Antibodies to glutamic acid decarboxylase define a form of limbic encephalitis
- PMID: 20437582
- DOI: 10.1002/ana.21917
Antibodies to glutamic acid decarboxylase define a form of limbic encephalitis
Abstract
Objective: Antibodies to glutamic acid decarboxylase (GAD) have been described in a few patients with temporal lobe epilepsies consistent with limbic encephalitis (LE). We studied a cohort of patients with recent-onset temporal lobe epilepsy caused by LE to test for GAD antibody positivity and response to immunotherapies.
Methods: Over a period of 3.75 years, 138 patients aged >or=18 years investigated at the Department of Epileptology, University of Bonn, for recent-onset epilepsy were prospectively collected and studied for cliniconeuroradiological features of LE, autoantibodies, and treatment responses.
Results: Fifty-three adult patients fulfilled the criteria for LE: (1) limbic signs and symptoms for <or=5 years and (2) brain MRI revealing mediotemporal encephalitis (T2/fluid attenuated inversion recovery hyperintensity without atrophy). Nine had high-titer GAD antibodies; 10 had voltage-gated potassium channel (VGKC) antibodies. Patients with GAD antibodies were younger (median age, 23 years; range, 17-66 years) (p = 0.003) and presented with seizures only, whereas polymorphic limbic features were more common in the VGKC antibody-positive group (p < 0.001). None had tumors. Patients with GAD antibodies more frequently had cerebrospinal fluid oligoclonal bands (p = 0.009) and intrathecal secretion of the specific antibody (p = 0.01). Following monthly intravenous methylprednisolone pulses, GAD antibodies remained highly elevated in 6/6 patients, whereas VGKC antibodies normalized in 6/9 patients (p = 0.03). Despite more intense anticonvulsive treatment in the GAD antibody-positive group (p = 0.01), none of these patients became seizure free, unlike all of the patients with VGKC antibodies (p < 0.001).
Interpretation: High-titer GAD antibodies define a form of nonparaneoplastic LE. This is a chronic, nonremitting disorder and should be included in the differential diagnosis of patients with TLE and mediotemporal encephalitis. Therapeutic trials of other immunotherapies should be undertaken.
Similar articles
-
Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis.Brain. 2004 Mar;127(Pt 3):701-12. doi: 10.1093/brain/awh077. Epub 2004 Feb 11. Brain. 2004. PMID: 14960497
-
Voltage-gated potassium channel antibodies in limbic encephalitis.Ann Neurol. 2003 Oct;54(4):530-3. doi: 10.1002/ana.10713. Ann Neurol. 2003. PMID: 14520669
-
Antibodies to voltage-gated potassium and calcium channels in epilepsy.Epilepsy Res. 2006 Oct;71(2-3):135-41. doi: 10.1016/j.eplepsyres.2006.06.003. Epub 2006 Jul 25. Epilepsy Res. 2006. PMID: 16870397
-
Diagnostic value of CSF findings in antibody-associated limbic and anti-NMDAR-encephalitis.Seizure. 2013 Mar;22(2):136-40. doi: 10.1016/j.seizure.2012.12.013. Epub 2013 Jan 11. Seizure. 2013. PMID: 23318046 Review.
-
Autoantibodies and epilepsy.Epilepsia. 2011 May;52 Suppl 3:18-22. doi: 10.1111/j.1528-1167.2011.03031.x. Epilepsia. 2011. PMID: 21542841 Review.
Cited by
-
Characterization of Anti-GAD65-Associated Neurological Syndromes: Clinical Features and Antibody Titers.NeuroSci. 2024 Jun 17;5(2):201-208. doi: 10.3390/neurosci5020015. eCollection 2024 Jun. NeuroSci. 2024. PMID: 39483498 Free PMC article.
-
GAD antibody-spectrum disorders: progress in clinical phenotypes, immunopathogenesis and therapeutic interventions.Ther Adv Neurol Disord. 2021 Mar 30;14:17562864211003486. doi: 10.1177/17562864211003486. eCollection 2021. Ther Adv Neurol Disord. 2021. PMID: 33854562 Free PMC article. Review.
-
Specific B- and T-cell populations are associated with cognition in patients with epilepsy and antibody positive and negative suspected limbic encephalitis.J Neurol. 2021 Feb;268(2):455-466. doi: 10.1007/s00415-020-10158-1. Epub 2020 Aug 20. J Neurol. 2021. PMID: 32816110 Free PMC article.
-
Isolated adrenocorticotropic hormone deficiency as a form of paraneoplastic syndrome.Pituitary. 2018 Oct;21(5):480-489. doi: 10.1007/s11102-018-0901-7. Pituitary. 2018. PMID: 30008158
-
MOG antibody-positive, benign, unilateral, cerebral cortical encephalitis with epilepsy.Neurol Neuroimmunol Neuroinflamm. 2017 Jan 16;4(2):e322. doi: 10.1212/NXI.0000000000000322. eCollection 2017 Mar. Neurol Neuroimmunol Neuroinflamm. 2017. PMID: 28105459 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources