Distinguishing autoimmune encephalitis from its mimics using brain [¹F]-FDG PET: real-world study

Hélène Rostand1, Fiene Marie Kuijper1, Cristina Birzu2

  • 1Department of Nuclear Medicine, Pitié-Salpêtrière Hospital, AP-HP, Sorbonne Université, Paris, France.

Abstract

Insights

Brain [¹⁸F]-FDG PET/CT shows a distinct metabolic pattern in autoimmune encephalitis (AE), aiding diagnosis. This imaging technique helps differentiate AE from other conditions, especially in younger individuals.

Area of Science:

  • Neuroimaging
  • Nuclear Medicine
  • Neurology

Background:

  • Diagnosing autoimmune encephalitis (AE) is challenging due to varied symptoms, seronegativity, and low MRI sensitivity.
  • Brain [¹⁸F]-FDG PET/CT is evaluated as a diagnostic tool for suspected AE in a real-world clinical setting.

Purpose of the Study:

  • To assess the diagnostic performance of brain [¹⁸F]-FDG PET/CT in patients with suspected autoimmune encephalitis.
  • To identify characteristic metabolic patterns of AE using [¹⁸F]-FDG PET/CT and differentiate it from mimics.

Main Methods:

  • Retrospective analysis of 141 patients undergoing [¹⁸F]-FDG PET/CT for suspected AE.
  • Final diagnoses established using international criteria and expert consensus.
  • PET findings analyzed visually and quantitatively, compared with healthy controls, and stratified by age.

Main Results:

  • Autoimmune encephalitis (AE) cases (33%) exhibited cortical hypometabolism and mesiotemporal lobe (MTL), basal ganglia, cerebellum, midbrain, and insula hypermetabolism.
  • [¹⁸F]-FDG PET/CT effectively discriminated AE from differential diagnoses (AUC 0.82-0.83), with MTL hypermetabolism being a key feature.
  • Diagnostic accuracy was highest in patients under 40, with positive/negative predictive values of 82%/81% for visual PET analysis.

Conclusions:

  • Brain [¹⁸F]-FDG PET/CT reveals a characteristic metabolic signature for AE, aiding in its differentiation from other neurological conditions.
  • The study supports [¹⁸F]-FDG PET/CT as a valuable complementary diagnostic biomarker for AE, particularly in younger patient populations.