In vivo Metabolic Profiles as Determined by 31 P and short TE 1 H MR-Spectroscopy

Abstract

Purpose

Previous ex vivo spectroscopic data from tissue samples revealed differences in phospholipid metabolites between isocitrate dehydrogenase mutated (IDHmut) and IDH wildtype (IDHwt) gliomas. We investigated whether these changes can be found in vivo using ¹H-decoupled ³¹P magnetic resonance spectroscopic imaging (MRSI) with 3D chemical shift imaging (CSI) at 3 T in patients with low and high-grade gliomas.

Methods

The study included 33 prospectively enrolled, mostly untreated patients who met spectral quality criteria according to the World Health Organization (WHO II n = 7, WHO III n = 17, WHO IV n = 9; 25 patients IDHmut, 8 patients IDHwt). The MRSI protocol included ¹H decoupled ³¹P MRSI with 3D CSI (3D ³¹P CSI), 2D ¹H CSI and a ¹H single voxel spectroscopy sequence (TE 30 ms) from the tumor area. For ¹H MRS, absolute metabolite concentration values were calculated (phantom replacement method). For ³¹P MRS, metabolite intensity ratios were calculated for the choline (C) and ethanolamine (E)-containing metabolites.

Results

In our patient cohort we did not find significant differences for the ratio of phosphocholine (PC) and phosphoethanolamine (PE), PC/PE, (p = 0.24) for IDHmut compared to IDHwt gliomas. Furthermore, we found no elevated ratios of glycerophosphocholine (GPC) and glycerophosphoethanolamine (GPE), GPC/GPE, (p = 0.68) or GPC/PE (p = 0.12) for IDHmut gliomas. Even the ratio (PC+GPC)/(PE+GPE) showed no significant differences with respect to mutation status (p = 0.16). Nonetheless, changes related to tumor grade regarding intracellular pH (pH_i) and phospholipid metabolism as well as absolute metabolite concentrations of co-registered 2D ¹H CSI data for tumor and control tissue showed the anticipated results.

Conclusion

Using 3D-CSI data acquisition, in vivo ³¹P MR spectroscopic measurement of phospholipid metabolites could not distinguish between IDHmut and IDHwt.

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