Acute and Postacute COVID-19 Outcomes Among Immunologically Naive Adults During Delta vs Omicron Waves.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 02 2023
Historique:
entrez: 28 2 2023
pubmed: 1 3 2023
medline: 3 3 2023
Statut: epublish

Résumé

The US arrival of the Omicron variant led to a rapid increase in SARS-CoV-2 infections. While numerous studies report characteristics of Omicron infections among vaccinated individuals or persons with previous infection, comprehensive data describing infections among adults who are immunologically naive are lacking. To examine COVID-19 acute and postacute clinical outcomes among a well-characterized cohort of unvaccinated and previously uninfected adults who contracted SARS-CoV-2 during the Omicron (BA.1/BA.2) surge, and to compare outcomes with infections that occurred during the Delta wave. This prospective multisite cohort study included community-dwelling adults undergoing high-resolution symptom and virologic monitoring in 8 US states between June 2021 and September 2022. Unvaccinated adults aged 30 to less than 65 years without an immunological history of SARS-CoV-2 who were at high risk of infection were recruited. Participants were followed for up to 48 weeks, submitting regular COVID-19 symptom surveys and nasal swabs for SARS-CoV-2 polymerase chain reaction (PCR) testing. Data were analyzed from May to October 2022. Omicron (BA.1/BA.2 lineages) vs Delta SARS-CoV-2 infection, defined as a positive PCR test result that occurred during a period when the variant represented at least 50% of circulating SARS-CoV-2 variants in the participant's geographic region. The main outcomes examined were the prevalence and severity of acute (≤28 days after onset) and postacute (≥5 weeks after onset) symptoms. Among 274 participants who were immunologically naive (mean [SD] age, 49 [9.7] years; 186 [68%] female; 19 [7%] Hispanic participants; 242 [88%] White participants), 166 (61%) contracted SARS-CoV-2. Of these, 137 infections (83%) occurred during the Omicron-predominant period and 29 infections (17%) occurred during the Delta-predominant period. Asymptomatic infections occurred among 7% (95% CI, 3%-12%) of Omicron-wave infections and 0% (95% CI, 0%-12%) of Delta-wave infections. Health care use among individuals with Omicron-wave infections was 79% (95% CI, 43%-92%) lower relative to individuals with Delta-wave infections (P = .001). Compared with individuals infected during the Delta wave, individuals infected during the Omicron wave also experienced a 56% (95% CI, 26%-74%, P = .004) relative reduction in the risk of postacute symptoms and a 79% (95% CI, 54%-91%, P < .001) relative reduction in the rate of postacute symptoms. These findings suggest that among adults who were previously immunologically naive, few Omicron-wave (BA.1/BA.2) and Delta-wave infections were asymptomatic. Compared with individuals with Delta-wave infections, individuals with Omicron-wave infections were less likely to seek health care and experience postacute symptoms.

Identifiants

pubmed: 36853602
pii: 2801781
doi: 10.1001/jamanetworkopen.2023.1181
pmc: PMC9975921
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e231181

Subventions

Organisme : NIAID NIH HHS
ID : R25 AI147376
Pays : United States
Organisme : NIAID NIH HHS
ID : K08 AI135078
Pays : United States

Commentaires et corrections

Type : UpdateOf

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Auteurs

Margaret K Doll (MK)

Department of Population Health Sciences, Albany College of Pharmacy & Health Sciences, Albany, New York.

Alpana Waghmare (A)

Division of Infectious Diseases, Department of Pediatrics, University of Washington, Seattle.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.

Antje Heit (A)

Amazon, Seattle, Washington.

Brianna Levenson Shakoor (B)

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California.

Louise E Kimball (LE)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.

Nina Ozbek (N)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.

Rachel L Blazevic (RL)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.

Larry Mose (L)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.

Jim Boonyaratanakornkit (J)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.

Terry L Stevens-Ayers (TL)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.

Kevin Cornell (K)

St Luke's Medical Center, Ketchum, Idaho.

Benjamin D Sheppard (BD)

St Luke's Medical Center, Ketchum, Idaho.

Emma Hampson (E)

St Luke's Medical Center, Ketchum, Idaho.

Faria Sharmin (F)

Department of Population Health Sciences, Albany College of Pharmacy & Health Sciences, Albany, New York.

Benjamin Goodwin (B)

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California.

Jennifer M Dan (JM)

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California.
Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California, San Diego, La Jolla.

Tom Archie (T)

St Luke's Medical Center, Ketchum, Idaho.

Terry O'Connor (T)

St Luke's Medical Center, Ketchum, Idaho.
Department of Emergency Medicine, University of Washington, Seattle.

David Heckerman (D)

Amazon, Seattle, Washington.

Frank Schmitz (F)

Amazon, Seattle, Washington.

Michael Boeckh (M)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle.

Shane Crotty (S)

Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California.
Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California, San Diego, La Jolla.

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