Proton magnetic resonance spectroscopy of the brain in patients with Prader-Willi syndrome

Pediatr Neurol. 1998 Jan;18(1):30-5. doi: 10.1016/s0887-8994(97)00139-2.

Abstract

Five patients with Prader-Willi syndrome underwent magnetic resonance imaging and proton magnetic resonance spectroscopy. Magnetic resonance images revealed mild abnormalities, including slight ventriculomegaly, cortical atrophy, and a small brainstem, in all cases. The N-acetylaspartate/Choline (NAA/Cho) and N-acetylaspartate/Creatine (NAA/Cr) ratios were decreased in one (Case 1) and two (Cases 1 and 4) patients, respectively. The Choline/Creatine (Cho/Cr) ratio did not differ from those in control subjects. Thus, in patients with Prader-Willi syndrome, it is thought that there may be neuron loss or a neuron dysfunction caused by a chromosome abnormality. Statistically significant relationships were observed between IQ (DQ) and the NAA/Cho and Cho/Cr ratios: r = 0.895 (P < .05, NAA/Cho ratio) and r = -0.898 (P < .05, Cho/Cr ratio). This suggests that the parietal lobe pathology detected on 1H-magnetic resonance spectroscopy may be associated with more global brain damage and with loss of cognitive functions.

MeSH terms

  • Adolescent
  • Brain / metabolism*
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Electroencephalography
  • Female
  • Humans
  • Infant
  • Linear Models
  • Magnetic Resonance Imaging
  • Magnetic Resonance Spectroscopy / methods*
  • Male
  • Prader-Willi Syndrome / diagnosis*
  • Prader-Willi Syndrome / metabolism
  • Protons

Substances

  • Protons