4.5 Article Proceedings Paper

Neuropathology of Parkinson disease

期刊

PARKINSONISM & RELATED DISORDERS
卷 46, 期 -, 页码 S30-S33

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.parkreldis.2017.07.033

关键词

Parkinson disease; Neuropathology; alpha-Synuclein; Lewy body

资金

  1. NINDS [P50-NS072187]
  2. Mangurian Foundation Lewy Body Dementia Program
  3. CurePSP/Tau Consortium Brain Bank
  4. Robert E. Jacoby Professorship
  5. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R21NS099757, U54NS100693, P50NS072187] Funding Source: NIH RePORTER

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Introduction: Parkinson's disease (PD) is characterized by bradykinesia, rigidity, postural instability and tremor. Several pathologic processes can produce this syndrome, but neurodegeneration accompanied by neuronal inclusions composed of alpha-synuclein (Lewy bodies) is considered the typical pathologic correlate of PD. Methods: The neuropathologic features of PD are reviewed based upon personal experience and review of the literature. Molecular pathology of PD is summarized from cell biological and animal studies. Results: The pathologic feature that correlates with signs and symptoms of PD is neuronal loss in the substantia nigra with dopaminergic denervation of the striatum. Neuronal degeneration in the substantia nigra preferentially affects the ventrolateral cell group that projects to posterolateral putamen and is accompanied by formation of Lewy bodies composed of aggregated alpha-synuclein. Some patients with PD are found at autopsy to have other pathologic processes, such as multiple system atrophy, progressive supranuclear palsy and cerebrovascular disease (vascular Parkinsonism). The peripheral autonomic nervous system is also affected. The triggering event in PD is unknown, but recent studies suggest a role for loss of nuclear membrane integrity. Once alpha-synuclein aggregates forms, evidence supports cell-to-cell propagation. Conclusion: PD is a multisystem synucleinopathy caused by poorly characterized genetic and environmental factors that produces degeneration in selectively vulnerable neuronal populations. (C) 2017 Elsevier Ltd. All rights reserved.

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