Laboratorio Antidoping, Federazione Medico Sportiva Italiana, Rome, Italy.
Institute of Pharmacy, Freie Universität Berlin, Berlin, Germany.
Rapid Commun Mass Spectrom. 2022 Jan 30;36(2):e9217. doi: 10.1002/rcm.9217.
This work demonstrates the high potential of combining high-resolution mass spectrometry with chemometric tools, using metabolomics as a guided tool for anti-doping analysis. The administration of 7-keto-DHEA was studied as a proof-of-concept of the effectiveness of the combination of knowledge-based and machine-learning approaches to differentiate the changes due to the athletic activities from those due to the recourse to doping substances and methods.
Urine samples were collected from five healthy volunteers before and after an oral administration by identifying three time intervals. Raw data were acquired by injecting less than 1 μL of derivatized samples into a model 8890 gas chromatograph coupled to a model 7250 accurate-mass quadrupole time-of-flight analyzer (both from Agilent Technologies), by using a low-energy electron ionization source; the samples were then preprocessed to align peak retention times with the same accurate mass. The resulting data table was subjected to multivariate analysis.
Multivariate analysis showed a high similarity between the samples belonging to the same collection interval and a clear separation between the different excretion intervals. The discrimination between blank and long excretion groups may suggest the presence of long excretion markers, which are particularly significant in anti-doping analysis. Furthermore, matching the most significant features with some of the metabolites reported in the literature data demonstrated the rationality of the proposed metabolomics-based approach.
The application of metabolomics tools as an investigation strategy could reduce the time and resources required to identify and characterize intake markers maximizing the information that can be extracted from the data and extending the research field by avoiding a priori bias. Therefore, metabolic fingerprinting of prohibited substance intakes could be an appropriate analytical approach to reduce the risk of false-positive/negative results, aiding in the interpretation of "abnormal" profiles and discrimination of pseudo-endogenous steroid intake in the anti-doping field.
本工作展示了将高分辨率质谱与化学计量学工具相结合的巨大潜力,将代谢组学作为指导分析兴奋剂的工具。本文以 7-酮去氢表雄酮(7-keto-DHEA)的给药为例,证明了基于知识和机器学习的方法相结合,区分因运动活动引起的变化和因使用兴奋剂物质和方法引起的变化的有效性。
通过确定三个时间间隔,从五名健康志愿者中采集口服给药前后的尿液样本。通过使用低能量电子电离源,将衍生化后的样品注射到小于 1μL 到模型 8890 气相色谱仪中,然后与模型 7250 精确质量四极杆飞行时间分析仪(均来自安捷伦科技公司)耦合,获取原始数据;对样品进行预处理,以将峰保留时间与相同的精确质量对齐。对得到的数据表进行多元分析。
多元分析表明,同一采集间隔的样本之间具有很高的相似性,不同排泄间隔之间有明显的分离。空白和长排泄组之间的区分可能表明存在长排泄标记物,这在兴奋剂分析中尤为重要。此外,将最显著的特征与文献数据中报道的一些代谢物相匹配,证明了基于代谢组学的方法的合理性。
代谢组学工具作为一种研究策略的应用可以减少识别和表征摄入标记物所需的时间和资源,最大限度地利用从数据中提取的信息,并通过避免先验偏见来扩展研究领域。因此,禁止物质摄入的代谢指纹分析可能是一种适当的分析方法,可以降低假阳性/阴性结果的风险,有助于解释“异常”谱并区分兴奋剂领域的伪内源性甾体摄入。