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阿尔茨海默病患者的脑结构和功能连接与神经病理学进展。

Brain structural and functional connectivity and the progression of neuropathology in Alzheimer's disease.

机构信息

Department of Medicine, Division of Brain Sciences, Imperial College, London, UK.

出版信息

J Alzheimers Dis. 2013;33 Suppl 1:S163-72. doi: 10.3233/JAD-2012-129012.

DOI:10.3233/JAD-2012-129012
PMID:22669012
Abstract

In our contribution to this special issue focusing on advances in Alzheimer's disease (AD) research since the centennial, we will briefly review some of our own studies applying magnetic resonance imaging (MRI) measures of function and connectivity for characterization of genetic contributions to the neuropathology of AD and as candidate biomarkers. We review how functional MRI during both memory encoding and at rest is able to define APOE4 genotype-dependent physiological changes decades before potential development of AD and demonstrate changes distinct from those with healthy aging. More generally, imaging provides a powerful quantitative measure of phenotype for understanding associations arising from whole genome studies in AD. Structural connectivity measures derived from diffusion tensor MRI (DTI) methods offer additional markers of neuropathology arising from the secondary changes in axonal caliber and myelination that accompany decreased neuronal activity and neurodegeneration. We illustrate applications of DTI for more finely mapping neurodegenerative changes with AD in the thalamus in vivo and for defining neuropathological changes in the white matter itself. The latter efforts have highlighted how sensitivity to the neuropathology can be enhanced by using more specific DTI measures and interpreting them relative to knowledge of local white matter anatomy in the healthy brain. Together, our studies and related work are helping to establish the exciting potential of a new range of MRI methods as neuropathological measures and as biomarkers of disease progression.

摘要

在我们为本期特刊撰写的关于阿尔茨海默病(AD)研究进展的贡献中,我们将简要回顾我们自己的一些研究,这些研究应用磁共振成像(MRI)来测量功能和连接,以描述 AD 神经病理学的遗传贡献,并作为候选生物标志物。我们回顾了在记忆编码和静息状态下进行功能 MRI 如何能够在 AD 潜在发展的几十年前定义 APOE4 基因型依赖性的生理变化,并证明这些变化与健康衰老不同。更一般地说,成像为理解 AD 全基因组研究中出现的关联提供了一种强大的表型定量测量方法。从扩散张量 MRI(DTI)方法得出的结构连接测量提供了轴突口径和髓鞘二次变化引起的神经病理学变化的额外标志物,这些变化伴随着神经元活动和神经退行性变的减少。我们举例说明了 DTI 在活体丘脑 AD 中更精细地映射神经退行性变化以及在白质本身中定义神经病理学变化的应用。这些努力强调了如何通过使用更特定的 DTI 测量并相对于健康大脑中局部白质解剖结构的知识来解释它们,从而提高对神经病理学的敏感性。总之,我们的研究和相关工作正在帮助确立一系列新的 MRI 方法作为神经病理学测量和疾病进展的生物标志物的令人兴奋的潜力。

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