Abstract

Uncoupling protein-2 (UCP2) regulates insulin secretion and may play an important role in linking obesity to diabetes type 2 (T2D) that represents a major public health problem in Saudi Arabia. The present study aimed to evaluate the association between the 45-bp insertion/deletion (ins/del) in 3′UTR exon 8 within the UCP2 gene as risk factors in T2D and obesity. This study assessed the body mass index (BMI) in 113 Saudi subjects (46 T2D, 38 obese and 29 healthy controls). The study genotyped for the UCP2 ins/del polymorphism using polymerase chain reaction, evaluated its association with T2D and obesity, and compared its prevalence with those reported for other ethnic populations. The genotype frequencies were 63% for the del/del genotype, 32% for the ins/del genotype and 4% ins/ins genotype. The ANOVA between groups and within groups in T2D, obese, and healthy controls is non-significant (p>0.05). The genotype distributions were figured in-between compared to those ethnic populations reported in the literature. Based on this Saudi study, the genetic variant UCP2 45-bp insertion/deletion do not influence T2D and obesity risks. These results were similar, but the insertion allele was modest relative to other ethnic populations.

Highlights

  • Production and hosting by ElsevierUncoupling proteins (UCPs) are mitochondrial membrane transporters that disrupt the coupling between the mitochondrial proton gradient and ATP synthesis

  • The Uncoupling protein-2 (UCP2) 45-bp insertion/deletion polymorphism was reported to be related to metabolic rate [19] and increased body mass index (BMI) [6,20,21], whereas the UCP3 -55T allele was associated with increased expression of UCP3 mRNA in the skeletal muscle [22]

  • Our diabetes mellitus is talented as a major public health trouble in Saudi Arabia in parallel with the worldwide diabetes pandemic, which is having a particular impact upon the Middle East and the third world [25,26]

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Summary

Introduction

Production and hosting by ElsevierUncoupling proteins (UCPs) are mitochondrial membrane transporters that disrupt the coupling between the mitochondrial proton gradient and ATP synthesis. UCP2 is widely distributed in human tissues The UCP2 45-bp insertion/deletion polymorphism was reported to be related to metabolic rate [19] and increased BMI [6,20,21], whereas the UCP3 -55T allele was associated with increased expression of UCP3 mRNA in the skeletal muscle [22]. The patho-physiological impact of both polymorphisms remains unknown

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