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髓鞘水平越高,阿尔茨海默病中对 tau 病理学的抵抗力就越强。

Higher levels of myelin are associated with higher resistance against tau pathology in Alzheimer's disease.

机构信息

Institute for Stroke and Dementia Research, University Hospital, LMU Munich, Munich, Germany.

Department of Neurology, Skåne University Hospital, Lund, Sweden.

出版信息

Alzheimers Res Ther. 2022 Sep 24;14(1):139. doi: 10.1186/s13195-022-01074-9.

Abstract

BACKGROUND

In Alzheimer's disease (AD), fibrillar tau initially occurs locally and progresses preferentially between closely connected regions. However, the underlying sources of regional vulnerability to tau pathology remain unclear. Previous brain-autopsy findings suggest that the myelin levels-which differ substantially between white matter tracts in the brain-are a key modulating factor of region-specific susceptibility to tau deposition. Here, we investigated whether myelination differences between fiber tracts of the human connectome are predictive of the interregional spreading of tau pathology in AD.

METHODS

We included two independently recruited samples consisting of amyloid-PET-positive asymptomatic and symptomatic elderly individuals, in whom tau-PET was obtained at baseline (ADNI: n = 275; BioFINDER-1: n = 102) and longitudinally in a subset (ADNI: n = 123, mean FU = 1.53 [0.69-3.95] years; BioFINDER-1: n = 39, mean FU = 1.87 [1.21-2.78] years). We constructed MRI templates of the myelin water fraction (MWF) in 200 gray matter ROIs and connecting fiber tracts obtained from adult cognitively normal participants. Using the same 200 ROI brain-parcellation atlas, we obtained tau-PET ROI values from each individual in ADNI and BioFINDER-1. In a spatial regression analysis, we first tested the association between cortical myelin and group-average tau-PET signal in the amyloid-positive and control groups. Secondly, employing a previously established approach of modeling tau-PET spreading based on functional connectivity between ROIs, we estimated in a linear regression analysis, whether the level of fiber-tract myelin modulates the association between functional connectivity and longitudinal tau-PET spreading (i.e., covariance) between ROIs.

RESULTS

We found that higher myelinated cortical regions show lower tau-PET uptake (ADNI: rho =  - 0.267, p < 0.001; BioFINDER-1: rho =  - 0.175, p = 0.013). Fiber-tract myelin levels modulated the association between functional connectivity and tau-PET spreading, such that at higher levels of fiber-tract myelin, the association between stronger connectivity and higher covariance of tau-PET between the connected ROIs was attenuated (interaction fiber-tract myelin × functional connectivity: ADNI: β =  - 0.185, p < 0.001; BioFINDER-1: β =  - 0.166, p < 0.001).

CONCLUSION

Higher levels of myelin are associated with lower susceptibility of the connected regions to accumulate fibrillar tau. These results enhance our understanding of brain substrates that explain regional variation in tau accumulation and encourage future studies to investigate potential underlying mechanisms.

摘要

背景

在阿尔茨海默病(AD)中,纤维状 tau 最初局部出现,并优先在紧密相连的区域之间进展。然而,tau 病理学对区域易感性的潜在来源仍不清楚。先前的脑尸检结果表明,髓鞘水平——大脑白质束之间存在显著差异——是调节 tau 沉积区域特异性易感性的关键调节因素。在这里,我们研究了人类连接组纤维束之间的髓鞘差异是否可以预测 AD 中 tau 病理学的区域间传播。

方法

我们纳入了两个独立招募的样本,包括淀粉样蛋白-PET 阳性的无症状和有症状的老年人,他们在基线(ADNI:n=275;BioFINDER-1:n=102)和亚组中进行了纵向 tau-PET 检测(ADNI:n=123,平均 FU=1.53[0.69-3.95]年;BioFINDER-1:n=39,平均 FU=1.87[1.21-2.78]年)。我们构建了 200 个灰质 ROI 和连接纤维束的髓鞘水分数(MWF)的 MRI 模板,这些模板来自成年认知正常参与者。使用相同的 200 个 ROI 脑分割图谱,我们从 ADNI 和 BioFINDER-1 中的每个个体获得了 tau-PET ROI 值。在空间回归分析中,我们首先测试了皮质髓鞘与淀粉样蛋白阳性组和对照组中群体平均 tau-PET 信号之间的关联。其次,采用先前建立的基于 ROI 间功能连接建模 tau-PET 扩散的方法,我们在线性回归分析中估计,纤维束髓鞘水平是否调节了 ROI 间功能连接与纵向 tau-PET 扩散(即协方差)之间的关联。

结果

我们发现,更高的髓鞘化皮质区域显示出较低的 tau-PET 摄取(ADNI:rho=-0.267,p<0.001;BioFINDER-1:rho=-0.175,p=0.013)。纤维束髓鞘水平调节了功能连接和 tau-PET 扩散之间的关联,使得在更高的纤维束髓鞘水平下,连接的 ROI 之间连接性更强与 tau-PET 协方差更高之间的关联减弱(纤维束髓鞘的交互作用:ADNI:β=-0.185,p<0.001;BioFINDER-1:β=-0.166,p<0.001)。

结论

较高的髓鞘水平与连接区域积累纤维状 tau 的易感性降低有关。这些结果增强了我们对解释 tau 积累区域变异性的脑基质的理解,并鼓励未来的研究调查潜在的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9aa/9508747/6617e0748145/13195_2022_1074_Fig1_HTML.jpg

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