Evidence map›Paper›PMID 41526946›Full record

ArticleAdvances in rheumatology (London, England)2026

Multidimensional contributors to disease burden in axial spondyloarthritis: role of central sensitization, catastrophizing and sleep disturbance.

Jeniffer Mirelli Dos Santos Lopes, Aline Ranzolin, Nara Gualberto Cavalcanti, Angela Luzia Branco Pinto Duarte, Claudia Diniz Lopes Marques

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Article in Advances in rheumatology (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jeniffer Mirelli Dos Santos LopesPrograma de Pós-Graduação em Saúde Translacional, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil. jeniffer.lopes15@gmail.com.ORCID 0000-0002-2027-1233
Aline RanzolinDepartment of Rheumatology, Hospital das Clínicas da Universidade Federal de Pernambuco/Ebserh, Recife, Pernambuco, Brazil.
Nara Gualberto CavalcantiDepartment of Rheumatology, Hospital das Clínicas da Universidade Federal de Pernambuco/Ebserh, Recife, Pernambuco, Brazil.
Angela Luzia Branco Pinto DuarteDepartment of Rheumatology, Hospital das Clínicas da Universidade Federal de Pernambuco/Ebserh, Recife, Pernambuco, Brazil.
Claudia Diniz Lopes MarquesDepartment of Rheumatology, Hospital das Clínicas da Universidade Federal de Pernambuco/Ebserh, Recife, Pernambuco, Brazil.ORCID 0000-0002-3333-2621

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAxial spondyloarthritis (axSpA) imposes a multidimensional burden that is not fully explained by inflammation. Central sensitization (CS), pain catastrophizing (PC), and sleep disturbance may amplify symptoms and worsen outcomes. This study aimed to assess the prevalence and impact of CS, PC, and sleep disturbances in axSpA patients and their associations with disease activity, function, and quality of life compared with controls.

methodsThis cross-sectional study included adults with axSpA (ASAS 2009) and healthy controls recruited from a tertiary clinic (April 2024-April 2025). The assessments included demographics; CSI, PCS, JSS, fibromyalgia (ACR-2016), fibromyalgianess (WPI + SSS); and axSpA outcomes (BASDAI, ASDAS, BASFI, BASMI, ASQoL, CRP, and MASES). Statistical analyses included group comparisons, correlations, and multivariable regressions.

resultsWe enrolled 100 axSpA patients and 50 controls. The median scores were greater in the axSpA patients for the CSI (42 vs. 28), PCS (32 vs. 12.5), and JSS (12 vs. 6) (all p < 0.001). The prevalence was greater for CS (59% vs. 20%), PC (53% vs. 18%), and fibromyalgia (43% vs. 18%). The WPI was strongly correlated with the SSS (r = 0.92). In the axSpA patients, the CSI was correlated with the BASDAI (r = 0.58), ASDAS (r = 0.43), BASFI (r = 0.45), and ASQoL (r = 0.68) (all p ≤ 0.001). The PCS and JSS are also correlated with disease activity, disease function, and ASQoL. Independent predictors were CSI-female sex, higher SSS, and worse ASQoL; PCS-ASQoL; JSS-higher SSS and arthritis, with lower scores in patients on TNF inhibitors or pain-modulating therapy.

conclusionCS, PC, sleep disturbance, and FM/FMness are highly prevalent in axSpA patients and are independently associated with worse outcomes. Incorporating nociplastic and psychosocial dimensions into assessment and care is crucial to reduce disease burden.

Indexed as

Axial SpondyloarthritisCatastrophizationCentral Nervous System SensitizationCost of IllnessSleep Wake DisordersAdultCase-Control StudiesCross-Sectional StudiesFemaleFibromyalgiaHumansMaleMiddle AgedNociplastic PainPrevalenceQuality of LifeAxial spondyloarthritisCentral sensitizationDisease activityPain catastrophizing

Identifiers

PMID41526946
PMCPMC13488833

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.