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Progress Toward an Integrated Understanding of Parkinson's Disease

Overview
Journal F1000Res
Date 2017 Jul 29
PMID 28751973
Citations 13
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Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease, affecting over 10 million individuals worldwide. While numerous effective symptomatic treatments are currently available, no curative or disease-modifying therapies exist. An integrated, comprehensive understanding of PD pathogenic mechanisms will likely address this unmet clinical need. Here, we highlight recent progress in PD research with an emphasis on promising translational findings, including (i) advances in our understanding of disease susceptibility, (ii) improved knowledge of cellular dysfunction, and (iii) insights into mechanisms of spread and propagation of PD pathology. We emphasize connections between these previously disparate strands of PD research and the development of an emerging systems-level understanding that will enable the next generation of PD therapeutics.

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References
1.
. The Parkinson Progression Marker Initiative (PPMI). Prog Neurobiol. 2011; 95(4):629-35. PMC: 9014725. DOI: 10.1016/j.pneurobio.2011.09.005. View

2.
Jansen I, Ye H, Heetveld S, Lechler M, Michels H, Seinstra R . Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome Biol. 2017; 18(1):22. PMC: 5282828. DOI: 10.1186/s13059-017-1147-9. View

3.
Valenca G, Srivastava G, Oliveira-Filho J, White C, Yu L, Schneider J . The Role of MAPT Haplotype H2 and Isoform 1N/4R in Parkinsonism of Older Adults. PLoS One. 2016; 11(7):e0157452. PMC: 4961370. DOI: 10.1371/journal.pone.0157452. View

4.
Migdalska-Richards A, Ko W, Li Q, Bezard E, Schapira A . Oral ambroxol increases brain glucocerebrosidase activity in a nonhuman primate. Synapse. 2017; 71(7). PMC: 5485051. DOI: 10.1002/syn.21967. View

5.
Davis M, Johnson C, Leverenz J, Weintraub D, Trojanowski J, Chen-Plotkin A . Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease. JAMA Neurol. 2016; 73(10):1217-1224. PMC: 5056861. DOI: 10.1001/jamaneurol.2016.2245. View