Psychological burden associated with incident persistent symptoms and their evolution during the COVID-19 pandemic: a prospective population-based study.


Journal

BMJ mental health
ISSN: 2755-9734
Titre abrégé: BMJ Ment Health
Pays: England
ID NLM: 9918521385306676

Informations de publication

Date de publication:
15 Mar 2024
Historique:
received: 16 10 2023
accepted: 01 02 2024
medline: 18 3 2024
pubmed: 16 3 2024
entrez: 15 3 2024
Statut: epublish

Résumé

Identifying factors that predict the course of persistent symptoms that occurred during the COVID-19 pandemic is a public health issue. Modifiable factors could be targeted in therapeutic interventions. This prospective study based on the population-based CONSTANCES cohort examined whether the psychological burden associated with incident persistent symptoms (ie, that first occurred from March 2020) would predict having ≥1 persistent symptom 6-10 months later. A total of 8424 participants (mean age=54.6 years (SD=12.6), 57.2% women) having ≥1 incident persistent symptom at baseline (ie, between December 2020 and February 2021) were included. The psychological burden associated with these persistent symptoms was assessed with the Somatic Symptom Disorder-B Criteria Scale (SSD-12). The outcome was having ≥1 persistent symptom at follow-up. Adjusted binary logistic regression models examined the association between the SSD-12 score and the outcome. At follow-up, 1124 participants (13.3%) still had ≥1 persistent symptom. The SSD-12 score at baseline was associated with persistent symptoms at follow-up in both participants with (OR (95% CI) for one IQR increase: 1.42 (1.09 to 1.84)) and without SARS-CoV-2 infection prior to baseline (1.39 (1.25 to 1.55)). Female gender, older age, poorer self-rated health and infection prior to baseline were also associated with persistent symptoms at follow-up. The psychological burden associated with persistent symptoms at baseline predicted the presence of ≥1 persistent symptom at follow-up regardless of infection prior to baseline. Intervention studies should test whether reducing the psychological burden associated with persistent symptoms could improve the course of these symptoms.

Sections du résumé

BACKGROUND BACKGROUND
Identifying factors that predict the course of persistent symptoms that occurred during the COVID-19 pandemic is a public health issue. Modifiable factors could be targeted in therapeutic interventions.
OBJECTIVE OBJECTIVE
This prospective study based on the population-based CONSTANCES cohort examined whether the psychological burden associated with incident persistent symptoms (ie, that first occurred from March 2020) would predict having ≥1 persistent symptom 6-10 months later.
METHODS METHODS
A total of 8424 participants (mean age=54.6 years (SD=12.6), 57.2% women) having ≥1 incident persistent symptom at baseline (ie, between December 2020 and February 2021) were included. The psychological burden associated with these persistent symptoms was assessed with the Somatic Symptom Disorder-B Criteria Scale (SSD-12). The outcome was having ≥1 persistent symptom at follow-up. Adjusted binary logistic regression models examined the association between the SSD-12 score and the outcome.
FINDINGS RESULTS
At follow-up, 1124 participants (13.3%) still had ≥1 persistent symptom. The SSD-12 score at baseline was associated with persistent symptoms at follow-up in both participants with (OR (95% CI) for one IQR increase: 1.42 (1.09 to 1.84)) and without SARS-CoV-2 infection prior to baseline (1.39 (1.25 to 1.55)). Female gender, older age, poorer self-rated health and infection prior to baseline were also associated with persistent symptoms at follow-up.
CONCLUSIONS CONCLUSIONS
The psychological burden associated with persistent symptoms at baseline predicted the presence of ≥1 persistent symptom at follow-up regardless of infection prior to baseline.
CLINICAL IMPLICATIONS CONCLUSIONS
Intervention studies should test whether reducing the psychological burden associated with persistent symptoms could improve the course of these symptoms.

Identifiants

pubmed: 38490690
pii: bmjment-2023-300907
doi: 10.1136/bmjment-2023-300907
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: OR reported personal fees and non-financial support from Gilead, ViiV Healthcare and Merck Sharp & Dohme Corp outside the submitted work. VP reported personal fees from Grunenthal, outside the submitted work. CL reported non-financial support from Nordic Pharma, outside the submitted work. No other disclosures were reported.

Auteurs

Baptiste Pignon (B)

Population-based Cohorts Unit, Paris Saclay University, Paris, France baptistepignon@yahoo.fr.

Joane Matta (J)

Population-based Cohorts Unit, Paris Saclay University, Paris, France.

Emmanuel Wiernik (E)

Population-based Cohorts Unit, Paris Saclay University, Paris, France.

Anne Toussaint (A)

Klinik und Poliklinik für Psychosomatische Medizin und Psychotherapie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

Bernd Loewe (B)

Klinik und Poliklinik für Psychosomatische Medizin und Psychotherapie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

Olivier Robineau (O)

Sorbonne Université, Inserm, Institut Pierre-Louis d'Epidémiologie et de Santé Publique, Paris, France.
EA2694, Univ Lille, Centre Hospitalier de Tourcoing, Tourcoing, Paris.

Fabrice Carrat (F)

Sorbonne Université, Inserm, Institut Pierre-Louis d'Epidémiologie et de Santé Publique, Paris, France.
Département de santé publique, AP-HP, Hôpital Saint-Antoine, Paris, France.

Gianluca Severi (G)

Université Paris-Saclay, UVSQ, INSERM, CESP U1018, Gustave Roussy, Villejuif, France.
Department of Statistics, University of Florence, Florence, Italy.

Mathilde Touvier (M)

Sorbonne Paris Nord University, Inserm U1153, Inrae U1125, Cnam, Nutritional Epidemiology Research Team (EREN), Centre of Research in Epidemiology and Statistics (CRESS) - Université Paris Cité (CRESS), Bobigny, France.

Clement Gouraud (C)

Service de Psychiatrie de l'adulte, AP-HP, Hôpital Hôtel-Dieu, Paris, France.
Université Paris Cité and Université Sorbonne Paris Nord, Inserm; INRAE, Center for Research in Epidemiology and StatisticS (CRESS), Paris, France.

Charles Ouazana Vedrines (C)

Service de Psychiatrie de l'adulte, AP-HP, Hôpital Hôtel-Dieu, Paris, France.

Victor Pitron (V)

Université Paris Cité, VIFASOM (Vigilance Fatigue Sommeil et Santé Publique), Paris, France.
Centre du Sommeil et de la Vigilance-Pathologie professionnelle, APHP, Hôtel-Dieu, Paris, France.

Brigitte Ranque (B)

Université Paris Cité, Service de Médecine interne, AP-HP, Hôpital européen Georges-Pompidou, Paris, France.

Nicolas Hoertel (N)

Université Paris Cité, INSERM U1266, Institut de Psychiatrie et Neuroscience de Paris, Paris, France.
Service de Psychiatrie et Addictologie, AP-HP, Hôpital Corentin-Celton, DMU Psychiatrie et Addictologie, Issy-les-Moulineaux, France.

Sofiane Kab (S)

Population-based Cohorts Unit, Paris Saclay University, Paris, France.

Marcel Goldberg (M)

Population-based Cohorts Unit, Paris Saclay University, Paris, France.

Marie Zins (M)

Population-based Cohorts Unit, Paris Saclay University, Paris, France.

Cédric Lemogne (C)

Service de Psychiatrie de l'adulte, AP-HP, Hôpital Hôtel-Dieu, Paris, France.
Université Paris Cité and Université Sorbonne Paris Nord, Inserm; INRAE, Center for Research in Epidemiology and StatisticS (CRESS), Paris, France.

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