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首页> 外文期刊>European review for medical and pharmacological sciences. >Lys656Asn polymorphism of leptin receptor gene and metabolic syndrome in obese patients.
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Lys656Asn polymorphism of leptin receptor gene and metabolic syndrome in obese patients.

机译:肥胖患者瘦素受体基因Lys656Asn多态性与代谢综合征的关系

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摘要

BACKGROUND: The etiology of common obesity is complex, because many genetic, environmental and metabolic factors might act. Alterations of the normal leptin receptor gene be involved in the development of obesity. The polymorphism on codon 656 produces a change in charge, making this change a possibility to be functional. OBJECTIVE: The aim of our study was to investigate the relationship between metabolic syndrome and Lys656Asn polymorphism in obese patients. DESIGN: A population of 714 obese patients (body mass index > 30) was analyzed in cross-sectional survey. A bioimpedance, blood pressure, a serial assessment of nutritional intake with 3 days written food records and biochemical analysis were performed. RESULTS: Four hundred and seventy eight patients (66.9%) had the genotype Lys656/Lys 656 (wild group), whereas 236 (33.1%) had either the genotype Lys656/Asn656 (212 patients, 29.7%) or the genotype Asn656/Asn656 (24 patients, 3.4%) (mutant group). Prevalence of metabolic syndrome (MS) with ATP III definition was 49.4% (353 patients; 35.1% males and 64.9% females) and 50.6% patients without MS (n = 361; 25.2% males and 75.8% females). Prevalence of leptin receptor (LEPR) genotypes was similar in patients with metabolic syndrome (65.5% wild genotype and 34.5% mutant genotype) and without metabolic syndrome (68.3% wild genotype and 31.7% mutant genotype). No differences in anthropometric and biochemical parameters were detected between genotypes in the same group of metabolic syndrome. CONCLUSION: The finding of our study is the lack of association of the Lys656/Asn656 and Asn656/ Asn656 genotypes with metabolic syndrome.
机译:背景:常见肥胖的病因很复杂,因为许多遗传,环境和代谢因素都可能起作用。正常的瘦素受体基因的改变与肥胖症的发展有关。密码子656上的多态性产生电荷变化,使这种变化成为可能的功能。目的:本研究旨在探讨肥胖患者代谢综合征与Lys656Asn多态性之间的关系。设计:在横断面调查中分析了714名肥胖患者(体重指数> 30)。进行了生物阻抗,血压,营养摄入量的连续评估以及3天的书面食物记录和生化分析。结果:478例患者(66.9%)具有Lys656 / Lys 656基因型(野生型),而236例患者(33.1%)具有Lys656 / Asn656基因型(212例患者,占29.7%)或Ans656 / Asn656基因型(24例,3.4%)(突变组)。 ATP III定义的代谢综合征(MS)的患病率为49.4%(353例患者;男性35.1%;女性64.9%);无MS的患病率为50.6%(n = 361;男性25.2%,女性75.8%)。瘦素受体(LEPR)基因型的患病率与代谢综合征(65.5%野生基因型和34.5%突变基因型)和无代谢综合征(68.3%野生基因型和31.7%突变基因型)的患者相似。在同一组代谢综合征的基因型之间,在人体测量学和生化参数方面未发现差异。结论:本研究的发现是Lys656 / Asn656和Asn656 / Asn656基因型与代谢综合征之间缺乏关联。

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