Abstract

BackgroundAround 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.MethodsThe 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.ResultsOne 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 (n = 347) and a smaller cluster (n = 32) with axial and peripheral disease, and in both groups more than half of members met criteria for fibromyalgia. The remaining two clusters (n = 437, n = 462) had overall less severe disease however the one which showed greater disease activity and poorer quality of life had a higher proportion meeting fibromyalgia criteria (16% v. 4%). Within those meeting fibromyalgia criteria there were three clusters. The two main groups were defined by level of symptom severity with a smaller third cluster noted to have high average swollen and tender joint counts and high levels of comorbidity.ConclusionsThe 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.

Highlights

  • Around 1 in 8 patients with axial spondyloarthritis meet criteria for fibromyalgia and such patients have considerable unmet need

  • If the co-morbid fibromyalgia-like symptoms are unrelated to disease activity and arise through distinct mechanisms, management should focus on the fibromyalgia. In this analysis, using BSRBR-AS, we aimed to establish if distinct clusters of patients with axial spondyloarthritis (axSpA) exist, and if so to a) ascertain whether such clusters exhibit important differences in the prevalence of fibromyalgia and b) determine features of the clusters which exhibit a high prevalence of fibromyalgia

  • In total 1338 participants were eligible for the current analysis of whom 65% were male, with a median age of 49 years, and median time since symptom onset of 18 years, and 36% had been recruited to the biologic cohort of the study

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Summary

Introduction

Around 1 in 8 patients with axial spondyloarthritis (axSpA) 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. There has been specific interest in the co-occurrence of fibromyalgia and axSpA for two reasons. The first is a result of a United States Food and Drug Administration Arthritis Advisory Committee meeting in 2013 which considered the case for expanding the use of Tumour Necrosis Factor inhibition (TNFi) therapy from ankylosing spondylitis to non-radiographic axSpA. An alternative possibility is that high levels of disease activity, and consequent pain, poor function and impact on quality of life including work, lead to emotional distress which itself has been shown to increase the risk of fibromyalgia. [3]

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