Method to correlate 1H MRSI and 18FDG-PET

Joseph O'Neill, Jamie Lynn Eberling, Norbert Schuff, William Jagust, Bruce R Reed, Gabriel Soto, Frank Ezekiel, Gregory Klein, Michael W. Weiner

Research output: Contribution to journalArticle

35 Scopus citations

Abstract

The in vivo neuronal contribution to human cerebral metabolic rate of glucose (CMRglc), measured by 18FDG-PET, is unknown. Examining the effect of 1H MRSI-derived N-acetyl aspartate (NAA) concentration on positron emission tomography (PET) measures of metabolic activity might indicate the relationship of CMRglc to neuron density. In a population of 19 demented, cognitively impaired, and control subjects, the Muller-Gartner algorithm was applied to whole-brain PET data to isolate the PET signal originating in cortical gray matter alone (GMPET). An analogous procedure applied to multislice proton MRSI data yielded the N-acetyl aspartate concentration in cortical gray matter (GMNAA). In 18 of 19 subjects, a significant linear regression (P < 0.05) resulted when GMPET was plotted against GMNAA, whereby GMPET was higher for higher GMNAA. This suggests that CMRglc rises linearly with increasing neuron density in gray matter. This method may be used to investigate the relationship of CMRglc to neurons in various conditions. (C) 2000 Wiley-Liss, Inc.

Original languageEnglish (US)
Pages (from-to)244-250
Number of pages7
JournalMagnetic Resonance in Medicine
Volume43
Issue number2
DOIs
StatePublished - 2000

    Fingerprint

Keywords

  • CMRglc
  • FDG-PET
  • NAA
  • Proton MRSI

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging
  • Radiological and Ultrasound Technology

Cite this

O'Neill, J., Eberling, J. L., Schuff, N., Jagust, W., Reed, B. R., Soto, G., Ezekiel, F., Klein, G., & Weiner, M. W. (2000). Method to correlate 1H MRSI and 18FDG-PET. Magnetic Resonance in Medicine, 43(2), 244-250. https://doi.org/10.1002/(SICI)1522-2594(200002)43:2<244::AID-MRM11>3.0.CO;2-2