Ayral Violette, Pastor-Bernier Alexandre, Daneault Véronique, Tremblay Christina, Filiatrault Marie, Haddad Celine, Gagnon Jean-François, Postuma Ronald B, Dušek Petr, Marecek Stanislav, Varga Zsoka, Klein Johannes C, Hu Michele T, Lehéricy Stéphane, Arnulf Isabelle, Vidailhet Marie, Corvol Jean-Christophe, Rahayel Shady
Centre for Advanced Research in Sleep Medicine, Hôpital du Sacré-Cœur de Montréal, CIUSSS du Nord-de-l'Île-de-Montréal, Quebec, Canada.
Department of Neuroscience, University of Montreal, Quebec, Canada.
Neurology. 2025 Oct 7;105(7):e214042. doi: 10.1212/WNL.0000000000214042. Epub 2025 Sep 16.
Isolated REM sleep behavior disorder (iRBD) is the strongest prodromal marker of synucleinopathies, including Parkinson disease (PD) and dementia with Lewy bodies (DLB). Identifying brain biomarkers that predict progression and distinguish phenoconversion trajectories remains a challenge. The glymphatic system is involved in interstitial waste clearance, and its dysfunction has been associated with pathologic protein accumulation and neurodegeneration. Diffusion tensor imaging along the perivascular space (DTI-ALPS) has been proposed as a noninvasive proxy for glymphatic function. The aim of this study was to determine whether patients with iRBD show a reduced DTI-ALPS index compared with controls and whether a lower DTI-ALPS index predicts future phenoconversion to PD or DLB.
We conducted a longitudinal, multicenter cohort study using brain MRI scans from patients with polysomnography-confirmed iRBD and healthy controls recruited across 5 international centers. All participants underwent T1-weighted and diffusion-weighted MRI. DTI-ALPS indices were computed from diffusivity along projection and associative fibers adjacent to the lateral ventricles. The primary outcome was time to phenoconversion to synucleinopathy. Linear models assessed baseline group differences and clinical correlates, and Cox proportional hazard models assessed the predictive value of DTI-ALPS for time to phenoconversion.
A total of 250 patients with iRBD (mean age: 66.5 ± 6.8 years; 87% male) and 178 controls (65.7 ± 6.8 years; 81% male) were included. Patients with iRBD showed a lower left DTI-ALPS index compared with controls (mean difference = -0.034, 95% CI -0.067 to -0.001; = 0.043). Of 224 patients with iRBD followed for a mean of 6.1 ± 3.5 years, 65 phenoconverted to a synucleinopathy. Converters had a lower left DTI-ALPS index than nonconverters (mean difference = -0.050, 95% CI -0.098 to -0.003; = 0.038). Lower left DTI-ALPS index was associated with an increased risk of conversion to PD over time (hazard ratio = 2.43, 95% CI 1.13-5.25; = 0.012). Other diffusion metrics inside periventricular masks, namely fractional anisotropy, diffusivity metrics, and free water, did not differ between groups.
Patients with iRBD exhibit a reduced DTI-ALPS index, suggesting altered glymphatic function. This reduction was associated with future phenoconversion to PD, supporting the DTI-ALPS index as a potential prognostic MRI biomarker of progression in prodromal synucleinopathies.
孤立性快速眼动睡眠行为障碍(iRBD)是突触核蛋白病(包括帕金森病(PD)和路易体痴呆(DLB))最强的前驱标志物。识别预测疾病进展并区分表型转化轨迹的脑生物标志物仍然是一项挑战。类淋巴系统参与间质废物清除,其功能障碍与病理性蛋白质积累和神经退行性变有关。沿血管周围间隙的扩散张量成像(DTI-ALPS)已被提议作为类淋巴功能的一种非侵入性替代指标。本研究的目的是确定iRBD患者与对照组相比是否表现出DTI-ALPS指数降低,以及较低的DTI-ALPS指数是否能预测未来向PD或DLB的表型转化。
我们进行了一项纵向、多中心队列研究,使用了来自5个国际中心招募的经多导睡眠图确诊的iRBD患者和健康对照的脑部MRI扫描数据。所有参与者均接受了T1加权和扩散加权MRI检查。DTI-ALPS指数是根据沿侧脑室相邻投射纤维和联合纤维的扩散率计算得出的。主要结局是向突触核蛋白病表型转化的时间。线性模型评估了基线组间差异和临床相关性,Cox比例风险模型评估了DTI-ALPS对表型转化时间的预测价值。
共纳入250例iRBD患者(平均年龄:66.5±6.8岁;87%为男性)和178例对照(65.7±6.8岁;81%为男性)。与对照组相比,iRBD患者的左侧DTI-ALPS指数较低(平均差异=-0.034,95%CI -0.067至-0.001;P=0.043)。在224例平均随访6.1±3.5年的iRBD患者中,65例发生了向突触核蛋白病的表型转化。转化者的左侧DTI-ALPS指数低于未转化者(平均差异=-0.050,95%CI -0.098至-0.003;P=0.038)。随着时间的推移,较低的左侧DTI-ALPS指数与转化为PD的风险增加相关(风险比=2.43,95%CI 1.13-5.25;P=0.012)。脑室周围区域内的其他扩散指标,即分数各向异性、扩散率指标和自由水,在组间没有差异。
iRBD患者表现出DTI-ALPS指数降低,提示类淋巴功能改变。这种降低与未来向PD的表型转化相关,支持DTI-ALPS指数作为前驱突触核蛋白病进展的一种潜在预后MRI生物标志物。