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Cluster-Partial Least Squares (C-Pls) Regression Analysis: Application to Mirna and Metabolomic Data

Analytica Chimica Acta(2023)

Hlth Res Inst La Fe | Hosp Univ Dr Peset | Univ Valencia | Hosp Univ & Politecn La Fe | Maastricht Univ | Leitat Technol Ctr

Cited 2|Views29
Abstract
BACKGROUND:Biomedicine and biological research frequently involve analyzing large datasets generated by high-throughput technologies like genomics, transcriptomics, miRNomics, and metabolomics. Pathway analysis is a common computational approach used to understand the impact of experimental conditions, phenotypes, or interventions on biological pathways and networks. This involves statistical analysis of omic data to identify differentially expressed variables and mapping them onto predefined pathways. Analyzing such datasets often requires multivariate techniques to extract meaningful insights such as Partial Least Squares (PLS). Variable selection strategies like interval-PLS (iPLS) help improve understanding and predictive performance by identifying informative variables or intervals. However, iPLS is suboptimal to treat omic data such as metabolic or miRNA profiles, where features cannot be distributed along a continuous dimension describing their relationships as in e.g., vibrational or nuclear magnetic resonance spectroscopy.RESULTS:This study introduces a novel variable selection approach called cluster PLS (c-PLS) that aims to assess the joint impact of variable groups selected based on biological characteristics (such as miRNA-regulated metabolic pathway or lipid classes) on the predictive performance of a multivariate model. The usefulness of c-PLS is shown using miRNomic and metabolomic datasets obtained from the analysis of 24 liver tissue biopsies collected in the frame of a clinical study of steatosis.SIGNIFICANCE AND NOVELTY:Results obtained show that c-PLS enables analyzing the effect of biologically relevant variable clusters, facilitating the identification of biological processes associated with the independent variable, and the prioritization of the biological factors influencing model performance, thereby improving the understanding of the biological factors driving model predictions. While the strategy is tested for the evaluation of PLS models, it could be extended to other linear and non-linear multivariate models.
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要点】:本研究提出了一种新的变量选择方法,即簇部分最小二乘法(c-PLS),用于评估基于生物学特征(如miRNA调控的代谢途径或脂质类)的变量组对多变量模型预测性能的联合影响。

方法】:该方法通过统计分析大规模的高通量技术生成数据,如基因组学、转录组学、miRNomics和代谢组学,来识别不同表达的变量,并将它们映射到预定义的途径上。

实验】:在24例肝组织活检的临床研究中,使用c-PLS分析了miRNomic和代谢组数据集,结果显示c-PLS能够分析生物相关变量簇的效果,有助于识别与自变量相关的生物过程,并优先考虑影响模型性能的生物因素,从而提高对驱动模型预测的生物学因素的理解。