Association of SARS-CoV-2 Seropositivity With Myalgic Encephalomyelitis and/or Chronic Fatigue Syndrome Among Children and Adolescents in Germany.


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 09 2022
Historique:
entrez: 27 9 2022
pubmed: 28 9 2022
medline: 30 9 2022
Statut: epublish

Résumé

During the COVID-19 pandemic, a reduction in quality of life and physical and mental health among children and adolescents has been reported that may be associated with SARS-CoV-2 infection and/or containment measures. To assess the association of SARS-CoV-2 seropositivity with symptoms that may be related to myalgic encephalomyelitis and/or chronic fatigue syndrome (ME/CFS) among children and adolescents. This substudy of the cross-sectional SARS-CoV-2 seroprevalence surveys in Germany (SARS-CoV-2 KIDS) was performed in 9 pediatric hospitals from May 1 to October 31, 2021. Pediatric patients were recruited during an inpatient or outpatient visit regardless of the purpose of the visit. Parental questionnaires and serum samples were collected during clinically indicated blood draws. The parental questionnaire on demographic and clinical information was extended by items according to the DePaul Symptom Questionnaire, a pediatric screening tool for ME/CFS in epidemiological studies in patients aged 5 to 17 years. Seropositivity was determined by SARS-CoV-2 IgG antibodies in serum samples using enzyme-linked immunosorbent assays. Key symptoms of ME/CFS were evaluated separately or as clustered ME/CFS symptoms according to the DePaul Symptom Questionnaire, including fatigue. Among 634 participants (294 male [46.4%] and 340 female [53.6%]; median age, 11.5 [IQR, 8-14] years), 198 (31.2%) reported clustered ME/CFS symptoms, including 40 of 100 SARS-CoV-2-seropositive (40.0%) and 158 of 534 SARS-CoV-2-seronegative (29.6%) children and adolescents. After adjustment for sex, age group, and preexisting disease, the risk ratio for reporting clustered ME/CFS symptoms decreased from 1.35 (95% CI, 1.03-1.78) to 1.18 (95% CI, 0.90-1.53) and for substantial fatigue from 2.45 (95% CI, 1.24-4.84) to 2.08 (95% CI, 1.05-4.13). Confinement to children and adolescents with unknown previous SARS-CoV-2 infection status (n = 610) yielded lower adjusted risks for all symptoms except joint pain ME/CFS-related symptoms. The adjusted risk ratio was 1.08 (95% CI, 0.80-1.46) for reporting clustered ME/CFS symptoms and 1.43 (95% CI, 0.63-3.23) for fatigue. These findings suggest that the risk of ME/CFS in children and adolescents owing to SARS-CoV-2 infection may be very small. Recall bias may contribute to risk estimates of long COVID-19 symptoms in children. Extensive lockdowns must be considered as an alternative explanation for complex unspecific symptoms during the COVID-19 pandemic.

Identifiants

pubmed: 36166227
pii: 2796733
doi: 10.1001/jamanetworkopen.2022.33454
pmc: PMC9516317
doi:

Substances chimiques

Immunoglobulin G 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2233454

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Auteurs

Anna-Lisa Sorg (AL)

Institute of Social Paediatrics and Adolescent Medicine, Division of Paediatric Epidemiology, Ludwig-Maximilians-University Munich, Munich, Germany.
University Children's Hospital, Eberhard Karls University, Tuebingen, Germany.

Selina Becht (S)

Institute of Social Paediatrics and Adolescent Medicine, Division of Paediatric Epidemiology, Ludwig-Maximilians-University Munich, Munich, Germany.

Marietta Jank (M)

Paediatric Infectious Diseases, Department of Paediatrics, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Jakob Armann (J)

Department of Pediatrics, University Hospital and Medical Faculty Carl Gustav Carus, Technical University Dresden, Dresden, Germany.

Ulrich von Both (U)

Dr von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.

Markus Hufnagel (M)

Department of Paediatrics and Adolescent Medicine, Medical Faculty, University Medical Centre, University of Freiburg, Freiburg, Germany.

Fabian Lander (F)

Department of Paediatrics, University Hospital and Medical Faculty Carl Gustav Carus, Technical University Dresden, Dresden, Germany.

Johannes G Liese (JG)

University Hospital of Wuerzburg, Division of Paediatric Infectious Diseases, Department of Paediatrics, Wuerzburg, Germany.

Tim Niehues (T)

Department of Paediatrics, Helios Klinikum Krefeld, Krefeld, Germany.

Eva Verjans (E)

Department of Paediatrics, Medical Faculty, University Hospital RWTH Aachen, Aachen, Germany.

Martin Wetzke (M)

Centre for Paediatrics and Adolescent Medicine, Hannover Medical School, Excellence Cluster RESIST (Resolving Infection Susceptibility), Deutsche Forschungsgemeinschaft, Hannover, Germany.

Silvia Stojanov (S)

Department of Paediatrics, Faculty of Medicine, Technical University Munich, Munich, Germany.

Uta Behrends (U)

Department of Paediatrics, Faculty of Medicine, Technical University Munich, Munich, Germany.

Christian Drosten (C)

Institute of Virology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Horst Schroten (H)

Paediatric Infectious Diseases, Department of Paediatrics, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Rüdiger von Kries (R)

Institute of Social Paediatrics and Adolescent Medicine, Division of Paediatric Epidemiology, Ludwig-Maximilians-University Munich, Munich, Germany.

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