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Polysubstance and alcohol dependence: unique abnormalities of magnetic resonance-derived brain metabolite levels
- Source :
- Drug and alcohol dependence, vol 130, iss 1-3, Abé, C; Mon, A; Durazzo, TC; Pennington, DL; Schmidt, TP; & Meyerhoff, DJ. (2013). Polysubstance and alcohol dependence: Unique abnormalities of magnetic resonance-derived brain metabolite levels. Drug and Alcohol Dependence, 130(1-3), 30-37. doi: 10.1016/j.drugalcdep.2012.10.004. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/2n41r2tb
- Publication Year :
- 2013
- Publisher :
- eScholarship, University of California, 2013.
-
Abstract
- Background: Although comorbid substance misuse is common in alcohol dependence, and polysubstance abusers (PSU) represent the largest group of individuals seeking treatment for drug abuse today, we know little about potential brain abnormalities in this population. Brain magnetic resonance spectroscopy studies of mono-substance use disorders (e.g., alcohol or cocaine) reveal abnormal levels of cortical metabolites (reflecting neuronal integrity, cell membrane turnover/synthesis, cellular bioenergetics, gliosis) and altered concentrations of glutamate and γ-aminobutyric acid (GABA). The concurrent misuse of several substances may have unique and different effects on brain biology and function compared to any mono-substance misuse. Methods: High field brain magnetic resonance spectroscopy at 4. T and neurocognitive testing were performed at one month of abstinence in 40 alcohol dependent individuals (ALC), 28 alcohol dependent PSU and 16 drug-free controls. Absolute metabolite concentrations were calculated in anterior cingulate (ACC), parieto-occipital (POC) and dorso-lateral prefrontal cortices (DLPFC). Results: Compared to ALC, PSU demonstrated significant metabolic abnormalities in the DLPFC and strong trends to lower GABA in the ACC. Metabolite levels in ALC and light drinking controls were statistically equivalent. Within PSU, lower DLPFC GABA levels are related to greater cocaine consumption. Several cortical metabolite concentrations were associated with cognitive performance. Conclusions: While metabolite concentrations in ALC at one month of abstinence were largely normal, PSU showed persistent and functionally significant metabolic abnormalities, primarily in the DLPFC. Our results point to specific metabolic deficits as biomarkers in polysubstance misuse and as targets for pharmacological and behavioral PSU-specific treatment. © 2012 Elsevier Ireland Ltd.
- Subjects :
- Male
Metabolite
Toxicology
Medical and Health Sciences
Cohort Studies
Alcohol Use and Health
chemistry.chemical_compound
2.1 Biological and endogenous factors
Pharmacology (medical)
Aetiology
education.field_of_study
Brain metabolite concentrations
Glutamate receptor
Substance Abuse
Brain
Alcohol dependence
Middle Aged
Magnetic Resonance Imaging
Substance abuse
Psychiatry and Mental health
Alcoholism
medicine.anatomical_structure
Polysubstance dependence
Mental health
Female
Substance Abuse Treatment Centers
Dorsolateral prefrontal cortex
Adult
Drug Abuse (NIDA Only)
medicine.medical_specialty
Substance-Related Disorders
Population
Biology
Article
Clinical Research
Internal medicine
Magnetic resonance spectroscopy
medicine
Humans
education
Neurocognition
Pharmacology
Prevention
Psychology and Cognitive Sciences
Neurosciences
Substance use comorbidity
medicine.disease
Brain Disorders
Good Health and Well Being
Endocrinology
chemistry
nervous system
Neuroscience
Neurocognitive
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Drug and alcohol dependence, vol 130, iss 1-3, Abé, C; Mon, A; Durazzo, TC; Pennington, DL; Schmidt, TP; & Meyerhoff, DJ. (2013). Polysubstance and alcohol dependence: Unique abnormalities of magnetic resonance-derived brain metabolite levels. Drug and Alcohol Dependence, 130(1-3), 30-37. doi: 10.1016/j.drugalcdep.2012.10.004. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/2n41r2tb
- Accession number :
- edsair.doi.dedup.....99b1f25dcbe21e3bafabc8ea3983dd2e
- Full Text :
- https://doi.org/10.1016/j.drugalcdep.2012.10.004.