Abstract

The aim of this study is to investigate the insulin-like growth factor type 2 (IGF2R) gene and circulating soluble IGF2R in relation to type 2 diabetes (T2DM). Six hundred fifty-four subjects without history of diabetes were screened for diabetes by oral glucose tolerance test. In addition, 145 subjects with known diabetes were recruited from a local diabetes clinic. Circulating IGF2R levels were measured by ELISA method; plasma glucose was measured by colorimetric method; insulin levels were determined by chemiluminescent method; IGF2R gene rs416572 was genotyped using real-time PCR. The distributions of IGF2R genotypes were 69.2% CC, 27.8% CT, and 3.0% TT. The C allele was more commonly found in diabetes subjects, with a significant difference (P < 0.01). In the presence of the T allele, circulating IGF2R levels were significantly lower (P < 0.05). There was no significant difference in other potential confounders including age, sex, and BMI. Only circulating IGF2R, age, and BMI were independently associated with the degree of insulin resistance, as assessed by the HOMA model. It was found that age, sex, and BMI were associated with beta cell function. In conclusion, IGF2R gene polymorphism and circulating IGF2R are associated with T2DM.

Highlights

  • The insulin-like growth factor (IGF) system and its binding proteins play important roles in a number of biological processes, including growth and development as well as energy homeostasis

  • We further explored the influence of both IGF type 2 receptor (IGF2R) gene polymorphism and IGF2R levels on insulin resistance as assessed by the homeostatic model assessment (HOMA) model

  • We have identified a genetic variant in IGF2R, another protein in the IGF system, as being associated with T2DM in Thais

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Summary

Introduction

The insulin-like growth factor (IGF) system and its binding proteins play important roles in a number of biological processes, including growth and development as well as energy homeostasis. A soluble form of IGF2R exists in the circulation and has been found to be related to body size in term infants [7]. Taken together, this suggests the importance of IGF2R in the pathogenesis of disorders related to glucose and energy metabolism. Whether circulating IGF2R is determined by IGF2R gene variants and how soluble IGR2R is related to diabetes in adults are currently unknown. It is the purpose of the present study to investigate the IGF2R gene and circulating soluble IGF2R in relation to T2DM in adults

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