Health-related quality of life in Marfan syndrome: a 10-year follow-up

Health and Quality of Life Outcomes

Thy Thy Vanem¹  Svend Rand-Hendriksen¹  Odd Ragnar Geiran¹  Cecilie Røe¹  Cathrine Brunborg² 

[1] Institute of Clinical Medicine, Faculty of Medicine, University of Oslo;Oslo Centre for Biostatistics & Epidemiology;

关键词: Marfan syndrome;    Follow-up;    Health-related quality of life;    SF-36;   

DOI  :  10.1186/s12955-020-01633-4

来源: DOAJ

【 摘 要 】

Abstract Background Marfan syndrome, a rare hereditary connective tissue disorder caused by mutations in fibrillin-1, can affect many organ systems, especially the cardiovascular system. Previous research has paid less attention to health-related quality of life and prospective studies on this topic are needed. The aim of this study was to assess changes in health-related quality of life after 10 years in a Norwegian Marfan syndrome cohort. Methods Forty-seven Marfan syndrome patients ≥ 18 years were investigated for all organ manifestations in the 1996 Ghent nosology and completed the self-reported questionnaire, Short-Form-36 Health Survey, at baseline in 2003–2004 and at follow-up in 2014–2015. Paired sample t tests were performed to compare means and multiple regression analyses were performed with age, sex, new cardiovascular and new non-cardiovascular pathology as predictors. Results At 10-year follow-up: a significant decline was found in the physical domain. The mental domain was unchanged. Older age predicted a larger decline in physical health-related quality of life. None of the chosen Marfan-related variables predicted changes in any of the subscales of the Short-Form 36 Health Survey or in the physical or the mental domain. Conclusion Knowledge of decline in the physical domain, not related to organ affections, may be important in the follow-up of Marfan syndrome patients.

【 授权许可】

Unknown