4.7 Article

A longitudinal study on α-synuclein in plasma neuronal exosomes as a biomarker for Parkinson's disease development and progression

期刊

EUROPEAN JOURNAL OF NEUROLOGY
卷 27, 期 6, 页码 967-974

出版社

WILEY
DOI: 10.1111/ene.14208

关键词

biomarker; diagnosis; disease progression; idiopathic rapid eye movement sleep behavior disorder; neuronal exosome; Parkinson's disease; plasma; alpha-synuclein

资金

  1. National Key Research and Development Program [2016YFC1306505]
  2. National Natural Science Foundation of China [81501097]

向作者/读者索取更多资源

Background and purpose The identification of reliable diagnostic and prognostic biomarkers for Parkinson's disease (PD) is urgently needed. Here, we explored the potential use of alpha-synuclein (alpha-syn) in plasma neuronal exosomes as a biomarker for early PD diagnosis and disease progression. Methods This study included both cross-sectional and longitudinal designs. The subjects included 36 patients with early-stage PD, 17 patients with advanced PD, 20 patients with idiopathic rapid eye movement sleep behavior disorder and 21 healthy controls (HCs). alpha-syn levels were measured by electrochemiluminescence immunoassay. A subgroup of patients with early-stage PD (n = 18) participated in a follow-up examination with repeated blood collection and clinical assessments after an average of 22 months. Results The alpha-syn levels in plasma neuronal exosomes were significantly higher in patients with early-stage PD compared with HCs (P = 0.007). Differences in alpha-syn levels between patients with idiopathic rapid eye movement sleep behavior disorder and HCs did not reach statistical significance (P = 0.08). In addition, Spearman correlation analysis revealed that neuronal exosomal alpha-syn concentrations were correlated with Movement Disorders Society Unified Parkinson's Disease Rating Scale III/(I + II + III) scores, Non-Motor Symptom Questionnaire scores and Sniffin' Sticks 16-item test scores of patients with PD (P < 0.05). After a mean follow-up of 22 months in patients with early-stage PD, a Cox regression analysis adjusted for age and gender showed that longitudinally increased alpha-syn rather than baseline alpha-syn levels were associated with higher risk for motor symptom progression in PD (P = 0.039). Conclusions Our results suggested that alpha-syn in plasma neuronal exosomes may serve as a biomarker to aid early diagnosis of PD and also as a prognostic marker for PD progression.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据