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Analysis of candidate genes in Polish families with obesity.

机译:分析波兰肥胖家庭的候选基因。

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摘要

This study analyzes the relationship between risk factors related to overweight/obesity, insulin resistance, lipid tolerance, hypertension, endothelial function and genetic polymorphisms associated with: i) appetite regulation (leptin, melanocortin-3-receptor (MCR-3), dopamine receptor 2 (D2R)); ii) adipocyte differentiation and insulin sensitivity (peroxisome proliferator-activated receptor-gamma2 (PPAR-gamma2), tumor necrosis factor-alpha (TNF-alpha)); iii) thermogenesis and free fatty acid (FFA) transport/catabolism (uncoupling protein-1 (UCP1), lipoprotein lipase (LPL), beta2- and beta3-adrenergic receptor (beta2AR, beta3AR), fatty acid transport protein-1 (FATP-1) and iv) lipoproteins (apoliprotein E (apoE), apo CIII). The 122 members of 40 obese Caucasian families from southern Poland participated in the study. The genotypes were analyzed by restriction fragment length polymorphism-polymerase chain reaction (RFLP-PCR) or by direct sequencing. Phenotypes related to obesity (body mass index (BMI), fat/lean body mass composition, waist-to-hip ratio (WHR)), fasting lipids, glucose, leptin and insulin, as well as insulin during oral glucose tolerance test (OGTT) (4 points within 2 hours) and during oral lipid tolerance test (OLTT) (5 points within 8 hours) were assessed. The insulin sensitivity indexes: homeostasis model assessment of insulin resistance, whole body insulin sensitivity index, hepatic insulin sensitivity and early secretory response to an oral glucose load (HOMA-IR, ISI-COMP, ISI-HOMA and DELTA) were calculated. The single gene mutations such as C105 T OB and Pro115 Gln PPAR-gamma2 linked to morbid obesity were not detected in our group. A weak correlation between obesity and certain gene polymorphisms was observed. Being overweight (25 < BMI > or = 30 kg/m2) significantly correlated with worse FFA tolerance in male PPAR-gamma2 12Pro, LPL-H (G) allele carriers. Insulin resistance was found in female PPAR-gamma2 Pro12, TNF-alpha (-308A) and LPL-H (G) allele carriers. Hypertension linked to the PPAR-gamma2 Pro allele carriers was characterized by high leptin output during OLTT. We conclude that the polymorphisms we investigated were weakly correlated with obesity but significantly modified the risk factors of the metabolic syndrome.
机译:这项研究分析了与超重/肥胖,胰岛素抵抗,脂质耐受,高血压,内皮功能和遗传多态性相关的危险因素之间的关系,这些因素与:i)食欲调节(瘦素,黑皮质素-3-受体(MCR-3),多巴胺受体2(D2R)); ii)脂肪细胞分化和胰岛素敏感性(过氧化物酶体增殖物激活受体-γ2(PPAR-γ2),肿瘤坏死因子-α(TNF-α)); iii)生热和游离脂肪酸(FFA)转运/分解代谢(解偶联蛋白1(UCP1),脂蛋白脂肪酶(LPL),β2-和β3-肾上腺素能受体(beta2AR,beta3AR),脂肪酸转运蛋白-1(FATP- 1)和iv)脂蛋白(载脂蛋白E(apoE),apo CIII)。来自波兰南部40个肥胖白种人家庭的122名成员参加了研究。通过限制性片段长度多态性-聚合酶链反应(RFLP-PCR)或直接测序来分析基因型。与肥胖有关的表型(体重指数(BMI),脂肪/瘦体重组成,腰臀比(WHR)),空腹血脂,葡萄糖,瘦素和胰岛素,以及口服葡萄糖耐量测试(OGTT)中的胰岛素)(2小时内4分)和口服脂质耐量测试(OLTT)期间(8小时内5分)进行了评估。胰岛素敏感性指数:计算胰岛素抵抗的稳态模型评估,全身胰岛素敏感性指数,肝胰岛素敏感性和对口服葡萄糖负荷的早期分泌反应(HOMA-IR,ISI-COMP,ISI-HOMA和DELTA)。在本组中未检测到与病态肥胖有关的单基因突变,例如C105 T OB和Pro115 Gln PPAR-gamma2。肥胖与某些基因多态性之间存在弱相关性。超重(25 或= 30 kg / m2)与男性PPAR-gamma2 12Pro,LPL-H(G)等位基因携带者的FFA耐受性差显着相关。在雌性PPAR-γ2Pro12,TNF-α(-308A)和LPL-H(G)等位基因携带者中发现了胰岛素抵抗。与PPAR-gamma2 Pro等位基因携带者相关的高血压的特征是在OLTT期间瘦素输出高。我们得出的结论是,我们研究的多态性与肥胖关系不大,但显着改变了代谢综合征的危险因素。

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