4.7 Article

An explainable model of host genetic interactions linked to COVID-19 severity

期刊

COMMUNICATIONS BIOLOGY
卷 5, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s42003-022-04073-6

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资金

  1. Italian Ministry of University and Research through the Department of excellence Faculty of Sciences of Scuola Normale Superiore
  2. EuroBioBank [GTB18001]
  3. Network for Italian Genomes (NIG)
  4. Intesa San Paolo [B/2020/0119]
  5. EU [101016775]

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A multifaceted computational strategy identified 16 genetic variants contributing to increased risk of severe COVID-19 infection from a Whole Exome Sequencing dataset of an Italian patient cohort. These variants, along with age, gender, and specific diseases, can predict COVID-19 severity with high accuracy. The study also revealed immune and inflammatory processes related to viral infection response, as well as other cross-talking signaling pathways, providing new opportunities for treatment and patient stratification.
We employed a multifaceted computational strategy to identify the genetic factors contributing to increased risk of severe COVID-19 infection from a Whole Exome Sequencing (WES) dataset of a cohort of 2000 Italian patients. We coupled a stratified k-fold screening, to rank variants more associated with severity, with the training of multiple supervised classifiers, to predict severity based on screened features. Feature importance analysis from tree-based models allowed us to identify 16 variants with the highest support which, together with age and gender covariates, were found to be most predictive of COVID-19 severity. When tested on a follow-up cohort, our ensemble of models predicted severity with high accuracy (ACC = 81.88%; AUCROC = 96%; MCC = 61.55%). Our model recapitulated a vast literature of emerging molecular mechanisms and genetic factors linked to COVID-19 response and extends previous landmark Genome-Wide Association Studies (GWAS). It revealed a network of interplaying genetic signatures converging on established immune system and inflammatory processes linked to viral infection response. It also identified additional processes cross-talking with immune pathways, such as GPCR signaling, which might offer additional opportunities for therapeutic intervention and patient stratification. Publicly available PheWAS datasets revealed that several variants were significantly associated with phenotypic traits such as Respiratory or thoracic disease, supporting their link with COVID-19 severity outcome. A multifaceted computational strategy identifies 16 genetic variants contributing to increased risk of severe COVID-19 infection from a Whole Exome Sequencing dataset of a cohort of Italian patients.

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