High energy phosphate abnormalities normalize after antipsychotic treatment in schizophrenia: a longitudinal 31P MRS study of basal ganglia

Peruvumba N Jayakumar, Bangalore N Gangadhar, Ganesan Venkatasubramanian, Sunali Desai, Latha Velayudhan, Dattathreya Subbakrishna, Matcheri S Keshavan

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)

Abstract

We reported increased high-energy phosphate metabolism in the basal ganglia of antipsychotic-naïve schizophrenia patients using (31)P Magnetic Resonance Spectroscopy (MRS). These patients were followed up for 1 year and and reassessed using (31)P MRS. Fourteen (8 males) patients with DSM-IV schizophrenia and 14 (11 males) healthy controls underwent (31)P MRS of sub-cortical structures (predominantly basal ganglia) twice (mean+/-S.D. interscan interval 1.15+/-0.17year) on a 1.5T scanner. Total scores on the Positive and Negative Syndrome Scale (PANSS) decreased significantly after treatment in schizophrenia patients. Patients had significantly lower mean PCr/ATP ratios than healthy controls at baseline but not during the follow-up. In patients, there was a significant positive correlation between the magnitude of improvement in PANSS total scores and the extent of change in the PCr/ATP ratio. Findings support the hypothesis that reduction of energy demand or induction of decreased energy-demanding processes might underlie the mechanism of action of antipsychotics in schizophrenia.

Original languageEnglish
Pages (from-to)237-40
Number of pages4
JournalPsychiatry Research
Volume181
Issue number3
DOIs
Publication statusPublished - 30 Mar 2010

Keywords

  • Adenosine Triphosphate
  • Adult
  • Analysis of Variance
  • Antipsychotic Agents
  • Aspartic Acid
  • Basal Ganglia
  • Female
  • Humans
  • Longitudinal Studies
  • Magnetic Resonance Spectroscopy
  • Male
  • Phosphocreatine
  • Phosphorus Isotopes
  • Psychiatric Status Rating Scales
  • Radionuclide Imaging
  • Schizophrenia
  • Young Adult
  • Clinical Trial
  • Journal Article
  • Research Support, Non-U.S. Gov't

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