Early-life adversity predicting the incidence of multisite chronic pain in the general population.
Détails
Télécharger: 39375924.pdf (338.17 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY-NC-ND 4.0
Etat: Public
Version: Final published version
Licence: CC BY-NC-ND 4.0
ID Serval
serval:BIB_9A2F2F97941A
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Early-life adversity predicting the incidence of multisite chronic pain in the general population.
Périodique
European psychiatry
ISSN
1778-3585 (Electronic)
ISSN-L
0924-9338
Statut éditorial
Publié
Date de publication
08/10/2024
Peer-reviewed
Oui
Volume
67
Numéro
1
Pages
e67
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Publication Status: epublish
Résumé
Adverse childhood events (ACEs) have been linked to widespread chronic pain (CP) in various cross-sectional studies, mainly in clinical populations. However, the independent role of different ACEs on the development of different types of CP remains elusive. Accordingly, we aimed to prospectively assess the associations between specific types of ACEs with the development of multisite CP in a large population-based cohort.
Data stemmed from the three first follow-up evaluations of CoLaus|PsyCoLaus, a prospective population-based cohort study of initially 6734 participants (age range: 35-75 years). The present sample included 1537 participants with 2161 analyzable intervals (49.7% men, mean age 57.3 years). Diagnostic criteria for ACEs were elicited using semi-structured interviews and CP was assessed by self-rating questionnaires. Multinomial logistic regressions with generalized estimating equations method analyzed the relationship between the different ACEs measured in the beginning of the interval and the risk of developing multisite CP during the follow-up. Sensitivity analyses were performed to assess the predictive value of ACEs on multisite CP with neuropathic features.
Participants with a history of parental divorce or separation had an increased risk of developing multisite CP at during follow-up in comparison to those without (RR1.98; 95% CI 1.13-3.47). A strong association was highlighted between parental divorce or separation and the risk of subsequent CP with neuropathic characteristics (RR 4.21, 95% CI 1.45-12.18).
These results highlight the importance of psychotherapeutic management of people experiencing parental separation to prevent CP in the future.
Data stemmed from the three first follow-up evaluations of CoLaus|PsyCoLaus, a prospective population-based cohort study of initially 6734 participants (age range: 35-75 years). The present sample included 1537 participants with 2161 analyzable intervals (49.7% men, mean age 57.3 years). Diagnostic criteria for ACEs were elicited using semi-structured interviews and CP was assessed by self-rating questionnaires. Multinomial logistic regressions with generalized estimating equations method analyzed the relationship between the different ACEs measured in the beginning of the interval and the risk of developing multisite CP during the follow-up. Sensitivity analyses were performed to assess the predictive value of ACEs on multisite CP with neuropathic features.
Participants with a history of parental divorce or separation had an increased risk of developing multisite CP at during follow-up in comparison to those without (RR1.98; 95% CI 1.13-3.47). A strong association was highlighted between parental divorce or separation and the risk of subsequent CP with neuropathic characteristics (RR 4.21, 95% CI 1.45-12.18).
These results highlight the importance of psychotherapeutic management of people experiencing parental separation to prevent CP in the future.
Mots-clé
Humans, Male, Female, Chronic Pain/epidemiology, Chronic Pain/psychology, Middle Aged, Adult, Adverse Childhood Experiences/statistics & numerical data, Aged, Incidence, Prospective Studies, Adult Survivors of Child Adverse Events/statistics & numerical data, Adult Survivors of Child Adverse Events/psychology, Risk Factors, Adverse childhood events, chronic pain, cohort, longitudinal
Pubmed
Web of science
Open Access
Oui
Création de la notice
11/10/2024 13:34
Dernière modification de la notice
31/10/2024 7:13