Lack of antibodies to NMDAR or VGKC-complex in GAD and cardiolipin antibody-positive refractory epilepsy

作者：Liimatainen Suvi^*; Peltola Jukka; Hietaharju Aki; Sabater Lidia; Lang Bethan

来源：Epilepsy Research, 2014, 108(3): 592-596.

DOI：10.1016/j.eplepsyres.2013.12.015

• Neuronal antibody
• Seizure
• Autoimmune encephalitis
• New-onset epilepsy
• Refractory epilepsy
• Polyautoimmunity

Background: Over the last few years autoantibodies against neuronal proteins have been identified in several forms of autoimmune encephalitis and epilepsy. NMDA receptor (NMDAR) and voltage gated potassium channel (VGKC) complex antibodies are mainly associated with limbic encephalitis (LE) whereas glutamic acid decarboxylase antibodies (GADA) and anticardiolipin (ACL) antibodies are more commonly detected in patients with chronic epilepsy. Clinical features vary between these antibodies suggesting the specificity of different neuronal antibodies in seizures. %26lt;br%26gt;Methods: Serum samples of 14 GADA positive and 24 ACL positive patients with refractory epilepsy were analyzed for the presence of VGKC or NMDAR antibodies. %26lt;br%26gt;Results: No positive VGKC or NMDAR antibodies were found in these patients. %26lt;br%26gt;Conclusions: The results confirm the different significance of these neuronal antibodies in seizure disorders. Different autoantibodies have different significance in seizures and probably have different pathophysiological mechanisms of actions.

• 出版日期2014-3