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Licensed Unlicensed Requires Authentication Published by De Gruyter March 19, 2019

Association of IRS1 genetic variants with glucose control and insulin resistance in type 2 diabetic patients from Bosnia and Herzegovina

  • Lejla Mahmutovic EMAIL logo , Tamer Bego , Maria Sterner , Gabriella Gremsperger , Emma Ahlqvist , Zelija Velija Asimi , Besim Prnjavorac , Nour Hamad , Adlija Causevic , Leif Groop and Sabina Semiz

Abstract

Background

Previous studies reported conflicting results regarding association of insulin receptor substrate 1 (IRS1) gene variation with type 2 diabetes (T2D) and insulin resistance (IR) in different ethnic groups. We examined the association of rs7578326, rs2943641, and rs4675095 in the IRS1 gene with T2D and related traits in a population from Bosnia and Herzegovina, which is one of the European countries with the highest T2D prevalence of 12.5%.

Methods

Our study included 390 T2D patients and 252 control subjects. Biochemical parameters, including fasting glucose (FG), fasting insulin (FI), homeostasis model assessment insulin resistance index (HOMA-IR), and HbA1c were measured in all participants. Genotyping analysis was performed by Mass Array Sequenom iPlex platform.

Results

Our results demonstrated that rs7578326 and rs4675095 variants were associated with increased FG levels. The rs7578326 was also associated with higher FI, HOMA-IR (B = 0.08, 95% CI [0.01, 0.15], padd = 0.025; B = 0.079, 95% CI [0.006, 0.150], padd = 0.033, respectively) in T2D, and with HbA1c (B = 0.034, 95% CI [0.003, 0.065], pdom = 0.035) in non-drug-treated T2D. In contrast, rs2943641 C allele was associated with lower FG levels in control subjects (B = −0.17, 95% CI [−0.03, −0.002], padd = 0.030) and HbA1c (B = 0.03, 95% CI [0.002, 0.06], pdom = 0.040) in non-drug-treated T2D.

Conclusions

We report the association between common variants in IRS1 gene with insulin resistance, glucose, and HbA1c levels in Bosnia and Herzegovina’s population.

Acknowledgments

Authors would like to thank medical doctors and paramedical staff from the Clinic of Endocrinology at the Clinical Center University of Sarajevo and General Hospital Tesanj for the recruitment of study subjects. We also acknowledge the invaluable contribution by the individuals who participated in this study. We thank Dr. Fadila Serdarevic and the Association South East European Network for Medical Research-SOVE for statistical consulting. This study was supported by grants from the Council of Ministers of Bosnia and Herzegovina/Ministry of Civil Affairs of Bosnia and Herzegovina, Grant Number: 190/14 and the Federal Ministry of Education and Science of Bosnia and Herzegovina awarded to S.S, Grant Number: 263/13.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: Declaration.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Supplementary Material

The online version of this article offers supplementary material (DOI: https://doi.org/10.1515/dmpt-2018-0031).


Received: 2018-10-17
Accepted: 2019-01-09
Published Online: 2019-03-19

©2019 Walter de Gruyter GmbH, Berlin/Boston

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