Department of Biomedical Sciences, University of Cagliari , Cagliari, Italy.
Department of Biochemistry, University of Cambridge , Cambridge, United Kingdom.
Anal Chem. 2016 Aug 16;88(16):7921-9. doi: 10.1021/acs.analchem.5b03078. Epub 2016 Aug 2.
In a typical metabolomics experiment, two or more conditions (e.g., treated versus untreated) are compared, in order to investigate the potential differences in the metabolic profiles. When dealing with complex biological systems, a two-class classification is often unsuitable, since it does not consider the unpredictable differences between samples (e.g., nonresponder to treatment). An approach based on statistical process control (SPC), which is able to monitor the response to a treatment or the development of a pathological condition, is proposed here. Such an approach has been applied to an experimental hepatocarcinogenesis model to discover early individual metabolic variations associated with a different response to the treatment. Liver study was performed by nuclear magnetic resonance (NMR) spectroscopy, followed by multivariate statistical analysis. By this approach, we were able to (1) identify which treated samples have a significantly different metabolic profile, compared to the control (in fact, as confirmed by immunohistochemistry, the method correctly classified 7 responders and 3 nonresponders among the 10 treated animals); (2) recognize, for each individual sample, the metabolites that are out of control (e.g., glutathione, acetate, betaine, and phosphocholine). The first point could be used for classification purposes, and the second point could be used for a better understanding of the mechanisms underlying the early phase of carcinogenesis. The statistical control approach can be used for diagnosis (e.g., healthy versus pathological, responder versus nonresponder) and for generation of an individual metabolic profile, leading to a better understanding of the individual pathological processes and to a personalized diagnosis and therapy.
在典型的代谢组学实验中,通常会比较两种或更多条件(例如,处理组与未处理组),以研究代谢谱中的潜在差异。当处理复杂的生物系统时,通常不适合采用两类分类法,因为它没有考虑到样本之间不可预测的差异(例如,对治疗无反应)。这里提出了一种基于统计过程控制(SPC)的方法,该方法能够监测对治疗的反应或病理状况的发展。该方法已应用于实验性肝癌发生模型,以发现与对治疗的不同反应相关的早期个体代谢变化。肝脏研究通过核磁共振(NMR)光谱法进行,随后进行多变量统计分析。通过这种方法,我们能够(1)确定与对照组相比,哪些处理后的样本具有明显不同的代谢谱(实际上,如免疫组织化学所证实的,该方法正确地对 10 只处理动物中的 7 个应答者和 3 个无应答者进行了分类);(2)识别每个个体样本中失控的代谢物(例如,谷胱甘肽、乙酸盐、甜菜碱和磷酸胆碱)。第一点可用于分类目的,第二点可用于更好地理解致癌作用早期阶段的机制。统计控制方法可用于诊断(例如,健康与病理、应答者与无应答者)和生成个体代谢谱,从而更好地理解个体病理过程并进行个性化诊断和治疗。