Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy.
IRCCS Istituto delle Scienze Neurologiche di Bologna, Programma di Patologia Neuromuscolare e Neuroimmunologia, Bologna, Italy.
J Parkinsons Dis. 2022;12(2):585-591. doi: 10.3233/JPD-212904.
Previous studies reported skin phosphorylated α-synuclein (p-syn) deposits in Parkinson's disease (PD) patients but not in patients with parkinsonism due to tauopathies, although data on the latter are limited.
We aimed to assess the presence of skin p-syn deposits in patients with clinical diagnosis of parkinsonism usually due to tauopathy and PD.
We consecutively recruited 26 patients, 18 fulfilling clinical diagnostic criteria of progressive supranuclear palsy (PSP) and 8 of corticobasal syndrome (CBS), 26 patients with PD, and 26 healthy controls (HC). All subjects underwent skin biopsy to study p-syn deposits in skin nerves by immunofluorescence.
Skin p-syn deposits were present in only two of the PSP/CBS patients and none of the HC. Conversely, all PD patients showed p-syn deposition (p < 0.001, Chi-square). The two p-syn positive patients were diagnosed with PSP and CBS, respectively. Although clinical and MRI findings supported these diagnoses, both patients had some atypical features more typical of synucleinopathies.
The detection of skin p-syn deposits may help in the differential diagnosis of parkinsonism. Indeed, in this study, all PD patients and only two out of 26 with a clinical diagnosis of PSP/CBS had skin p-syn deposits. Furthermore, these two patients showed clinical features that could suggest an atypical synucleinopathy presentation or a mixed pathology.
先前的研究报告称帕金森病(PD)患者存在皮肤磷酸化 α-突触核蛋白(p-syn)沉积,但tau 病引起的帕金森综合征患者不存在,尽管后者的数据有限。
我们旨在评估临床诊断为通常由 tau 病引起的帕金森综合征患者和 PD 患者皮肤 p-syn 沉积的存在情况。
我们连续招募了 26 名患者,18 名符合进行性核上性麻痹(PSP)的临床诊断标准,8 名符合皮质基底节综合征(CBS)的临床诊断标准,26 名 PD 患者和 26 名健康对照者(HC)。所有受试者均接受皮肤活检,通过免疫荧光法研究皮肤神经中的 p-syn 沉积。
仅在两名 PSP/CBS 患者中存在皮肤 p-syn 沉积,而在 HC 中均不存在。相反,所有 PD 患者均显示 p-syn 沉积(p<0.001,卡方检验)。两名 p-syn 阳性患者分别被诊断为 PSP 和 CBS。尽管临床和 MRI 发现支持这些诊断,但这两名患者均具有一些更典型的突触核蛋白病的非典型特征。
皮肤 p-syn 沉积的检测可能有助于帕金森综合征的鉴别诊断。事实上,在这项研究中,所有 PD 患者和 26 名临床诊断为 PSP/CBS 的患者中仅有 2 名患者存在皮肤 p-syn 沉积。此外,这两名患者表现出的临床特征可能提示存在非典型的突触核蛋白病表现或混合性病理。