AxSpA patients who also meet criteria for fibromyalgia: identifying distinct patient clusters using data from a UK national register (BSRBR-AS).

Axial spondyloarthritis Cluster analysis Comorbidity Criteria Disease register Fibromyalgia

Journal

BMC rheumatology
ISSN: 2520-1026
Titre abrégé: BMC Rheumatol
Pays: England
ID NLM: 101738571

Informations de publication

Date de publication:
2019
Historique:
received: 22 11 2018
accepted: 25 04 2019
entrez: 31 5 2019
pubmed: 31 5 2019
medline: 31 5 2019
Statut: epublish

Résumé

Around 1 in 8 patients with axial spondyloarthritis (axSpA) also meet criteria for fibromyalgia and such patients have considerable unmet need. Identifying effective therapy is important but to what extent fibromyalgia-like symptoms relate to axSpA disease severity has not been established. The aim of the current analysis was to determine whether distinct clusters of axSpA patients exist and if so to determine a) whether they differ in terms of prevalence of fibromyalgia and b) the features of patients in clusters with high prevalence. The British Society for Rheumatology Biologics Register (BSRBR-AS) recruited axSpA patients from 83 centres 2012-2017. Clinical data, and information from patients was collected (including research criteria for fibromyalgia). Cluster analysis was undertaken using split samples for development and validation both in the whole population and the sub-group which met fibromyalgia criteria. One thousand three hundred thirty-eight participants were included of whom 23% met research criteria for fibromyalgia. Four clusters were identified. Two exhibited very high disease activity, one which was primarily axial ( The major feature defining clusters with a high proportion of persons meeting criteria for fibromyalgia is high axSpA disease activity although clusters with features of fibromyalgia in the absence of high disease activity also show moderately high prevalence. Management may be most successful with pharmacologic therapy to target inflammation but enhanced by the concurrent use of non-pharmacologic therapy in such patients.

Sections du résumé

BACKGROUND BACKGROUND
Around 1 in 8 patients with axial spondyloarthritis (axSpA) also meet criteria for fibromyalgia and such patients have considerable unmet need. Identifying effective therapy is important but to what extent fibromyalgia-like symptoms relate to axSpA disease severity has not been established. The aim of the current analysis was to determine whether distinct clusters of axSpA patients exist and if so to determine a) whether they differ in terms of prevalence of fibromyalgia and b) the features of patients in clusters with high prevalence.
METHODS METHODS
The British Society for Rheumatology Biologics Register (BSRBR-AS) recruited axSpA patients from 83 centres 2012-2017. Clinical data, and information from patients was collected (including research criteria for fibromyalgia). Cluster analysis was undertaken using split samples for development and validation both in the whole population and the sub-group which met fibromyalgia criteria.
RESULTS RESULTS
One thousand three hundred thirty-eight participants were included of whom 23% met research criteria for fibromyalgia. Four clusters were identified. Two exhibited very high disease activity, one which was primarily axial (
CONCLUSIONS CONCLUSIONS
The major feature defining clusters with a high proportion of persons meeting criteria for fibromyalgia is high axSpA disease activity although clusters with features of fibromyalgia in the absence of high disease activity also show moderately high prevalence. Management may be most successful with pharmacologic therapy to target inflammation but enhanced by the concurrent use of non-pharmacologic therapy in such patients.

Identifiants

pubmed: 31143851
doi: 10.1186/s41927-019-0066-7
pii: 66
pmc: PMC6532149
doi:

Types de publication

Journal Article

Langues

eng

Pagination

19

Subventions

Organisme : Versus Arthritis
ID : 21378
Pays : United Kingdom

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

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Auteurs

Gary J Macfarlane (GJ)

1Epidemiology Group, School of Medicine, Medical Sciences and Nutrition and The Aberdeen Centre for Arthritis and Musculoskeletal Health, University of Aberdeen, Health Sciences Building, Foresterhill, Aberdeen, AB25 2ZD UK.

Ejaz Pathan (E)

2Department of Rheumatology, Spondylitis Program, Toronto Western Hospital, University Health Network, Toronto, Ontario Canada.

Stefan Siebert (S)

3Institute of Infection, Immunity & Inflammation, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, UK.

Jonathan Packham (J)

4Institute of Primary Care and Health Sciences, Keele University, Keele, UK.

Karl Gaffney (K)

5Department of Rheumatology, Norfolk & Norwich University Hospitals NHS Foundation Trust, Norwich, UK.

Ernest Choy (E)

6CREATE Centre, Section of Rheumatology, Division of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.

Raj Sengupta (R)

7Royal National Hospital for Rheumatic Diseases, Bath, UK.

Fabiola Atzeni (F)

8Rheumatology Unit, L. Sacco University Hospital, Milan, Italy.

Kathryn R Martin (KR)

1Epidemiology Group, School of Medicine, Medical Sciences and Nutrition and The Aberdeen Centre for Arthritis and Musculoskeletal Health, University of Aberdeen, Health Sciences Building, Foresterhill, Aberdeen, AB25 2ZD UK.

Gareth T Jones (GT)

1Epidemiology Group, School of Medicine, Medical Sciences and Nutrition and The Aberdeen Centre for Arthritis and Musculoskeletal Health, University of Aberdeen, Health Sciences Building, Foresterhill, Aberdeen, AB25 2ZD UK.

Linda E Dean (LE)

1Epidemiology Group, School of Medicine, Medical Sciences and Nutrition and The Aberdeen Centre for Arthritis and Musculoskeletal Health, University of Aberdeen, Health Sciences Building, Foresterhill, Aberdeen, AB25 2ZD UK.

Classifications MeSH