Comparison of conventional and diffusion-weighted MRI and proton MR spectroscopy in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like events

Neuroradiology. 2004 Feb;46(2):113-7. doi: 10.1007/s00234-003-1138-2. Epub 2003 Dec 12.

Abstract

The mechanism of neurological disturbances in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is controversial. We studied 12 patients with MELAS using conventional and diffusion weighted MRI (DWI) and MR spectroscopy (MRS), to look at the physiopathology of the stroke-like events. Although conventional MRI showed lesions in all patients, DWI was more sensitive. One patient did not show high signal on DWI 48 h after a from stroke-like episode, but MRS demonstrated a lactate peak in left occipital lobe; 2 weeks after the attack, high signal was demonstrated on the right frontal lobe where MRS had shown a lactate peak. Our findings suggest a possible predictive ability of (1)H-MRS, in showing early MELAS lesions and supports the hypothesis that mitochondrial metabolic dysfunction may precedes abnormalities on DWI.

Publication types

  • Comparative Study

MeSH terms

  • Adolescent
  • Adult
  • Cerebral Cortex / pathology*
  • Cerebral Cortex / physiopathology
  • Diagnosis, Differential
  • Diffusion Magnetic Resonance Imaging*
  • Disease Progression
  • Dominance, Cerebral / physiology
  • Female
  • Frontal Lobe / pathology
  • Frontal Lobe / physiopathology
  • Humans
  • Image Enhancement*
  • Image Processing, Computer-Assisted*
  • Lactic Acid / metabolism
  • MELAS Syndrome / diagnosis*
  • MELAS Syndrome / physiopathology
  • Magnetic Resonance Imaging*
  • Magnetic Resonance Spectroscopy*
  • Male
  • Middle Aged
  • Neurologic Examination
  • Occipital Lobe / pathology
  • Occipital Lobe / physiopathology
  • Sensitivity and Specificity

Substances

  • Lactic Acid