Diabetes and Cognitive Impairment

被引:362
作者
Zilliox, Lindsay A. [1 ,2 ]
Chadrasekaran, Krish [1 ,2 ]
Kwan, Justin Y. [1 ,2 ]
Russell, James W. [1 ,2 ,3 ]
机构
[1] Maryland VA Healthcare Syst, Dept Neurol, 110 South Paca St, Baltimore, MD 21201 USA
[2] Univ Maryland, 110 South Paca St, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Neurol, 3S-129,110 South Paca St, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
Diabetes; Brain; Dementia; Encephalopathy; Neuropathy; Mitochondria; MRI; Treatment; BRAIN MITOCHONDRIAL-FUNCTION; GLUCOSE-TOLERANCE STATUS; ALZHEIMERS-DISEASE; INSULIN-RESISTANCE; GENE-EXPRESSION; OLDER-ADULTS; INTRANASAL INSULIN; MOUSE MODEL; FOLLOW-UP; MEMORY;
D O I
10.1007/s11892-016-0775-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 1a (SIRT-PGC-1 alpha) axis, and Tau signaling. Several promising therapies have been identified in preclinical studies, but remain to be validated in clinical trials.
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页数:11
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