Patient stratification reveals the molecular basis of disease co-occurrences

Epidemiological evidence shows that some diseases tend to co-occur; more exactly, certain groups of patients with a given disease are at a higher risk of developing a specific secondary condition. Here, we develop an approach to generate a disease network that uses the accumulating RNA-seq data on human diseases to significantly match an unprecedented proportion of known comorbidities, providing plausible biological models for such co-occurrences and effectively mirroring the underlying structure of complex disease relationships. Furthermore, 64% of the known disease pairs can be explained by analyzing groups of patients with similar expression profiles, highlighting the importance of patient stratification in the study of comorbidities. These results solidly support the existence of molecular mechanisms behind many of the known comorbidities, with most captured co-occurrences implicating the immune system. Additionally, we identified new and potentially underdiagnosed comorbidities, providing molecular insights that could inform targeted therapeutic strategies. We provide a functional and comprehensive resource to explore diseases, disease co-occurrences, and their underlying molecular processes at different resolution levels at http://disease-perception.bsc.es/rgenexcom/.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-08-29
DOI
https://doi.org/10.1073/pnas.2421060122
Citations
4
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
3.22

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article

Patient stratification reveals the molecular basis of disease co-occurrences

Alfonso Valencia, Beatriz Urda-García, Rosalba Lepore, Jon Sánchez-Valle
4 citations
Proceedings of the National Academy of Sciences
Bioinformatics and Genomic Networks
3.22
article

Patient stratification reveals the molecular basis of disease co-occurrences

Alfonso Valencia, Beatriz Urda-García, Rosalba Lepore, Jon Sánchez-Valle
article en
4 citations

Abstract

Epidemiological evidence shows that some diseases tend to co-occur; more exactly, certain groups of patients with a given disease are at a higher risk of developing a specific secondary condition. Here, we develop an approach to generate a disease network that uses the accumulating RNA-seq data on human diseases to significantly match an unprecedented proportion of known comorbidities, providing plausible biological models for such co-occurrences and effectively mirroring the underlying structure of complex disease relationships. Furthermore, 64% of the known disease pairs can be explained by analyzing groups of patients with similar expression profiles, highlighting the importance of patient stratification in the study of comorbidities. These results solidly support the existence of molecular mechanisms behind many of the known comorbidities, with most captured co-occurrences implicating the immune system. Additionally, we identified new and potentially underdiagnosed comorbidities, providing molecular insights that could inform targeted therapeutic strategies. We provide a functional and comprehensive resource to explore diseases, disease co-occurrences, and their underlying molecular processes at different resolution levels at http://disease-perception.bsc.es/rgenexcom/.

Proceedings of the National Academy of SciencesVol. 122(35)
Institució Catalana de Recerca i Estudis Avançats (ES), Universitat Pompeu Fabra (ES), University of Basel (CH), Barcelona Supercomputing Center (ES), University Hospital of Basel (CH), Department of Biomedicine Basel (CH), Universitat Politècnica de Catalunya (ES)
European Commission, Ministerio de Economía y Competitividad, Ministerio de Ciencia e Innovación, HORIZON EUROPE Framework Programme, European Regional Development Fund, Agencia Estatal de Investigación, European Social Fund
Openalex Percentile: Top 8%
Bioinformatics and Genomic Networks
3.22
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