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Updated: Dec 29, 2025

Technique for Intranasal Administration of α-Synuclein Aggregates
Published on: November 8, 2024
Traumatic brain injury preceding clinically diagnosed α-synucleinopathies: A case-control study
Shemonti Hasan1, Michelle M Mielke1, Pierpaolo Turcano1
1From the Alix School of Medicine (S.H.), Department of Health Sciences Research (M.M.M., R.S.), and Department of Neurology (P.T., J.E.A., J.H.B., R.S.), Mayo Clinic, Rochester, MN.
Traumatic brain injury (TBI) was not linked to developing Parkinson disease (PD) or other synucleinopathies. This study found no association between TBI and these neurodegenerative conditions, regardless of injury severity or timing.
Area of Science:
- Neurology
- Neuroscience
- Epidemiology
Background:
- Traumatic brain injury (TBI) is a potential risk factor for neurodegenerative diseases.
- α-synucleinopathies, including Parkinson disease (PD), dementia with Lewy bodies (DLB), PD dementia (PDD), and multiple system atrophy (MSA), are characterized by the accumulation of α-synuclein protein.
- The relationship between TBI and α-synucleinopathies requires further investigation.
Purpose of the Study:
- To investigate the association between traumatic brain injury (TBI) and the risk of developing clinically diagnosed α-synucleinopathies.
- To examine specific associations between TBI and individual α-synucleinopathies: PD, DLB, PDD, and MSA.
Main Methods:
- A nested case-control study was conducted using the Rochester Epidemiology Project medical records.
- Incident cases of α-synucleinopathies (1991-2010) were identified and matched to controls by age and sex.
- TBI history, severity, and timing were assessed, and conditional-logistic regression was used to calculate odds ratios, adjusting for coffee intake and smoking.
Main Results:
- TBI occurred less frequently in cases (7.0%) than controls (8.2%).
- No significant association was found between TBI and all α-synucleinopathies combined (OR 0.90, 95% CI 0.54-1.52) in multivariable analyses.
- No associations were identified for TBI with PD, DLB, or PDD. A single case of TBI was noted in the MSA group, precluding robust analysis.
Conclusions:
- This population-based study found no evidence of an association between TBI and the subsequent development of α-synucleinopathies.
- The lack of association persisted regardless of TBI temporality or severity.
- Study findings may be limited by statistical power.
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