Distinct temporal trajectories and risk factors for Post-acute sequelae of SARS-CoV-2 infection.

COVID-19 PASC SARS-CoV-2 long COVID symptom clusters

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2023
Historique:
received: 23 05 2023
accepted: 19 09 2023
medline: 1 11 2023
pubmed: 1 11 2023
entrez: 1 11 2023
Statut: epublish

Résumé

The understanding of Post-acute sequelae of SARS-CoV-2 infection (PASC) can be improved by longitudinal assessment of symptoms encompassing the acute illness period. To gain insight into the various disease trajectories of PASC, we assessed symptom evolution and clinical factors associated with the development of PASC over 3 months, starting with the acute illness period. We conducted a prospective cohort study to identify parameters associated with PASC. We performed cluster and case control analyses of clinical data, including symptomatology collected over 3 months following infection. We identified three phenotypic clusters associated with PASC that could be characterized as remittent, persistent, or incident based on the 3-month change in symptom number compared to study entry: remittent (median; min, max: -4; -17, 3), persistent (-2; -14, 7), or incident (4.5; -5, 17) ( An incident disease phenotype characterized by symptoms that were absent during acute illness and the observed association with high dose steroids during acute illness have potential critical implications for preventing PASC.

Sections du résumé

Background UNASSIGNED
The understanding of Post-acute sequelae of SARS-CoV-2 infection (PASC) can be improved by longitudinal assessment of symptoms encompassing the acute illness period. To gain insight into the various disease trajectories of PASC, we assessed symptom evolution and clinical factors associated with the development of PASC over 3 months, starting with the acute illness period.
Methods UNASSIGNED
We conducted a prospective cohort study to identify parameters associated with PASC. We performed cluster and case control analyses of clinical data, including symptomatology collected over 3 months following infection.
Results UNASSIGNED
We identified three phenotypic clusters associated with PASC that could be characterized as remittent, persistent, or incident based on the 3-month change in symptom number compared to study entry: remittent (median; min, max: -4; -17, 3), persistent (-2; -14, 7), or incident (4.5; -5, 17) (
Conclusion UNASSIGNED
An incident disease phenotype characterized by symptoms that were absent during acute illness and the observed association with high dose steroids during acute illness have potential critical implications for preventing PASC.

Identifiants

pubmed: 37908849
doi: 10.3389/fmed.2023.1227883
pmc: PMC10614284
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1227883

Informations de copyright

Copyright © 2023 Chen, Parthasarathy, Leung, Wu, Drake, Ridaura, Zisser, Conrad, Tapson, Moy, deFilippi, Rosas, Prabhakar, Basit, Salvatore, Krishnan and Kim.

Déclaration de conflit d'intérêts

CC, JL, MW, KD, and CK maintain equity ownership and employment at Verily Life Sciences. SP reports personal fees from Jazz Pharmaceuticals, Inc., and UpToDate, Inc., and grants from Philips, Inc., Sommetrics, Inc., and Regeneron. CRd serves on advisory boards for Abbott Diagnostics, Ortho/Quidel Diagnostics, and Roche Diagnostics. JK receives research funding from Regeneron. JK has also provided consulting for GlaxoSmithKline, AstraZeneca, CereVu Medical, Propeller/ResMed, and BData, Inc. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer RP declared a past co-authorship with the author SP to the handling editor.

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Auteurs

Chen Chen (C)

Verily Life Sciences, South San Francisco, CA, United States.

Sairam Parthasarathy (S)

Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, University of Arizona, Tucson, AZ, United States.

Jacqueline M Leung (JM)

Verily Life Sciences, South San Francisco, CA, United States.

Michelle J Wu (MJ)

Verily Life Sciences, South San Francisco, CA, United States.

Katherine A Drake (KA)

Verily Life Sciences, South San Francisco, CA, United States.

Vanessa K Ridaura (VK)

Verily Life Sciences, South San Francisco, CA, United States.

Howard C Zisser (HC)

Verily Life Sciences, South San Francisco, CA, United States.

William A Conrad (WA)

Providence Little Company of Mary Medical Center Torrance, Torrance, CA, United States.

Victor F Tapson (VF)

Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, United States.

James N Moy (JN)

Department of Internal Medicine, Rush University Medical Center, Chicago, IL, United States.

Christopher R deFilippi (CR)

Inova Heart and Vascular Institute, Falls Church, VA, United States.

Ivan O Rosas (IO)

Department of Medicine, Baylor College of Medicine, Houston, TX, United States.

Bellur S Prabhakar (BS)

Department of Microbiology and Immunology, University of Illinois-College of Medicine, Chicago, IL, United States.

Mujeeb Basit (M)

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.

Mirella Salvatore (M)

Department of Medicine, Weill Cornell Medicine, New York, NY, United States.
Department of Population Health Sciences, Weill Cornell Medicine, New York, NY, United States.

Jerry A Krishnan (JA)

Breathe Chicago Center, University of Illinois Chicago, Chicago, IL, United States.

Charles C Kim (CC)

Verily Life Sciences, South San Francisco, CA, United States.

Classifications MeSH