He Xiao-Song, Wang Zhao-Xin, Zhu You-Zhi, Wang Nan, Hu Xiaoping, Zhang Da-Ren, Zhu De-Fa, Zhou Jiang-Ning
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.
Acta Diabetol. 2015 Feb;52(1):133-42. doi: 10.1007/s00592-014-0618-7. Epub 2014 Jul 4.
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.
2型糖尿病(T2DM)因其对大脑和认知的不利影响而广为人知,这些影响会导致多维度认知缺陷和广泛的脑结构异常。然而,现有文献主要关注老年患者或T2DM病程较长的患者。因此,在相对年轻的人群中,T2DM发病初期大脑功能是否以及如何受到影响仍不清楚。在本研究中,招募了12名新诊断的、既往无糖尿病治疗史的中年T2DM患者和12名匹配的对照组。通过功能磁共振成像获得工作记忆任务(数字n-back范式,即0-back、1-back和2-back)期间的大脑激活情况,并通过重复测量方差分析进行测试。虽然患者在执行n-back任务时与对照组表现相当,但在右侧背外侧前额叶皮层(DLPFC)、左侧额中/下回和左侧顶叶皮层发现了显著的负荷-组交互作用的大脑激活,与对照组相比,患者在2-back条件下表现出过度激活,但在0-back或1-back条件下没有。此外,将糖化血红蛋白(HbA1c)水平估计的慢性高血糖严重程度纳入与任务相关的大脑激活的偏相关分析中,同时控制扫描前即时血浆葡萄糖水平估计的葡萄糖的实时影响。仅在患者中发现HbA1c与前扣带回皮层和双侧DLPFC的大脑激活之间存在显著正相关。综上所述,这些发现表明,在T2DM发病初期,可能存在一种因慢性高血糖导致大脑效率低下而产生的代偿机制。