4.6 Article

SARS-CoV-2 Genomic Characteristics and Clinical Impact of SARS-CoV-2 Viral Diversity in Critically Ill COVID-19 Patients: A Prospective Multicenter Cohort Study

期刊

VIRUSES-BASEL
卷 14, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/v14071529

关键词

COVID-19; SARS-CoV-2; variant of concern; acute respiratory failure; intensive care unit

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资金

  1. Agence Nationale de la Recherche [ANR-21-COVR-0022]

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This study aimed to investigate the relationship between SARS-CoV-2 variants and clinical outcomes. The findings showed that the alpha variant did not increase the risk of mortality compared to other variants. Additionally, there was no association between specific variants or mutations and day-28 mortality.
The SARS-CoV-2 variant of concern, alpha, spread worldwide at the beginning of 2021. It was suggested that this variant was associated with a higher risk of mortality than other variants. We aimed to characterize the genetic diversity of SARS-CoV-2 variants isolated from patients with severe COVID-19 and unravel the relationships between specific viral mutations/mutational patterns and clinical outcomes. This is a prospective multicenter observational cohort study. Patients aged >= 18 years admitted to 11 intensive care units (ICUs) in hospitals in the Greater Paris area for SARS-CoV-2 infection and acute respiratory failure between 1 October 2020 and 30 May 2021 were included. The primary clinical endpoint was day-28 mortality. Full-length SARS-CoV-2 genomes were sequenced by means of next-generation sequencing (Illumina COVIDSeq). In total, 413 patients were included, 183 (44.3%) were infected with pre-existing variants, 197 (47.7%) were infected with variant alpha, and 33 (8.0%) were infected with other variants. The patients infected with pre-existing variants were significantly older (64.9 +/- 11.9 vs. 60.5 +/- 11.8 years; p = 0.0005) and had more frequent COPD (11.5% vs. 4.1%; p = 0.009) and higher SOFA scores (4 [3-8] vs. 3 [2-4]; 0.0002). The day-28 mortality was no different between the patients infected with pre-existing, alpha, or other variants (31.1% vs. 26.2% vs. 30.3%; p = 0.550). There was no association between day-28 mortality and specific variants or the presence of specific mutations. At ICU admission, the patients infected with pre-existing variants had a different clinical presentation from those infected with variant alpha, but mortality did not differ between these groups. There was no association between specific variants or SARS-CoV-2 genome mutational pattern and day-28 mortality.

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