Journal of neuroimmunology · 2016
Autoantibody profile and clinical characteristics in a cohort of Chinese adult myasthenia gravis patients.
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Hong Yu, Li Hai-Feng, Skeie Geir Olve, Romi Fredrik, Hao Hong-Jun, Zhang Xu, Gao Xiang, Owe Jone Furlund, Gilhus Nils Erik
Аннотация
Myasthenia gravis (MG) is an autoimmune disorder with heterogeneity. Antibodies against acetylcholine receptor (AChR), muscle-specific kinase (MuSK), titin and ryanodine receptor (RyR) were examined in 437 adult Chinese MG patients. The AChR, MuSK, titin and RyR antibodies were found in 82.2%, 2.3%, 28.4% and 23.8% of all patients. Autoantibody profiles vary among different MG subgroups. Thymoma MG patients had high frequencies of AChR (99.2%), titin (50.8%) and RyR antibodies (46.9%). The titin and RyR antibodies also showed high frequencies in late onset patients (54.4% and 33.3%, respectively). These two antibodies may indicate an underlying thymoma when combined. The patients with titin and RyR antibodies tend to have more severe disease and worse outcome, and may need more active immunosuppressive treatment.
Предметные рубрики MeSH
AdolescentAdultAgedAged, 80 and overAsian PeopleAutoantibodiesCohort StudiesFemaleHumansMaleMiddle AgedMyasthenia GravisRadioimmunoassayReceptor Protein-Tyrosine KinasesReceptors, CholinergicRetrospective StudiesRyanodine Receptor Calcium Release ChannelSeverity of Illness IndexShelterin ComplexTelomere-Binding ProteinsThymomaYoung Adult