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A blood microRNA classifier for the prediction of ICU mortality in COVID-19 patients: a multicenter validation study

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URI: http://hdl.handle.net/10498/29728

DOI: 10.1186/s12931-023-02462-x

ISSN: 1465-9921

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SC_2023_0536.pdf (3.148Mb)
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de Gonzalo Calvo, David; Molinero, Marta; Benítez, Iván D.; Perez Pons, Manel; García Mateo, Nadia; Ortega, Alicia; Postigo, Tamara; García Hidalgo, María C.; Belmonte, Thalía; Rodríguez Muñoz, Carlos; González, Jessica; Torres, Gerard; Gort Paniello, Clara; Moncusí Moix, Anna; Estella García, ÁngelAuthority UCA; Tamayo Lomas, Luis; Martínez de la Gándara, Amalia; Socias, Lorenzo; Peñasco, Yhivian; de la Torre, María del Carmen; Bustamante Munguira, Elena; Gallego Curto, Elena; Martínez Varela, Ignacio; Martín Delgado, María Cruz; Vidal Cortés, Pablo; López Messa, Juan; Pérez García, Felipe; Caballero, Jesús; Añón, José Manuel; Loza Vázquez, Ana; Carbonell, Nieves; Marin Corral, Judith; Jorge García, Ruth Noemí; Barberà, Carmen; Ceccato, Adrián; Fernández Barat, Laia; Ferrer, Ricard; García Gasulla, Dario; Lorente Balanza, Jose Ángel; Menéndez, Rosario; Motos, Ana; Peñuelas, Oscar; Riera, Jordi; Bermejo Martin, Jesús F.; Torres, Antoni; Barbé, Ferrán
Date
2023-06-17
Department
Medicina
Source
Respiratory Research. Vol. 24, nº 1, December 2023, 159
Abstract
Background: The identification of critically ill COVID-19 patients at risk of fatal outcomes remains a challenge. Here, we first validated candidate microRNAs (miRNAs) as biomarkers for clinical decision-making in critically ill patients. Second, we constructed a blood miRNA classifier for the early prediction of adverse outcomes in the ICU. Methods: This was a multicenter, observational and retrospective/prospective study including 503 critically ill patients admitted to the ICU from 19 hospitals. qPCR assays were performed in plasma samples collected within the first 48 h upon admission. A 16-miRNA panel was designed based on recently published data from our group. Results: Nine miRNAs were validated as biomarkers of all-cause in-ICU mortality in the independent cohort of critically ill patients (FDR < 0.05). Cox regression analysis revealed that low expression levels of eight miRNAs were associated with a higher risk of death (HR from 1.56 to 2.61). LASSO regression for variable selection was used to construct a miRNA classifier. A 4-blood miRNA signature composed of miR-16-5p, miR-192-5p, miR-323a-3p and miR-451a predicts the risk of all-cause in-ICU mortality (HR 2.5). Kaplan‒Meier analysis confirmed these findings. The miRNA signature provides a significant increase in the prognostic capacity of conventional scores, APACHE-II (C-index 0.71, DeLong test p-value 0.055) and SOFA (C-index 0.67, DeLong test p-value 0.001), and a risk model based on clinical predictors (C-index 0.74, DeLong test-p-value 0.035). For 28-day and 90-day mortality, the classifier also improved the prognostic value of APACHE-II, SOFA and the clinical model. The association between the classifier and mortality persisted even after multivariable adjustment. The functional analysis reported biological pathways involved in SARS-CoV infection and inflammatory, fibrotic and transcriptional pathways. Conclusions: A blood miRNA classifier improves the early prediction of fatal outcomes in critically ill COVID-19 patients.
Subjects
COVID-19; Biomarker; ICU; microRNA; Prognosis; SARS-CoV-2
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  • Articulos Científicos Medicina [306]
Atribución 4.0 Internacional
This work is under a Creative Commons License Atribución 4.0 Internacional

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