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Selected findings from the Religious Orders Study and Rush Memory and Aging Project.宗教机构研究和拉什记忆与衰老项目的部分研究结果。
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Toward defining the preclinical stages of Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease.为了定义阿尔茨海默病的临床前阶段:来自美国国家老龄化研究所-阿尔茨海默病协会工作组关于阿尔茨海默病诊断指南的建议。
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Alzheimer-signature MRI biomarker predicts AD dementia in cognitively normal adults.阿尔茨海默氏症特征 MRI 生物标志物可预测认知正常成年人的 AD 痴呆。
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Ultrahigh-resolution microstructural diffusion tensor imaging reveals perforant path degradation in aged humans in vivo.超高分辨率微结构弥散张量成像揭示了体内老年人类穿通纤维束的退化。
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Atrophy and dysfunction of parahippocampal white matter in mild Alzheimer's disease.轻度阿尔茨海默病中海马旁回白质的萎缩和功能障碍。
Neurobiol Aging. 2012 Jan;33(1):43-52. doi: 10.1016/j.neurobiolaging.2010.01.020. Epub 2010 Apr 1.
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Changes in parahippocampal white matter integrity in amnestic mild cognitive impairment: a diffusion tensor imaging study.遗忘型轻度认知障碍患者海马旁回白质完整性的变化:一项扩散张量成像研究
Behav Neurol. 2009;21(1):51-61. doi: 10.3233/BEN-2009-0235.

海马旁回白质体积可预测认知正常老年人患阿尔茨海默病的风险。

Parahippocampal white matter volume predicts Alzheimer's disease risk in cognitively normal old adults.

作者信息

Stoub Travis R, Detoledo-Morrell Leyla, Dickerson Bradford C

机构信息

Department of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.

Department of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.

出版信息

Neurobiol Aging. 2014 Aug;35(8):1855-61. doi: 10.1016/j.neurobiolaging.2014.01.153. Epub 2014 Feb 18.

DOI:10.1016/j.neurobiolaging.2014.01.153
PMID:24656833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4069055/
Abstract

An in vivo marker of the underlying pathology in Alzheimer's disease (AD) is atrophy in select brain regions detected with quantitative magnetic resonance imaging (MRI). Although gray matter changes have been documented to be predictive of cognitive decline culminating in AD among healthy older adults, very little attention has been given to alterations in white matter as a possible MRI biomarker predictive of AD. In this investigation, we examined parahippocampal white matter (PWM) volume derived from baseline MRI scans in 2 independent samples of 65 cognitively normal older adults, followed longitudinally, to determine if it was predictive of AD risk. The average follow-up period for the 2 samples was 8.5 years. Comparisons between the stable participants (N = 50) and those who declined to AD (N = 15) over time revealed a significant difference in baseline PWM volume (p < 0.001). Furthermore, baseline PWM volume was predictive not only of time to AD (hazard ratio = 3.1, p < 0.05), but also of baseline episodic memory performance (p = 0.041). These results demonstrate that PWM atrophy provides a sensitive MRI biomarker of AD dementia risk among those with normal cognitive function.

摘要

阿尔茨海默病(AD)潜在病理的一种体内标志物是通过定量磁共振成像(MRI)检测到的特定脑区萎缩。尽管已有文献记载,在健康的老年人中,灰质变化可预测最终发展为AD的认知衰退,但作为可能预测AD的MRI生物标志物,白质改变却很少受到关注。在这项研究中,我们检查了来自65名认知正常的老年人的两个独立样本的基线MRI扫描得出的海马旁白质(PWM)体积,并对其进行纵向跟踪,以确定它是否能预测AD风险。这两个样本的平均随访期为8.5年。随着时间的推移,对稳定参与者(N = 50)和发展为AD的参与者(N = 15)进行比较,结果显示基线PWM体积存在显著差异(p < 0.001)。此外,基线PWM体积不仅能预测发展为AD的时间(风险比 = 3.1,p < 0.05),还能预测基线情景记忆表现(p = 0.041)。这些结果表明,PWM萎缩为认知功能正常者中的AD痴呆风险提供了一种敏感的MRI生物标志物。