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Assessing the Impact of SARS-CoV-2 Lineages and Mutations on Patient Survival

Objectives: More than two years into the COVID-19 pandemic, SARS-CoV-2 still remains a global public health problem. Successive waves of infection have produced new SARS-CoV-2 variants with new mutations for which the impact on COVID-19 severity and patient survival is uncertain. Methods: A total of...

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Detalles Bibliográficos
Autores principales: Loucera, Carlos, Perez-Florido, Javier, Casimiro-Soriguer, Carlos S., Ortuño, Francisco M., Carmona, Rosario, Bostelmann, Gerrit, Martínez-González, L. Javier, Muñoyerro-Muñiz, Dolores, Villegas, Román, Rodriguez-Baño, Jesus, Romero-Gomez, Manuel, Lorusso, Nicola, Garcia-León, Javier, Navarro-Marí, Jose M., Camacho-Martinez, Pedro, Merino-Diaz, Laura, de Salazar, Adolfo, Viñuela, Laura, Lepe, Jose A., Garcia, Federico, Dopazo, Joaquin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500738/
https://www.ncbi.nlm.nih.gov/pubmed/36146700
http://dx.doi.org/10.3390/v14091893
Descripción
Sumario:Objectives: More than two years into the COVID-19 pandemic, SARS-CoV-2 still remains a global public health problem. Successive waves of infection have produced new SARS-CoV-2 variants with new mutations for which the impact on COVID-19 severity and patient survival is uncertain. Methods: A total of 764 SARS-CoV-2 genomes, sequenced from COVID-19 patients, hospitalized from 19th February 2020 to 30 April 2021, along with their clinical data, were used for survival analysis. Results: A significant association of B.1.1.7, the alpha lineage, with patient mortality (log hazard ratio (LHR) = 0.51, C.I. = [0.14,0.88]) was found upon adjustment by all the covariates known to affect COVID-19 prognosis. Moreover, survival analysis of mutations in the SARS-CoV-2 genome revealed 27 of them were significantly associated with higher mortality of patients. Most of these mutations were located in the genes coding for the S, ORF8, and N proteins. Conclusions: This study illustrates how a combination of genomic and clinical data can provide solid evidence for the impact of viral lineage on patient survival.