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Glucose metabolism in sporadic Creutzfeldt-Jakob disease: A statistical parametric mapping analysis of 18F-FDG PET

  • E. J. Kim
  • , S. S. Cho
  • , B. H. Jeong
  • , Y. S. Kim
  • , S. W. Seo
  • , D. L. Na
  • , M. D. Geschwind
  • , Y. Jeong*
  • *Corresponding author for this work
  • Pusan National University
  • University of Toronto
  • Hayllym University
  • Sungkyunkwan University
  • University of California at San Francisco
  • Korea Advanced Institute of Science and Technology

Research output: Contribution to journalJournal articlepeer-review

Abstract

Background and purpose: Reports describing functional neuroimaging techniques, such as positron emission tomography (PET) and single-photon emission computed tomography (SPECT), in sporadic Creutzfeldt-Jakob disease (sCJD) have consistently suggested that these tools are sensitive for the identification of areas of hypoperfusion or hypometabolism, even in the early stages of sCJD. However, there are few reports on the use of [18F]fluoro-2-deoxy-D-glucose (FDG) PET in sCJD, and most of them are single case reports. Only two small cohort studies based on visual inspection or a region of interest method have been published to date. Using a statistical parametric mapping (SPM) analysis of 18F-FDG PET, we investigated whether there are brain regions preferentially affected in sCJD. Methods: After controlling for age and gender, using SPM 2, we compared the glucose metabolism between (i) 11 patients with sCJD and 35 controls and (ii) the subset of five patients with the Heidenhain variant of sCJD and 35 controls. Results: The patients with sCJD showed decreased glucose metabolism in bilateral parietal, frontal and occipital cortices. The Heidenhain variant of sCJD showed glucose hypometabolism mainly in bilateral occipital areas. Conclusions: Glucose hypometabolism in sCJD was detected in extensive cortical regions; however, it was not found in the basal ganglia or thalamus, which are frequently reported to be affected on diffusion-weighted images. The medial temporal area, which is possibly resistant to the prion deposits, was also less involved in sCJD.

Original languageEnglish
Pages (from-to)488-493
Number of pages6
JournalEuropean Journal of Neurology
Volume19
Issue number3
DOIs
StatePublished - 2012.03

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Creutzfeldt-Jakob disease
  • Positron emission tomography
  • Prion disease

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