Cargando…

Association between chronic pain and risk of incident dementia: findings from a prospective cohort

BACKGROUND: Chronic musculoskeletal pain has been linked to dementia; however, chronic pain typically occurs in multiple sites; therefore, this study was to investigate whether greater number of chronic pain sites is associated with a higher risk of dementia and its subtypes. METHODS: Participants (...

Descripción completa

Detalles Bibliográficos
Autores principales: Tian, Jing, Jones, Graeme, Lin, Xin, Zhou, Yuan, King, Anna, Vickers, James, Pan, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161483/
https://www.ncbi.nlm.nih.gov/pubmed/37143042
http://dx.doi.org/10.1186/s12916-023-02875-x
_version_ 1785037504343179264
author Tian, Jing
Jones, Graeme
Lin, Xin
Zhou, Yuan
King, Anna
Vickers, James
Pan, Feng
author_facet Tian, Jing
Jones, Graeme
Lin, Xin
Zhou, Yuan
King, Anna
Vickers, James
Pan, Feng
author_sort Tian, Jing
collection PubMed
description BACKGROUND: Chronic musculoskeletal pain has been linked to dementia; however, chronic pain typically occurs in multiple sites; therefore, this study was to investigate whether greater number of chronic pain sites is associated with a higher risk of dementia and its subtypes. METHODS: Participants (N = 356,383) in the UK Biobank who were dementia-free at baseline were included. Pain in the hip, knee, back, and neck/shoulder or ‘all over the body’ and its duration were assessed. Participants were categorised into six groups: no chronic pain; chronic pain in 1, 2, 3, and 4 sites, and ‘all over the body’. All-cause dementia and its subtypes were ascertained using hospital inpatient and death registry records. Cox regression was used to investigate the associations between the number of chronic pain sites and the incidence of all-cause dementia and its subtypes. RESULTS: Over a median follow-up of 13 years, 4959 participants developed dementia. After adjustment for sociodemographic, lifestyle, comorbidities, pain medications, psychological problems, and sleep factors, greater number of chronic pain sites was associated with an increased risk of incident all-cause dementia (hazard ratio [HR] = 1.08 per 1 site increase, 95% CI 1.05–1.11) and Alzheimer’s disease (AD) (HR = 1.09 per 1-site increase, 95% CI 1.04–1.13) in a dose–response manner but not vascular and frontotemporal dementia. No significant association was found between the number of chronic pain sites and the risk of incident all-cause dementia among a subsample that underwent a fluid intelligence test. CONCLUSIONS: Greater number of chronic pain sites was associated with an increased risk of incident all-cause dementia and AD, suggesting that chronic pain in multiple sites may contribute to individuals’ dementia risk and is an underestimated risk factor for dementia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-02875-x.
format Online
Article
Text
id pubmed-10161483
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-101614832023-05-06 Association between chronic pain and risk of incident dementia: findings from a prospective cohort Tian, Jing Jones, Graeme Lin, Xin Zhou, Yuan King, Anna Vickers, James Pan, Feng BMC Med Research Article BACKGROUND: Chronic musculoskeletal pain has been linked to dementia; however, chronic pain typically occurs in multiple sites; therefore, this study was to investigate whether greater number of chronic pain sites is associated with a higher risk of dementia and its subtypes. METHODS: Participants (N = 356,383) in the UK Biobank who were dementia-free at baseline were included. Pain in the hip, knee, back, and neck/shoulder or ‘all over the body’ and its duration were assessed. Participants were categorised into six groups: no chronic pain; chronic pain in 1, 2, 3, and 4 sites, and ‘all over the body’. All-cause dementia and its subtypes were ascertained using hospital inpatient and death registry records. Cox regression was used to investigate the associations between the number of chronic pain sites and the incidence of all-cause dementia and its subtypes. RESULTS: Over a median follow-up of 13 years, 4959 participants developed dementia. After adjustment for sociodemographic, lifestyle, comorbidities, pain medications, psychological problems, and sleep factors, greater number of chronic pain sites was associated with an increased risk of incident all-cause dementia (hazard ratio [HR] = 1.08 per 1 site increase, 95% CI 1.05–1.11) and Alzheimer’s disease (AD) (HR = 1.09 per 1-site increase, 95% CI 1.04–1.13) in a dose–response manner but not vascular and frontotemporal dementia. No significant association was found between the number of chronic pain sites and the risk of incident all-cause dementia among a subsample that underwent a fluid intelligence test. CONCLUSIONS: Greater number of chronic pain sites was associated with an increased risk of incident all-cause dementia and AD, suggesting that chronic pain in multiple sites may contribute to individuals’ dementia risk and is an underestimated risk factor for dementia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-02875-x. BioMed Central 2023-05-04 /pmc/articles/PMC10161483/ /pubmed/37143042 http://dx.doi.org/10.1186/s12916-023-02875-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Tian, Jing
Jones, Graeme
Lin, Xin
Zhou, Yuan
King, Anna
Vickers, James
Pan, Feng
Association between chronic pain and risk of incident dementia: findings from a prospective cohort
title Association between chronic pain and risk of incident dementia: findings from a prospective cohort
title_full Association between chronic pain and risk of incident dementia: findings from a prospective cohort
title_fullStr Association between chronic pain and risk of incident dementia: findings from a prospective cohort
title_full_unstemmed Association between chronic pain and risk of incident dementia: findings from a prospective cohort
title_short Association between chronic pain and risk of incident dementia: findings from a prospective cohort
title_sort association between chronic pain and risk of incident dementia: findings from a prospective cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161483/
https://www.ncbi.nlm.nih.gov/pubmed/37143042
http://dx.doi.org/10.1186/s12916-023-02875-x
work_keys_str_mv AT tianjing associationbetweenchronicpainandriskofincidentdementiafindingsfromaprospectivecohort
AT jonesgraeme associationbetweenchronicpainandriskofincidentdementiafindingsfromaprospectivecohort
AT linxin associationbetweenchronicpainandriskofincidentdementiafindingsfromaprospectivecohort
AT zhouyuan associationbetweenchronicpainandriskofincidentdementiafindingsfromaprospectivecohort
AT kinganna associationbetweenchronicpainandriskofincidentdementiafindingsfromaprospectivecohort
AT vickersjames associationbetweenchronicpainandriskofincidentdementiafindingsfromaprospectivecohort
AT panfeng associationbetweenchronicpainandriskofincidentdementiafindingsfromaprospectivecohort