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Peer-reviewed veterinary case report

Distinctive seizure signature in the first video case-control study of a naturally-occurring feline autoimmune encephalitis model.

Journal:
Brain, behavior, and immunity
Year:
2025
Authors:
Binks, S N M et al.
Affiliation:
Nuffield Department of Clinical Neurosciences · United Kingdom
Species:
cat

Abstract

BACKGROUND AND OBJECTIVE: Autoimmune encephalitis (AE) is a form of brain inflammation where pathogenic autoantibodies bind surface proteins. In humans, AE is at least as common as infective encephalitis, and seizures are a prominent manifestation. The most common adult human AE is associated with antibodies to leucine-rich glioma-inactivated 1 (LGI1-Ab-E). AE in non-human mammals is also recognised, notably the polar bear 'Knut', diagnosed with N-methyl D-aspartate receptor antibody encephalitis. LGI1-Ab-E is an emerging cause of spontaneously-arising AE in domestic cats. Our objective was to phenotype the seizure profile of feline LGI1-Ab-E and probe parallels to its human counterpart. METHODS: We characterised seizures in naturally-occurring feline LGI1-Ab-E. Three veterinary and two human neurologists independently blind-rated 35 LGI1-antibody positive and negative feline seizure videos from 24 cats (16 LGI1-Ab-E positive, 8 negative). Data analysed included seizure frequency, semiologies and their co-occurrence, localisation, inter-rater agreement, and predictive factors. RESULTS: The mean number of daily seizures at peak was significantly higher in LGI1-antibody positive compared to LGI1-antibody-negative cats (12.6 vs. 1.9/day, pcorr&#xa0;=&#xa0;0.011). Semiologies statistically significantly enriched in LGI1-Ab-E observations included orofacial automatisms (88/120, 73&#xa0;% vs. 26/55, 47&#xa0;%, pcorr&#xa0;=&#xa0;0.024), salivation (87/120, 73&#xa0;% vs. 23/55, 42&#xa0;%, pcorr&#xa0;=&#xa0;0.004); and mydriasis (79/120, 66&#xa0;% vs 19/55, 35&#xa0;%, pcorr&#xa0;=&#xa0;0.004), and almost exclusively seen in LGI1-Ab-E were circling (39/120, 33&#xa0;% vs. 1/55, 2&#xa0;%, pcorr=<0.001) and aggression (14/120, 12&#xa0;% vs. 0/55, 0&#xa0;%, non significant after correction). A temporal lobe onset was proposed in 67&#xa0;% (80/120) of seropositive ratings, compared to 28&#xa0;% (15/55) LGI1-Ab-E negative (p&#xa0;<&#xa0;0.0001). Network analysis depicted complex and overlapping relationships between features, akin to the frequent and multifaceted seizures of human LGI1-Ab-E. Orofacial automatisms, mydriasis and temporal lobe localisation were predictive semiological features of feline LGI1-Ab-E. SIGNIFICANCE: Feline LGI1-Ab-E represents a clinically distinctive seizure disorder. Our findings highlight the value of studying naturally-occurring, biologically representative animal models which closely mimic human diseases. This bidirectional translational approach confers benefits across species and unites human and veterinary neurology.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/39984138/