Abstract
AbstractWe aimed to synthesize evidence on (1) the prevalence of mood and anxiety disorders and (2) factors associated with symptoms in systemic sclerosis (SSc). We searched MEDLINE, CINAHL, EMBASE, Cochrane CENTRAL, and PsycINFO via an ongoing living systematic review with automated monthly searches. We identified 6 eligible studies through March 1, 2023. Based on 3 studies (N = 93 to 345), current or 30-day major depressive disorder prevalence was 4% (95% confidence interval [CI] 2%, 6%) in a sample of Canadian outpatients (N = 345), 18% (95% CI 12%, 27%) in a study of Indian outpatients (N = 93), 10% (95% CI 4%, 21%) for French patient conference attendees (N = 51), and 29% (95% CI 18%, 42%) for French inpatients (N = 49). Current or 30-day prevalence of any anxiety disorder was 49% (95% CI 36%, 62%) for French conference attendees and 51% (95% CI 38%, 64%) for French inpatients; current or 30-day prevalence of generalized anxiety disorder was 3% for Indian outpatients (95% CI 1%, 9%; N = 93). In 3 studies (N = 114 to 376) that examined factors associated with depressive symptoms, higher education and being married or living as married were associated with lower symptoms and pulmonary involvement, breathing problems, and tender joint counts with higher symptoms; age and disease severity markers were not associated. Only 1 study (N = 114) assessed factors associated with anxiety symptoms and found no statistically significant associations. Limitations included heterogeneous populations and assessment methods, small samples, and substantial risk of bias concerns. Mood and anxiety disorder prevalence appear high in SSc, but estimates vary, and existing studies have important limitations. Future research should assess mood and anxiety prevalence and factors associated with symptoms using large representative samples and validated classification and assessment methods.Review registration: PROSPERO (CRD 42021251339).
Funder
Fonds de Recherche du Québec-Société et Culture
Canada Research Chairs
Publisher
Springer Science and Business Media LLC
Reference41 articles.
1. Wigley, F.M., Hummers, L.K. Clinical features of systemic sclerosis in Rheumatology 3rd ed (ed. Hochberg, M.C.) 1463–1480 (Philadelphia: Mosby, 2003).
2. Allanore, Y. et al. Systemic sclerosis. Nat Rev Dis Primers. 1, 15002 (2015).
3. Mayes, M.D. Systemic sclerosis: clinical features in Primer on the Rheumatic Diseases (ed. Klippel, J.H., Stone, J.H., White, P.H.) 343–350 (New York, NY: Springer, 2008).
4. Gelber, A. C. et al. Race and association with disease manifestations and mortality in scleroderma: A 20-year experience at the Johns Hopkins Scleroderma Center and review of the literature. Medicine 92, 191–205 (2013).
5. Kwakkenbos, L. et al. Psychosocial aspects of scleroderma. Rheum. Dis. Clin. N. Am. 41, 519–528 (2015).