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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 |
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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 |
doi_str_mv | 10.1016/j.msard.2023.105244 |
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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<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<0,001).
The physical and psychological burden of NMOSD in patients daily life is an underestimated dimension of the disease. Thus, it should be considered in the early management of NMOSD patients.</description><identifier>ISSN: 2211-0348</identifier><identifier>DOI: 10.1016/j.msard.2023.105244</identifier><language>eng</language><publisher>Elsevier B.V</publisher><ispartof>Multiple sclerosis and related disorders, 2023-12, Vol.80, p.105244, Article 105244</ispartof><rights>2023</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Chaibi, Azza</creatorcontrib><creatorcontrib>Mohamed, Dina Ben</creatorcontrib><creatorcontrib>Majoul, Slim</creatorcontrib><creatorcontrib>Zouari, Rania</creatorcontrib><creatorcontrib>Rachdi, Amine</creatorcontrib><creatorcontrib>Said, Zakari</creatorcontrib><creatorcontrib>Nabli, Fatma</creatorcontrib><creatorcontrib>Sassi, Samia Ben</creatorcontrib><title>Factors Associated with Altered Quality of Life in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort</title><title>Multiple sclerosis and related disorders</title><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<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<0,001).
The physical and psychological burden of NMOSD in patients daily life is an underestimated dimension of the disease. Thus, it should be considered in the early management of NMOSD patients.</description><issn>2211-0348</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhnNQsNT-Ai_5A1s3H_t18FCq1UKxiL2HbDJLp3Q3Jckq_fem1rMDwzAv8w4zDyEPLJ-znJWPh3kftLdznnORlIJLeUMmnDOW5ULWd2QWwiFPURZMlmxChpU20flAFyE4gzqCpd8Y93RxjOBT8zHqI8YzdR3dYAcUB_oOo3f9GZKOgW5PEY2mnycw0Y89fcbgvAV_mdR0Nw4YUA906fbOx3ty2-ljgNlfnZLd6mW3fMs229f1crHJTFPLrBWiFaWppJFGA2taK6yRTDa85bXUTcNrYzmwosqrynLNUooW6tZWjSwLLaZEXNca70Lw0KmTx177s2K5uoBSB_ULSl1AqSuo5Hq6uiBd9oXgVTAIgwGLPj2nrMN__T8TGHWX</recordid><startdate>202312</startdate><enddate>202312</enddate><creator>Chaibi, Azza</creator><creator>Mohamed, Dina Ben</creator><creator>Majoul, Slim</creator><creator>Zouari, Rania</creator><creator>Rachdi, Amine</creator><creator>Said, Zakari</creator><creator>Nabli, Fatma</creator><creator>Sassi, Samia Ben</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>202312</creationdate><title>Factors Associated with Altered Quality of Life in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort</title><author>Chaibi, Azza ; Mohamed, Dina Ben ; Majoul, Slim ; Zouari, Rania ; Rachdi, Amine ; Said, Zakari ; Nabli, Fatma ; Sassi, Samia Ben</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c984-b33b36c74c4cae19bd3dc41492b284a9928cd2e157077d2a1d2a3be8bd79465a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Chaibi, Azza</creatorcontrib><creatorcontrib>Mohamed, Dina Ben</creatorcontrib><creatorcontrib>Majoul, Slim</creatorcontrib><creatorcontrib>Zouari, Rania</creatorcontrib><creatorcontrib>Rachdi, Amine</creatorcontrib><creatorcontrib>Said, Zakari</creatorcontrib><creatorcontrib>Nabli, Fatma</creatorcontrib><creatorcontrib>Sassi, Samia Ben</creatorcontrib><collection>CrossRef</collection><jtitle>Multiple sclerosis and related disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chaibi, Azza</au><au>Mohamed, Dina Ben</au><au>Majoul, Slim</au><au>Zouari, Rania</au><au>Rachdi, Amine</au><au>Said, Zakari</au><au>Nabli, Fatma</au><au>Sassi, Samia Ben</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Factors Associated with Altered Quality of Life in Neuromyelitis Optica Spectrum Disorder in a Tunisian Cohort</atitle><jtitle>Multiple sclerosis and related disorders</jtitle><date>2023-12</date><risdate>2023</risdate><volume>80</volume><spage>105244</spage><pages>105244-</pages><artnum>105244</artnum><issn>2211-0348</issn><abstract>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<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<0,001).
The physical and psychological burden of NMOSD in patients daily life is an underestimated dimension of the disease. Thus, it should be considered in the early management of NMOSD patients.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.msard.2023.105244</doi></addata></record> |
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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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