期刊
MOVEMENT DISORDERS
卷 30, 期 13, 页码 1794-1801出版社
WILEY
DOI: 10.1002/mds.26319
关键词
Parkinson's disease; alpha-synuclein; DNA methylation; blood; L-dopa
资金
- Deutsche Parkinson Vereinigung (dPV)
- Hans Tauber Stiftung
- Internationale Parkinson Fonds
- EU/EFPIA Innovative Medicines Initiative Joint Undertaking [115568]
Background: Increasing gene dosages of alpha-synuclein induce familial Parkinson's disease (PD); thus, the hypothesis has been put forward that regulation of gene expression, in particular altered alpha-synuclein gene methylation, might be associated with sporadic PD and could be used as a biological marker. Methods: We performed a thorough analysis of alpha-synuclein methylation in bisulfite-treated DNA from peripheral blood of 490 sporadic PD patients and 485 healthy controls and in addition analyzed the effect of levodopa (L-dopa) on alpha-synuclein methylation and expression in cultured mononuclear cells. Results: alpha-Synuclein was hypomethylated in sporadic PD patients, correlated with sex, age, and a polymorphism in the analyzed sequence stretch (rs3756063). alpha-Synuclein methylation separated healthy individuals from sporadic PD with a specificity of 74% (male) and 78% (female), respectively. alpha-Synuclein methylation was increased in sporadic PD patients with higher L-dopa dosage, and L-dopa specifically induced methylation of alpha-synuclein intron 1 in cultured mononuclear cells. Conclusions: alpha-Synuclein methylation levels depended on disease status, sex, age, and the genotype of rs3756063. The pharmacological action of L-dopa was not limited to the dopamine precursor function but included epigenetic off-target effects. The hypomethylation of alpha-synuclein in sporadic PD patients' blood already observed in previous studies was probably underestimated because of effect of L-dopa, which was not known previously. The analysis of alpha-synuclein methylation can help to identify nonparkinsonian individuals with reasonable specificity, which offers a valuable tool for researchers and clinicians. (C) 2015 International Parkinson and Movement Disorder Society
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