SARS-CoV-2 viral load is associated with increased disease severity and mortality.
SARS-CoV-2 viral load is associated with increased disease severity and mortality.
复制标题
DOI:
10.1038/s41467-020-19057-5
复制
发表时间:
2020-10-30
影响因子:
16.6
通讯作者:
Massachusetts Consortium for Pathogen Readiness
中科院分区:
文献类型:
--
作者:
Fajnzylber J;Regan J;Coxen K;Corry H;Wong C;Rosenthal A;Worrall D;Giguel F;Piechocka-Trocha A;Atyeo C;Fischinger S;Chan A;Flaherty KT;Hall K;Dougan M;Ryan ET;Gillespie E;Chishti R;Li Y;Jilg N;Hanidziar D;Baron RM;Baden L;Tsibris AM;Armstrong KA;Kuritzkes DR;Alter G;Walker BD;Yu X;Li JZ;Massachusetts Consortium for Pathogen Readiness
The relationship between SARS-CoV-2 viral load and risk of disease progression remains largely undefined in coronavirus disease 2019 (COVID-19). Here, we quantify SARS-CoV-2 viral load from participants with a diverse range of COVID-19 disease severity, including those requiring hospitalization, outpatients with mild disease, and individuals with resolved infection. We detected SARS-CoV-2 plasma RNA in 27% of hospitalized participants, and 13% of outpatients diagnosed with COVID-19. Amongst the participants hospitalized with COVID-19, we report that a higher prevalence of detectable SARS-CoV-2 plasma viral load is associated with worse respiratory disease severity, lower absolute lymphocyte counts, and increased markers of inflammation, including C-reactive protein and IL-6. SARS-CoV-2 viral loads, especially plasma viremia, are associated with increased risk of mortality. Our data show that SARS-CoV-2 viral loads may aid in the risk stratification of patients with COVID-19, and therefore its role in disease pathogenesis should be further explored. In this study, Massachusetts Consortium for Pathogen Readiness (MassCPR) investigators assess the relationship between SARS-CoV-2 viral load and COVID-19 disease severity and report that the levels of detectable viral RNA, especially in plasma, correlates with severity of respiratory disease, inflammatory markers and predicted risk of death.
登录
查看更多内容
影响因子:
5.4
作者:
Towner, JS;Rollin, PE;Nichol, ST
通讯作者:
Nichol, ST
影响因子:
158.5
作者:
Ackermann, Maximilian;Verleden, Stijn E.;Jonigk, Danny
通讯作者:
Jonigk, Danny
影响因子:
7.3
作者:
Hamming, I;Timens, W;van Goor, H
通讯作者:
van Goor, H
影响因子:
82.9
作者:
He, Xi;Lau, Eric H. Y.;Leung, Gabriel M.
通讯作者:
Leung, Gabriel M.
影响因子:
8
作者:
Boudreault, Francis;Pinilla-Vera, Miguel;Baron, Rebecca M.
通讯作者:
Baron, Rebecca M.