4.6 Article

Decreased frontal N-acetylaspartate levels in adolescents concurrently using both methamphetamine and marijuana

Journal

BEHAVIOURAL BRAIN RESEARCH
Volume 246, Issue 1, Pages 154-161

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbr.2013.02.028

Keywords

Methamphetamine; Marijuana; Adolescent; Imaging; Magnetic resonance spectroscopy

Funding

  1. Kyowa Hakko
  2. Eli Lilly
  3. Hoffman-La Roche
  4. GlaxoSmithKline
  5. Abbott
  6. Astrazeneca
  7. Eli-Lilly
  8. Jazz Pharmaceuticals
  9. Johnson Johnson
  10. Lundbeck
  11. Orion
  12. Pfizer
  13. Pharmacia
  14. Roche
  15. Servier
  16. Solvay
  17. Sumitomo
  18. Takeda
  19. Tikvah
  20. Wyeth
  21. NIH [R21 DA021422, 1R01 DA020269]

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Introduction: The potential neurochemical toxicity associated with methamphetamine (MA) or marijuana (MJ) use on the developing adolescent brain is unclear, particularly with regard to individuals with concomitant use of MA and MJ (MA+MJ). In this study, proton magnetic resonance spectroscopy (MRS) was utilized to measure in vivo brain N-acetylaspartate plus N-acetylaspartyl glutamate (tNAA, an indicator of intact neuronal integrity) levels. Methods: Three adolescent groups from Cape Town, South Africa completed MRS scans as well as clinical measures including a drug use history. Subjects included (I) nine MA (age = 15.7 +/- 1.37), (2) eight MA+MJ (age = 16.2 +/- 1.16) using adolescents and (3) ten healthy controls (age = 16.8 +/- 0.62). Single voxel spectra were acquired from midfrontal gray matter using a point-resolved spectroscopy sequence (PRESS). The MRS data were post-processed in the fully automated approach for quantitation of metabolite ratios to phosphocreatine plus creatine (PCr+Cr). Results: A significant reduction in frontal tNAA/PCr+Cr ratios was seen in the MA+MJ group compared to the healthy controls (p = 0.01, by 7.2%) and to the MA group (p = 0.04, by 6.9%). Significant relationships were also observed between decreased tNAA/PCr+Cr ratios and drug use history of MA or MJ (total cumulative lifetime dose, age of onset, and duration of MA and MJ exposure) only in the MA+MJ group (all p<0.05). Conclusions: These findings suggest that in adolescents, concomitant heavy MA+MJ use may contribute to altered brain metabolites in frontal gray matter. The significant associations between the abnormal tNAA/PCr+Cr ratios and the drug use history suggest that MA+MJ abuse may induce neurotoxicity in a dose-responsive manner in adolescent brain. (C) 2013 Elsevier B.V. All rights reserved.

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