Suppr超能文献

1443名捷克青少年中肥胖易感性基因变异与代谢综合征及相关特征的关联

Association of obesity susceptibility gene variants with metabolic syndrome and related traits in 1,443 Czech adolescents.

作者信息

Dušátková L, Zamrazilová H, Sedláčková B, Včelák J, Hlavatý P, Aldhoon Hainerová I, Korenková V, Bradnová O, Bendlová B, Kunešová M, Hainer V

机构信息

Institute of Endocrinology, Obesity Management Centre, Prague, Czech Republic.

出版信息

Folia Biol (Praha). 2013;59(3):123-33.

Abstract

Genome-wide association studies have revealed several gene variants associated with obesity; however, only a few studies have further investigated their association with metabolic syndrome. We performed a study of eleven variants in/near genes TMEM18, SH2B1, KCTD15, PCSK1, BDNF, SEC16B, MC4R, and FTO in Czech adolescents and analysed their association with obesity, metabolic syndrome and related traits. Genotyping was performed in 1,443 adolescents aged 13.0-17.9 years. Anthropometric parameters, biochemical parameters and blood pressure were assessed. Metabolic syndrome was defined according to the International Diabetes Federation. The FTO rs9939609 variant was associated with overweight/obesity (OR 1.40, 95% CI 1.21-1.63, P < 0.001). The minor allele of TMEM18 rs7561317 was related to underweight (OR 1.78, 95% CI 1.14-2.79, P = 0.015). BDNF rs925946 and MC4R rs17782313 were associated with metabolic syndrome (OR 1.53, 95% CI 1.14-2.04, P = 0.005; 1.51, 95% CI 1.12-2.04, P = 0.009). The PCSK1 rs6235 variant was negatively related to increased blood glucose (OR 0.69, 95% CI 0.49-0.97, P = 0.040). In conclusion, the FTO variant was associated with overweight/obesity in Czech adolescents. Moreover, MC4R and BDNF variants increased the risk of metabolic syndrome, probably through their effect on abdominal obesity. The PCSK1 variant may have a protective role in the development of type 2 diabetes.

摘要

全基因组关联研究已经揭示了几种与肥胖相关的基因变异;然而,只有少数研究进一步探究了它们与代谢综合征的关联。我们对捷克青少年中TMEM18、SH2B1、KCTD15、PCSK1、BDNF、SEC16B、MC4R和FTO基因内部或附近的11种变异进行了研究,并分析了它们与肥胖、代谢综合征及相关特征的关联。对1443名年龄在13.0 - 17.9岁的青少年进行了基因分型。评估了人体测量参数、生化参数和血压。代谢综合征根据国际糖尿病联盟的标准进行定义。FTO基因的rs9939609变异与超重/肥胖相关(比值比1.40,95%置信区间1.21 - 1.63,P < 0.001)。TMEM18基因rs7561317的次要等位基因与体重过轻有关(比值比1.78,95%置信区间1.14 - 2.79,P = 0.015)。BDNF基因的rs925946和MC4R基因的rs17782313与代谢综合征相关(比值比1.53,95%置信区间1.14 - 2.04,P = 0.005;1.51,95%置信区间1.12 - 2.04,P = 0.009)。PCSK1基因的rs6235变异与血糖升高呈负相关(比值比0.69,95%置信区间0.49 - 0.97,P = 0.040)。总之,FTO变异与捷克青少年的超重/肥胖相关。此外,MC4R和BDNF变异可能通过对腹部肥胖的影响增加了代谢综合征的风险。PCSK1变异可能在2型糖尿病的发生发展中具有保护作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验