ArticleJournal of neurology2026
Sensitivity of the UT-Hopkins Score in 350 patients with antibody-mediated autoimmune encephalitis.
Article in Journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundEarly recognition of autoimmune encephalitis (AE) is critical but remains challenging because of overlapping clinical features with viral encephalitis (VE) and delays in antibody testing. The UT-Hopkins Score was recently developed to assist in the clinical differentiation of AE from VE at presentation. We aimed to assess the sensitivity of this score in a large national cohort of antibody-mediated AE and across major antibody-defined subgroups.
methodsWe conducted a retrospective cohort study including 350 patients with antibody-mediated AE diagnosed according to international consensus criteria at the French Reference Center. Antibodies included anti-N-methyl-D-aspartate receptor (NMDAR), leucine-rich glioma-inactivated 1 (LGI1), contactin-associated protein-like 2 (CASPR2), γ-aminobutyric acid type B receptor (GABA
resultsOverall, 90.3% (95% CI, 86.7-93.0) of patients scored ≥ 2. In the reweighted model, sensitivity increased to 92.9% (95% CI, 86.3-96.6). Sensitivity was highest in GAD65 (100%) and NMDAR (99%) subgroups, remained high in LGI1 (94%) and CASPR2 (90%), but was lower in GABA
conclusionsIn this large cohort of antibody-mediated AE, the UT-Hopkins Score demonstrated high sensitivity across most antibody subtypes, supporting its use to detect autoimmune causes early in patients presenting with encephalitis.
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