Striatal Creatine and Glutamate/Glutamine in Attention-Deficit/Hyperactivity Disorder
The glutamatergic prefrontal-striatal pathway has been implicated previously in the neurobiology of attention-deficit/hyperactivity disorder (ADHD). We used short echo proton magnetic resonance spectroscopy (1H-MRS) to examine glutamate in the prefrontal cortex, left striatum, and, as a control area...
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Published in | Journal of child and adolescent psychopharmacology Vol. 17; no. 1; pp. 11 - 17 |
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Language | English |
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Mary Ann Liebert, Inc
01.02.2007
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Abstract | The glutamatergic prefrontal-striatal pathway has been implicated previously in the neurobiology of attention-deficit/hyperactivity disorder (ADHD). We used short echo proton magnetic resonance spectroscopy (1H-MRS) to examine glutamate in the prefrontal cortex, left striatum, and, as a control area, the occipital lobe.
Thirteen treatment-naïve ADHD children and 10 healthy comparison subjects participated. All were males between the ages of 6 to 11 years of age. Twelve ADHD subjects were scanned after 8 weeks of treatment.
Striatal glutamate, glutamate/glutamine (Glx) and creatine concentrations were greater in the ADHD subjects at baseline as compared to controls. Only striatal creatine, not glutamate or Glx, was reduced after stimulant treatment in the ADHD patients. No significant differences between groups were noted in the remainder of the striatal metabolites or any of the occipital lobe or prefrontal cortex metabolites.
These findings provide initial evidence of a striatal creatine/glutamatergic dysregulation in ADHD. |
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AbstractList | The glutamatergic prefrontal-striatal pathway has been implicated previously in the neurobiology of attention-deficit/hyperactivity disorder (ADHD). We used short echo proton magnetic resonance spectroscopy (1H-MRS) to examine glutamate in the prefrontal cortex, left striatum, and, as a control area, the occipital lobe. Thirteen treatment-naïve ADHD children and 10 healthy comparison subjects participated. All were males between the ages of 6 to 11 years of age. Twelve ADHD subjects were scanned after 8 weeks of treatment. Striatal glutamate, glutamate/glutamine (Glx) and creatine concentrations were greater in the ADHD subjects at baseline as compared to controls. Only striatal creatine, not glutamate or Glx, was reduced after stimulant treatment in the ADHD patients. No significant differences between groups were noted in the remainder of the striatal metabolites or any of the occipital lobe or prefrontal cortex metabolites. These findings provide initial evidence of a striatal creatine/glutamatergic dysregulation in ADHD. The glutamatergic prefrontal-striatal pathway has been implicated previously in the neurobiology of attention-deficit/hyperactivity disorder (ADHD). We used short echo proton magnetic resonance spectroscopy (1H-MRS) to examine glutamate in the prefrontal cortex, left striatum, and, as a control area, the occipital lobe. Thirteen treatment-naïve ADHD children and 10 healthy comparison subjects participated. All were males between the ages of 6 to 11 years of age. Twelve ADHD subjects were scanned after 8 weeks of treatment. Striatal glutamate, glutamate/glutamine (Glx) and creatine concentrations were greater in the ADHD subjects at baseline as compared to controls. Only striatal creatine, not glutamate or Glx, was reduced after stimulant treatment in the ADHD patients. No significant differences between groups were noted in the remainder of the striatal metabolites or any of the occipital lobe or prefrontal cortex metabolites. These findings provide initial evidence of a striatal creatine/glutamatergic dysregulation in ADHD. The glutamatergic prefrontal-striatal pathway has been implicated previously in the neurobiology of attention-deficit/hyperactivity disorder (ADHD). We used short echo proton magnetic resonance spectroscopy (1H-MRS) to examine glutamate in the prefrontal cortex, left striatum, and, as a control area, the occipital lobe.OBJECTIVEThe glutamatergic prefrontal-striatal pathway has been implicated previously in the neurobiology of attention-deficit/hyperactivity disorder (ADHD). We used short echo proton magnetic resonance spectroscopy (1H-MRS) to examine glutamate in the prefrontal cortex, left striatum, and, as a control area, the occipital lobe.Thirteen treatment-naïve ADHD children and 10 healthy comparison subjects participated. All were males between the ages of 6 to 11 years of age. Twelve ADHD subjects were scanned after 8 weeks of treatment.METHODThirteen treatment-naïve ADHD children and 10 healthy comparison subjects participated. All were males between the ages of 6 to 11 years of age. Twelve ADHD subjects were scanned after 8 weeks of treatment.Striatal glutamate, glutamate/glutamine (Glx) and creatine concentrations were greater in the ADHD subjects at baseline as compared to controls. Only striatal creatine, not glutamate or Glx, was reduced after stimulant treatment in the ADHD patients. No significant differences between groups were noted in the remainder of the striatal metabolites or any of the occipital lobe or prefrontal cortex metabolites.RESULTSStriatal glutamate, glutamate/glutamine (Glx) and creatine concentrations were greater in the ADHD subjects at baseline as compared to controls. Only striatal creatine, not glutamate or Glx, was reduced after stimulant treatment in the ADHD patients. No significant differences between groups were noted in the remainder of the striatal metabolites or any of the occipital lobe or prefrontal cortex metabolites.These findings provide initial evidence of a striatal creatine/glutamatergic dysregulation in ADHD.CONCLUSIONSThese findings provide initial evidence of a striatal creatine/glutamatergic dysregulation in ADHD. |
Author | Schmidt, Matthias H. Carrey, Normand J. MacMaster, Frank P. Gaudet, Laura |
Author_xml | – sequence: 1 givenname: Normand J. surname: Carrey fullname: Carrey, Normand J. organization: Department of Psychiatry, Dalhousie University, Halifax, Nova Scotia, Canada – sequence: 2 givenname: Frank P. surname: MacMaster fullname: MacMaster, Frank P. organization: Department of Anatomy and Neurobiology, Dalhousie University, Halifax, Nova Scotia, Canada., Psychiatry & Behavioral Neurosciences, Wayne State University, Detroit, Michigan – sequence: 3 givenname: Laura surname: Gaudet fullname: Gaudet, Laura organization: Department of Psychiatry, Dalhousie University, Halifax, Nova Scotia, Canada – sequence: 4 givenname: Matthias H. surname: Schmidt fullname: Schmidt, Matthias H. organization: Departments of Psychiatry, and Radiology Dalhousie University, Halifax, Nova Scotia, Canada |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17343550$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Attention Deficit Disorder with Hyperactivity - drug therapy Attention Deficit Disorder with Hyperactivity - physiopathology Attention deficit hyperactivity disorder Boys Brain Central Nervous System Stimulants - therapeutic use Child Child psychology Choline - metabolism Comparative studies Corpus Striatum - drug effects Corpus Striatum - physiopathology Creatine - metabolism Dose-Response Relationship, Drug Glutamic Acid - metabolism Glutamine - metabolism Humans Inositol - metabolism Magnetic Resonance Imaging Magnetic Resonance Spectroscopy Male Methylphenidate - therapeutic use Neural Pathways - drug effects Neural Pathways - physiopathology Neurology Occipital Lobe - drug effects Occipital Lobe - physiopathology Pharmacology Phosphocreatine - metabolism Prefrontal Cortex - drug effects Prefrontal Cortex - physiopathology Reference Values Spectrum analysis |
Title | Striatal Creatine and Glutamate/Glutamine in Attention-Deficit/Hyperactivity Disorder |
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