Multivariate analysis of metabolomic data to identify biological pathways modified by a clinical intervention.

IF 3.5 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Rachel M Wood, Laura J Corbin, Jane M Blazeby, Chris A Rogers, Nicholas J Timpson, Daniel J Lawson
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引用次数: 0

Abstract

Introduction: High throughput metabolomic assays offer a huge opportunity to quantify the cellular processes underlying disease and intervention pathways. However, the multi-dimensional inter-relatedness between these processes coupled with the complex noisy measurement environment create a need for generation of new methods that move beyond simple pairwise associations.

Objectives: To evaluate the utility of a simple, multivariate, relational comparison method called CLARITY in the context of metabolomics data.

Methods: Nuclear magnetic resonance (NMR)-derived metabolomics data collected from the same individuals (N = 125) before and after a weight management intervention in By-Band-Sleeve (BBS), a clinical trial of metabolic and bariatric surgery, were used. First a traditional (univariate) linear mixed model approach was taken to identify metabolites that were changed post-intervention. The CLARITY method was then used to generate a covariance-based relational anomaly score with a view to increasing classification performance of the underlying cause of changes to the levels of and covariances between metabolites.

Results: CLARITY enabled further characterisation of metabolites identified in univariate linear regression analyses, differentiating those that exhibited covariance changes from those with mean changes only. An additional cluster of metabolites were identified as undergoing a relational change that would not have been detected using traditional methods.

Conclusions: Gathering insights about biological pathways from large-scale metabolomics data has the potential to inform the future design of modelling and laboratory experiments aimed at capturing the underlying biological processes relevant to disease.

代谢组学数据的多变量分析,以确定临床干预改变的生物学途径。
高通量代谢组学分析为量化潜在疾病和干预途径的细胞过程提供了巨大的机会。然而,这些过程之间的多维相互关系与复杂的噪声测量环境相结合,需要产生超越简单成对关联的新方法。目的:评估一种简单、多变量、关联比较方法CLARITY在代谢组学数据中的实用性。方法:采用代谢和减肥手术临床试验By-Band-Sleeve (BBS)体重管理干预前后收集的来自同一个体(N = 125)的核磁共振(NMR)衍生代谢组学数据。首先,采用传统的(单变量)线性混合模型方法来识别干预后改变的代谢物。然后使用CLARITY方法生成基于协方差的关系异常评分,以期提高对代谢物水平和协方差变化的潜在原因的分类性能。结果:CLARITY能够进一步表征单变量线性回归分析中鉴定的代谢物,区分那些显示协方差变化的代谢物和那些仅显示平均值变化的代谢物。另外一组代谢物被确定为经历了使用传统方法无法检测到的关系变化。结论:从大规模代谢组学数据中收集有关生物学途径的见解,有可能为未来设计旨在捕获与疾病相关的潜在生物学过程的建模和实验室实验提供信息。
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来源期刊
Metabolomics
Metabolomics 医学-内分泌学与代谢
CiteScore
6.60
自引率
2.80%
发文量
84
审稿时长
2 months
期刊介绍: Metabolomics publishes current research regarding the development of technology platforms for metabolomics. This includes, but is not limited to: metabolomic applications within man, including pre-clinical and clinical pharmacometabolomics for precision medicine metabolic profiling and fingerprinting metabolite target analysis metabolomic applications within animals, plants and microbes transcriptomics and proteomics in systems biology Metabolomics is an indispensable platform for researchers using new post-genomics approaches, to discover networks and interactions between metabolites, pharmaceuticals, SNPs, proteins and more. Its articles go beyond the genome and metabolome, by including original clinical study material together with big data from new emerging technologies.
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