Neuropathic-like pain symptoms in inflammatory hand osteoarthritis lower quality of life and may not decrease under prednisolone treatment.


Journal

European journal of pain (London, England)
ISSN: 1532-2149
Titre abrégé: Eur J Pain
Pays: England
ID NLM: 9801774

Informations de publication

Date de publication:
09 2022
Historique:
revised: 25 05 2022
received: 22 11 2021
accepted: 30 05 2022
pubmed: 8 6 2022
medline: 17 8 2022
entrez: 7 6 2022
Statut: ppublish

Résumé

Pain is common in hand osteoarthritis (OA) and multiple types may occur. We investigated the prevalence, associated patient characteristics, influence on health-related quality of life (HR-QoL) and response to anti-inflammatory treatment of neuropathic-like pain in inflammatory hand OA. Data were analysed from a 6-week, randomized, double-blind, placebo-controlled trial investigating prednisolone treatment in 92 patients with painful inflammatory hand OA. Neuropathic-like pain was measured with the painDETECT questionnaire. Associations between baseline characteristics and baseline neuropathic-like pain were analysed with ordinal logistic regression, association of baseline neuropathic-like pain symptoms with baseline HR-QoL with linear regression, painDETECT and visual analogue scale (VAS) change from baseline to week 6 and interaction of painDETECT with prednisolone efficacy on VAS pain change from baseline to week 6 with generalized estimating equations (GEE). Of 91 patients (79% female, mean age 64) with complete painDETECT data at baseline, 53% were unlikely to have neuropathic-like pain, 31% were indeterminate and 16% were likely to have neuropathic-like pain. Neuropathic-like pain was associated with female sex, less radiographic damage and more comorbidities. Patients with neuropathic-like pain had lower HR-QoL (PCS-6.5 [95% CI -10.4 to -2.6]) than those without. Neuropathic-like pain symptoms remained under prednisolone treatment and no interaction was seen between painDETECT and prednisolone efficacy on VAS pain. In this study, 16% of inflammatory hand OA patients had neuropathic-like pain. They were more often female, had more comorbidities and had lower QoL than those without. Neuropathic-like pain symptoms remained despite prednisolone treatment and did not seem to affect the outcome of prednisolone treatment. Pain is the dominant symptom in hand OA, with an unclear aetiology. In this study, we found that neuropathic-like pain may play a role in hand OA, that it showed associations with female sex, younger age and more comorbidities and that it lowered health-related quality of life in hand OA. Neuropathic-like pain in hand OA seems resistant to prednisolone therapy but did not seem to interfere with the treatment of inflammatory pain with prednisolone.

Sections du résumé

BACKGROUND
Pain is common in hand osteoarthritis (OA) and multiple types may occur. We investigated the prevalence, associated patient characteristics, influence on health-related quality of life (HR-QoL) and response to anti-inflammatory treatment of neuropathic-like pain in inflammatory hand OA.
METHODS
Data were analysed from a 6-week, randomized, double-blind, placebo-controlled trial investigating prednisolone treatment in 92 patients with painful inflammatory hand OA. Neuropathic-like pain was measured with the painDETECT questionnaire. Associations between baseline characteristics and baseline neuropathic-like pain were analysed with ordinal logistic regression, association of baseline neuropathic-like pain symptoms with baseline HR-QoL with linear regression, painDETECT and visual analogue scale (VAS) change from baseline to week 6 and interaction of painDETECT with prednisolone efficacy on VAS pain change from baseline to week 6 with generalized estimating equations (GEE).
RESULTS
Of 91 patients (79% female, mean age 64) with complete painDETECT data at baseline, 53% were unlikely to have neuropathic-like pain, 31% were indeterminate and 16% were likely to have neuropathic-like pain. Neuropathic-like pain was associated with female sex, less radiographic damage and more comorbidities. Patients with neuropathic-like pain had lower HR-QoL (PCS-6.5 [95% CI -10.4 to -2.6]) than those without. Neuropathic-like pain symptoms remained under prednisolone treatment and no interaction was seen between painDETECT and prednisolone efficacy on VAS pain.
CONCLUSIONS
In this study, 16% of inflammatory hand OA patients had neuropathic-like pain. They were more often female, had more comorbidities and had lower QoL than those without. Neuropathic-like pain symptoms remained despite prednisolone treatment and did not seem to affect the outcome of prednisolone treatment.
SIGNIFICANCE
Pain is the dominant symptom in hand OA, with an unclear aetiology. In this study, we found that neuropathic-like pain may play a role in hand OA, that it showed associations with female sex, younger age and more comorbidities and that it lowered health-related quality of life in hand OA. Neuropathic-like pain in hand OA seems resistant to prednisolone therapy but did not seem to interfere with the treatment of inflammatory pain with prednisolone.

Identifiants

pubmed: 35671123
doi: 10.1002/ejp.1991
pmc: PMC9541664
doi:

Substances chimiques

Prednisolone 9PHQ9Y1OLM

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1691-1701

Informations de copyright

© 2022 The Authors. European Journal of Pain published by John Wiley & Sons Ltd on behalf of European Pain Federation - EFIC®.

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Auteurs

Coen van der Meulen (C)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

Lotte A van de Stadt (LA)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

Féline P B Kroon (FPB)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
Department of Rheumatology, Zuyderland Medical Center, Heerlen, The Netherlands.

Marion C Kortekaas (MC)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

Annelies E R C H Boonen (AERCH)

Department of Rheumatology, Maastricht University Medical Center and Care and Public Health Research Institute, Maastricht, The Netherlands.

Stefan Böhringer (S)

Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, The Netherlands.

Marieke Niesters (M)

Department of Anaesthesiology, Leiden University Medical Center, Leiden, The Netherlands.

Monique Reijnierse (M)

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

Frits R Rosendaal (FR)

Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.

Naghmeh Riyazi (N)

Department of Rheumatology, Haga Hospital, The Hague, The Netherlands.

Mirian Starmans-Kool (M)

Department of Rheumatology, Zuyderland Medical Center, Heerlen, The Netherlands.

Franktien Turkstra (F)

Amsterdam Rheumatology and Immunology Center - Reade, Amsterdam, The Netherlands.

Jendé van Zeben (J)

Department of Rheumatology, Sint Franciscus Vlietland Groep, Rotterdam, The Netherlands.

Cornelia F Allaart (CF)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

Margreet Kloppenburg (M)

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

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