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早期阿尔茨海默病中黄斑视网膜变化与脑白质完整性的相互作用。

Interplay Between Macular Retinal Changes and White Matter Integrity in Early Alzheimer's Disease.

机构信息

CIBIT - Coimbra Institute for Biomedical Imaging and Life Sciences, Coimbra, Portugal.

Institute for Nuclear Sciences Applied to Health (ICNAS), University of Coimbra, Coimbra, Portugal.

出版信息

J Alzheimers Dis. 2019;70(3):723-732. doi: 10.3233/JAD-190152.

Abstract

This study aims to investigate the relationship between structural changes in the retina and white matter in the brain, in early Alzheimer's disease (AD). Twenty-three healthy controls (mean age = 63.4±7.5 years) and seventeen AD patients (mean age = 66.5±6.6 years) were recruited for this study. By combining two imaging techniques-optical coherence tomography and diffusion tensor imaging (DTI)-the association between changes in the thickness of individual retinal layers and white matter dysfunction in early AD was assessed. Retinal layers were segmented, and thickness measurements were obtained for each layer. DTI images were analyzed with a quantitative data-driven approach to evaluating whole-brain diffusion metrics, using tract-based spatial statistics. Diffusion metrics, such as fractional anisotropy, are markers for white matter integrity. Multivariate and partial correlation analyses evaluating the association between individual retinal layers thickness and diffusion metrics were performed. We found that axial diffusivity, indexing axonal integrity, was significantly reduced in AD (p = 0.016, Cohen's d = 1.004) while in the retina, only a marginal trend for significance was found for the outer plexiform layer (p = 0.084, Cohen's d = 0.688). Furthermore, a positive association was found in the AD group between fractional anisotropy and the inner nuclear layer thickness (p < 0.05, r = 0.419, corrected for multiple comparisons by controlling family-wise error rate). Our findings suggest that axonal damage in the brain dominates early on in this condition and shows an association with retinal structural integrity already at initial stages of AD. These findings are consistent with an early axonal degeneration mechanism in AD.

摘要

本研究旨在探讨早期阿尔茨海默病(AD)中视网膜结构变化与大脑白质之间的关系。本研究纳入了 23 名健康对照者(平均年龄 63.4±7.5 岁)和 17 名 AD 患者(平均年龄 66.5±6.6 岁)。通过结合两种成像技术——光学相干断层扫描和弥散张量成像(DTI),评估了早期 AD 中个体视网膜层厚度变化与白质功能障碍之间的相关性。对视网膜层进行分割,并获得每个层的厚度测量值。使用基于体素的空间统计学方法对弥散张量成像图像进行分析,以评估全脑弥散指标。各向异性分数等弥散指标是白质完整性的标志物。进行了多元和偏相关分析,以评估个体视网膜层厚度与弥散指标之间的关联。我们发现,AD 患者的轴向弥散率(轴突完整性的标志物)显著降低(p=0.016,Cohen's d=1.004),而在视网膜中,仅在外丛状层发现了有意义的趋势(p=0.084,Cohen's d=0.688)。此外,在 AD 组中,发现各向异性分数与内核层厚度之间存在正相关(p<0.05,r=0.419,通过控制组间错误率校正多重比较)。我们的研究结果表明,大脑中的轴突损伤在这种情况下早期占主导地位,并且在 AD 的初始阶段就与视网膜结构完整性存在关联。这些发现与 AD 中的早期轴突退化机制一致。

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