4.6 Article

Network Analysis for Uncovering the Relationship between Host Response and Clinical Factors to Virus Pathogen: Lessons from SARS-CoV-2

期刊

VIRUSES-BASEL
卷 14, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/v14112422

关键词

patient similarity network; multivariate data analysis; COVID-19 severity; minimal immune signature; data visualisation; IgM and IgG levels

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资金

  1. Ministry of Health of the Czech Republic [NU22-A-105]

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This study utilized a patient similarity network approach to uncover the relationships between immune and clinical factors in COVID-19 patients, providing insights into disease severity. Multivariate network approaches play a crucial role in analyzing complex datasets.
Analysing complex datasets while maintaining the interpretability and explainability of outcomes for clinicians and patients is challenging, not only in viral infections. These datasets often include a variety of heterogeneous clinical, demographic, laboratory, and personal data, and it is not a single factor but a combination of multiple factors that contribute to patient characterisation and host response. Therefore, multivariate approaches are needed to analyse these complex patient datasets, which are impossible to analyse with univariate comparisons (e.g., one immune cell subset versus one clinical factor). Using a SARS-CoV-2 infection as an example, we employed a patient similarity network (PSN) approach to assess the relationship between host immune factors and the clinical course of infection and performed visualisation and data interpretation. A PSN analysis of similar to 85 immunological (cellular and humoral) and similar to 70 clinical factors in 250 recruited patients with coronavirus disease (COVID-19) who were sampled four to eight weeks after a PCR-confirmed SARS-CoV-2 infection identified a minimal immune signature, as well as clinical and laboratory factors strongly associated with disease severity. Our study demonstrates the benefits of implementing multivariate network approaches to identify relevant factors and visualise their relationships in a SARS-CoV-2 infection, but the model is generally applicable to any complex dataset.

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