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Dietary exposure biomarker-lead discovery based on metabolomics analysis of urine samples

机译:基于尿液样品代谢组学分析的饮食暴露生物标志物发现

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Although robust associations between dietary intake and population health are evident from conventional observational epidemiology, the outcomes of large-scale intervention studies testing the causality of those links have often proved inconclusive or have failed to demonstrate causality. This apparent conflict may be due to the well-recognised difficulty in measuring habitual food intake which may lead to confounding in observational epidemiology. Urine biomarkers indicative of exposure to specific foods offer information supplementary to the reliance on dietary intake self-assessment tools, such as FFQ, which are subject to individual bias. Biomarker discovery strategies using non-targeted metabolomics have been used recently to analyse urine from either short-term food intervention studies or from cohort studies in which participants consumed a freely-chosen diet. In the latter, the analysis of diet diary or FFQ information allowed classification of individuals in terms of the frequency of consumption of specific diet constituents. We review these approaches for biomarker discovery and illustrate both with particular reference to two studies carried out by the authors using approaches combining metabolite fingerprinting by MS with supervised multivariate data analysis. In both approaches, urine signals responsible for distinguishing between specific foods were identified and could be related to the chemical composition of the original foods. When using dietary data, both food distinctiveness and consumption frequency influenced whether differential dietary exposure could be discriminated adequately. We conclude that metabolomics methods for fingerprinting or profiling of overnight void urine, in particular, provide a robust strategy for dietary exposure biomarker-lead discovery.
机译:尽管从常规观察流行病学中可以明显看出饮食摄入量与人群健康之间的密切联系,但测试这些联系的因果关系的大规模干预研究的结果常常没有定论,或未能证明因果关系。这种明显的冲突可能是由于众所周知的测量习惯性食物摄入量的困难,这可能导致观察流行病学混淆。指示暴露于特定食物的尿液生物标志物提供了对依赖饮食摄入自我评估工具(例如FFQ)的依赖的补充信息,这些工具会受到个体偏见的影响。最近,使用非目标代谢组学的生物标志物发现策略已用于分析短期食物干预研究或参加者食用自由选择饮食的队列研究中的尿液。在后者中,通过饮食日记或FFQ信息的分析,可以根据特定饮食成分的食用频率对个体进行分类。我们回顾了这些用于生物标志物发现的方法,并特别参考了两位作者进行的两项研究,这些研究使用了结合了MS代谢物指纹和监督性多变量数据分析的方法进行。在这两种方法中,都识别出负责区分特定食物的尿液信号,并且可能与原始食物的化学成分有关。在使用饮食数据时,食物的独特性和食用频率都会影响是否可以适当地区分不同的饮食摄入量。我们得出的结论是,代谢组学方法尤其可以为过夜空尿进行指纹识别或分析,为饮食暴露生物标志物铅的发现提供了可靠的策略。

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