PMID- 24993663 OWN - NLM STAT- MEDLINE DCOM- 20151125 LR - 20211021 IS - 1432-5233 (Electronic) IS - 0940-5429 (Print) IS - 0940-5429 (Linking) VI - 52 IP - 1 DP - 2015 Feb TI - Hyperactivation of working memory-related brain circuits in newly diagnosed middle-aged type 2 diabetics. PG - 133-42 LID - 10.1007/s00592-014-0618-7 [doi] AB - Type 2 diabetes mellitus (T2DM) is well known for its adverse impacts on brain and cognition, which leads to multidimensional cognitive deficits and wildly spread cerebral structure abnormalities. However, existing literatures are mainly focused on patients with advanced age or extended T2DM duration. Therefore, it remains unclear whether and how brain function would be affected at the initial onset stage of T2DM in relatively younger population. In current study, twelve newly diagnosed middle-aged T2DM patients with no previous diabetic treatment history and twelve matched controls were recruited. Brain activations during a working memory task, the digit n-back paradigm (0-, 1- and 2-back), were obtained with functional magnetic resonance imaging and tested by repeated measures ANOVA. Whereas patients performed the n-back task comparably well as controls, significant load-by-group interactions of brain activation were found in the right dorsolateral prefrontal cortex (DLPFC), left middle/inferior frontal gyrus, and left parietal cortex, where patients exhibited hyperactivation in the 2-back, but not the 0-back or 1-back condition compared to controls. Furthermore, the severity of chronic hyperglycemia, estimated by glycosylated hemoglobin (HbA1c) level, was entered into partial correlational analyses with task-related brain activations, while controlling for the real-time influence of glucose, estimated by instant plasma glucose level measured before scanning. Significant positive correlations were found between HbA1c and brain activations in the anterior cingulate cortex and bilateral DLPFC only in patients. Taken together, these findings suggest there might be a compensatory mechanism due to brain inefficiency related to chronic hyperglycemia at the initial onset stage of T2DM. FAU - He, Xiao-Song AU - He XS AD - CAS Key Laboratory of Brain Function and Diseases, School of Life Science, University of Science and Technology of China, 433 Huangshan Road, Hefei, 230027, Anhui, China. FAU - Wang, Zhao-Xin AU - Wang ZX FAU - Zhu, You-Zhi AU - Zhu YZ FAU - Wang, Nan AU - Wang N FAU - Hu, Xiaoping AU - Hu X FAU - Zhang, Da-Ren AU - Zhang DR FAU - Zhu, De-Fa AU - Zhu DF FAU - Zhou, Jiang-Ning AU - Zhou JN LA - eng GR - R01 EB002009/EB/NIBIB NIH HHS/United States GR - R01EB002009/EB/NIBIB NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20140704 PL - Germany TA - Acta Diabetol JT - Acta diabetologica JID - 9200299 RN - 0 (Blood Glucose) SB - IM MH - Adult MH - Blood Glucose/metabolism MH - Brain/diagnostic imaging/*physiopathology MH - Case-Control Studies MH - Diabetes Mellitus, Type 2/diagnosis/metabolism/physiopathology/*psychology MH - Female MH - Humans MH - Magnetic Resonance Imaging MH - Male MH - *Memory, Short-Term MH - Middle Aged MH - Radiography PMC - PMC4416650 MID - NIHMS611134 COIS- Conflict of Interest: Xiao-Song He, Zhao-Xin Wang, You-Zhi Zhu, Nan Wang, Xiaoping Hu, Da-Ren Zhang, De-Fa Zhu, Jiang-Ning Zhou declare that they have no conflict of interest. EDAT- 2014/07/06 06:00 MHDA- 2015/12/15 06:00 PMCR- 2016/02/01 CRDT- 2014/07/05 06:00 PHST- 2014/03/17 00:00 [received] PHST- 2014/06/16 00:00 [accepted] PHST- 2014/07/05 06:00 [entrez] PHST- 2014/07/06 06:00 [pubmed] PHST- 2015/12/15 06:00 [medline] PHST- 2016/02/01 00:00 [pmc-release] AID - 10.1007/s00592-014-0618-7 [doi] PST - ppublish SO - Acta Diabetol. 2015 Feb;52(1):133-42. doi: 10.1007/s00592-014-0618-7. Epub 2014 Jul 4.