Association Between Anterior Nasal and Plasma SARS-CoV-2 RNA Levels and Hospitalization or Death in Nonhospitalized Adults With Mild-to-Moderate COVID-19

Author:

Giganti Mark J1ORCID,Chew Kara W2,Eron Joseph J3,Li Jonathan Z4ORCID,Pinilla Mauricio1,Moser Carlee1ORCID,Javan Arzhang Cyrus5,Fischer William A3,Klekotka Paul6,Margolis David7,Wohl David Alain3,Coombs Robert W8,Daar Eric S9,Smith Davey M10,Currier Judith S2,Hughes Michael D1,Hosey Lara,Roa Jhoanna,Patel Nilam,Greninger Alexander,Degli-Angeli Emily,Goecker Erin,Daza Glenda,Harb Socorro,Dragavon Joan,Aldrovandi Grace,Murtaugh William,Science Frontier,Cooper Marlene,Gutzman Howard,Knowles Kevin,Bowman Rachel,Erhardt Bill,Waring Lorraine,Hessinger Diane,Adams Stacey,

Affiliation:

1. Center for Biostatistics in AIDS Research, Harvard T. H. Chan School of Public Health , Boston, Massachusetts

2. Department of Medicine, David Geffen School of Medicine, University of California , Los Angeles

3. Department of Medicine, University of North Carolina , Chapel Hill

4. Department of Medicine, Brigham & Women's Hospital, Harvard Medical School , Boston, Massachusetts

5. National Institute of Allergy and Infectious Diseases, National Institutes of Health , Rockville, Maryland

6. Eli Lilly and Company , San Diego, California

7. Brii Biosciences , Durham, North Carolina

8. Department of Laboratory Medicine and Pathology, University of Washington , Seattle

9. Lundquist Institute, Harbor-UCLA Medical Center , Torrance, California

10. Department of Medicine, University of California, San Diego , La Jolla

Abstract

Abstract Background There is little information regarding severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA as a predictor for clinical outcomes in outpatients with mild-to-moderate coronavirus disease 2019 (COVID-19). Methods Anterior nasal (AN) and plasma SARS-CoV-2 RNA data from 2115 nonhospitalized adults who received monoclonal antibodies (mAbs) or placebo in the ACTIV-2/A5401 trial were analyzed for associations with hospitalization or death. Results One hundred two participants were hospitalized or died through 28 days of follow-up. Higher day 0 (pretreatment) AN RNA was associated with increasing risk of hospitalization/death (risk ratio [RR], 1.24 per log10 copies/mL [95% confidence interval {CI}, 1.04–1.49]) among placebo recipients, ranging from 3% to 16% for <2 to ≥6 log10 copies/mL. Although only 1% had quantifiable levels, there was a similar trend across day 0 plasma RNA categories. Higher day 3 AN RNA was associated with subsequent hospitalization/death among placebo recipients (RR, 1.42 per log10 copies/mL [95% CI, 1.00–2.03]), but not mAb recipients (RR, 1.02 per log10 copies/mL [95% CI, 0.68–1.56]). The proportion of treatment effect (reduction in hospitalizations/deaths after day 3 for mAb vs placebo) explained by day 3 AN RNA was 8%. Conclusions SARS-CoV-2 RNA levels are predictive of hospitalization/death in the natural history setting, but AN RNA levels may not be a reliable surrogate marker of mAb treatment effect in COVID-19 trials. Clinical Trials Registration. NCT04518410.

Funder

NIH

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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