Comprehensive data for studying serum exosome microRNA transcriptome in Parkinson's disease patients

被引:0
|
作者
Yu, Zhiyang [1 ]
Saiki, Shinji [1 ,2 ]
Shiina, Kenta [1 ]
Iseki, Tatou [1 ]
Sasazawa, Yukiko [1 ,3 ,4 ]
Ishikawa, Kei-Ichi [1 ]
Nishikawa, Noriko [1 ]
Sako, Wataru [1 ]
Oyama, Genko [1 ]
Hatano, Taku [1 ]
Suzuki, Ayami [1 ,2 ]
Souma, Sanae [1 ]
Kataura, Tetsushi [2 ]
Hattori, Nobutaka [1 ,3 ,4 ,5 ]
机构
[1] Juntendo Univ, Grad Sch Med, Dept Neurol, Tokyo, Japan
[2] Univ Tsukuba, Inst Med, Dept Neurol, Ibaraki, Japan
[3] Juntendo Univ, Fac Med, Div Dev Autophagy Modulating Drugs, Tokyo, Japan
[4] Juntendo Univ, Grad Sch Med, Res Inst Dis Old Age, Tokyo, Japan
[5] RIKEN Ctr Brain Sci, Neurodegenerat Disorders Collaborat Lab, Saitama, Japan
关键词
DELAYED-START TRIAL; ENRICHMENT ANALYSIS; ALPHA-SYNUCLEIN; DOUBLE-BLIND; MIRNAS; RASAGILINE; EXPRESSION; HALLMARKS;
D O I
10.1038/s41597-024-03909-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Parkinson's disease (PD), the second most prevalent neurodegenerative disorder, was classically attributed to alpha-synuclein aggregation and consequent loss of dopaminergic neurons in the substantia nigra pars compacta. Recently, emerging evidence suggested a broader spectrum of contributing factors, including exosome-mediated intercellular communication, which can potentially serve as biomarkers and therapeutic targets. However, there is a remarkable lack of comprehensive studies that connect the serum exosome microRNA (miRNA) transcriptome with demographic, clinical, and neuroimaging data in PD patients. Here, we present serum exosome miRNA transcriptome data generated from four cohort studies. Two of these studies include 96 PD patients and 80 age- and gender-matched controls, with anonymised demographic, clinical, and neuroimaging data provided for PD patients. The other two studies involve 96 PD patients who were evaluated both before and after one year of treatment with rasagiline, a widely prescribed anti-parkinsonism drug. Together, the datasets provide a valuable source for understanding pathogenesis and discovering biomarkers and therapeutic targets in PD.
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页数:9
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