Association of Obesity with Proteasomal Gene Polymorphisms in Children

Author:

Kupca Sarmite123,Sjakste Tatjana2ORCID,Paramonova Natalija2,Sugoka Olga2,Rinkuza Irena1,Trapina Ilva12,Daugule Ilva1,Sipols Alfred J.13,Rumba-Rozenfelde Ingrida1

Affiliation:

1. Faculty of Medicine, University of Latvia, Sarlotes Street 1a, Riga 1001, Latvia

2. Institute of Biology, University of Latvia, Miera Street 3, Salaspils 2169, Latvia

3. Institute of Experimental and Clinical Medicine, University of Latvia, No. 4 Ojara Vaciesa Street, Riga 1004, Latvia

Abstract

The aim of this study was to ascertain possible associations between childhood obesity, its anthropometric and clinical parameters, and three loci of proteasomal genes rs2277460 (PSMA6c.-110C>A), rs1048990 (PSMA6c.-8C>G), and rs2348071 (PSMA3c. 543+138G>A) implicated in obesity-related diseases. Obese subjects included 94 otherwise healthy children in Latvia. Loci were genotyped and then analyzed using polymerase chain reactions, with results compared to those of 191 nonobese controls.PSMA3SNP frequency differences between obese children and controls, while not reaching significance, suggested a trend. These differences, however, proved highly significant (P<0.002) in the subset of children reporting a family history of obesity. Among obese children denying such history,PSMA6c.-8C>G SNP differences, while being nonsignificant, likewise suggested a trend in comparison to the nonobese controls. NoPSMA6c.-110C>A SNP differences were detected in the obese group or its subsets. Finally,PSMA3SNP differences were significantly associated (P<0.05) with circulating low-density lipoprotein cholesterol (LDL) levels. Our results clearly implicate thePSMA3gene locus as an obesity risk factor in those Latvian children with a family history of obesity. While being speculative, the clinical results are suggestive of altered circulatory LDL levels playing a possible role in the etiology of obesity in the young.

Funder

The Latvian National Research Program

Publisher

Hindawi Limited

Subject

Endocrinology, Diabetes and Metabolism

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