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胰岛素抵抗与认知正常成年人特定认知领域的下降和 CSF tau 的增加有关。

Insulin resistance is associated with reductions in specific cognitive domains and increases in CSF tau in cognitively normal adults.

机构信息

Collaborative Genomics Group, Centre of Excellence for Alzheimer's Disease Research and Care, School of Medical and Health Sciences, Edith Cowan University, Joondalup, Western Australia, Australia.

School of Biomedical Sciences, Faculty of Health Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, Western Australia, Australia.

出版信息

Sci Rep. 2017 Aug 29;7(1):9766. doi: 10.1038/s41598-017-09577-4.

Abstract

Growing evidence supports the hypothesis that type 2 diabetes (T2D) increases the risk of developing dementia. Experimental evidence from mouse models demonstrates that the induction of T2D/insulin resistance (IR) can promote the accumulation of Alzheimer's disease (AD) pathological features. However, the association of T2D with pathological and clinical phenotypes in humans is unclear. Here we investigate the relationship of indices of IR (HOMA-IR) and pancreatic β-cell function (HOMA-B) with cognitive performance across several domains (Verbal/Visual Episodic Memory, Executive Function, Language and a measure of Global cognition) and AD biomarkers (CSF Aβ42, T-tau/P-tau, hippocampal volume and neocortical Aβ-amyloid burden). We reveal that HOMA-IR (p < 0.001) incrementally increases across diagnostic groups, becoming significantly elevated in the AD group compared with cognitively normal (CN) adults. In CN adults, higher HOMA-IR was associated with poorer performance on measures of verbal episodic memory (p = 0.010), executive function (p = 0.046) and global cognition (p = 0.007), as well as with higher CSF T-tau (p = 0.008) and P-tau (p = 0.014) levels. No association was observed with CSF Aβ or imaging modalities. Together our data suggest that IR may contribute to reduced cognitive performance and the accumulation of CSF tau biomarkers in cognitively normal adults.

摘要

越来越多的证据支持 2 型糖尿病(T2D)会增加痴呆风险的假说。来自小鼠模型的实验证据表明,T2D/胰岛素抵抗(IR)的诱导可以促进阿尔茨海默病(AD)病理特征的积累。然而,T2D 与人类病理和临床表型的关联尚不清楚。在这里,我们研究了 IR(HOMA-IR)和胰岛β细胞功能(HOMA-B)指数与认知表现(包括口头/视觉情节记忆、执行功能、语言和整体认知测量)和 AD 生物标志物(CSF Aβ42、T-tau/P-tau、海马体积和新皮质 Aβ-淀粉样蛋白负担)之间的关系。我们发现,HOMA-IR(p<0.001)在整个诊断组中呈递增趋势,在 AD 组中与认知正常(CN)成年人相比显著升高。在 CN 成年人中,较高的 HOMA-IR 与口头情节记忆(p=0.010)、执行功能(p=0.046)和整体认知(p=0.007)的测量结果较差相关,与更高的 CSF T-tau(p=0.008)和 P-tau(p=0.014)水平相关。与 CSF Aβ 或成像方式无关联。我们的数据表明,IR 可能导致认知正常成年人认知表现下降和 CSF tau 生物标志物积累。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a641/5575049/03fd8ee5a49d/41598_2017_9577_Fig1_HTML.jpg

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