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胰岛素抵抗是否会影响非糖尿病阿尔茨海默病患者的神经退行性变?

Does insulin resistance influence neurodegeneration in non-diabetic Alzheimer's subjects?

机构信息

Division of Neurology, Neurology Imaging Unit, Department of Brain Sciences, Imperial College London, 1st Floor B Block, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.

University of Oxford, Oxford, UK.

出版信息

Alzheimers Res Ther. 2021 Feb 17;13(1):47. doi: 10.1186/s13195-021-00784-w.

Abstract

BACKGROUND

Type 2 diabetes is a risk factor for Alzheimer's disease (AD), and AD brain shows impaired insulin signalling. The role of peripheral insulin resistance on AD aetiopathogenesis in non-diabetic patients is still debated. Here we evaluated the influence of insulin resistance on brain glucose metabolism, grey matter volume and white matter lesions (WMLs) in non-diabetic AD subjects.

METHODS

In total, 130 non-diabetic AD subjects underwent MRI and [18F]FDG PET scans with arterial cannula insertion for radioactivity measurement. T1 Volumetric and FLAIR sequences were acquired on a 3-T MRI scanner. These subjects also had measurement of glucose and insulin levels after a 4-h fast on the same day of the scan. Insulin resistance was calculated by the updated homeostatic model assessment (HOMA2). For [18F]FDG analysis, cerebral glucose metabolic rate (rCMRGlc) parametric images were generated using spectral analysis with arterial plasma input function.

RESULTS

In this non-diabetic AD population, HOMA2 was negatively associated with hippocampal rCMRGlc, along with total grey matter volumes. No significant correlation was observed between HOMA2, hippocampal volume and WMLs.

CONCLUSIONS

In non-diabetic AD, peripheral insulin resistance is independently associated with reduced hippocampal glucose metabolism and with lower grey matter volume, suggesting that peripheral insulin resistance might influence AD pathology by its action on cerebral glucose metabolism and on neurodegeneration.

摘要

背景

2 型糖尿病是阿尔茨海默病(AD)的一个风险因素,AD 大脑表现出胰岛素信号受损。外周胰岛素抵抗在非糖尿病患者 AD 发病机制中的作用仍存在争议。在这里,我们评估了胰岛素抵抗对非糖尿病 AD 患者脑葡萄糖代谢、灰质体积和白质病变(WML)的影响。

方法

总共 130 名非糖尿病 AD 患者接受了 MRI 和 [18F]FDG PET 扫描,并插入动脉插管进行放射性测量。T1 容积和 FLAIR 序列在 3T MRI 扫描仪上采集。这些患者还在扫描当天禁食 4 小时后测量血糖和胰岛素水平。胰岛素抵抗通过更新的稳态模型评估(HOMA2)计算。对于 [18F]FDG 分析,使用动脉血浆输入函数的光谱分析生成脑葡萄糖代谢率(rCMRGlc)参数图像。

结果

在非糖尿病 AD 人群中,HOMA2 与海马体 rCMRGlc 以及总灰质体积呈负相关。HOMA2 与海马体体积和 WML 之间没有观察到显著相关性。

结论

在非糖尿病 AD 中,外周胰岛素抵抗与海马葡萄糖代谢降低以及灰质体积降低独立相关,这表明外周胰岛素抵抗可能通过其对脑葡萄糖代谢和神经退行性变的作用影响 AD 病理学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ce/7890851/715a0d5abc36/13195_2021_784_Fig1_HTML.jpg

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