Magnetic Resonance in Medicine · 1994 · 30 citations · 15 references
Life SciencesBiochemistryNeuroscienceMagnetic Resonance BiophysicsMineral MetabolismNeurochemistryAmino Acid Metabolism DisordersMagnetic Resonance SpectroscopyAromatic Amino Acid Metabolism DisordersIn Vivo Nmr SpectroscopyMagnetic Resonance Spectroscopic ImagingMedian AgeMetabolic Deficiency DisordersPhenylalanine MetabolismWhite Matter Abnormalities
Localized proton magnetic resonance spectroscopy with short echo time (TE = 20 ms) was used to investigate biochemical changes in the cerebral white matter of 20 young adult patients (median 19 years) with phenylketonuria (PKU). Results were compared with those of a group of 12 age-matched healthy volunteers (median 25 years). Concentrations of N-acetyl-aspartate (NAA) and choline (Cho) relative to creatine (Cr) were unchanged. However, concentrations of inositol (Ins) relative to creatine were found to be significantly lower (P < 0.001) in the PKU patients (0.30 +/- 0.09 versus 0.57 +/- 0.17). Individual inositol concentrations did not correlate with age, diet, serum phenylalanine (Phe) levels or extent of pathological regions in the T2-weighted images. The lack of correlation with individual data suggests that the decreased inositol concentration could be related to a metabolic deficiency during fetal development. No signal from the phenyl ring protons of phenylalanine was detected in the PKU patients (phenylalanine serum concentration < or = 1.27 mM), which suggests that concentration of phenylalanine may be lower in brain than in serum.
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The Metabolic Basis of Inherited Disease.
Annals of Internal Medicine · 1988 · 7.8K citations
The Metabolic Basis of Inherited Disease
Annals of Internal Medicine · 1990 · 4K citations
Neurological deterioration in young adults with phenylketonuria
Alan J. Thompson, B.D. Youl, B. E. Kendall et al. · The Lancet · 1990 · 198 citations