The Myasthenia Gravis Activities of Daily Living score and associated factors to distinguish the refractory phase in generalized myasthenia gravis patients with 5 years or more disease duration

Associated factors of the Myasthenia Gravis Activities of Daily Living (MG-ADL) score were investigated in 55 patients who had had generalized MG for more than 5 years. In multivariate analysis, correlates of the MG-ADL score at the last follow-up were the total number of fast-acting treatments (FTs...

Full description

Saved in:
Bibliographic Details
Published inRinsho Shinkeigaku Vol. 62; no. 12; pp. 915 - 921
Main Authors Sugimoto, Takamichi, Yamawaki, Takemori, Naito, Hiroyuki, Ohno, Narumi, Giga, Mayumi, Kono, Tomoyuki, Ochi, Kazuhide, Kohriyama, Tatsuo, Nomura, Eiichi, Maruyama, Hirofumi
Format Journal Article
LanguageJapanese
Published Japan Societas Neurologica Japonica 17.12.2022
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Associated factors of the Myasthenia Gravis Activities of Daily Living (MG-ADL) score were investigated in 55 patients who had had generalized MG for more than 5 years. In multivariate analysis, correlates of the MG-ADL score at the last follow-up were the total number of fast-acting treatments (FTs) (standardized regression coefficient 0.617,P < 0.001) and Myasthenia Gravis Foundation of America (MGFA) classification (standardized regression coefficient 0.227,P = 0.032) (F = 32.7,P < 0.001). In patients with a score of 5 or more on MG-ADL at the last follow-up, tendency as follows were seen: 1) early-onset (P = 0.002), 2) longer duration (P = 0.014), 3) high frequency of MGFA classification V (P = 0.017), 4) high frequency of the total number of FTs (P < 0.001), and 5) higher dose of prednisolone at the last follow-up (P = 0.003). MGFA V, early-onset without depending on E-L-T classification, or difficulty of reduction for high doses of prednisolone can be the target of novel treatment for MG, and future prospective study will be expected.
ISSN:0009-918X
1882-0654
DOI:10.5692/clinicalneurol.cn-001790