Reduced N-acetylaspartate levels in the frontal cortex of 3,4-methylenedioxymethamphetamine (Ecstasy) users: preliminary results

AJNR Am J Neuroradiol. 2002 Feb;23(2):231-7.

Abstract

Background and purpose: The perceived safety of the recreational drug methylenedioxymethamphetamine (MDMA), or Ecstasy, conflicts with animal evidence indicating that MDMA damages cortical serotonin (5-HT) neurons at doses similar to those used by humans. Few data are available about the effects of MDMA on the human brain. This study was designed to evaluate MDMA-related alterations in metabolite ratios with single-voxel proton ((1)H) MR spectroscopy.

Methods: Fifteen male MDMA users (mean lifetime exposure, 723 tablets; mean time since last tablet, 12.0 weeks) and 12 age-matched control subjects underwent single-voxel (1)H MR spectroscopy. N-Acetylaspartate (NAA)/creatine (Cr), NAA/Choline (Cho), and myoinositol (MI)/Cr ratios were measured in midfrontal gray matter, midoccipital gray matter, and right parietal white matter. Data were analyzed with linear model-based multivariate analysis of variance.

Results: NAA/Cr (P =.04) and NAA/Cho (P =.03) ratios, markers associated with neuronal loss or dysfunction, were reduced in the frontal cortex of MDMA users. Neither NAA/Cr (P =.72) nor NAA/Cho (P =.12) ratios were different between both groups in occipital gray matter and parietal white matter (P =.18). Extent of previous MDMA use and frontal cortical NAA/Cr (rho = -.50, P =.012) or NAA/Cho (rho = -.550, P <.01) ratios were significantly associated.

Conclusion: Reduced NAA/Cr and NAA/Cho ratios at (1)H MR spectroscopy provide evidence for neuronal abnormality in the frontal cortex of MDMA users; these are correlated with the degree of MDMA exposure. These data suggest that MDMA may be a neurotoxin in humans, as it is in animals.

MeSH terms

  • Adult
  • Aspartic Acid / analogs & derivatives*
  • Aspartic Acid / metabolism*
  • Choline / metabolism
  • Creatine / metabolism
  • Frontal Lobe / metabolism*
  • Hallucinogens / adverse effects*
  • Humans
  • Magnetic Resonance Spectroscopy*
  • Male
  • N-Methyl-3,4-methylenedioxyamphetamine / adverse effects*
  • Occipital Lobe / metabolism
  • Parietal Lobe / metabolism
  • Periaqueductal Gray / metabolism
  • Reference Values
  • Substance-Related Disorders / metabolism*

Substances

  • Hallucinogens
  • Aspartic Acid
  • N-acetylaspartate
  • N-Methyl-3,4-methylenedioxyamphetamine
  • Creatine
  • Choline