Zilliox Lindsay A, Chadrasekaran Krish, Kwan Justin Y, Russell James W
Department of Neurology, Maryland VA Healthcare System and University of Maryland, 110 South Paca Street, Baltimore, MD, 21201, USA.
School of Medicine, Department of Neurology, University of Maryland, 3S-129, 110 South Paca Street, Baltimore, MD, 21201-1595, USA.
Curr Diab Rep. 2016 Sep;16(9):87. doi: 10.1007/s11892-016-0775-x.
Both type 1 (T1DM) and type 2 diabetes mellitus (T2DM) have been associated with reduced performance on multiple domains of cognitive function and with evidence of abnormal structural and functional brain magnetic resonance imaging (MRI). Cognitive deficits may occur at the very earliest stages of diabetes and are further exacerbated by the metabolic syndrome. The duration of diabetes and glycemic control may have an impact on the type and severity of cognitive impairment, but as yet we cannot predict who is at greatest risk of developing cognitive impairment. The pathophysiology of cognitive impairment is multifactorial, although dysfunction in each interconnecting pathway ultimately leads to discordance in metabolic signaling. The pathophysiology includes defects in insulin signaling, autonomic function, neuroinflammatory pathways, mitochondrial (Mt) metabolism, the sirtuin-peroxisome proliferator-activated receptor-gamma co-activator 1α (SIRT-PGC-1α) axis, and Tau signaling. Several promising therapies have been identified in pre-clinical studies, but remain to be validated in clinical trials.
1型糖尿病(T1DM)和2型糖尿病(T2DM)均与认知功能多个领域的表现下降以及脑磁共振成像(MRI)结构和功能异常的证据有关。认知缺陷可能在糖尿病的最早阶段就出现,并且会因代谢综合征而进一步加重。糖尿病病程和血糖控制可能会对认知障碍的类型和严重程度产生影响,但目前我们尚无法预测谁发生认知障碍的风险最高。认知障碍的病理生理学是多因素的,尽管每个相互连接途径的功能障碍最终都会导致代谢信号的失调。病理生理学包括胰岛素信号传导、自主神经功能、神经炎症途径、线粒体(Mt)代谢、沉默调节蛋白-过氧化物酶体增殖物激活受体-γ共激活因子1α(SIRT-PGC-1α)轴和Tau信号传导缺陷。在临床前研究中已确定了几种有前景的疗法,但仍有待在临床试验中验证。