Glutamic acid decarboxylase autoantibodies and neurological disorders |
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Authors: | M. Vianello B. Tavolato B. Giometto |
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Affiliation: | (1) Department of Neurology and Psychiatry Sciences, Second Clinic, University of Padua, Via Vendramini 7, I-35121 Padua, Italy, IT |
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Abstract: | 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 GADAb 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. Received: 16 May 2002 / Accepted in revised form: 10 July 2002 Correspondence to B. Giometto |
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Keywords: | GAD autoantibodies Stiff-person syndrome Chronic cerebellar ataxia Epilepsy Polyglandular autoimmunity |
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