Evidence map›Paper›PMID 37464077›Full record

ArticleMolecular psychiatry2023

Depression and anxiety before and at the beginning of the COVID-19 pandemic and incident persistent symptoms: a prospective population-based cohort study.

Joane Matta, Olivier Robineau, Emmanuel Wiernik, Fabrice Carrat, Gianluca Severi, Mathilde Touvier, Clément Gouraud, Charles Ouazana Vedrines, Victor Pitron, Brigitte Ranque and 6 more

Abstract read
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In one paragraph

Article in Molecular psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

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  14. Complex association between post-COVID-19 condition and anxiety and depression symptoms.European psychiatry : the journal of the Association of European Psychiatrists · 2023
    Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Joane MattaUniversité Paris Cité, « Population-based Cohorts Unit », INSERM, Paris Saclay University, UVSQ, UMS 011, Paris, France.ORCID 0000-0002-9123-6726
Olivier RobineauSorbonne Université, Inserm, Institut Pierre-Louis d'Epidémiologie et de Santé Publique, Paris, France.
Emmanuel WiernikUniversité Paris Cité, « Population-based Cohorts Unit », INSERM, Paris Saclay University, UVSQ, UMS 011, Paris, France.ORCID 0000-0001-8046-7919
Fabrice CarratSorbonne Université, Inserm, Institut Pierre-Louis d'Epidémiologie et de Santé Publique, Paris, France.
Gianluca SeveriUniversité Paris-Saclay, UVSQ, INSERM, CESP U1018, Gustave Roussy, Villejuif, France.
Mathilde TouvierSorbonne Paris Nord University, Inserm U1153, Inrae U1125, Cnam, Nutritional Epidemiology Research Team (EREN), Centre of Research in Epidemiology and StatisticS (CRESS) - Université Paris Cité, Bobigny, France.ORCID 0000-0002-8322-8857
Clément GouraudService de Psychiatrie de l'adulte, AP-HP, Hôpital Hôtel-Dieu, Paris, France.
Charles Ouazana VedrinesService de Psychiatrie de l'adulte, AP-HP, Hôpital Hôtel-Dieu, Paris, France.ORCID 0000-0002-3587-7182
Victor PitronUniversité Paris Cité, VIFASOM (Vigilance Fatigue Sommeil et Santé Publique), Paris, France.
Brigitte RanqueUniversité de Paris, Service de Médecine interne, AP-HP, Hôpital européen Georges-Pompidou, Paris, France.
Baptiste PignonUniversité Paris Cité, « Population-based Cohorts Unit », INSERM, Paris Saclay University, UVSQ, UMS 011, Paris, France.
Nicolas HoertelUniversité Paris Cité, INSERM U1266, Institut de Psychiatrie et Neuroscience de Paris, Paris, France.
Sofiane KabUniversité Paris Cité, « Population-based Cohorts Unit », INSERM, Paris Saclay University, UVSQ, UMS 011, Paris, France.
Marcel GoldbergUniversité Paris Cité, « Population-based Cohorts Unit », INSERM, Paris Saclay University, UVSQ, UMS 011, Paris, France.ORCID 0000-0002-6161-5880
Marie ZinsUniversité Paris Cité, « Population-based Cohorts Unit », INSERM, Paris Saclay University, UVSQ, UMS 011, Paris, France.ORCID 0000-0002-4540-4282
Cédric LemogneService de Psychiatrie de l'adulte, AP-HP, Hôpital Hôtel-Dieu, Paris, France. cedric.lemogne@aphp.fr.ORCID 0000-0002-3487-4721

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-COHO-06Agence Nationale de la Recherche (French National Research Agency) ANR-11-INBS-0002Agence Nationale de la Recherche (French National Research Agency) ANR-20-COVI-000Agence Nationale de Recherches sur le Sida et les Hépatites Virales (National Agency for AIDS Research) AAP Covid long 2022-1
6 · The paper itself

Abstract

Many patients affected by COVID-19 suffer from debilitating persistent symptoms whose risk factors remained poorly understood. This prospective study examined the association of depression and anxiety symptoms measured before and at the beginning of the COVID-19 pandemic with the incidence of persistent symptoms. Among 25,114 participants [mean (SD) age, 48.72 years (12.82); 51.1% women] from the SAPRIS and SAPRIS-Sérologie surveys nested in the French CONSTANCES population-based cohort, depression and anxiety symptoms were measured with the Center for Epidemiologic Studies-Depression scale and the 12-item General Health Questionnaire before the pandemic, and with the 9-item Patient Health Questionnaire and the 7-Item Generalized Anxiety Disorder scale at the beginning of the pandemic (i.e., between April 6, 2020 and May 4, 2020). Incident persistent symptoms were self-reported between December 2020 and January 2021. The following variables were also considered: gender, age, educational level, household income, smoking status, BMI, hypertension, diabetes, self-rated health, and SARS-CoV-2 infection according to serology/PCR test results. After a follow-up of seven to ten months, 2329 participants (9.3%) had been infected with SARS-CoV-2 and 4262 (17.0%) reported at least one incident persistent symptom that emerged from March 2020, regardless of SARS-CoV-2 infection. In multi-adjusted logistic regression models, participants in the highest (versus the lowest) quartile of depressive or anxiety symptom levels before or at the beginning of the pandemic were more likely to have at least one incident persistent symptom (versus none) at follow-up [OR (95%CI) ranging from 2.10 (1.89-2.32) to 3.01 (2.68-3.37)], with dose-response relationships (p for linear trend <0.001). Overall, these associations were significantly stronger in non-infected versus infected participants, except for depressive symptoms at the beginning of the pandemic. Depressive symptoms at the beginning of the pandemic were the strongest predictor of incident persistent symptoms in both infected and non-infected participants [OR (95%CI): 2.88 (2.01-4.14) and 3.03 (2.69-3.42), respectively]. In exploratory analyses, similar associations were found for each symptom taken separately in different models. Depression and anxiety symptoms should be tested as a potential target for preventive interventions against persistent symptoms after an infection with SARS-CoV-2.

Indexed as

COVID-19PandemicsAnxietyCohort StudiesDepressionFemaleHumansMaleMiddle AgedProspective StudiesSARS-CoV-2

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.