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  3. Post-acute sequelae after SARS-CoV-2 infection by viral variant and vaccination status: a multicenter cross-sectional study.
 

Post-acute sequelae after SARS-CoV-2 infection by viral variant and vaccination status: a multicenter cross-sectional study.

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BORIS DOI
10.48350/179910
Date of Publication
July 26, 2023
Publication Type
Article
Division/Institute

Universitätsinstitut ...

Contributor
Kahlert, Christian R
Strahm, Carol
Güsewell, Sabine
Cusini, Alexia
Brucher, Angela
Goppel, Stephan
Möller, Elisabeth
Möller, J Carsten
Ortner, Manuela
Ruetti, Markus
Stocker, Reto
Vuichard-Gysin, Danielle
Besold, Ulrike
McGeer, Allison
Risch, Lorenzorcid-logo
Universitätsinstitut für Klinische Chemie (UKC)
Friedl, Andrée
Schlegel, Matthias
Vernazza, Pietro
Kuster, Stefan P
Kohler, Philipp
Subject(s)

600 - Technology::610...

Series
Clinical infectious diseases
ISSN or ISBN (if monograph)
1537-6591
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/cid/ciad143
PubMed ID
36905145
Uncontrolled Keywords

Long-COVID Post-Acute...

Description
BACKGROUND

Disentangling the effects of SARS-CoV-2 variants and vaccination on the occurrence of post-acute sequelae of SARS-CoV-2 (PASC) is crucial to estimate and reduce the burden of PASC.

METHODS

We performed a cross-sectional analysis (May/June 2022) within a prospective multicenter healthcare worker (HCW) cohort in North-Eastern Switzerland. HCW were stratified by viral variant and vaccination status at time of their first positive SARS-CoV-2 nasopharyngeal swab. HCW without positive swab and with negative serology served as controls. The sum of eighteen self-reported PASC symptoms was modeled with univariable and multivariable negative-binomial regression to analyse the association of mean symptom number with viral variant and vaccination status.

RESULTS

Among 2'912 participants (median age 44 years, 81.3% female), PASC symptoms were significantly more frequent after wild-type infection (estimated mean symptom number 1.12, p<0.001; median time since infection 18.3 months), after Alpha/Delta infection (0.67 symptoms, p<0.001; 6.5 months), and after Omicron BA.1 infections (0.52 symptoms, p=0.005; 3.1 months) compared to uninfected controls (0.39 symptoms). After Omicron BA.1 infection, the estimated mean symptom number was 0.36 for unvaccinated individuals, compared to 0.71 with 1-2 vaccinations (p=0.028) and 0.49 with ≥3 prior vaccinations (p=0.30). Adjusting for confounders, only wild-type (adjusted rate ratio [aRR] 2.81, 95% confidence interval [CI] 2.08-3.83) and Alpha/Delta infection (aRR 1.93, 95% CI 1.10-3.46) were significantly associated with the outcome.

CONCLUSIONS

Previous infection with pre-Omicron variants was the strongest risk factor for PASC symptoms among our HCW. Vaccination prior to Omicron BA.1 infection was not associated with a clear protective effect against PASC symptoms in this population.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/165020
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