From the IRCCS Institute of Neurological Sciences (V.D., A.I., G.R., S.C., R.P., M.S.M., F.M., A.B., R.L.); Department of Biomedical and Neuromotor Sciences (G.R., S.C., R.L.), University of Bologna; Neurological Unit (G. Devigili, R.E.), Department of Neurosciences, "Santa Maria della Misericordia" University Hospital Udine; and Department of Basic Medical Sciences (G. Defazio), Neuroscience and Sense Organs, "Aldo Moro" University of Bari, Italy.
Neurology. 2017 Jul 25;89(4):318-326. doi: 10.1212/WNL.0000000000004146. Epub 2017 Jun 30.
To investigate whether (1) phosphorylated α-synuclein (p-syn) deposits in skin nerves could be useful in differentiating dementia with Lewy bodies (DLB) from different forms of dementia and (2) small fiber neuropathy (SFN) is associated with DLB.
We studied 18 well-characterized patients with DLB (11 with autonomic dysfunction), 23 patients with nonsynucleinopathy dementia (NSD; 13 with young-onset Alzheimer disease dementia, 6 frontotemporal dementia, and 4 vascular dementia), and 25 healthy controls. All participants underwent skin biopsies from proximal (i.e., cervical) and distal (i.e., thigh and distal leg) sites to study small nerve fibers and deposits of p-syn, considered the pathologic form of α-synuclein.
No p-syn was detected in any skin sample in patients with NSD and controls but was found in all patients with DLB. SFN was found in patients with DLB and the autonomic denervation of skin was more severe in patients with autonomic dysfunctions.
(1) In autonomic skin nerves, p-syn is a sensitive biomarker for DLB diagnosis, helping to differentiate DLB from other forms of dementia, although this needs to be confirmed in a larger, more representative sample; and (2) skin autonomic neuropathy is part of the DLB pathology and may contribute to autonomic symptoms.
This study provides Class III evidence that p-syn in skin nerve fibers on skin biopsy accurately distinguishes DLB from other forms of dementia.
研究(1)皮肤神经中磷酸化的α-突触核蛋白(p-syn)是否有助于将路易体痴呆(DLB)与其他类型痴呆区分开来,(2)小纤维神经病(SFN)是否与 DLB 相关。
我们研究了 18 名特征明确的 DLB 患者(11 名伴有自主神经功能障碍)、23 名非突触核蛋白病性痴呆(NSD;13 名早发性阿尔茨海默病性痴呆、6 名额颞叶痴呆、4 名血管性痴呆)和 25 名健康对照者。所有参与者均接受了来自近端(即颈部)和远端(即大腿和小腿)部位的皮肤活检,以研究小神经纤维和 p-syn 的沉积,后者被认为是α-synuclein 的病理形式。
在 NSD 患者和对照组的任何皮肤样本中均未检测到 p-syn,但在所有 DLB 患者中均发现了 p-syn。在 DLB 患者中发现了 SFN,且自主神经支配皮肤的去神经支配在伴有自主神经功能障碍的患者中更为严重。
(1)在自主神经皮肤神经中,p-syn 是 DLB 诊断的敏感生物标志物,有助于将 DLB 与其他类型的痴呆区分开来,尽管这需要在更大、更具代表性的样本中得到证实;(2)皮肤自主神经病变是 DLB 病理的一部分,可能导致自主症状。
本研究提供了 III 级证据,表明皮肤神经纤维活检中的 p-syn 可准确区分 DLB 与其他类型的痴呆。