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Myelitis in inflammatory disorders associated with myelin oligodendrocyte glycoprotein antibody and aquaporin-4 antibody: A comparative study in Chinese Han patients.
ZhangBao, Jingzi; Huang, Wenjuan; Zhou, Lei; Wang, Liang; Chang, Xuechun; Lu, Chuanzhen; Zhao, Chongbo; Lu, Jiahong; Quan, Chao.
Afiliação
  • ZhangBao J; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Huang W; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Zhou L; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Wang L; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Chang X; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Lu C; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Zhao C; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Lu J; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
  • Quan C; Department of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Eur J Neurol ; 28(4): 1308-1315, 2021 04.
Article em En | MEDLINE | ID: mdl-33220172
BACKGROUND AND PURPOSE: Myelitis is an important clinical component of myelin oligodendrocyte glycoprotein antibody (MOG-ab)-associated disease (MOGAD) and aquaporin-4 antibody (AQP4-ab)-positive neuromyelitis optica spectrum disorder (NMOSD). The aim of this work was to evaluate the differentiating features of myelitis between the two diseases. METHODS: Myelitis-related clinical and radiologic data from 130 patients with MOGAD and 125 patients with AQP4-ab-positive NMOSD were retrospectively reviewed and compared. A scoring model was established to differentiate MOG-ab-associated myelitis from AQP4-ab-associated myelitis. RESULTS: Overall, 29.2% (38/130) of patients with MOGAD and 66.4% (83/125) of patients with AQP4-ab-positive NMOSD had ever experienced myelitis. Compared with those with NMOSD, patients with MOGAD exhibited a lower frequency of myelitis, either during the first episode (p < 0.0001) or throughout the disease duration (p < 0.0001). Compared with AQP4-ab-associated myelitis, MOG-ab-associated myelitis manifested a higher male-to-female ratio (p < 0.0001), younger age at disease onset (p = 0.0004), more prodromic influenza-like symptoms (p = 0.030), more prodromic fever (p = 0.0003), more bowel and bladder dysfunction (p = 0.011), less painful tonic spasms (p < 0.0001), and lower Expanded Disability Status Scale scores after treatment (p < 0.0001). On magnetic resonance imaging, lower spinal cord lesions (p = 0.023), short-segment lesions (p = 0.021), conus involvement (p = 0.0001), and H sign (p < 0.0001) were more common in MOG-ab-associated myelitis. A scoring model with a cutoff value of 4 differentiated MOG-ab-associated myelitis from AQP4-ab-associated myelitis with a sensitivity of 87.9% and a specificity of 90.1%. CONCLUSIONS: Myelitis was less commonly observed in MOGAD and exhibited distinct features compared to those of AQP4-ab-positive NMOSD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuromielite Óptica / Mielite Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuromielite Óptica / Mielite Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article