Glutamic acid decarboxylase autoantibodies and neurological disorders

被引:73
作者
Vianello, M [1 ]
Tavolato, B [1 ]
Giometto, B [1 ]
机构
[1] Univ Padua, Clin 2, Dept Neurol & Psychiat Sci, I-35121 Padua, Italy
关键词
GAD autoantibodies; stiff-person syndrome; chronic cerebellar ataxia; epilepsy; polyglandular autoimmunity;
D O I
10.1007/s100720200055
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Glutamic acid decarboxylase (GAD) is the enzyme that catalyses the production of GABA, a major neurotransmitter of the central nervous system. Antibodies to GAD (GAD-Ab) were first recognised in a patient affected by stiff-person syndrome; subsequently they were reported in a large number of cases with type 1 diabetes. Recently GAD-Ab have been described in a number of patients affected by chronic cerebellar ataxia, drug-resistant epilepsy and myoclonus. These cases usually harbour other autoantibodies or are affected by organ-specific autoimmune diseases. The role of GAD-Ab is still unclear; the lack of experimental models makes it difficult to investigate their potential pathogenetic role. However two mechanisms have been suggested: the reduction by GAD-Ab of GABA synthesis in nerve terminals or the interference with exocytosis of GABA.
引用
收藏
页码:145 / 151
页数:7
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