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Braz. j. med. biol. res ; 44(4): 345-353, Apr. 2011. ilus, tab
Article in English | LILACS | ID: lil-581486

ABSTRACT

In vivo proton magnetic resonance spectroscopy (¹H-MRS) is a technique capable of assessing biochemical content and pathways in normal and pathological tissue. In the brain, ¹H-MRS complements the information given by magnetic resonance images. The main goal of the present study was to assess the accuracy of ¹H-MRS for the classification of brain tumors in a pilot study comparing results obtained by manual and semi-automatic quantification of metabolites. In vivo single-voxel ¹H-MRS was performed in 24 control subjects and 26 patients with brain neoplasms that included meningiomas, high-grade neuroglial tumors and pilocytic astrocytomas. Seven metabolite groups (lactate, lipids, N-acetyl-aspartate, glutamate and glutamine group, total creatine, total choline, myo-inositol) were evaluated in all spectra by two methods: a manual one consisting of integration of manually defined peak areas, and the advanced method for accurate, robust and efficient spectral fitting (AMARES), a semi-automatic quantification method implemented in the jMRUI software. Statistical methods included discriminant analysis and the leave-one-out cross-validation method. Both manual and semi-automatic analyses detected differences in metabolite content between tumor groups and controls (P < 0.005). The classification accuracy obtained with the manual method was 75 percent for high-grade neuroglial tumors, 55 percent for meningiomas and 56 percent for pilocytic astrocytomas, while for the semi-automatic method it was 78, 70, and 98 percent, respectively. Both methods classified all control subjects correctly. The study demonstrated that ¹H-MRS accurately differentiated normal from tumoral brain tissue and confirmed the superiority of the semi-automatic quantification method.


Subject(s)
Adolescent , Adult , Aged , Humans , Middle Aged , Young Adult , Brain Neoplasms/classification , Brain Neoplasms/metabolism , Brain Neoplasms/pathology , Case-Control Studies , Magnetic Resonance Spectroscopy/methods , Neoplasm Staging , Pilot Projects , Sensitivity and Specificity
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