Seizure control and cognitive improvement via immunotherapy in late onset epilepsy patients with paraneoplastic versus GAD65 autoantibody-associated limbic encephalitis

• Published in: Epilepsy & behavior Vol. 65; pp. 18 - 24
• Main Authors: Hansen, N, Widman, G, Witt, J.-A, Wagner, J, Becker, A.J, Elger, C.E, Helmstaedter, C
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-12-2016
• Subjects: Adult; Autoantibodies - blood; Brain - diagnostic imaging; Brain - metabolism; Case-Control Studies; Cognition Disorders - blood; Cognition Disorders - immunology; Cognition Disorders - therapy; Epilepsy; Epilepsy - blood; Epilepsy - immunology; Epilepsy - therapy; Female; Follow-Up Studies; GAD65 autoantibodies; Glutamate Decarboxylase - blood; Humans; Immunotherapy; Immunotherapy - methods; Limbic encephalitis; Limbic Encephalitis - blood; Limbic Encephalitis - immunology; Limbic Encephalitis - therapy; Magnetic Resonance Imaging - methods; Male; Middle Aged; Neurology; Paraneoplastic autoantibodies; Retrospective Studies; Seizures - blood; Seizures - immunology; Seizures - therapy; Paraneoplastic autoantibodies; Immunotherapy; Epilepsy; GAD65 autoantibodies; Limbic encephalitis
• ISSN: 1525-5050; 1525-5069
• DOI: 10.1016/j.yebeh.2016.10.016

Abstract Objective To determine the efficacy of immunotherapy in limbic encephalitis (LE) associated epilepsies with autoantibodies against intracellular antigens in the forms of paraneoplastic autoantibodies versus glutamic acid decarboxylase 65 (GAD)-autoantibodies. Methods Eleven paraneoplastic-antibodies + and eleven age- and gender-matched GAD-antibodies + patients with LE were compared regarding EEG, seizure frequency, MRI volumetry of the brain, and cognition. All patients received immunotherapy with corticosteroids add-on to antiepileptic therapy. A few patients underwent additional interventions like immunoglobulins or immunoadsorption. Results Immunotherapy led to a significantly greater proportion of seizure-free patients in the paraneoplastic antibodies + (55%) as compared to GAD-antibodies + (18%) patients (p < 0.05). Impaired cognition was evident initially (total cognitive performance score based on attentional-executive function, figural/verbal memory and word fluency) in 100% of the paraneoplastic-antibodies + and 73% of the GAD-antibodies + group. After therapy, cognition improved significantly in the paraneoplastic-antibodies +, but not in the GAD-antibodies + patients (p < 0.05). Cognitive change did not correlate with the change in the number of antiepileptic drugs over time. MRI showed larger and unchanged volumes of the amygdala, presubiculum and subiculum in GAD-antibodies + as compared to paraneoplastic-antibodies + patients (p < 0.05) over time. Conclusions Our data provide evidence of a beneficial effect of immunotherapy added to antiepileptic drugs on seizure frequency and cognition only in the paraneoplastic-antibodies + subgroup of LE presenting autoantibodies against intracellular antigens.