External Factors Modulating Pain and Pain-Related Functional Impairment in Cervical Dystonia.

Pain in Dystonia Scale (PIDS) cervical dystonia external factors pain relieving factors trigger

Journal

Movement disorders clinical practice
ISSN: 2330-1619
Titre abrégé: Mov Disord Clin Pract
Pays: United States
ID NLM: 101630279

Informations de publication

Date de publication:
23 Oct 2024
Historique:
revised: 09 09 2024
received: 03 07 2024
accepted: 04 10 2024
medline: 23 10 2024
pubmed: 23 10 2024
entrez: 23 10 2024
Statut: aheadofprint

Résumé

Little is known about factors modulating pain and pain-related functional impairment in isolated cervical dystonia (CD). The aim was to assess the prevalence and interrelationship between pain-modulating factors and pain-related determinants of functional impairment and quality of life in CD. We analyzed pain-aggravating and pain-relieving external factors, the degree of pain-related functional impact on routine activities, and the relationship between these and pain severity, using cross-sectional data collected using the Pain in Dystonia Scale (PIDS) from 85 participants with CD. Pairwise correlation analyses and age- and sex-adjusted linear regression models estimated the relationship between pain-modulating factors and pain severity, and the impact of pain severity, dystonia severity, and psychiatric symptoms on pain-related functional impairment and disease-specific quality of life (measured using the Craniocervical Dystonia Questionnaire-24). Stress and prolonged fixed position were the most frequent and impacting pain triggers, with women reporting larger impact. The average impact of pain-relieving factors was lower than that of pain triggers. Physical exercise and social gatherings were the most impacted activities by pain in CD. The intensity of external modulating factors was a predictor of pain severity. Severity of pain, CD, and psychiatric symptoms independently predicted pain-related functional impairment, whereas quality of life was predicted by pain severity, pain-related functional impairment, and psychiatric symptom severity, but not dystonia severity. The PIDS provides insight into external modulation and functional impact of pain in CD. The pattern of external modulation of pain in CD is in line with a multifactorial modulation and complex physiology.

Sections du résumé

BACKGROUND BACKGROUND
Little is known about factors modulating pain and pain-related functional impairment in isolated cervical dystonia (CD).
OBJECTIVE OBJECTIVE
The aim was to assess the prevalence and interrelationship between pain-modulating factors and pain-related determinants of functional impairment and quality of life in CD.
METHODS METHODS
We analyzed pain-aggravating and pain-relieving external factors, the degree of pain-related functional impact on routine activities, and the relationship between these and pain severity, using cross-sectional data collected using the Pain in Dystonia Scale (PIDS) from 85 participants with CD. Pairwise correlation analyses and age- and sex-adjusted linear regression models estimated the relationship between pain-modulating factors and pain severity, and the impact of pain severity, dystonia severity, and psychiatric symptoms on pain-related functional impairment and disease-specific quality of life (measured using the Craniocervical Dystonia Questionnaire-24).
RESULTS RESULTS
Stress and prolonged fixed position were the most frequent and impacting pain triggers, with women reporting larger impact. The average impact of pain-relieving factors was lower than that of pain triggers. Physical exercise and social gatherings were the most impacted activities by pain in CD. The intensity of external modulating factors was a predictor of pain severity. Severity of pain, CD, and psychiatric symptoms independently predicted pain-related functional impairment, whereas quality of life was predicted by pain severity, pain-related functional impairment, and psychiatric symptom severity, but not dystonia severity.
CONCLUSION CONCLUSIONS
The PIDS provides insight into external modulation and functional impact of pain in CD. The pattern of external modulation of pain in CD is in line with a multifactorial modulation and complex physiology.

Identifiants

pubmed: 39440662
doi: 10.1002/mdc3.14235
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Ipsen Pharmaceuticals

Informations de copyright

© 2024 The Author(s). Movement Disorders Clinical Practice published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Auteurs

Davide Martino (D)

University of Calgary, Department of Clinical Neurosciences, Faculty of Medicine, Calgary, Alberta, Canada.
Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.

Beatrice M C Achen (BMC)

University of Calgary, Department of Clinical Neurosciences, Faculty of Medicine, Calgary, Alberta, Canada.
Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.

Francesca Morgante (F)

Neurosciences and Cell Biology Institute, Neuromodulation and Motor Control Section, St George's University of London, London, United Kingdom.

Roberto Erro (R)

Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana," University of Salerno, Baronissi, Italy.

Susan H Fox (SH)

Movement Disorder Clinic, Krembil Brain Institute, University Health Network, Toronto, Ontario, Canada.

Mark J Edwards (MJ)

Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, United Kingdom.

Anette Schrag (A)

Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.

Maria Stamelou (M)

Parkinson's Disease and Movement Disorders Department, HYGEIA Hospital and First Department of Neurology, National and Kapodistrian University of Athens, Athens, Greece.

Silke Appel-Cresswell (S)

Pacific Parkinson's Research Centre, Djavad Mowafaghian Centre for Brain Health, University of British Columbia, Vancouver, British Columbia, Canada.

Giovanni Defazio (G)

Department of Neurological and Psychiatric Sciences, University of Bari, Bari, Italy.

Kallol Ray-Chaudhuri (K)

Parkinson's Foundation Centre of Excellence, King's College Hospital and Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, United Kingdom.

Karolina Poplawska-Domaszewicz (K)

Parkinson's Foundation Centre of Excellence, King's College Hospital and Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, United Kingdom.
Department of Neurology, Poznan University of Medical Sciences, Poznan, Poland.

Sarah Pirio Richardson (SP)

Department of Neurology, University of New Mexico, New Mexico VA Healthcare System, Albuquerque, New Mexico, USA.

Hyder A Jinnah (HA)

Department of Neurology, Human Genetics and Pediatrics, Emory University School of Medicine, Atlanta, Georgia, USA.

Veronica A Bruno (VA)

University of Calgary, Department of Clinical Neurosciences, Faculty of Medicine, Calgary, Alberta, Canada.
Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.

Classifications MeSH