Residual Disease in Patients with Axial Spondyloarthritis: A Post-Hoc Analysis of the QUASAR Study.

ASDAS ASQoL BASDAI EQ-5D-5L HRQoL ankylosing spondylitis low disease activity pain/discomfort remission residual disease tiredness/fatigue

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
20 Jun 2022
Historique:
received: 08 06 2022
accepted: 15 06 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 25 6 2022
Statut: epublish

Résumé

In this study, we evaluated the presence of residual disease in patients with axial spondyloarthritis (axSpA) in remission/low disease activity (LDA) status. This cross-sectional post-hoc analysis of the QUASAR study involving 23 rheumatology centres across Italy included adults with axSpA classified according to the Assessment of SpondyloArthritis International Society criteria. Patients with inactive disease (score < 1.3) or at least LDA status (score < 2.1) at baseline visit according to Ankylosing Spondylitis Disease Activity Score were investigated to evaluate how residual disease activity impacts patients’ quality of life. They were assessed using the Ankylosing Spondylitis Quality of Life (ASQoL) and EuroQoL 5-Dimension 5-Level (EQ-5D-5L) questionnaires. This study included 480 patients with axSpA (mean age, 47.5 ± 12.9 years, 64% male). In total, 123 patients (25.6%) had inactive disease and 262 (54.6%) had at least LDA. Using the ASQoL, ranges of 10−25% and 20−40% of patients with inactive disease and with LDA status, respectively, experienced tiredness/fatigue. Despite being classified with inactive disease, 48.8% of patients reported light pain/discomfort according to the EQ-5D-5L, with 4.1% reporting moderate pain/discomfort, whereas 55.7% of patients with LDA reported light pain/discomfort and 13% had moderate pain/discomfort. Using the ASQoL questionnaire, in patients with at least LDA, a higher proportion of women compared with males and a higher proportion of patients > 48 years of age (vs. patients ≤ 48 years) experienced tiredness. In this post-hoc analysis, ≥25% of axSpA patients in remission/LDA status were still burdened by residual disease, mainly characterised by pain and fatigue.

Identifiants

pubmed: 35743623
pii: jcm11123553
doi: 10.3390/jcm11123553
pmc: PMC9224866
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Abbvie SrL
ID : N/A

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Auteurs

Salvatore D'Angelo (S)

Rheumatology Department of Lucania, San Carlo Hospital of Potenza, 85100 Potenza, Italy.

Carlo Salvarani (C)

Rheumatology Unit, Azienda USL-IRCCS di Reggio Emilia and Università di Modena and Reggio Emilia, 42123 Reggio Emilia, Italy.

Francesca Marando (F)

AbbVie Srl, 00185 Rome, Italy.

Lucia Novelli (L)

AbbVie Srl, 00185 Rome, Italy.

Giacomo Curradi (G)

AbbVie Srl, 00185 Rome, Italy.

Giovanni Tripepi (G)

National Research Council-Institute of Clinical Physiology (CNR-IFC), 89124 Reggio Calabria, Italy.

Annalisa Pitino (A)

Institute of Clinical Physiology (IFC-CNR), 00185 Rome, Italy.

Roberta Ramonda (R)

Rheumatology Unit, Department of Medicine-DIMED, University of Padova, 35131 Padova, Italy.

Antonio Marchesoni (A)

Rheumatology, Humanitas San Pio X, 20122 Milan, Italy.

Classifications MeSH