ArticleEuropean journal of nuclear medicine and molecular imaging2026
Distinguishing autoimmune encephalitis from its mimics using brain [¹⁸F]-FDG PET: real-world study.
Article in European journal of nuclear medicine and molecular imaging, 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
backgroundDiagnosing autoimmune encephalitis (AE) remains challenging due to heterogeneous clinical presentations, frequent seronegativity, and limited MRI sensitivity. We evaluated the diagnostic performance of brain [¹⁸F]-FDG PET/CT in a real-world cohort of patients with suspected AE.
methodsConsecutive patients referred for [¹⁸F]-FDG PET/CT for suspected AE between January 2020 and July 2023 were retrospectively included. Final diagnoses were established using international criteria, expert consensus, and follow-up. PET findings were assessed visually, with voxel-wise and regional analyses, compared with 54 healthy controls, and stratified by age and treatment.
resultsAmong 141 patients (48 ± 21 years), 33% had AE, 43% differential diagnoses (DD), and 24% remained undetermined. Of AE cases, 70% were definite, 63% seropositive, and 35% had supportive MRI findings. AE showed cortical hypometabolism with mesiotemporal lobe (MTL), basal ganglia, cerebellum, midbrain, and insula hypermetabolism (p < 0.05). Compared with DD, AE exhibited lower occipital/prefrontal and higher MTL, insular, and midbrain metabolism (p < 0.001), with good discrimination versus DD (AUC 0.82-0.83). MTL hypermetabolism, alone or with cortical hypometabolism, emerged as the most specific feature, whereas other regional metrics and ratios were less reliable (AUC ≤ 0.73). Accuracy of visual PET analysis was high in patients under 40 years (positive/negative predictive values 82%/81%) and declined with age to 81%/69% at 40-65 years and 79%/64% over 65 years.
conclusions[¹⁸F]-FDG PET/CT identifies a characteristic metabolic signature of AE and differentiates it from relevant mimics, supporting its role as a complementary diagnostic biomarker, particularly in younger patients.
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