Defining at-risk populations for Parkinson's disease: Lessons from ongoing studies

被引:101
作者
Berg, Daniela [1 ,2 ]
Marek, Ken [3 ]
Ross, George W. [4 ,5 ]
Poewe, Werner [6 ]
机构
[1] Univ Tubingen, Dept Neurodegenerat, Hertie Inst Clin Brain Res, D-72076 Tubingen, Germany
[2] Univ Tubingen, German Ctr Neurodegenerat Dis, D-72076 Tubingen, Germany
[3] Inst Neurodegenerat Disorders, New Haven, CT USA
[4] Kuakini Med Ctr, Honolulu, HI USA
[5] VA Pacific Isl Hlth Care Syst, Honolulu, HI USA
[6] Univ Innsbruck, Dept Neurol, A-6020 Innsbruck, Austria
关键词
preclinical Parkinson's disease; at-risk populations; population-based cohorts; enriched risk cohorts; SLEEP BEHAVIOR DISORDER; DOPAMINE TRANSPORTERS; LEWY BODY; OLFACTORY DYSFUNCTION; IDENTIFICATION TEST; IMPAIRED OLFACTION; SUBSTANTIA-NIGRA; DIAGNOSIS; SPECT; ASSOCIATION;
D O I
10.1002/mds.24985
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
It is currently widely acknowledged that the natural history of PD includes a preclinical phase, and there are increasing efforts to identify markers that would allow the identification of individuals at risk for PD. Here, we discuss the issues related to defining at-risk populations for PD and review findings of current population-based cohorts that have reported potential biomarkers for PD, such as the Honolulu-Asia Aging Study (HAAS) and the PRIPS (Prospective Validation of Risk factors for the development of Parkinson Syndromes) study. We also discuss enriched risk cohorts designed to evaluate specificity and predictive value of markers exemplified by the PARS (Parkinson Associated Risk Study) and the TREND (Tubinger evaluation of Risk factors for the Early detection of NeuroDegeneration) study. Although there is still a long way to go, studies designed according to these concepts might eventually provide sufficient data to form the basis for future screening programs for PD risk to be applied at a population level. (C) 2012 Movement Disorder Society
引用
收藏
页码:656 / 665
页数:10
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