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Factors Associated with Altered Quality of Life in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort

Neuromyelitis optica spectrum disease (NMOSD) is a chronic autoimmune disorder that negatively affect the quality of life during patient's life time. A cross-sectional study was conducted in the neurology department of the National Institute of Neurology Mongi Ben Hamida of Tunis among patients...

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Published in:Multiple sclerosis and related disorders 2023-12, Vol.80, p.105244, Article 105244
Main Authors: Chaibi, Azza, Mohamed, Dina Ben, Majoul, Slim, Zouari, Rania, Rachdi, Amine, Said, Zakari, Nabli, Fatma, Sassi, Samia Ben
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container_title Multiple sclerosis and related disorders
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creator Chaibi, Azza
Mohamed, Dina Ben
Majoul, Slim
Zouari, Rania
Rachdi, Amine
Said, Zakari
Nabli, Fatma
Sassi, Samia Ben
description Neuromyelitis optica spectrum disease (NMOSD) is a chronic autoimmune disorder that negatively affect the quality of life during patient's life time. A cross-sectional study was conducted in the neurology department of the National Institute of Neurology Mongi Ben Hamida of Tunis among patients meeting Wingerchuck et al (2015) criteria for anti-aquaporine 4 positive (AQP4+) NMOSD and Banwell et al (2023) for myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). The demographic, clinical and radiological data were assessed. The arabic version of the Short Form-36 (SF-36) score was applied. Written consent was obtained from all participants. Among the 43 patients included, 24 female participants were diagnosed with AQP4+ NMOSD and 3 male patients met the criteria for double seronegative NMOSD. Sixteen patients had MOGAD with a sex-ratio of 0.33. The mean age of onset was 38 years (interquartile range (IQR) =19) with myelitis being the inaugural in 55.8% (n=24) of patients. The mean Expanded Disability status scale (EDSS) at the first evaluation was 2 (IQR=2.25). The mean SF-36 score in our population was 59 (IQR=8.5). Our study found that the lack of social and familial support was strongly correlated to higher SF-36 total score (p=0.007),lower mental health subscore (0.012), a higher EDSS score at the moment of evaluation (p
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A cross-sectional study was conducted in the neurology department of the National Institute of Neurology Mongi Ben Hamida of Tunis among patients meeting Wingerchuck et al (2015) criteria for anti-aquaporine 4 positive (AQP4+) NMOSD and Banwell et al (2023) for myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). The demographic, clinical and radiological data were assessed. The arabic version of the Short Form-36 (SF-36) score was applied. Written consent was obtained from all participants. Among the 43 patients included, 24 female participants were diagnosed with AQP4+ NMOSD and 3 male patients met the criteria for double seronegative NMOSD. Sixteen patients had MOGAD with a sex-ratio of 0.33. The mean age of onset was 38 years (interquartile range (IQR) =19) with myelitis being the inaugural in 55.8% (n=24) of patients. The mean Expanded Disability status scale (EDSS) at the first evaluation was 2 (IQR=2.25). The mean SF-36 score in our population was 59 (IQR=8.5). Our study found that the lack of social and familial support was strongly correlated to higher SF-36 total score (p=0.007),lower mental health subscore (0.012), a higher EDSS score at the moment of evaluation (p&lt;0.001), and a higher general health component (p=0,033). Radiological data assessement showed a correlation between worse SF-36 total score and patients with extensive myelitis (p&lt;0,001). The physical and psychological burden of NMOSD in patients daily life is an underestimated dimension of the disease. 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title Factors Associated with Altered Quality of Life in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort
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