Increase of α-Synuclein in the Peripheral Blood of Subjects with Methamphetamine Use Disorder
- Authors
- Choi, Mi Ran; Chon, Younghoon; Cho, Joongbum; Han, Changwoo; Jin, Yeung-Bae; Lee, Sang-Rae; Kim, Dai-Jin
- Issue Date
- Jul-2025
- Publisher
- 대한신경정신의학회
- Keywords
- Addiction; Methamphetamine; Neurotoxicity; Alpha-synuclein
- Citation
- Psychiatry Investigation, v.22, no.7, pp 786 - 795
- Pages
- 10
- Indexed
- SCIE
SSCI
SCOPUS
KCI
- Journal Title
- Psychiatry Investigation
- Volume
- 22
- Number
- 7
- Start Page
- 786
- End Page
- 795
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/79616
- DOI
- 10.30773/pi.2023.0389
- ISSN
- 1738-3684
1976-3026
- Abstract
- Objective Methamphetamine (MA) use has created significant public health problems worldwide. Its chronic abuse causes neurotoxicity resulting in disruption of neural plasticity and early onset of neurodegenerative diseases. Therefore, there is need for a biomarker to evaluate the neurotoxicity caused by MA. This study investigates the expression levels of alpha-synuclein (alpha-Syn), brain-derived neurotrophic factor (BDNF), and neuron-specific enolase (NSE) in the blood of patients with MA use disorder to identify potential biomarkers. Methods We collected blood samples from 60 subjects (30 normal healthy controls and 30 patients with MA use disorder [MA group]). We used multiplex assay kits to analyze the expression levels of alpha-Syn, BDNF, and NSE in the blood of these subjects. Results Beck Depression Inventory and Beck Anxiety Inventory scale scores were significantly different between the control and MA groups. The expression level of alpha-Syn in the MA group was significantly increased compared to that in the control group (z value=-1.986, p=0.0473). In contrast, BDNF in the MA group tended to increase as the duration of MA use increased (r=0.323, p=0.082). Conclusion We identified an increase of alpha-Syn in the blood of the MA group. This finding suggests that the alpha-Syn level increases in the brain after exposure to MA by passing through the blood brain barrier. This result provides useful information for potential biomarkers in diagnosis of neurodegenerative diseases caused by MA abuse. Psychiatry Investig 2025;22(7):786-795
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