Stoub Travis R, Detoledo-Morrell Leyla, Dickerson Bradford C
Department of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.
Department of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.
Neurobiol Aging. 2014 Aug;35(8):1855-61. doi: 10.1016/j.neurobiolaging.2014.01.153. Epub 2014 Feb 18.
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.
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。