Publication: Discovering potential interactions between rare diseases and COVID-19 by combining mechanistic models of viral infection with statistical modeling.
dc.contributor.author | López-Sánchez, Macarena | |
dc.contributor.author | Loucera, Carlos | |
dc.contributor.author | Peña-Chilet, María | |
dc.contributor.author | Dopazo, Joaquín | |
dc.date.accessioned | 2023-05-03T13:27:31Z | |
dc.date.available | 2023-05-03T13:27:31Z | |
dc.date.issued | 2022 | |
dc.description.abstract | Recent studies have demonstrated a relevant role of the host genetics in the coronavirus disease 2019 (COVID-19) prognosis. Most of the 7000 rare diseases described to date have a genetic component, typically highly penetrant. However, this vast spectrum of genetic variability remains yet unexplored with respect to possible interactions with COVID-19. Here, a mathematical mechanistic model of the COVID-19 molecular disease mechanism has been used to detect potential interactions between rare disease genes and the COVID-19 infection process and downstream consequences. Out of the 2518 disease genes analyzed, causative of 3854 rare diseases, a total of 254 genes have a direct effect on the COVID-19 molecular disease mechanism and 207 have an indirect effect revealed by a significant strong correlation. This remarkable potential of interaction occurs for >300 rare diseases. Mechanistic modeling of COVID-19 disease map has allowed a holistic systematic analysis of the potential interactions between the loss of function in known rare disease genes and the pathological consequences of COVID-19 infection. The results identify links between disease genes and COVID-19 hallmarks and demonstrate the usefulness of the proposed approach for future preventive measures in some rare diseases. | |
dc.identifier.doi | 10.1093/hmg/ddac007 | |
dc.identifier.essn | 1460-2083 | |
dc.identifier.pmc | PMC9239744 | |
dc.identifier.pmid | 35022696 | |
dc.identifier.pubmedURL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239744/pdf | |
dc.identifier.unpaywallURL | https://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddac007/42366554/ddac007.pdf | |
dc.identifier.uri | http://hdl.handle.net/10668/19784 | |
dc.issue.number | 12 | |
dc.journal.title | Human molecular genetics | |
dc.journal.titleabbreviation | Hum Mol Genet | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.organization | Fundación Pública Andaluz Progreso y Salud-FPS | |
dc.organization | Instituto de Biomedicina de Sevilla-IBIS | |
dc.page.number | 2078-2089 | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.rights | Attribution 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Models, Statistical | |
dc.subject.mesh | Rare Diseases | |
dc.subject.mesh | Virus Diseases | |
dc.title | Discovering potential interactions between rare diseases and COVID-19 by combining mechanistic models of viral infection with statistical modeling. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 31 | |
dspace.entity.type | Publication |
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