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Health-related quality of life in systemic sclerosis compared with other rheumatic diseases: a cross-sectional study

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dc.contributor.authorPark, Eun Hye-
dc.contributor.authorStrand, Vibeke-
dc.contributor.authorOh, Yoon Jeong-
dc.contributor.authorSong, Yeong Wook-
dc.contributor.authorLee, Eun Bong-
dc.date.accessioned2019-03-20T05:34:02Z-
dc.date.available2019-03-20T14:36:45Z-
dc.date.issued2019-02-15-
dc.identifier.citationArthritis Research & Therapy. 2019 Feb 15;21(1):61ko_KR
dc.identifier.issn1478-6362-
dc.identifier.urihttps://hdl.handle.net/10371/147189-
dc.description.abstractBackground
Systemic sclerosis (SSc) is a rare autoimmune disease characterized by fibrosis of the skin and the involvement of multiple internal organs. Previous studies reported poorer health-related quality of life (HRQoL) in patients with SSc compared with the general population. However, very little is known about how HRQoL in SSc patients compares with that in patients with other systemic autoimmune diseases, such as rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and Sjogrens syndrome (SjS). Thus, the main aim of this study was to compare HRQoL in SSc patients, patients with other rheumatic diseases, and the general population.

Methods
In this cross-sectional study, patients from the rheumatology clinics of Seoul National University Hospital with SSc, RA, SLE, and SjS were enrolled via a random sampling technique. HRQoL was captured by the Short Form (36) health survey (SF-36), the Short Form Six-Dimensional health index (SF-6D), and the EuroQol Five-Dimensional descriptive system (EQ-5D). Demographic characteristics and standardized disease activity for each disease were also obtained. Previously reported data from 600 healthy Koreans were used for the healthy controls. An ANCOVA test was used to compare the SF-36, SF-6D, and EQ-5D values between study subjects with adjustments for age, sex, disease duration, comorbidities, and disease activity status.

Results
One hundred twenty patients were included in each of the SSc, RA, SLE, and SjS cohorts. Patients with rheumatic diseases had significantly lower SF-36, SF-6D, and EQ-5D scores than healthy controls (all P < 0.001). After statistical adjustments, SSc patients reported significantly lower mental component summary (MCS) scores than patients with RA (P < 0.001) or SLE (P = 0.001). Specifically, the mental health and general health domains were significantly lower in SSc patients than reported in RA or SLE patients (P < 0.001 and P = 0.001, respectively, in both domains). In SSc patients, higher modified Rodnan skin scores (mRSS) correlated with lower MCS scores.

Conclusions
SSc patients report poorer HRQoL than patients with RA or SLE. The extent of skin involvement is associated with poorer HRQoL in SSc patients.

Trial registration

NCT03257878. Registered 22 August 2017
ko_KR
dc.description.sponsorshipThis research was partly supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2016R1D1A1A02937044).ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.subjectSystemic sclerosisko_KR
dc.subjectQuality of lifeko_KR
dc.subjectDisabilityko_KR
dc.titleHealth-related quality of life in systemic sclerosis compared with other rheumatic diseases: a cross-sectional studyko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor박은혜-
dc.contributor.AlternativeAuthor오윤정-
dc.contributor.AlternativeAuthor송영욱-
dc.contributor.AlternativeAuthor이은봉-
dc.identifier.doi10.1186/s13075-019-1842-x-
dc.language.rfc3066en-
dc.rights.holderThe Author(s).-
dc.date.updated2019-02-17T04:19:23Z-
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