Affiliation:
1. Center for Advanced Imaging Research University of Maryland School of Medicine Baltimore Maryland USA
2. Department of Diagnostic Radiology and Nuclear Medicine University of Maryland School of Medicine Baltimore Maryland USA
3. Lurie Family Foundations MEG Imaging Center, Department of Radiology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA
4. Department of Radiology, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA
5. Department of Neurology University of Maryland School of Medicine Baltimore Maryland USA
Abstract
BackgroundMR spectroscopy (MRS) is a noninvasive tool for evaluating biochemical alterations, such as glutamate (Glu)/gamma‐aminobutyric acid (GABA) imbalance and depletion of antioxidative glutathione (GSH) after traumatic brain injury (TBI). Thalamus, a critical and vulnerable region post‐TBI, is challenging for MRS acquisitions, necessitating optimization to simultaneously measure GABA/Glu and GSH.PurposeTo assess the feasibility and optimize acquisition and processing approaches for simultaneously measuring GABA, Glx (Glu + glutamine (Gln)), and GSH in the thalamus, employing Hadamard encoding and reconstruction of MEscher–GArwood (MEGA)‐edited spectroscopy (HERMES).Study TypeProspective.Subjects28 control subjects (age: 35.9 ± 15.1 years), and 17 mild TBI (mTBI) patients (age: 32.4 ± 11.3 years).Field Strength/Sequence3T/T1‐weighted magnetization‐prepared rapid gradient‐echo (MP‐RAGE), HERMES.AssessmentWe evaluated the impact of acquisition with spatial saturation bands and post‐processing with spectral alignment on HERMES performance in the thalamus among controls. Within‐subject variability was examined in five controls through repeated scans within a week. The HERMES spectra in the posterior cingulate cortex (PCC) of controls were used as a reference for assessing HERMES performance in a reliable target. Furthermore, we compared metabolite levels and fitting quality in the thalamus between mTBI patients and controls.Statistical TestsUnpaired t‐tests and within‐subject coefficient‐of‐variation (CV). A P‐value <0.05 was deemed significant.ResultsHERMES spectra, acquired with saturation bands and processed with spectral alignment, yielded reliable metabolite measurements in the thalamus. The mean within‐subject CV for GABA, Glx, and GSH levels were 18%, 10%, and 16% in the thalamus (7%, 9%, and 16% in the PCC). GABA (3.20 ± 0.60 vs 2.51 ± 0.55, P < 0.01) and Glx (8.69 ± 1.23 vs 7.72 ± 1.19, P = 0.03) levels in the thalamus were significantly higher in mTBI patients than in controls, with GSH (1.27 ± 0.35 vs 1.22 ± 0.28, P = 0.65) levels showing no significant difference.Data ConclusionSimultaneous measuring GABA/Glx and GSH using HERMES is feasible in the thalamus, providing valuable insight into TBI.Level of Evidence2Technical EfficacyStage 2
Funder
National Institute on Drug Abuse
National Institute of Neurological Disorders and Stroke
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