PMID- 24331546 OWN - NLM STAT- MEDLINE DCOM- 20150824 LR - 20220310 IS - 1873-2402 (Electronic) IS - 0006-3223 (Linking) VI - 77 IP - 3 DP - 2015 Feb 1 TI - Type 2 diabetes mellitus: a potentially modifiable risk factor for neurochemical brain changes in bipolar disorders. PG - 295-303 LID - S0006-3223(13)00988-8 [pii] LID - 10.1016/j.biopsych.2013.11.007 [doi] AB - BACKGROUND: Neuroimaging changes in bipolar disorder (BD) may be secondary to the presence of certain clinical factors. Type 2 diabetes mellitus (T2DM) damages the brain and frequently co-occurs with BD. Studying patients with both T2DM and BD could help identify preventable risk factors for neuroimaging changes in BD. METHODS: We used 1.5T magnetic resonance spectroscopy to measure prefrontal N-acetylaspartate (NAA), which is mainly localized in neurons, and total creatine (tCr), an energy metabolite, in 19 BD patients with insulin resistance/glucose intolerance (BD + IR/GI), 14 BD subjects with T2DM (BD + T2DM), 15 euglycemic BD participants, and 11 euglycemic, nonpsychiatric control. RESULTS: The levels of NAA and tCr were lowest among BD + T2DM, intermediate in the BD + IR/GI, and highest among the euglycemic BD and control subjects (F(3),(5)(5) = 4.57, p = .006; F(3),(5)(5) = 2.92, p = .04, respectively). Even the BD + IR/GI subjects had lower NAA than the euglycemic participants (t(4)(3) = 2.13, p = .04). Total Cr was associated with NAA (beta = .52, t(5)(6) = 5.57, p = .000001). Both NAA and tCr correlated with Global Assessment of Functioning scores (r(4)(6) = .28, p = .05; r(4)(6) = .48, p = .0004, respectively). CONCLUSIONS: T2DM, but also prediabetes, may be risk factors for prefrontal neurochemical alterations in BD. These changes were associated with poor psychosocial functioning and could indicate impaired energy metabolism. The findings emphasize the importance of improving diabetes care in BD and suggest potential options for treatment of neuroimaging alterations. CI - (c) 2014 Society of Biological Psychiatry Published by Society of Biological Psychiatry All rights reserved. FAU - Hajek, Tomas AU - Hajek T AD - Department of Psychiatry (TH, CC, RB, CS, MA), Dalhousie University, Halifax, Nova Scotia, Canada; Prague Psychiatric Center (TH, MA), Department of Psychiatry and Medical Psychology, 3rd School of Medicine, Charles University, Prague, Czech Republic. Electronic address: tomas.hajek@dal.ca. FAU - Calkin, Cynthia AU - Calkin C AD - Department of Psychiatry (TH, CC, RB, CS, MA), Dalhousie University, Halifax, Nova Scotia, Canada. FAU - Blagdon, Ryan AU - Blagdon R AD - Department of Psychiatry (TH, CC, RB, CS, MA), Dalhousie University, Halifax, Nova Scotia, Canada. FAU - Slaney, Claire AU - Slaney C AD - Department of Psychiatry (TH, CC, RB, CS, MA), Dalhousie University, Halifax, Nova Scotia, Canada. FAU - Alda, Martin AU - Alda M AD - Department of Psychiatry (TH, CC, RB, CS, MA), Dalhousie University, Halifax, Nova Scotia, Canada; Prague Psychiatric Center (TH, MA), Department of Psychiatry and Medical Psychology, 3rd School of Medicine, Charles University, Prague, Czech Republic. LA - eng GR - 103703/Canadian Institutes of Health Research/Canada GR - 106469/Canadian Institutes of Health Research/Canada GR - 64410/Canadian Institutes of Health Research/Canada PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20131113 PL - United States TA - Biol Psychiatry JT - Biological psychiatry JID - 0213264 RN - 30KYC7MIAI (Aspartic Acid) RN - 997-55-7 (N-acetylaspartate) RN - MU72812GK0 (Creatine) SB - IM MH - Adult MH - Aspartic Acid/*analogs & derivatives/metabolism MH - Bipolar Disorder/complications/*metabolism MH - Brain/*metabolism MH - Creatine/*metabolism MH - Cross-Sectional Studies MH - Diabetes Mellitus, Type 2/complications/*metabolism MH - Female MH - Humans MH - Magnetic Resonance Spectroscopy MH - Male MH - Middle Aged MH - Psychiatric Status Rating Scales MH - Risk Factors OTO - NOTNLM OT - Bipolar disorder OT - Global assessment of functioning OT - N-acetylaspartate OT - Prefrontal cortex OT - Total creatine OT - Type 2 diabetes mellitus EDAT- 2013/12/18 06:00 MHDA- 2015/08/25 06:00 CRDT- 2013/12/17 06:00 PHST- 2013/08/18 00:00 [received] PHST- 2013/11/08 00:00 [revised] PHST- 2013/11/08 00:00 [accepted] PHST- 2013/12/17 06:00 [entrez] PHST- 2013/12/18 06:00 [pubmed] PHST- 2015/08/25 06:00 [medline] AID - S0006-3223(13)00988-8 [pii] AID - 10.1016/j.biopsych.2013.11.007 [doi] PST - ppublish SO - Biol Psychiatry. 2015 Feb 1;77(3):295-303. doi: 10.1016/j.biopsych.2013.11.007. Epub 2013 Nov 13.