| Literature DB >> 33762651 |
Yang Li1, Yongzhong Jiang2, Yi Zhang1, Naizhe Li1, Qiangling Yin1, Linlin Liu2, Xin Lv3, Yan Liu4, Aqian Li1, Bin Fang2, Jiajia Li5, Hengping Ye6, Gang Yang7, Xiaoxian Cui8, Yang Liu1, Yuanyuan Qu1, Chuan Li1, Jiandong Li1, Dexin Li1, Zhongtao Gai3, Shiwen Wang9,10, Faxian Zhan11, Mifang Liang12,13.
Abstract
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.Entities:
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Year: 2021 PMID: 33762651 PMCID: PMC7990942 DOI: 10.1038/s41598-021-85848-5
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379