Longitudinal Metabolomics Data Analysis Informed by Mechanistic Models.

IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Metabolites Pub Date : 2024-12-24 DOI:10.3390/metabo15010002
Lu Li, Huub Hoefsloot, Barbara M Bakker, David Horner, Morten A Rasmussen, Age K Smilde, Evrim Acar
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Abstract

Background: Metabolomics measurements are noisy, often characterized by a small sample size and missing entries. While data-driven methods have shown promise in terms of analyzing metabolomics data, e.g., revealing biomarkers of various phenotypes, metabolomics data analysis can significantly benefit from incorporating prior information about metabolic mechanisms. This paper introduces a novel data analysis approach to incorporate mechanistic models in metabolomics data analysis. Methods: We arranged time-resolved metabolomics measurements of plasma samples collected during a meal challenge test from the COPSAC2000 cohort as a third-order tensor: subjects by metabolites by time samples. Simulated challenge test data generated using a human whole-body metabolic model were also arranged as a third-order tensor: virtual subjects by metabolites by time samples. Real and simulated data sets were coupled in the metabolites mode and jointly analyzed using coupled tensor factorizations to reveal the underlying patterns. Results: Our experiments demonstrated that the joint analysis of simulated and real data had better performance in terms of pattern discovery, achieving higher correlations with a BMI (body mass index)-related phenotype compared to the analysis of only real data in males, while in females, the performance was comparable. We also demonstrated the advantages of such a joint analysis approach in the presence of incomplete measurements and its limitations in the presence of wrong prior information. Conclusions: The joint analysis of real measurements and simulated data (generated using a mechanistic model) through coupled tensor factorizations guides real data analysis with prior information encapsulated in mechanistic models and reveals interpretable patterns.

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基于机制模型的纵向代谢组学数据分析。
背景:代谢组学测量是有噪声的,通常以小样本量和缺失条目为特征。虽然数据驱动的方法在分析代谢组学数据方面显示出前景,例如,揭示各种表型的生物标志物,代谢组学数据分析可以从纳入有关代谢机制的先验信息中显著受益。本文介绍了一种新的数据分析方法,将机制模型纳入代谢组学数据分析。方法:我们将COPSAC2000队列中膳食激发试验中收集的血浆样本的时间分辨代谢组学测量作为三阶张量:受试者按代谢物按时间样本排列。利用人体全身代谢模型生成的模拟激射试验数据也被排列成三阶张量:虚拟受试者按代谢物按时间样本排列。真实数据集和模拟数据集以代谢物模式耦合,并使用耦合张量分解进行联合分析,以揭示潜在的模式。结果:我们的实验表明,与仅分析男性真实数据相比,模拟数据和真实数据的联合分析在模式发现方面具有更好的性能,与BMI(身体质量指数)相关表型具有更高的相关性,而在女性中,性能具有可比性。我们还证明了这种联合分析方法在存在不完整测量和存在错误先验信息时的局限性的优点。结论:通过耦合张量分解对实际测量和模拟数据(使用机制模型生成)进行联合分析,可以指导将先验信息封装在机制模型中的真实数据分析,并揭示可解释的模式。
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来源期刊
Metabolites
Metabolites Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
5.70
自引率
7.30%
发文量
1070
审稿时长
17.17 days
期刊介绍: Metabolites (ISSN 2218-1989) is an international, peer-reviewed open access journal of metabolism and metabolomics. Metabolites publishes original research articles and review articles in all molecular aspects of metabolism relevant to the fields of metabolomics, metabolic biochemistry, computational and systems biology, biotechnology and medicine, with a particular focus on the biological roles of metabolites and small molecule biomarkers. Metabolites encourages scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on article length. Sufficient experimental details must be provided to enable the results to be accurately reproduced. Electronic material representing additional figures, materials and methods explanation, or supporting results and evidence can be submitted with the main manuscript as supplementary material.
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