Comparative study of quality of life, anxiety, depression, and fatigue among patients with neuromyelitis optica spectrum disorder and multiple sclerosis: The first report from Iran

Neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS) are associated with reduced Health Related Quality of Life (HRQOL). To the best of our knowledge, change of HRQOL in patients with NMOSD has not been yet measure in Iran. The objective of this study was to assess HRQOL in NMO...

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Veröffentlicht in:Multiple sclerosis and related disorders 2018-05, Vol.22, p.161-165
Hauptverfasser: Barzegar, Mahdi, Badihian, Shervin, Mirmosayyeb, Omid, Ashtari, Fereshteh, Jamadi, Maryam, Emami, Shohreh, Jahani, Leila, Safavi, Armaghan, Shaygannejad, Vahid
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Sprache:eng
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Zusammenfassung:Neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS) are associated with reduced Health Related Quality of Life (HRQOL). To the best of our knowledge, change of HRQOL in patients with NMOSD has not been yet measure in Iran. The objective of this study was to assess HRQOL in NMOSD and MS patients and identify related factors A cross sectional study of 41 patients with NMOSD and 136 age and sex-match MS patients was performed. A series of questionnaires including Persian validated questionnaires on HRQOL (SF-36), fatigue (MFIS), depression (BDI-II), anxiety (HAM-A) and sleep quality (PSQI) were record. All demographic variables, socioeconomic status and clinical data were also obtained. Student's T test and Mann–Whitney U test used to compare variables between groups and multivariate regression analysis applied to assay predictor factors. The mean scores of mental (MCS) and physical (PCS) components of QOL were statistically lower in patients with NMOSD compare with MS patients (β = −4.49, P = 0.004; β = −3.52, P = 0.015). Multivariate analysis indicated fatigue, depression and anxiety were independent, significant predictor of MCS (β = −0.229, P = 0.002; β = −0.229, P = 0.002; β = −0.258, P = 0.020 respectively). However, PCS was significantly predicted by fatigue (β = −0.258 P 
ISSN:2211-0348
2211-0356
DOI:10.1016/j.msard.2018.04.009