Key result
Unsupervised machine learning applied to multi-omics data can identify mechanistically distinct endotypes of heart failure, potentially guiding individualized treatment and clinical trial selection.
Why the study?
Heart failure encompasses multiple endotypes with differential risks and treatment responses, requiring multi-omics approaches and machine-learning methods to identify mechanistically meaningful disease subtypes.
The integration of multi-omics data with machine learning enables the identification of distinct molecular endotypes in heart failure, paving the way for individualized treatment strategies.
Endotyping is an emerging concept in which diseases are classified into distinct subtypes based on underlying molecular mechanisms. Heart failure (HF) is a complex clinical syndrome that encompasses multiple endotypes with differential risks of adverse events, and varying responses to treatment. Identifying these distinct endotypes requires molecular-level investigation involving multi-"omics" approaches, including genomics, transcriptomics, proteomics, and metabolomics. The derivation of these HF endotypes has important implications in promoting individualized treatment and facilitating more targeted selection of patients for clinical trials, as well as in potentially revealing new pathways of disease that may serve as therapeutic targets. One challenge in the integrated analysis of high-throughput omics and detailed clinical data is that it requires the ability to handle "big data", a task for which machine learning is well suited. In particular, unsupervised machine learning has the ability to uncover novel endotypes of disease in an unbiased approach. In this review, we will discuss recent efforts to identify HF endotypes and cover approaches involving proteomics, transcriptomics, and genomics, with a focus on machine-learning methods.
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A 2021 study conducted a review in Heart Failure. Endotyping using multi-omics and machine learning was evaluated. Unsupervised machine learning applied to multi-omics data can identify mechanistically distinct endotypes of heart failure, potentially guiding individualized treatment and clinical trial selection.
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