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Main Effects of Diagnoses, Brain Regions, and their Interaction Effects for Cerebral Metabolites in Bipolar and Unipolar Depressive Disorders. | LitMetric

AI Article Synopsis

  • Previous studies indicated that patients with bipolar depressive disorder (BDd) or unipolar depressive disorder (UDd) exhibit abnormalities in cerebral metabolites due to issues in specific brain regions.
  • A study involving 13 BDd patients, 20 UDd patients, and 20 healthy controls analyzed the concentrations of 5 cerebral metabolites across different subregions of gray matter, including key areas like the medial frontal cortex and anterior cingulate cortex.
  • Results showed significant differences in metabolite levels (like higher glutamate-glutamine in BDd compared to UDd) and highlighted various interactions, suggesting that cerebral metabolite concentrations relate to the severity of the conditions in different brain regions.

Article Abstract

Previous studies suggested patients with bipolar depressive disorder (BDd) or unipolar depressive disorder (UDd) have cerebral metabolites abnormalities. These abnormalities may stem from multiple sub-regions of gray matter in brain regions. Thirteen BDd patients, 20 UDd patients and 20 healthy controls (HC) were enrolled to investigate these abnormalities. Absolute concentrations of 5 cerebral metabolites (glutamate-glutamine (Glx), N-acetylaspartate (NAA), choline (Cho), myo-inositol (mI), creatine (Cr), parietal cortex (PC)) were measured from 4 subregions (the medial frontal cortex (mPFC), anterior cingulate cortex (ACC), posterior cingulate cortex (PCC), and parietal cortex (PC)) of gray matter. Main and interaction effects of cerebral metabolites across subregions of gray matter were evaluated. For example, the Glx was significantly higher in BDd compared with UDd, and so on. As the interaction analyses showed, some interaction effects existed. The concentrations of BDds' Glx, Cho, Cr in the ACC and HCs' mI and Cr in the PC were higher than that of other interaction effects. In addition, the concentrations of BDds' Glx and Cr in the PC and HCs' mI in the ACC were statistically significant lower than that of other interaction effects. These findings point to region-related abnormalities of cerebral metabolites across subjects with BDd and UDd.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116758PMC
http://dx.doi.org/10.1038/srep37343DOI Listing

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