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Sci Rep ; 11(1): 6811, 2021 03 24.
Artigo em Inglês | MEDLINE | ID: mdl-33762651

RESUMO

High rate of cardiovascular disease (CVD) has been reported among patients with coronavirus disease 2019 (COVID-19). Importantly, CVD, as one of the comorbidities, could also increase the risks of the severity of COVID-19. Here we identified phospholipase A2 group VII (PLA2G7), a well-studied CVD biomarker, as a hub gene in COVID-19 though an integrated hypothesis-free genomic analysis on nasal swabs (n = 486) from patients with COVID-19. PLA2G7 was further found to be predominantly expressed by proinflammatory macrophages in lungs emerging with progression of COVID-19. In the validation stage, RNA level of PLA2G7 was identified in nasal swabs from both COVID-19 and pneumonia patients, other than health individuals. The positive rate of PLA2G7 were correlated with not only viral loads but also severity of pneumonia in non-COVID-19 patients. Serum protein levels of PLA2G7 were found to be elevated and beyond the normal limit in COVID-19 patients, especially among those re-positive patients. We identified and validated PLA2G7, a biomarker for CVD, was abnormally enhanced in COVID-19 at both nucleotide and protein aspects. These findings provided indications into the prevalence of cardiovascular involvements seen in patients with COVID-19. PLA2G7 could be a potential prognostic and therapeutic target in COVID-19.


Assuntos
1-Alquil-2-acetilglicerofosfocolina Esterase/metabolismo , COVID-19/metabolismo , Doenças Cardiovasculares/metabolismo , Macrófagos/metabolismo , 1-Alquil-2-acetilglicerofosfocolina Esterase/sangue , 1-Alquil-2-acetilglicerofosfocolina Esterase/genética , Biomarcadores/metabolismo , COVID-19/epidemiologia , COVID-19/imunologia , COVID-19/patologia , Doenças Cardiovasculares/epidemiologia , Doenças Cardiovasculares/virologia , China/epidemiologia , Mineração de Dados/métodos , Humanos , Macrófagos/imunologia , Macrófagos/patologia , Polimorfismo de Nucleotídeo Único , SARS-CoV-2/isolamento & purificação , Ativação Transcricional , Regulação para Cima
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