School of Pharmaceutical Sciences, University of Geneva and Lausanne, 20 Bd d'Yvoy, 1211 Geneva 4, Switzerland.
Forensic Sci Int. 2011 Dec 10;213(1-3):85-94. doi: 10.1016/j.forsciint.2011.07.023. Epub 2011 Aug 9.
Anti-doping authorities have high expectations of the athlete steroidal passport (ASP) for anabolic-androgenic steroids misuse detection. However, it is still limited to the monitoring of known well-established compounds and might greatly benefit from the discovery of new relevant biomarkers candidates. In this context, steroidomics opens the way to the untargeted simultaneous evaluation of a high number of compounds. Analytical platforms associating the performance of ultra-high pressure liquid chromatography (UHPLC) and the high mass-resolving power of quadrupole time-of-flight (QTOF) mass spectrometers are particularly adapted for such purpose. An untargeted steroidomic approach was proposed to analyse urine samples from a clinical trial for the discovery of relevant biomarkers of testosterone undecanoate oral intake. Automatic peak detection was performed and a filter of reference steroid metabolites mass-to-charge ratio (m/z) values was applied to the raw data to ensure the selection of a subset of steroid-related features. Chemometric tools were applied for the filtering and the analysis of UHPLC-QTOF-MS(E) data. Time kinetics could be assessed with N-way projections to latent structures discriminant analysis (N-PLS-DA) and a detection window was confirmed. Orthogonal projections to latent structures discriminant analysis (O-PLS-DA) classification models were evaluated in a second step to assess the predictive power of both known metabolites and unknown compounds. A shared and unique structure plot (SUS-plot) analysis was performed to select the most promising unknown candidates and receiver operating characteristic (ROC) curves were computed to assess specificity criteria applied in routine doping control. This approach underlined the pertinence to monitor both glucuronide and sulphate steroid conjugates and include them in the athletes passport, while promising biomarkers were also highlighted.
反兴奋剂机构对运动员类固醇护照(ASP)在检测合成代谢雄激素类滥用方面寄予厚望。然而,它仍然仅限于监测已知的成熟化合物,并且可能会极大地受益于新的相关生物标志物候选物的发现。在这种情况下,类固醇组学为非靶向同时评估大量化合物开辟了道路。将超高效液相色谱(UHPLC)的性能与四极杆飞行时间(QTOF)质谱联用的分析平台特别适合于这种目的。提出了一种非靶向类固醇组学方法,用于分析来自临床试验的尿液样本,以发现十一酸睾酮口服摄入的相关生物标志物。自动进行了峰检测,并应用了参考类固醇代谢物质荷比(m/z)值的过滤器对原始数据进行过滤,以确保选择与类固醇相关的特征子集。应用化学计量学工具对 UHPLC-QTOF-MS(E)数据进行过滤和分析。可以通过 N 向投影到潜在结构判别分析(N-PLS-DA)评估时间动力学,并且确认了检测窗口。在第二步中评估正交投影到潜在结构判别分析(O-PLS-DA)分类模型,以评估已知代谢物和未知化合物的预测能力。进行了共享和独特结构图(SUS-plot)分析,以选择最有前途的未知候选物,并计算接收者操作特征(ROC)曲线,以评估在常规兴奋剂控制中应用的特异性标准。这种方法强调了监测葡萄糖醛酸和硫酸盐类固醇缀合物的相关性,并将其纳入运动员护照,同时还突出了有前途的生物标志物。