Imaging of Dementia and Aging Laboratory, University of California, Davis, Davis, California, USA.
AJNR Am J Neuroradiol. 2013 Jan;34(1):54-61. doi: 10.3174/ajnr.A3146. Epub 2012 Jun 14.
WMH, associated with cognitive decline and cardiovascular risk factors, may represent only the extreme end of a more widespread continuous WM injury process that progresses during aging and is poorly understood. We investigated the ability of FLAIR and DTI to characterize the longitudinal course of WMH development.
One hundred nineteen participants (mean age, 74.5 ± 7.4), including cognitively healthy elders and subjects diagnosed with Alzheimer disease and mild cognitive impairment, received a comprehensive clinical evaluation and brain MR imaging, including FLAIR and DTI on 2 dates. The risk for each baseline normal-appearing WM voxel to convert into WMH was modeled as a function of baseline FA (model M1) and both baseline FA and standardized FLAIR (M2). Sensitivity, specificity, accuracy, and AUC for predicting conversion to WMH were compared between models.
Independent of clinical diagnosis, lower baseline FA (P < .001, both models) and higher baseline FLAIR intensity (P < .001, M2) were independently associated with increased risk for conversion from normal WM to WMH. M1 exhibited higher sensitivity but lower specificity, accuracy, and AUC compared with M2.
These findings provide further evidence that WMH result from a continuous process of WM degeneration with time. Stepwise decreases in WM integrity as measured by both DTI and FLAIR were independently associated with stepwise increases in WMH risk, emphasizing that these modalities may provide complementary information for understanding the time course of aging-associated WM degeneration.
与认知能力下降和心血管危险因素相关的脑白质高信号(WMH)可能仅代表更广泛的脑白质损伤过程的极端表现,该过程在衰老过程中进展,目前了解甚少。我们研究了 FLAIR 和 DTI 对 WMH 发展的纵向过程的特征描述能力。
119 名参与者(平均年龄 74.5 ± 7.4 岁),包括认知健康的老年人和被诊断为阿尔茨海默病和轻度认知障碍的患者,接受了全面的临床评估和脑 MRI 检查,包括两次 FLAIR 和 DTI。将每个基线正常表现的脑白质体素转变为 WMH 的风险建模为基线 FA(模型 M1)和基线 FA 和标准化 FLAIR(M2)的函数。比较了模型之间预测向 WMH 转化的敏感性、特异性、准确性和 AUC。
与临床诊断无关,较低的基线 FA(P <.001,两种模型)和较高的基线 FLAIR 强度(P <.001,M2)与从正常脑白质向 WMH 转化的风险增加独立相关。M1 与 M2 相比,表现出更高的敏感性但更低的特异性、准确性和 AUC。
这些发现进一步证明了 WMH 是脑白质随时间进行性退化的结果。DTI 和 FLAIR 测量的脑白质完整性的逐步下降与 WMH 风险的逐步增加独立相关,强调这些方法可能为理解与年龄相关的脑白质退化的时间过程提供补充信息。