Jh. Anderson et al., MULTIMODALITY CORRELATIVE STUDY OF CANINE BRAIN-TUMORS - PROTON MAGNETIC-RESONANCE SPECTROSCOPY - POSITRON EMISSION TOMOGRAPHY, AND HISTOLOGY, Investigative radiology, 29(6), 1994, pp. 597-605
RATIONALE AND OBJECTIVES. Structural/functional relationships in an in
duced canine brain tumor were studied using proton-magnetic resonance
spectroscopy (H-1-MRS), positron emission tomography (PET), and histol
ogy. METHODS. Proton-MRS and PET data of implanted canine brain tumors
were correlated with quantitative analysis of the tissue composition
within the MRS and PET regions of interest (ROIs). Linear regression a
nalysis was employed to correlate the H-1-MRS and PET data with the pe
rcent tumor and the percent total lesion (comprising tumor plus associ
ated pathology ie, edema, cysts, hemorrhage, inflammation) within the
ROI. RESULTS. Using H-1-MRS, N-acetyl aspartate concentrations were in
directly correlated with the amount of tumor (P = .058), as well as th
e amount of tumor plus associated pathology (P = .032) within the ROI.
Total creatine concentrations were indirectly correlated with the amo
unt of tumor and the amount of tumor plus associated pathology within
the ROI (P < .05). Lactate concentrations were directly correlated wit
h the amount of tumor (P = .053) and the amount of tumor plus associat
ed pathology (P = .058) within the ROI. Using PET, Oxygen metabolic ra
tes were indirectly correlated with the amount of tumor and with the a
mount of tumor plus associated pathology within the ROI (P < .05). Glu
cose metabolic rates were directly correlated with both the amount of
tumor and with the amount of tumor plus associated pathology at P < .0
5. Proton-MRS measured concentrations of choline and PET measured valu
es for blood flow, and oxygen extraction showed correlations with the
amount of tumor and with the amount of tumor plus associated pathology
at P greater than or equal to .080. CONCLUSIONS. The PET and MRS data
were complementary with respect to suggesting anaerobic glucose metab
olism for the tumor. Unlike other tumors, no increase in choline was n
oted in the canine tumor.