Link between type 2 diabetes and Alzheimer's disease: from epidemiology to mechanism and treatment

被引:194
|
作者
Li, Xiaohua [1 ]
Song, Dalin [2 ]
Leng, Sean X. [3 ]
机构
[1] Dalian Med Univ, Dalian, Peoples R China
[2] Qingdao Municipal Hosp, Dept Geriatr, Qingdao 266071, Peoples R China
[3] Johns Hopkins Univ, Sch Med, Dept Med, Div Geriatr Med & Gerontol, Baltimore, MD 21205 USA
关键词
type 2 diabetes mellitus; Alzheimer's disease; insulin; MILD COGNITIVE IMPAIRMENT; VASCULAR RISK-FACTORS; LIFE-STYLE INTERVENTION; GROWTH-FACTOR-I; DIPEPTIDYL PEPTIDASE-4 INHIBITORS; BRAIN MITOCHONDRIAL-FUNCTION; CEREBRAL GLUCOSE-METABOLISM; INSULIN-RESISTANCE; INTRANASAL INSULIN; C-PEPTIDE;
D O I
10.2147/CIA.S74042
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The aim of this paper is to provide a comprehensive review of the epidemiological evidence linking type 2 diabetes mellitus and its related conditions, including obesity, hyperinsulinemia, and metabolic syndrome, to Alzheimer's disease (AD). Several mechanisms could help to explain this proposed link; however, our focus is on insulin resistance and deficiency. Studies have shown that insulin resistance and deficiency can interact with amyloid-beta protein and tau protein phosphorylation, each leading to the onset and development of AD. Based on those epidemiological data and basic research, it was recently proposed that AD can be considered as "type 3 diabetes". Special attention has been paid to determining whether antidiabetic agents might be effective in treating AD. There has been much research both experimental and clinical on this topic. We mainly discuss the clinical trials on insulin, metformin, thiazolidinediones, glucagon-like peptide-1 receptor agonists, and dipeptidyl peptidase-4 inhibitors in the treatment of AD. Although the results of these trials seem to be contradictory, this approach is also full of promise. It is worth mentioning that the therapeutic effects of these drugs are influenced by the apolipoprotein E (APOE)epsilon 4 genotype. Patients without the APOE-epsilon 4 allele showed better treatment effects than those with this allele.
引用
收藏
页码:549 / 560
页数:12
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