In vivo 13C magnetic resonance spectroscopy of a human brain tumor after application of 13C-1-enriched glucose

Objectives nique tool to assess metabolic fluxes noninvasively, 13C magnetic resonance spectroscopy (MRS) could help to characterize and understand malignancy in human tumors. However, its low sensitivity has hampered applications in patients. The aim of this study was to demonstrate that with sensitivity-optimized localized 13C MRS and intravenous infusion of [1-13C]glucose under euglycemia, it is possible to assess the dynamic conversion of glucose into its metabolic products in vivo in human glioma tissue. als and Methods ements were done at 3 T with a broadband single RF channel and a quadrature 13C surface coil inserted in a 1H volume coil. A 1H/13C polarization transfer sequence was applied, modified for localized acquisition, alternatively in two (50 ml) voxels, one encompassing the tumor and the other normal brain tissue. s about 20 min of [1-13C]glucose infusion, a [3-13C]lactate signal appeared among several resonances of metabolic products of glucose in MR spectra of the tumor voxel. The resonance of [3-13C]lactate was absent in MR spectra from contralateral tissue. In addition, the intensity of [1-13C]glucose signals in the tumor area was about 50% higher than that in normal tissue, likely reflecting more glucose in extracellular space due to a defective blood–brain barrier. The signal intensity for metabolites produced in or via the tricarboxylic acid (TCA) cycle was lower in the tumor than in the contralateral area, albeit that the ratios of isotopomer signals were comparable. sion n improved 13C MRS approach, the uptake of glucose and its conversion into metabolites such as lactate can be monitored noninvasively in vivo in human brain tumors. This opens the way to assessing metabolic activity in human tumor tissue.