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Impact of UGT2B17 gene deletion on the steroid profile of an athlete

机译:UGT2B17基因缺失对运动员类固醇谱的影响

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AbstractThe measurement of the testosterone to epitestosterone ratio (T/E ratio) in urine is often used as a marker for testosterone administration in the doping control field. This study examines the frequencies of the different expression forms of the UGT2B17 gene, and assesses their effects on this marker in volunteer subjects. The sample for this descriptive study was composed of male and female athletes aged between 16 and 55 years old who practiced different sports disciplines. All participants underwent a sports-medical physical examination, and subsequently provided 10 urine samples consecutively over a period of 48 h. The dependent variable examined was T/E and the main independent variable was the UGT2B17 gene polymorphism. During 1 year, 1410 urine samples were obtained from 141 athletes. The frequencies of the three genotypes were as follows: wt homozygotes (ins/ins) 48.2% (n = 68), mutant homozygotes (del/del) 12.1% (n = 17), and heterozygotes (ins/del) 39.7% (n = 56). Genotype distributions varied significantly (P  0.001) according to ethnicity, 80% of Asian subjects being homozygous for the gene deletion (del/del) compared to 6.9% of Caucasian subjects. A multivariate analysis adjusted for genotype, age, sex, and sports discipline revealed that athletes with the del/del polymorphism showed a significantly lower mean T/E than heterozygotes (ins/del). In contrast, homozygous athletes for the gene insertion (ins/ins) showed higher mean T/E ratios than heterozygotes (ins/del). UGT2B17 gene deletion has a strong influence on the T/E ratio in urine, which is the most efficient indicator of testosterone prohormone misuse. Others factors studied seem not to have such an impact. The genotyping of UGT2B17 is an important source of information for understanding steroid profiling in the doping control field; therefore it is suggested that it be included in the Athletes Biological Passport.
机译:摘要尿液中睾酮与表睾酮之比(T / E比)的测量通常被用作兴奋剂控制领​​域中睾丸激素给药的标志物。这项研究检查了UGT2B17基因不同表达形式的频率,并评估了它们在志愿者受试者中对该标记的影响。此描述性研究的样本由年龄在16至55岁之间,从事不同运动学科的男女运动员组成。所有参与者均接受了运动医学体格检查,随后在48小时内连续提供了10个尿液样本。检查的因变量是T / E,主要的自变量是UGT2B17基因多态性。在1年中,从141名运动员中获得了1410尿液样本。三种基因型的频率如下:wt纯合子(ins / ins)48.2%(n = 68),突变纯合子(del / del)12.1%(n = 17)和杂合子(ins / del)39.7%( n = 56)。基因型分布根据种族而有显着差异(P <0.001),而80%的亚洲受试者是基因缺失纯合子(del / del),而白人受试者为6.9%。根据基因型,年龄,性别和运动纪律进行的多变量分析显示,具有del / del多态性的运动员的平均T / E显着低于杂合子(ins / del)。相反,用于基因插入的纯合运动员(ins / ins)显示出比杂合子(ins / del)更高的平均T / E比。 UGT2B17基因缺失对尿液中的T / E比有很大影响,这是滥用睾丸激素的最有效指标。研究的其他因素似乎没有产生这样的影响。 UGT2B17的基因分型是了解掺杂控制领域中类固醇谱的重要信息来源。因此,建议将其包括在运动员生物护照中。

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