Chiu Shannon Y, Chen Robin, Wang Wei-En, Armstrong Melissa J, Boeve Bradley F, Savica Rodolfo, Ramanan Vijay, Fields Julie A, Graff-Radford Neill, Ferman Tanis J, Kantarci Kejal, Vaillancourt David E
Department of Neurology, University of Florida, Gainesville, Florida, USA.
Department of Neurology, Mayo Clinic, Scottsdale, Arizona, USA.
Mov Disord. 2024 May;39(5):836-846. doi: 10.1002/mds.29763. Epub 2024 Mar 13.
Diffusion-weighted magnetic resonance imaging (dMRI) examines tissue microstructure integrity in vivo. Prior dementia with Lewy bodies (DLB) diffusion tensor imaging studies yielded mixed results.
We employed free-water (FW) imaging to assess DLB progression and correlate with clinical decline in DLB.
Baseline and follow-up MRIs were obtained at 12 and/or 24 months for 27 individuals with DLB or mild cognitive impairment with Lewy bodies (MCI-LB). FW was analyzed using the Mayo Clinic Adult Lifespan Template. Primary outcomes were FW differences between baseline and 12 or 24 months. To compare FW change longitudinally, we included 20 cognitively unimpaired individuals from the Alzheimer's Disease Neuroimaging Initiative.
We followed 23 participants to 12 months and 16 participants to 24 months. Both groups had worsening in Montreal Cognitive Assessment (MoCA) and Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) scores. We found significant FW increases at both time points compared to baseline in the insula, amygdala, posterior cingulum, parahippocampal, entorhinal, supramarginal, fusiform, retrosplenial, and Rolandic operculum regions. At 24 months, we found more widespread microstructural changes in regions implicated in visuospatial processing, motor, and cholinergic functions. Between-group analyses (DLB vs. controls) confirmed significant FW changes over 24 months in most of these regions. FW changes were associated with longitudinal worsening of MDS-UPDRS and MoCA scores.
FW increased in gray and white matter regions in DLB, likely due to neurodegenerative pathology associated with disease progression. FW change was associated with clinical decline. The findings support dMRI as a promising tool to track disease progression in DLB. © 2024 International Parkinson and Movement Disorder Society.
扩散加权磁共振成像(dMRI)可在体内检查组织微观结构完整性。先前关于路易体痴呆(DLB)的扩散张量成像研究结果不一。
我们采用自由水(FW)成像来评估DLB的进展,并将其与DLB的临床衰退相关联。
对27例DLB或路易体轻度认知障碍(MCI-LB)患者在12个月和/或24个月时进行了基线和随访磁共振成像检查。使用梅奥诊所成人寿命模板分析FW。主要结局是基线与12个月或24个月之间的FW差异。为了纵向比较FW变化,我们纳入了来自阿尔茨海默病神经影像倡议的20名认知未受损个体。
我们对23名参与者进行了12个月的随访,对16名参与者进行了24个月的随访。两组的蒙特利尔认知评估(MoCA)和运动障碍协会统一帕金森病评定量表(MDS-UPDRS)评分均有所恶化。我们发现,与基线相比,在岛叶、杏仁核、后扣带回、海马旁回、内嗅区、缘上回、梭状回、压后皮质和中央沟盖区,两个时间点的FW均显著增加。在24个月时,我们发现涉及视觉空间处理、运动和胆碱能功能的区域有更广泛的微观结构变化。组间分析(DLB与对照组)证实,在24个月内,这些区域中的大多数都有显著的FW变化。FW变化与MDS-UPDRS和MoCA评分的纵向恶化相关。
DLB的灰质和白质区域中FW增加,可能是由于与疾病进展相关的神经退行性病变所致。FW变化与临床衰退相关。这些发现支持dMRI作为追踪DLB疾病进展的一种有前景的工具。© 2024国际帕金森和运动障碍协会