From the Department of Neurology (Y.-W.C.), National Taiwan University Hospital, Hsin-Chu Branch; Graduate Institute of Clinical Medicine (Y.-W.C.), College of Medicine, National Taiwan University; Department of Neurology (C.-C.C., C.-H.C., J.-S.J., S.-C.T., S.-T.H.), National Taiwan University Hospital; Department of Anatomy and Cell Biology (T.-Y.Y., S.-T.H.), College of Medicine, National Taiwan University; Graduate Institute of Brain and Mind Sciences (S.-T.H.), College of Medicine, National Taiwan University; and Center of Precision Medicine (S.-T.H.), National Taiwan University College of Medicine, Taipei.
Neurology. 2022 Aug 9;99(6):e583-e593. doi: 10.1212/WNL.0000000000200672. Epub 2022 May 18.
This study investigated the cutaneous small fiber pathology of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and its clinical significance, that is, the NOTCH3 deposition in cutaneous vasculatures and CNS neurodegeneration focusing on cognitive impairment.
Thirty-seven patients with CADASIL and 59 age-matched healthy controls were enrolled to evaluate cutaneous small fiber pathology by quantitative measures of intraepidermal nerve fiber density (IENFD), sweat gland innervation, and vascular innervation. Cognitive performance of patients with CADASIL was evaluated by a comprehensive neuropsychological assessment, and its association with small fiber pathology was tested using multivariable linear regression analysis adjusted for age and diabetes mellitus. We further assessed the relationships of IENFD with cutaneous vascular NOTCH3 ectodomain (NOTCH3ECD) deposition and biomarkers of neurodegeneration including structural brain MRI measures, serum neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), tau, and ubiquitin carboxy-terminal hydrolase L1.
Patients with CADASIL showed reduced IENFD (5.22 ± 2.42 vs 7.88 ± 2.89 fibers/mm, = 0.0001) and reduced sweat gland ( < 0.0001) and vascular ( < 0.0001) innervations compared with age-matched controls. Reduced IENFD was associated with impaired global cognition measured by Mini-Mental State Examination ( = 1.062, 95% CI = 0.370-1.753, = 0.004), and this association remained after adjustment for age and diabetes mellitus ( = 0.043). In addition, IENFD in patients with CADASIL was associated with mean cortical thickness (Pearson = 0.565, = 0.0023) but not white matter hyperintensity volume, total lacune count, or total microbleed count. Reduced IENFD was associated with cutaneous vascular NOTCH3ECD deposition amount among patients harboring pathogenic variants in exon 11 (mainly p.R544C) ( = -0.092, 95% CI = -0.175 to -0.009, = 0.031). Compared with those with normal cognition, patients with CADASIL with cognitive impairment had an elevated plasma NfL level regardless of concurrent small fiber denervation, whereas only patients with both cognitive impairment and small fiber denervation showed an elevated plasma GFAP level.
Cutaneous small fiber pathology correlates with cognitive impairment and CNS neurodegeneration in patients with CADASIL, indicating a peripheral neurodegenerative process related to NOTCH3ECD aggregation.
本研究旨在探讨伴有皮质下梗死和白质脑病的常染色体显性脑动脉病(CADASIL)的皮肤小纤维病理及其临床意义,即 Notch3 在皮肤血管和中枢神经系统神经退行性变中的沉积与认知障碍的关系。
纳入 37 例 CADASIL 患者和 59 名年龄匹配的健康对照者,通过表皮内神经纤维密度(IENFD)、汗腺神经支配和血管神经支配的定量测量来评估皮肤小纤维病理。采用全面的神经心理学评估评估 CADASIL 患者的认知功能,并通过多变量线性回归分析,调整年龄和糖尿病,检验其与小纤维病理的关系。我们进一步评估了 IENFD 与皮肤血管 Notch3 外显子(NOTCH3ECD)沉积和神经退行性变的生物标志物之间的关系,包括结构脑 MRI 测量、血清神经丝轻链(NfL)、神经胶质纤维酸性蛋白(GFAP)、tau 和泛素羧基末端水解酶 L1。
CADASIL 患者的 IENFD(5.22±2.42 比 7.88±2.89 纤维/mm, = 0.0001)和汗腺(<0.0001)及血管(<0.0001)支配均降低,与年龄匹配的对照组相比。IENFD 降低与通过简易精神状态检查( = 1.062,95%CI=0.370-1.753, = 0.004)测量的全球认知能力受损相关,并且在调整年龄和糖尿病后,这种相关性仍然存在( = 0.043)。此外,CADASIL 患者的 IENFD 与皮质平均厚度相关(Pearson = 0.565, = 0.0023),但与脑白质高信号体积、总腔隙计数或总微出血计数无关。在携带外显子 11(主要为 p.R544C)致病性变异的患者中,IENFD 与皮肤血管 NOTCH3ECD 沉积量相关( = -0.092,95%CI=-0.175 至-0.009, = 0.031)。与认知正常的患者相比,CADASIL 患者无论是否伴有小纤维去神经支配,认知障碍患者的血浆 NfL 水平均升高,而只有认知障碍和小纤维去神经支配的患者血浆 GFAP 水平升高。
CADASIL 患者的皮肤小纤维病理与认知障碍和中枢神经系统神经退行性变相关,表明与 Notch3ECD 聚集相关的周围神经退行性过程。