Nelson Anne E, Ho Ken K
Pituitary Research Unit, Garvan Institute of Medical Research, 384 Victoria St, Darlinghurst, NSW 2010, Australia.
Asian J Androl. 2008 May;10(3):416-25. doi: 10.1111/j.1745-7262.2008.00395.x.
Although doping with growth hormone (GH) is banned, there is anecdotal evidence that it is widely abused. GH is reportedly used often in combination with anabolic steroids at high doses for several months. Development of a robust test for GH has been challenging because recombinant human 22 kDa (22K) GH used in doping is indistinguishable analytically from endogenous GH and there are wide physiological fluctuations in circulating GH concentrations. One approach to GH testing is based on measurement of different circulating GH isoforms using immunoassays that differentiate between 22K and other GH isoforms. Administration of 22K GH results in a change in its abundance relative to other endogenous pituitary GH isoforms. The differential isoform method has been implemented; however, its utility is limited because of the short window of opportunity of detection. The second approach, which will extend the window of opportunity of detection, is based on the detection of increased levels of circulating GH-responsive proteins, such as insulin-like growth factor (IGF) axis and collagen peptides. Age and gender are the major determinants of variability for IGF-I and the collagen markers; therefore, a test based on these markers must take age into account for men and women. Extensive data is now available that validates the GH-responsive marker approach and implementation is now largely dependent on establishing an assured supply of standardized assays. Future directions will include more widespread implementation of both approaches by the World Anti-Doping Agency, possible use of other platforms for measurement and an athlete's passport to establish individual reference levels for biological parameters such as GH-responsive markers. Novel approaches include gene expression and proteomic profiling.
尽管使用生长激素(GH)进行兴奋剂 doping 是被禁止的,但有传闻证据表明其被广泛滥用。据报道,GH 经常与合成代谢类固醇高剂量联合使用数月。开发一种可靠的 GH 检测方法具有挑战性,因为用于 doping 的重组人 22 kDa(22K)GH 在分析上与内源性 GH 无法区分,并且循环 GH 浓度存在广泛的生理波动。GH 检测的一种方法是基于使用免疫测定法测量不同的循环 GH 异构体,该方法可区分 22K 和其他 GH 异构体。给予 22K GH 会导致其相对于其他内源性垂体 GH 异构体的丰度发生变化。差异异构体方法已经实施;然而,由于检测机会窗口较短,其效用有限。第二种方法将延长检测机会窗口,基于检测循环中 GH 反应性蛋白水平的增加,如胰岛素样生长因子(IGF)轴和胶原蛋白肽。年龄和性别是 IGF-I 和胶原蛋白标志物变异性的主要决定因素;因此,基于这些标志物的检测必须考虑男性和女性的年龄。现在有大量数据验证了 GH 反应性标志物方法,其实施现在很大程度上取决于建立标准化检测的可靠供应。未来的方向将包括世界反兴奋剂机构更广泛地实施这两种方法,可能使用其他测量平台以及运动员护照来建立生物参数(如 GH 反应性标志物)的个体参考水平。新方法包括基因表达和蛋白质组学分析。