenterology. 2007;132(6):2131-2157. doi: 10.1053/j.gastro.2007.03.054

5. UniProtKB - [cited 2016 May 8]. Available from: http://www.uniprot.org/uniprot/P48546.

6. Nielsen ST, Janum S, Krogh-Madsen R, et al. The incretin effect in critically ill patients: a case-control study. Crit Care. 2015;19:402. doi: 10.1186/s13054-015-1118-z

7. Al-Sabah S, Al-Fulaij M, Shaaban G, et al. The GIP receptor displays higher basal activity than the GLP-1 receptor but does not recruit GRK2 or arrestin3 effectively. PLoS One. 2014;9(9):e106890. doi: 10.1371/journal.pone.0106890

8. Yabe D, Seino Y. Incretin actions beyond the pancreas: lessons from knockout mice. Curr Opin Pharmacol. 2013;13(6):946-953. doi: 10.1016/j.coph.2013.09.013

9. Vogel CI, Scherag A, Bronner G, et al. Gastric inhibitory polypeptide receptor: association analyses for obesity of several polymorphisms in large study groups. BMC Med Genet. 2009;10:19. doi: 10.1186/1471-2350-10-19

10. Дедов И.И., Шестакова М.В., Галстян Г.Р., и др. Алгоритмы специализированной медицинской помощи больным сахарным диабетом. Под редакцией И.И. Дедова, М.В. Шестаковой (7-й выпуск) // Сахарный диабет. – 2015. – Т. 18. – №1S – C. 1-112. [Dedov II, Shestakova MV, Galstyan GR, et al. Standards of specialized diabetes care. Edited by Dedov I.I., Shestakova M.V. (7th edition). Diabetes mellitus. 2015;18(1S):1-112. (in Russ)] doi: 10.14341/DM20151S1-112

11. Онлайн-калькулятор для расчета отношения шансов – [Onlayn-kal’kulyator dlya rascheta otnosheniya shansov (in Russ)] - [cited 2016 Aug 8]. Available from: http://gen-exp.ru/calculator_or.php

12. Sauber J, Grothe J, Behm M, et al. Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin. Eur J Endocrinol. 2010;163(2):259-264. doi: 10.1530/EJE-10-0444

13. Gogebakan O, Osterhoff MA, Schuler R, et al. GIP increases adipose tissue expression and blood levels of MCP-1 in humans and links high energy diets to inflammation: a randomised trial. Diabetologia. 2015;58(8):1759-1768. doi: 10.1007/s00125-015-3618-4

14. Al-Sabah S. Molecular Pharmacology of the Incretin Receptors. Med Princ Pract. 2016;25 Suppl 1:15-21. doi: 10.1159/000433437

15. Almind K, Ambye L, Urhammer SA, et al. Discovery of amino acid variants in the human glucose-dependent insulinotropic polypeptide (GIP) receptor: the impact on the pancreatic beta cell responses and functional expression studies in Chinese hamster fibroblast cells. Diabetologia. 1998;41(10):1194-1198. doi: 10.1007/s001250051051

16. Al-Sabah S, Al-Fulaij M, Shaaban G, et al. The GIP receptor displays higher basal activity than the GLP-1 receptor but does not recruit GRK2 or arrestin3 effectively. PLoS One. 2014;9(9):e106890. doi: 10.1371/journal.pone.0106890

17. Fortin JP, Schroeder JC, Zhu Y, et al. Pharmacological characterization of human incretin receptor missense variants. J Pharmacol Exp Ther. 2010;332(1):274-280. doi: 10.1124/jpet.109.160531


Supplementary files

Review

For citations:


Skuratovskaia D.S., Vasilenko M.A., Fattakhov N.S., Kirienkova E.V., Mironyuk N.I., Zatolokin P.A., Litvinova L.S. Pathogenetic significance of single nucleotide polymorphisms in the gastric inhibitory polypeptide receptor gene for the development of carbohydrate metabolism disorders in obesity. Diabetes mellitus. 2016;19(6):457-463. (In Russ.) https://doi.org/10.14341/DM7927

Views: 1095


ISSN 2072-0351 (Print)
ISSN 2072-0378 (Online)