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Published on: November 8, 2024
MicroRNA association with synucleinopathy conversion in rapid eye movement behavior disorder
Rubén Fernández-Santiago1, Alex Iranzo, Carles Gaig
1Laboratory of Neurodegenerative Disorders, Department of Neurology, Hospital Clínic of Barcelona, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), University of Barcelona, Barcelona; Center for Biomedical Research in Neurodegenerative Diseases, Madrid.
Downregulated miR-19b levels in serum indicate early Parkinson disease risk. This microRNA dysregulation occurs in the prodromal stage of synucleinopathies, preceding clinical diagnosis.
Area of Science:
- Neuroscience
- Genetics
- Biochemistry
Background:
- Parkinson disease is a synucleinopathy characterized by motor and non-motor symptoms.
- Previous research indicated decreased levels of miR-19b, miR-29a, and miR-29c in Parkinson disease patients.
- Idiopathic rapid eye movement sleep behavior disorder (iRBD) is a prodromal synucleinopathy.
Purpose of the Study:
- To investigate the expression of miR-19b, miR-29a, and miR-29c in serum from patients with iRBD.
- To determine if miR-19b dysregulation precedes the clinical diagnosis of synucleinopathies like Parkinson disease and dementia with Lewy bodies.
Main Methods:
- Serum samples were collected from 56 patients diagnosed with iRBD.
- MicroRNA expression levels were analyzed using quantitative real-time PCR.
- Patients were followed over time to track conversion to synucleinopathies.
Main Results:
- A significant downregulation of miR-19b was observed in patients with iRBD compared to controls.
- This downregulation of miR-19b was found to antedate the diagnosis of Parkinson disease and dementia with Lewy bodies by an average of 4.67 years.
- No significant changes were noted for miR-29a and miR-29c in this cohort.
Conclusions:
- Dysregulation of miR-19b occurs during the prodromal stage of synucleinopathies.
- miR-19b may serve as a potential biomarker for early detection of synucleinopathies.
- Further research is warranted to explore the role of miR-19b in neurodegenerative disease pathogenesis.
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