AI Article Synopsis

  • The study examined how outcome measures from EULAR relate to quality of life (QoL), fatigue, anxiety, and depression in patients with primary Sjögren's syndrome (pSS) and aimed to identify factors impacting QoL.
  • The research involved 105 pSS patients and 72 healthy controls, utilizing various clinical assessments, including anxiety and depression scales, fatigue measures, and QoL indices.
  • Results indicated that patients with pSS reported significantly lower QoL and higher levels of anxiety, depression, and fatigue compared to controls, with specific correlations found between disease activity measures and these psychological and physical symptoms.

Article Abstract

Introduction: The aim of the study was to investigate whether there is a relationship between the European League Against Rheumatism (EULAR) outcome measures and quality of life (QoL), fatigue, anxiety and depression in patients with pSS and to define determinants which could affect quality of life.

Material And Methods: The study included 105 pSS patients and 72 age/sex-matched healthy controls (HCs). Cross-sectional clinical data were collected, including the Hospital Anxiety and Depression Scale (HADS), the Multidimensional Assessment of Fatigue (MAF) scale, the Short Form (SF-36), EULAR Sjögren's syndrome disease activity index (ESSDAI) and EULAR Sjögren's syndrome patient reported index (ESSPRI).

Results: The SF-36 scores were significantly lower and anxiety, depression and fatigue scores were significantly higher in the pSS group than in the control group (all -value < 0.05). ESSDAI was negatively correlated with SF-36 scores and positively with MAF. ESSPRI was negatively correlated with SF-36 scores except for the mental health subdimension, and a positive correlation was determined with MAF, HADS-A and HADS-D. Multiple linear regression analysis revealed that HADS-A, HADS-D, MAF, ESSPRI and ESSDAI were associated with most SF-36 subscales.

Conclusions: The results of this study provide further evidence supporting the use of ESSDAI and ESSPRI in daily practice. Quality of life was diminished in patients with pSS and was associated with different symptoms. This should be taken into account when managing patients with pSS.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6040141PMC
http://dx.doi.org/10.5114/aoms.2017.70300DOI Listing

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