Characteristic MR imaging changes in severe hypermethioninemic states.

In a recent report in this journal (1), Tada et al described a patient with markedly elevated plasma methionine (740 M) and slightly elevated total homocysteine (tHcy) (37 M) who was diagnosed with possible cystathionine beta-synthase (CBS) deficiency. During dietary methionine restriction with supplemental betaine and, later, pyridoxine, his plasma methionine rose to 960–1560 M. His tHcy level was normal (6.3–14.9 M). Decreased appetite and daytime sleepiness developed, and MR imaging revealed diffuse T1 and T2 prolongation in subcortical areas extending to deep white matter with relative sparing of the corticospinal tracts, corpus callosum, optic radiations, ventral brain stem, and cerebellar white matter. Symmetrical lesions in the dorsal brain stem were recognized. Diffusion-weighted imaging (DWI) demonstrated a decreased apparent diffusion coefficient (ADC) in the white matter. These findings were considered by the authors to be less suggestive of CBS deficiency than of an alternative consistent with the metabolite findings, that is, methionine adenosyltransferase I/III (MAT I/III) deficiency (2). MAT I/III deficiency was then confirmed by demonstration of compound heterozygosity for 2 mutations in the gene encoding this enzyme. Therapy was discontinued, plasma methionine decreased to 570–1090 M, and brain imaging studies largely normalized. We suggest that the MR imaging abnormalities in question are similar to those already reported in other children with extreme elevations of methionine who developed clinical signs or symptoms of cerebral edema, thus prompting neuroimaging studies: Patient 1. A 10-year-old girl with homocystinuria due to CBS deficiency increased her plasma methionine from 800 to 3000 M while on betaine therapy (3). MR imaging showed T2 prolongation throughout the supratentorial white matter extending into the brain stem, with relative sparing of the cerebellum. There was striking involvement of the dorsal brain stem, particularly in the region of the midbrain and pons tegmentum (Fig 1A). MR spectroscopy was normal. Patients 2 and 3. Two normal infants developed hypermethioninemia from inadvertent, excessive methionine intake, with levels of 2154 M and 6830 M (3). MR imaging findings in both were similar to those in patient 1, and DWI in one showed decreased ADC values in regions corresponding to T2 prolongation within the brain stem (Fig 1B–D). Patient 4. A 4-year-old boy with CBS deficiency was placed on betaine, and his plasma methionine levels rose from 200 to 1190 M. Methionine was elevated also in CSF (4). MR imaging revealed diffusely abnormal signal within white matter bilaterally, but further imaging was not reported. Thus, in each of the above-reported patients, hypermethioninemia was associated with similar clinical and distinctive MR imaging abnormalities: widespread edema in subcortical