J Alzheimers Dis. 2016;51(4):961-77. doi: 10.3233/JAD-150980.
Numerous studies have documented a strong association between diabetes and Alzheimer's disease (AD). The nature of the relationship, however, has remained a puzzle, in part because of seemingly incongruent findings. For example, some studies have concluded that insulin deficiency is primarily at fault, suggesting that intranasal insulin or inhibiting the insulin-degrading enzyme (IDE) could be beneficial. Other research has concluded that hyperinsulinemia is to blame, which implies that intranasal insulin or the inhibition of IDE would exacerbate the disease. Such antithetical conclusions pose a serious obstacle to making progress on treatments. However, careful integration of multiple strands of research, with attention to the methods used in different studies, makes it possible to disentangle the research on AD. This integration suggests that there is an important relationship between insulin, IDE, and AD that yields multiple pathways to AD depending on the where deficiency or excess in the cycle occurs. I review evidence for each of these pathways here. The results suggest that avoiding excess insulin, and supporting robust IDE levels, could be important ways of preventing and lessening the impact of AD. I also describe what further tests need to be conducted to verify the arguments made in the paper, and their implications for treating AD.
大量研究记录了糖尿病与阿尔茨海默病(AD)之间存在很强的关联。然而,这种关系的本质一直是个谜,部分原因是研究结果似乎不一致。例如,一些研究得出结论认为胰岛素缺乏是主要原因,这表明鼻内胰岛素或抑制胰岛素降解酶(IDE)可能有益。其他研究得出结论认为是高胰岛素血症导致了这种情况,这意味着鼻内胰岛素或 IDE 的抑制会使疾病恶化。这些相互矛盾的结论给治疗研究带来了严重的障碍。然而,通过仔细整合多方面的研究,并注意不同研究中使用的方法,可以梳理 AD 相关研究。这种整合表明,胰岛素、IDE 和 AD 之间存在着重要的关系,根据该循环中出现的不足或过剩,会产生多种通向 AD 的途径。我在这里回顾了这些途径的证据。结果表明,避免胰岛素过多,并支持强健的 IDE 水平,可能是预防和减轻 AD 影响的重要方法。我还描述了需要进行哪些进一步的测试来验证本文中的论点及其对 AD 治疗的影响。