Biomarkers of Parkinson's disease and Dementia with Lewy bodies

被引:30
|
作者
Henchcliffe, Claire [1 ]
Dodel, Richard [2 ]
Beal, M. Flint [1 ]
机构
[1] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[2] Univ Marburg, Dept Neurol, Marburg, Germany
关键词
Parkinson's disease; Dementia with Lewy bodies; Parkinson's disease dementia; Biomarkers; CARDIAC SYMPATHETIC DENERVATION; HUMAN CEREBROSPINAL-FLUID; GENOME-WIDE ASSOCIATION; SLEEP BEHAVIOR DISORDER; HUMAN SUBSTANTIA-NIGRA; GENETIC RISK-FACTORS; ALPHA-SYNUCLEIN; CLINICAL-DIAGNOSIS; OXIDATIVE STRESS; ALZHEIMERS-DISEASE;
D O I
10.1016/j.pneurobio.2011.09.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Parkinson's disease (PD) and Dementia with Lewy bodies (DLB) are progressive and disabling neurodegenerative disorders, in which signs and symptoms overlap with each other and with other neurodegenerative conditions. Currently, diagnosis, measurement of progression, and response to therapeutic intervention rely upon clinical observation. However, there remains a critical need for validated biomarkers in each of these areas. A definitive diagnostic test would improve clinical management and enrollment into clinical trials. An objective measure of progression is vitally important in identifying neuroprotective interventions. Biomarkers may also provide insight into pathogenesis, and might therefore suggest possible novel targets for therapeutic intervention. In addition, certain biomarkers might be of use in monitoring the biochemical and physiological effects of therapeutic interventions. Development of diagnostic biomarkers has focused until recently upon imaging techniques based upon measuring loss of dopamine neurons. Additionally, advances in understanding the genetic contribution to neurodegenerative disorders, in particular in PD, have identified multiple causative genes and risk factors that in some cases may help estimate PD risk. However, recent availability of increasingly sophisticated bioinformatics technology has rendered development of fluid biomarkers feasible, opening the possibility of generally accessible blood or cerebrospinal fluid (CSF) tests that could impact upon diagnosis, management, and research in PD, PDD, and DLB. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:601 / 613
页数:13
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