4.5 Article

Glutamic Acid and Total Creatine as Predictive Markers for Epilepsy in Glioblastoma by Using Magnetic Resonance Spectroscopy Before Surgery

Journal

WORLD NEUROSURGERY
Volume 160, Issue -, Pages E501-E510

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.wneu.2022.01.056

Keywords

Creatine; Epilepsy; Glioblastoma; Glutamate; Magnetic resonance spectroscopy

Funding

  1. Japanese Ministry of Education, Culture, Sports, Science, and Technology [20K09389, 20K09369, 19K18391, 17K10898]
  2. Grants-in-Aid for Scientific Research [20K09369, 20K09389, 19K18391, 17K10898] Funding Source: KAKEN

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This study investigates the association between predicting epilepsy and metabolites in tumors using 3.0-T MRI and H-1-MRS. The results suggest that the Glu/tCr ratio in tumors has reliable predictive value for epilepsy. Pretreatment MRS is a minimally invasive and simple procedure that can provide useful information for glioblastoma patients.
OBJECTIVE: Epilepsy in glioblastoma patients significantly reduces their quality of life; however, little is known about the association between predicting epilepsy and metabolites in tumors. In this study, we used 3.0-T magnetic resonance imaging and H-1-magnetic resonance spectroscopy (MRS) to quantify metabolite concentrations in patients with varying epilepsy histories. METHODS: Fifty-one patients with glioblastoma underwent pretreatment 3.0-T MRI/H-1-MRS scanning. Single-voxel (1.5 cm(3)) MRS, in an enhanced lesion, was acquired using a double-echo point-resolved spectroscopic sequence with chemical-shift selective water suppression. MRS data were quantified with linear combination model (LC-Model) software. We compared the MRS data between groups with and without epilepsy during the postoperative course (EP). RESULTS: The ratios of glutamate (Glu) and glutamate + glutamine (Glx) to total creatine (Glu/tCr and Glx/tCr) in the tumor were associated with epilepsy history. The receiver operating characteristic curve analysis showed that a Glu/tCr value of 1.81 was 70% sensitive and 90% specific for the prediction of EP (area under curve: 0.82). In the analysis excluding patients with preoperative epilepsy, a Glu/tCr value of 1.81 was 75% sensitive and 88% specific for the prediction (area under curve: 0.87). CONCLUSIONS: Intratumoral metabolite concentrations measured using pretreatment 3.0-T MRI/H-1-MRS changed characteristically in the group with EP. Our study suggests that the Glu/tCr ratio in tumors has adequate reliability in predicting EP. Pretreatment MRS is a minimally invasive and simple procedure that can provide useful information on glioblastoma patients.

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