Effect of SARS-CoV2 infection on disease flares in patients with systemic lupus erythematosus: a case-control study.

COVID-19 flares lupus outcome viral trigger

Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
08 Nov 2023
Historique:
accepted: 27 10 2023
received: 06 08 2023
revised: 08 10 2023
medline: 10 11 2023
pubmed: 10 11 2023
entrez: 10 11 2023
Statut: aheadofprint

Résumé

To study the effect of SARS-CoV2 infection on flares of systemic lupus erythematosus (SLE). Patients who fulfilled the ACR/SLICC criteria for SLE and had documented COVID-19 between February and November 2022 were identified retrospectively from our hospital COVID-19 registry. SLE controls who did not have SARS-CoV2 infection were randomly matched for age, sex and the time of infection in a 2:1 ratio with those infected. The primary outcome of interest was clinical flare of SLE within 90 days of COVID-19. The rate of SLE flares (mild/moderate or severe) was compared between SARS-CoV2-infected SLE patients and controls. 91 SLE patients with COVID-19 (age 48.6 ± 14.0 years; 95.6% women) and 182 SLE controls (age 48.7 ± 13.8 years; 95.6% women) were studied. Eleven of 91 (12.1%) SARS-CoV2-infected patients had serious manifestations. One (1.1%) patient died and 7(7.7%) developed severe complications. Within 90 days of SARS-CoV2 infection, 14(15.4%) patients developed mild/moderate clinical SLE flares and 2(2.2%) patients had severe SLE flares. The incidence of SLE flares in SARS-CoV2-infected patients was significantly higher than those without the infection (17.6% vs 5.5%; odds ratio 3.67[1.59-8.46]; p = 0.001). The changes in anti-dsDNA and complement levels, however, were not significantly different between the two groups. Among SARS-CoV2-infected SLE patients, those with clinical SLE flares had significantly lower C3 values (p = 0.004) before the infection than those without. Clinical flares within 90 days were significantly more common in SLE patients infected with SARS-CoV2 than matched non-infected SLE controls.

Identifiants

pubmed: 37947324
pii: 7382220
doi: 10.1093/rheumatology/kead601
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Chi Chiu Mok (CC)

Department of Medicine, Tuen Mun Hospital, Hong Kong, SAR China.

Chris Ching Lam Cheung (CCL)

Fellow in Rheumatology, Rutonjee Hospital, Hong Kong.

Kar Li Chan (KL)

Associate consultant in Rheumatology, Tuen Mun Hospital, Hong Kong.

Sau Mei Tse (SM)

Associate consultant in Rheumatology, Tuen Mun Hospital, Hong Kong.

Chi Hung To (CH)

Consultant in Rheumatology, Pok Oi Hospital, Hong Kong.

Classifications MeSH