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Article type: Review Article
Authors: Swerdlow, Russell H.; *
Affiliations: Departments of Neurology, Molecular & Integrative Physiology, University of Kansas School of Medicine, Kansas City, KS, USA
Correspondence: [*] Address for correspondence: Russell Swerdlow, MD, Department of Neurology, University of Kansas, MS 2012, Landon Center on Aging, 3901 Rainbow Boulevard, Kansas City, KS 66160, USA. Tel.: +1 913 945 6632; E-mail: rswerdlow@kumc.edu.
Note: [] Communicated by Xiongwei Zhu
Abstract: Mitochondria are physically or functionally altered in many neurodegenerative diseases. This is the case for very rare neurodegenerative disorders as well as extremely common age-related ones such as Alzheimer's disease and Parkinson's disease. In some disorders very specific patterns of altered mitochondrial function or systemic mitochondrial dysfunction are demonstrable. Some disorders arise from mitochondrial DNA mutation, some from nuclear gene mutation, and for some the etiology is not definitively known. This review classifies neurodegenerative diseases using mitochondrial dysfunction as a unifying feature, and in doing so defines a group of disorders called the neurodegenerative mitochondriopathies. It discusses what mitochondrial abnormalities have been identified in various neurodegenerative diseases, what is currently known about the mitochondria-neurodegeneration nexus, and speculates on the significance of mitochondrial function in some disorders not classically thought of as mitochondriopathies.
Keywords: Alzheimer's disease, cybrid, mitochondria, mitochondriopathy, neurodegeneration, neurodegenerative, Parkinson's disease
DOI: 10.3233/JAD-2009-1095
Journal: Journal of Alzheimer's Disease, vol. 17, no. 4, pp. 737-751, 2009
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