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Many individuals with <jats:styled-content style=\"fixed-case\">BD<\/jats:styled-content> are initially misdiagnosed and treated for unipolar depression (<jats:styled-content style=\"fixed-case\">UD<\/jats:styled-content>). In this study, we report direct comparisons between medication\u2010free individuals with <jats:styled-content style=\"fixed-case\">BD<\/jats:styled-content> and those with <jats:styled-content style=\"fixed-case\">UD<\/jats:styled-content> in terms of the neurometabolites in the anterior cingulate cortex (<jats:styled-content style=\"fixed-case\">ACC<\/jats:styled-content>), medial prefrontal cortex (<jats:styled-content style=\"fixed-case\">mPFC<\/jats:styled-content>), parietal cortex (<jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>), and posterior cingulate cortex (<jats:styled-content style=\"fixed-case\">PCC<\/jats:styled-content>) of the brain.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Participants included medication\u2010free patients with <jats:styled-content style=\"fixed-case\">BD<\/jats:styled-content> or <jats:styled-content style=\"fixed-case\">UD<\/jats:styled-content>, and matched healthy controls. All patients were in the depressive state and had similar symptoms. All subjects were subjected to a multi\u2010voxel proton magnetic resonance spectroscopy procedure with a 3.0 T <jats:styled-content style=\"fixed-case\">GE<\/jats:styled-content> Signa <jats:styled-content style=\"fixed-case\">MR<\/jats:styled-content> scanner. After post\u2010processing, the absolute concentrations of glycerophosphocholine + phosphocholine (<jats:styled-content style=\"fixed-case\">GPC<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>), phosphocreatine + creatine (<jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>r\u00a0+\u00a0Cr), Glx (glutamate + glutamine), myo\u2010inositol (<jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content>), and <jats:italic>N<\/jats:italic>\u2010acetyl aspartate (<jats:styled-content style=\"fixed-case\">NAA<\/jats:styled-content>) from the above brain regions were compared across the three groups.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Patients with <jats:styled-content style=\"fixed-case\">BD<\/jats:styled-content> showed significantly higher levels of Glx in their <jats:styled-content style=\"fixed-case\">ACC<\/jats:styled-content>, lower <jats:styled-content style=\"fixed-case\">GPC<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> PC<\/jats:styled-content>r\u00a0+\u00a0Cr, <jats:styled-content style=\"fixed-case\">MI<\/jats:styled-content>, and <jats:styled-content style=\"fixed-case\">NAA<\/jats:styled-content> in their <jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>, and lower <jats:styled-content style=\"fixed-case\">NAA<\/jats:styled-content> in their <jats:styled-content style=\"fixed-case\">mPFC<\/jats:styled-content>, compared to healthy controls; patients with <jats:styled-content style=\"fixed-case\">UD<\/jats:styled-content> presented significantly lower levels of <jats:styled-content style=\"fixed-case\">GPC<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> PC<\/jats:styled-content>r\u00a0+\u00a0Cr, and <jats:styled-content style=\"fixed-case\">NAA<\/jats:styled-content> in their <jats:styled-content style=\"fixed-case\">PCC<\/jats:styled-content>, and lower Glx in their <jats:styled-content style=\"fixed-case\">mPFC<\/jats:styled-content>. All analyzed brain metabolites, except Glx, were significantly lower in the <jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content> of patients with <jats:styled-content style=\"fixed-case\">BD<\/jats:styled-content>, whereas levels of <jats:styled-content style=\"fixed-case\">GPC<\/jats:styled-content>\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">PC<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> PC<\/jats:styled-content>r\u00a0+\u00a0Cr, and <jats:styled-content style=\"fixed-case\">NAA<\/jats:styled-content> were significantly reduced in the <jats:styled-content style=\"fixed-case\">PCC<\/jats:styled-content> of patients with <jats:styled-content style=\"fixed-case\">UD<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>These results add to the evidence of brain metabolite differences in brains of patients with <jats:styled-content style=\"fixed-case\">UD<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">BD<\/jats:styled-content> which may be of help in differentiating these two mood disorders.<\/jats:p><\/jats:sec>","DOI":"10.1111\/bdi.12445","type":"journal-article","created":{"date-parts":[[2016,11,16]],"date-time":"2016-11-16T18:25:19Z","timestamp":1479320719000},"page":"583-590","source":"Crossref","is-referenced-by-count":39,"title":["Differential neurometabolite alterations in brains of medication\u2010free individuals with bipolar disorder and those with unipolar depression: a two\u2010dimensional proton magnetic resonance spectroscopy study"],"prefix":"10.1111","volume":"18","author":[{"given":"Hui","family":"Li","sequence":"first","affiliation":[{"name":"Mental Health Center Shantou University Medical College  Shantou China"},{"name":"Department of Medical Imaging The 2nd Affiliated Hospital Shantou University Medical College  Shantou 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