Back to Search
Start Over
Neurological Syndromes Associated with Anti-GAD Antibodies.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2020 May 24; Vol. 21 (10). Date of Electronic Publication: 2020 May 24. - Publication Year :
- 2020
-
Abstract
- Glutamic acid decarboxylase (GAD) is an intracellular enzyme whose physiologic function is the decarboxylation of glutamate to gamma-aminobutyric acid (GABA), the main inhibitory neurotransmitter within the central nervous system. GAD antibodies (Ab) have been associated with multiple neurological syndromes, including stiff-person syndrome, cerebellar ataxia, and limbic encephalitis, which are all considered to result from reduced GABAergic transmission. The pathogenic role of GAD Ab is still debated, and some evidence suggests that GAD autoimmunity might primarily be cell-mediated. Diagnosis relies on the detection of high titers of GAD Ab in serum and/or in the detection of GAD Ab in the cerebrospinal fluid. Due to the relative rarity of these syndromes, treatment schemes and predictors of response are poorly defined, highlighting the unmet need for multicentric prospective trials in this population. Here, we reviewed the main clinical characteristics of neurological syndromes associated with GAD Ab, focusing on pathophysiologic mechanisms.
- Subjects :
- Autoimmune Diseases of the Nervous System diagnosis
Autoimmune Diseases of the Nervous System therapy
Cerebellar Ataxia diagnosis
Cerebellar Ataxia immunology
Cerebellar Ataxia therapy
Humans
Limbic Encephalitis diagnosis
Limbic Encephalitis immunology
Limbic Encephalitis therapy
Neurons immunology
Stiff-Person Syndrome diagnosis
Stiff-Person Syndrome immunology
Stiff-Person Syndrome therapy
Autoimmune Diseases of the Nervous System immunology
Autoimmunity
Glutamate Decarboxylase immunology
Neurons enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 21
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 32456344
- Full Text :
- https://doi.org/10.3390/ijms21103701