Zeestraten Eva A, Lawrence Andrew J, Lambert Christian, Benjamin Philip, Brookes Rebecca L, Mackinnon Andrew D, Morris Robin G, Barrick Thomas R, Markus Hugh S
From the Neuroscience Research Centre (E.A.Z., C.L., P.B., T.R.B.), Cardiovascular and Cell Sciences Research Institute, St George's University of London; Stroke Research Group (A.J.L., R.L.B., H.S.M.), Clinical Neurosciences, University of Cambridge; Atkinson Morley Regional Neuroscience Centre (A.D.M.), St George's NHS Healthcare Trust; and Department of Psychology (R.G.M.), King's College Institute of Psychiatry, Psychology, and Neuroscience, London, UK.
Neurology. 2017 Oct 31;89(18):1869-1876. doi: 10.1212/WNL.0000000000004594. Epub 2017 Oct 4.
To determine whether MRI markers, including diffusion tensor imaging (DTI), can predict cognitive decline and dementia in patients with cerebral small vessel disease (SVD).
In the prospective St George's Cognition and Neuroimaging in Stroke study, multimodal MRI was performed annually for 3 years and cognitive assessments annually for 5 years in a cohort of 99 patients with SVD, defined as symptomatic lacunar stroke and confluent white matter hyperintensities (WMH). Progression to dementia was determined in all patients. Progression of WMH, brain volume, lacunes, cerebral microbleeds, and a DTI measure (the normalized peak height of the mean diffusivity histogram distribution) as a marker of white matter microstructural damage were determined.
Over 5 years of follow-up, 18 patients (18.2%) progressed to dementia. A significant change in all MRI markers, representing deterioration, was observed. The presence of new lacunes, and rate of increase in white matter microstructural damage on DTI, correlated with both decline in executive function and global functioning. Growth of WMH and deterioration of white matter microstructure on DTI predicted progression to dementia. A model including change in MRI variables together with their baseline values correctly classified progression to dementia with a C statistic of 0.85.
This longitudinal prospective study provides evidence that change in MRI measures including DTI, over time durations during which cognitive change is not detectable, predicts cognitive decline and progression to dementia. It supports the use of MRI measures, including DTI, as useful surrogate biomarkers to monitor disease and assess therapeutic interventions.
确定包括弥散张量成像(DTI)在内的MRI标志物能否预测脑小血管病(SVD)患者的认知功能衰退和痴呆。
在“圣乔治卒中认知与神经影像学”前瞻性研究中,对99例SVD患者队列进行了为期3年的年度多模态MRI检查和为期5年的年度认知评估,SVD定义为有症状的腔隙性卒中及融合性白质高信号(WMH)。确定所有患者是否进展为痴呆。测定WMH、脑体积、腔隙、脑微出血的进展情况,以及作为白质微结构损伤标志物的DTI测量值(平均扩散率直方图分布的标准化峰值高度)。
在5年的随访中,18例患者(18.2%)进展为痴呆。观察到所有MRI标志物均有显著变化,提示病情恶化。新腔隙的出现以及DTI上白质微结构损伤的增加率与执行功能和整体功能的衰退均相关。WMH的增长和DTI上白质微结构的恶化可预测痴呆的进展。一个包含MRI变量变化及其基线值的模型正确分类痴呆进展的C统计量为0.85。
这项纵向前瞻性研究提供了证据,表明在无法检测到认知变化的时间段内,包括DTI在内的MRI测量值的变化可预测认知衰退和痴呆进展。它支持将包括DTI在内的MRI测量值用作监测疾病和评估治疗干预的有用替代生物标志物。