Since mild traumatic brain injury (mTBI) often leads to neurological symptoms even without clinical MRI findings, our goal was to test whether diffuse axonal injury is quantifiable with multivoxel proton MR spectroscopic imaging (1H-MRSI). T1- and T2-weighted MRI and three dimensional 1H-MRSI (480 voxels over 360 cm3, ∼30% of the brain) were acquired at 3 Tesla from 26 mTBI patients (mean Glasgow Coma Scale score 14.7), 18–56 years old, 3–55 days post injury and 13 healthy matched contemporaries. The N-acetylaspartate (NAA), choline (Cho), creatine (Cr) and myo-inositol (mI) concentrations and gray-, white-matter (GM/WM) and cerebrospinal fluid fractions were obtained in each voxel. Global GM and WM absolute metabolic concentrations were estimated using linear regression, and patients were compared with controls using two-way analysis of variance. Patients' mean NAA, Cr, Cho and mI concentrations in GM (8.4±0.7, 6.9±0.6, 1.3±0.2, 5.5±0.6 mM) and Cr, Cho and mI in WM (4.8±0.5, 1.4±0.2, 4.6±0.7 mM) were not different from controls'. NAA, however, was significantly lower in patients' than controls' WM (7.2±0.8 versus 7.7±0.6 mM, p=0.0125). The Cho and Cr levels in patients' WM positively correlated with time from mTBI. This 1H-MRSI approach allowed us to ascertain that early mTBI sequelae are (i) diffuse (not merely local), (ii) neuronal (not glial) and (iii) in the global white (not gray) matter. These findings support the hypothesis that, similarly to more severe head trauma, mTBI also results in diffuse axonal injury, but that dysfunction, rather than cell death, dominates shortly after injury.