(1)H-magnetic resonance spectroscopy ((1)H-MRS) in methamphetamine dependence and methamphetamine induced psychosis
Fleur M Howells1, Anne Uhlmann1, Henk Temmingh1
1Department of Psychiatry and Mental Health, Faculty of Health Sciences, University of Cape Town, South Africa.
Background:
Methamphetamine (MA) use has been shown to decrease n-acetyl-aspartate (NAA), a marker of neuronal integrity and viability, on (1)H magnetic resonance spectroscopy ((1)H-MRS). However, little work has compared (1)H-MRS in MA dependent individuals and MA dependent individuals with MA induced psychotic disorder (MAP).
Methods:
Twenty six participants with MA dependence (sixteen without psychosis, ten with psychosis - MAP) and nineteen healthy controls underwent 2D-chemical shift imaging (1)H-MRS, which included voxels in the anterior cingulate cortices (ACC), dorsolateral prefrontal cortices (DLPFC), and frontal white matter. We compared metabolite concentrations relative to phosphocreatine+creatine (PCr+Cr) for n-acetyl-aspartate (NAA), n-acetyl-aspartate+n-acetyl-aspartyl-glutamate (NAA+NAAG), glutamate (Glu), glutamate+glutamine (Glu+Gln), myo-inositol, and glycerophosphocholine+phosphocholine (GPC+PCh) across groups.
Results:
The MA groups showed significantly decreased relative NAA metabolite concentrations for right ACC and right DLPFC, compared with control group. The MA dependent group only showed significantly decreased choline metabolites for right DLPFC, compared with control group. The MAP group's relative NAA metabolite concentrations were significantly correlated with age of initial use and duration of MA use, these correlates were not apparent in MA dependent group.
Conclusion:
MA use is associated with decreased neuronal integrity and viability, specifically in the right ACC and right DLPFC. MA dependence showed active neurodegeneration in the right DLPFC, this was not apparent in the MAP group and may be related to the use of antipsychotic medication in the MAP group. The effects of MA use in MAP suggest that age of initial use presents a mismatch of neuronal plasticity, in frontal white vs. gray matter and duration of use relates to decreased neuronal integrity and viability. Further study is warranted from this initial study of (1)H-MRS in MAP, in particular longitudinal assessment of these individuals both neurobiologically ((1)H-MRS) and clinically - to determine disease progression.
Insights
Methamphetamine (MA) use significantly reduces neuronal integrity markers in the brain. Early MA initiation and prolonged use correlate with neurodegeneration in MA-dependent individuals, especially those with psychosis.
Area of Science:
- Neuroimaging
- Neuroscience
- Psychiatry
Background:
- Methamphetamine (MA) use is linked to reduced n-acetyl-aspartate (NAA), a marker of neuronal integrity.
- Limited research has compared brain metabolites in MA-dependent individuals versus those with MA-induced psychotic disorder (MAP).
Purpose of the Study:
- To compare (1)H-MRS metabolite concentrations in individuals with MA dependence and MAP, and healthy controls.
- To investigate the relationship between MA use patterns and neurochemical changes.
Main Methods:
- 2D-chemical shift imaging (1)H-MRS was performed on 26 MA-dependent individuals (16 without psychosis, 10 with psychosis) and 19 healthy controls.
- Metabolite concentrations (NAA, NAA+NAAG, Glu, Glu+Gln, myo-inositol, GPC+PCh) were measured relative to PCr+Cr in the ACC, DLPFC, and frontal white matter.
Main Results:
- MA groups showed decreased relative NAA in the right ACC and right DLPFC compared to controls.
- MA dependence was associated with decreased choline metabolites in the right DLPFC compared to controls.
- In the MAP group, NAA concentrations correlated with age of initial MA use and duration of use, unlike in the MA-dependent group.
Conclusions:
- MA use is associated with reduced neuronal integrity in the right ACC and DLPFC.
- MA dependence may involve active neurodegeneration in the right DLPFC, potentially mitigated by antipsychotic use in the MAP group.
- Early MA initiation and prolonged use in MAP may indicate altered neuronal plasticity and integrity.
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