Kupca Sarmite, Sjakste Tatjana, Paramonova Natalija, Sugoka Olga, Rinkuza Irena, Trapina Ilva, Daugule Ilva, Sipols Alfred J, Rumba-Rozenfelde Ingrida
Faculty of Medicine, University of Latvia, Sarlotes Street 1a, Riga 1001, Latvia ; Institute of Biology, University of Latvia, Miera Street 3, Salaspils 2169, Latvia ; Institute of Experimental and Clinical Medicine, University of Latvia, No. 4 Ojara Vaciesa Street, Riga 1004, Latvia.
Institute of Biology, University of Latvia, Miera Street 3, Salaspils 2169, Latvia.
J Obes. 2013;2013:638154. doi: 10.1155/2013/638154. Epub 2013 Dec 21.
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 (PSMA6 c.-110C>A), rs1048990 (PSMA6 c.-8C>G), and rs2348071 (PSMA3 c. 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. PSMA3 SNP 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, PSMA6 c.-8C>G SNP differences, while being nonsignificant, likewise suggested a trend in comparison to the nonobese controls. No PSMA6 c.-110C>A SNP differences were detected in the obese group or its subsets. Finally, PSMA3 SNP differences were significantly associated (P < 0.05) with circulating low-density lipoprotein cholesterol (LDL) levels. Our results clearly implicate the PSMA3 gene 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.
本研究旨在确定儿童肥胖症、其人体测量学和临床参数与三个蛋白酶体基因位点rs2277460(PSMA6 c.-110C>A)、rs1048990(PSMA6 c.-8C>G)和rs2348071(PSMA3 c. 543+138G>A)之间可能存在的关联,这些位点与肥胖相关疾病有关。肥胖受试者包括94名拉脱维亚其他方面均健康的儿童。对这些位点进行基因分型,然后使用聚合酶链反应进行分析,并将结果与191名非肥胖对照者的结果进行比较。肥胖儿童与对照者之间PSMA3单核苷酸多态性(SNP)频率差异虽未达到显著水平,但显示出一种趋势。然而,在报告有肥胖家族史的儿童亚组中,这些差异被证明具有高度显著性(P < 0.002)。在否认有此类家族史的肥胖儿童中,PSMA6 c.-8C>G SNP差异虽不显著,但与非肥胖对照者相比同样显示出一种趋势。在肥胖组或其亚组中未检测到PSMA6 c.-110C>A SNP差异。最后,PSMA3 SNP差异与循环低密度脂蛋白胆固醇(LDL)水平显著相关(P < 0.05)。我们的结果清楚地表明,在那些有肥胖家族史的拉脱维亚儿童中,PSMA3基因位点是一个肥胖风险因素。虽然具有推测性,但临床结果提示循环LDL水平的改变可能在年轻人肥胖的病因中起作用。