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海马体退化与阿尔茨海默病的时间和边缘灰质/白质组织对比有关。

Hippocampal degeneration is associated with temporal and limbic gray matter/white matter tissue contrast in Alzheimer's disease.

机构信息

MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging, MGH Department of Radiology, Charlestown, MA 02129-2060, USA.

出版信息

Neuroimage. 2011 Feb 1;54(3):1795-802. doi: 10.1016/j.neuroimage.2010.10.034. Epub 2010 Oct 18.

Abstract

Recent studies have demonstrated alterations in cortical gray to white matter tissue contrast with nondemented aging and in individuals with Alzheimer's disease (AD). However, little information exists about the clinical relevance of such changes. It is possible that changes in MRI tissue contrast occur via independent mechanisms from those traditionally used in the assessment of AD associated degeneration such as hippocampal degeneration measured by more traditional volumetric magnetic resonance imaging (MRI). We created cortical surface models of 95 cognitively healthy individuals and 98 individuals with AD to characterize changes in regional gray and white matter T1-weighted signal intensities in dementia and to evaluate how such measures related to classically described hippocampal and cortical atrophy. We found a reduction in gray matter to white matter tissue contrast throughout portions of medial and lateral temporal cortical regions as well as in anatomically associated regions including the posterior cingulate, precuneus, and medial frontal cortex. Decreases in tissue contrast were associated with hippocampal volume, however, the regional patterns of these associations differed for demented and nondemented individuals. In nondemented controls, lower hippocampal volume was associated with decreased gray/white matter tissue contrast globally across the cortical mantle. In contrast, in individuals with AD, selective associations were found between hippocampal volume and tissue contrast in temporal and limbic tissue. These results demonstrate that there are strong regional changes in neural tissue properties in AD which follow a spatial pattern including regions known to be affected from pathology studies. Such changes are associated with traditional imaging metrics of degeneration and may provide a unique biomarker of the tissue loss that occurs as a result of AD.

摘要

最近的研究表明,皮质灰质与白质组织对比度在无痴呆性衰老和阿尔茨海默病(AD)个体中发生改变。然而,关于这些变化的临床相关性的信息很少。MRI 组织对比度的变化可能通过与传统用于评估 AD 相关变性的机制不同的机制发生,例如通过更传统的容积磁共振成像(MRI)测量的海马体变性。我们创建了 95 名认知健康个体和 98 名 AD 个体的皮质表面模型,以描述痴呆症中区域灰质和白质 T1 加权信号强度的变化,并评估这些测量值与经典描述的海马体和皮质萎缩的相关性。我们发现内侧和外侧颞叶皮质区域以及解剖相关区域(包括后扣带回、楔前叶和内侧额皮质)的灰质与白质组织对比度降低。组织对比度的降低与海马体体积有关,但是,这些关联的区域模式在痴呆和非痴呆个体中有所不同。在非痴呆对照组中,较低的海马体体积与皮质盖内的整体灰质/白质组织对比度降低有关。相比之下,在 AD 个体中,海马体体积与颞叶和边缘组织中的组织对比度之间存在选择性关联。这些结果表明,AD 中存在强烈的神经组织特性的区域性变化,其遵循包括已知受病理学研究影响的区域的空间模式。这些变化与传统的退化成像指标相关,并且可能为 AD 引起的组织损失提供独特的生物标志物。

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