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ObjectivesThe objective of this study was to evaluate the occurrence of voltage-gated potassium channel (VGKC) antibodies and the pattern of MRI changes in cats with complex partial seizures with orofacial involvement (CPSOFI), as well as to investigate whether there are factors influencing survival that could be used as prognostic markers in those cats.MethodsCats with CPSOFI were identified retrospectively. The following data were retrieved from the hospital database: signalment, age at first seizure and presentation, the presence of antibodies against VGKC (leucine-rich glioma inactivating factor 1 (LGI1), contactin-associated protein 2 (CASPR2)) and cerebrospinal fluid (CSF) analysis findings. Brain MRI scans were evaluated for T2 and/or fluid-attenuated inversion recovery (FLAIR) hippocampal hyperintensity and hippocampal contrast enhancement by a radiologist. The correlation between being positive for VGKC antibodies and MRI hippocampal hyperintensity was investigated.ResultsSerum antibodies against VGKC were found in 31.4% of cats, with 10/11 positive cats having antibodies against LGI1 and 1/11 against CASPR2. MRI T2/FLAIR hippocampal hyperintensities and T1 contrast enhancement were seen in 57.1% and 27.1% of cats, respectively. There was a weak correlation between those antibodies and MRI changes (phi coefficient 0.12). The following factors did not influence survival on multivariable regression analysis either for all cats together or when the cats that died were evaluated separately: age at first seizure, breed, sex, T2/FLAIR hippocampal hyperintensity, being positive for VGKC antibodies and prednisolone treatment.Conclusions and relevanceThere are no consistent findings on MRI or on testing for VGKC antibodies in all cats with CPSOFI. None of the factors investigated can be used to predict outcomes.
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http://dx.doi.org/10.1177/1098612X251365423 | DOI Listing |
J Feline Med Surg
September 2025
Department for Small Animals, Veterinary Faculty, Leipzig University, Leipzig, Germany.
ObjectivesThe objective of this study was to evaluate the occurrence of voltage-gated potassium channel (VGKC) antibodies and the pattern of MRI changes in cats with complex partial seizures with orofacial involvement (CPSOFI), as well as to investigate whether there are factors influencing survival that could be used as prognostic markers in those cats.MethodsCats with CPSOFI were identified retrospectively. The following data were retrieved from the hospital database: signalment, age at first seizure and presentation, the presence of antibodies against VGKC (leucine-rich glioma inactivating factor 1 (LGI1), contactin-associated protein 2 (CASPR2)) and cerebrospinal fluid (CSF) analysis findings.
View Article and Find Full Text PDFNeurol Neuroimmunol Neuroinflamm
July 2025
Institute for Clinical Neurobiology, University Hospital Wuerzburg, Germany.
Background And Objectives: Patients with autoantibodies (aAbs) against the contactin-associated protein-like 2 (CASPR2) suffer from a variety of clinical syndromes including neuropathic pain. CASPR2 is an adhesion protein of the neurexin family and part of the voltage-gated potassium channel complex (VGKC complex) in dorsal root ganglia (DRG) neurons. The pathologic mechanisms following the binding of CASPR2 aAbs and their association with pain are only partially understood.
View Article and Find Full Text PDFFront Immunol
June 2025
Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Objectives: Antibodies against voltage-gated potassium channel (VGKC) complexes include anti-LGI1 and anti-CASPR2. Anti-ADAM23 antibodies have not been previously reported in autoimmune encephalitis (AE).
Case Report: We report a 71-year-old female patient who presented with rapidly progressive short-term memory loss, psychobehavioural abnormalities, and impaired consciousness.
Ideggyogy Sz
May 2025
Department of Neurology, Gulhane Medical Faculty, University of Health Sciences, Turkey.
Isaacs' syndrome is an immune-mediated primary peripheral nerve hyperexcitability syndrome characterized by muscle twitches, cramps, and muscle stiffness. In 30-50% of cases, antibodies against voltage-gated potassium channel (VGKC) complex proteins are present. Symptomatic treatment, intravenous immunoglobulin (IVIg), plasma exchange (PE), and intravenous methylprednisolone (IVMP) are generally effective in controlling symptoms.
View Article and Find Full Text PDFJ Neurol
April 2025
Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases; National Key Clinical Department and Key Discipline of Neurology, Guangzhou, China.
Objective: Morvan Syndrome is a rare autoimmune-mediated clinical condition. This retrospective study aims at assessing the effectiveness and safety of intravenous Efgartigimod in 2 cases of the Morvan Syndrome with positive LGI1 and CASPR2 antibodies.
Methods: We reviewed the clinical manifestations, autoantibodies detection, electromyography (EMG) characteristics, treatments and follow-up outcomes in 2 patients of Morvan Syndrome with positive LGI1 and CASPR2 antibodies.