Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Ann Neurol. 2023 Jun;93(6):1130-1141. doi: 10.1002/ana.26615. Epub 2023 Feb 23.
Cerebral small vessel disease (SVD) is associated with motor impairments and parkinsonian signs cross-sectionally, however, there are little longitudinal data on whether SVD increases risk of incident parkinsonism itself. We investigated the relation between baseline SVD severity as well as SVD progression, and incident parkinsonism over a follow-up of 14 years.
This study included 503 participants with SVD, and without parkinsonism at baseline, from the RUN DMC prospective cohort study. Baseline inclusion was performed in 2006 and follow-up took place in 2011, 2015, and 2020, including magnetic resonance imaging (MRI) and motor assessments. Parkinsonism was diagnosed according to the UK Brain Bank criteria, and stratified into vascular parkinsonism (VaP) and idiopathic Parkinson's disease (IPD). Linear mixed-effect models were constructed to estimate individual rate changes of MRI-characteristics.
Follow-up for incident parkinsonism was near-complete (99%). In total, 51 (10.2%) participants developed parkinsonism (33 VaP, 17 IPD, and 1 progressive supranuclear palsy). Patients with incident VaP had higher SVD burden compared with patients with IPD. Higher baseline white matter hyperintensities (hazard ratio [HR] = 1.46 per 1-SD increase, 95% confidence interval [CI] = 1.21-1.78), peak width of skeletonized mean diffusivity (HR = 1.66 per 1-SD increase, 95% CI = 1.34-2.05), and presence of lacunes (HR = 1.84, 95% CI = 0.99-3.42) were associated with increased risk of all-cause parkinsonism. Incident lacunes were associated with incident VaP (HR = 4.64, 95% CI = 1.32-16.32).
Both baseline SVD severity and SVD progression are independently associated with long-term parkinsonism. Our findings indicate a causal role of SVD in parkinsonism. Future studies are needed to examine the underlying pathophysiology of this relation. ANN NEUROL 2023;93:1130-1141.
脑小血管病(SVD)与横断面运动障碍和帕金森病体征有关,但关于 SVD 是否会增加帕金森病本身的发病风险,纵向数据较少。我们研究了基线 SVD 严重程度以及 SVD 进展与 14 年随访期间新发帕金森病之间的关系。
这项研究纳入了来自 RUN DMC 前瞻性队列研究的 503 名基线时无帕金森病且存在 SVD 的参与者。基线纳入于 2006 年进行,随访于 2011 年、2015 年和 2020 年进行,包括磁共振成像(MRI)和运动评估。帕金森病根据英国脑库标准诊断,并分为血管性帕金森病(VaP)和特发性帕金森病(IPD)。构建线性混合效应模型来估计 MRI 特征的个体变化率。
新发帕金森病的随访几乎是完整的(99%)。共有 51 名(10.2%)参与者发生帕金森病(33 名 VaP,17 名 IPD,1 名进行性核上性麻痹)。新发 VaP 患者的 SVD 负担高于新发 IPD 患者。较高的基线白质高信号(HR=每增加 1-SD 1.46,95%CI=1.21-1.78)、骨架化平均弥散峰值宽度(HR=每增加 1-SD 1.66,95%CI=1.34-2.05)和腔隙存在(HR=1.84,95%CI=0.99-3.42)与全因帕金森病风险增加相关。新发腔隙与新发 VaP 相关(HR=4.64,95%CI=1.32-16.32)。
基线 SVD 严重程度和 SVD 进展均与长期帕金森病独立相关。我们的研究结果表明 SVD 在帕金森病中起因果作用。需要进一步研究来探讨这种关系的潜在病理生理学。