Molecular beacon–based detection of circulating microRNA-containing extracellular vesicle as an α-synucleinopathy biomarker

Author:

Yu Zhenwei12ORCID,Zheng Yuanchu23ORCID,Cai Huihui23,Li Siming23,Liu Genliang23,Kou Wenyi23,Yang Chen23,Cao Shuangshuang4,Chen Lei5,Liu Xuedong6ORCID,Wan Zhirong7,Zhang Ning8ORCID,Li Xiaohong9,Cui Guiyun10ORCID,Chang Ying11ORCID,Huang Yue21213ORCID,Lv Hong14,Feng Tao23ORCID

Affiliation:

1. Department of Pathophysiology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.

2. Center for Movement Disorders, Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

3. China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

4. Department of Neurology, Yidu Central Hospital of Weifang, Shandong, China.

5. Department of Neurology, Tianjin Huanhu Hospital, Tianjin, China.

6. Department of Neurology, Fourth Military Medical University, Xi’an, China.

7. Department of Neurology, Aerospace Center Hospital, Beijing, China.

8. Department of Neuropsychiatry and Behavioral Neurology and Clinical Psychology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

9. Department of Neurology, Dalian Friendship Hospital, Dalian, China.

10. Department of Neurology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.

11. Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, China.

12. Human Brain and Tissue Bank, China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

13. Department of Pharmacology, School of Biomedical Sciences, Faculty of Medicine and Health, UNSW Sydney, Sydney, NSW, Australia.

14. Department of Clinical Diagnosis, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

Abstract

Early and precise diagnosis of α-synucleinopathies is challenging but critical. In this study, we developed a molecular beacon–based assay to evaluate microRNA-containing extracellular vesicles (EVs) in plasma. We recruited 1203 participants including healthy controls (HCs) and patients with isolated REM sleep behavior disorder (iRBD), α-synucleinopathies, or non–α-synucleinopathies from eight centers across China. Plasma miR-44438–containing EV levels were significantly increased in α-synucleinopathies, including those in the prodromal stage (e.g., iRBD), compared to both non–α-synucleinopathy patients and HCs. However, there are no significant differences between Parkinson’s disease (PD) and multiple system atrophy. The miR-44438–containing EV levels negatively correlated with age and the Hoehn and Yahr stage of PD patients, suggesting a potential association with disease progression. Furthermore, a longitudinal analysis over 16.3 months demonstrated a significant decline in miR-44438–containing EV levels in patients with PD. These results highlight the potential of plasma miR-44438–containing EV as a biomarker for early detection and progress monitoring of α-synucleinopathies.

Publisher

American Association for the Advancement of Science (AAAS)

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