A Longitudinal Program for Biomarker Development in Parkinson's Disease: A Feasibility Study

被引:44
作者
Ravina, Bernard [1 ]
Tanner, Caroline [2 ]
DiEuliis, Diane [3 ]
Eberly, Shirley [1 ]
Flagg, Emily [1 ]
Galpern, Wendy R. [3 ]
Fahn, Stanley [4 ]
Goetz, Christopher G. [5 ]
Grate, Stephen [6 ]
Kurlan, Roger [1 ]
Lang, Anthony E. [7 ]
Marek, Kenneth [8 ]
Kieburtz, Karl [1 ]
Oakes, David [1 ]
Elliott, Robin [9 ]
Shoulson, Ira [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Dept Neurol, Rochester, NY 14642 USA
[2] Parkinsons Inst, Sunnyvale, CA USA
[3] NINDS, Bethesda, MD 20892 USA
[4] Columbia Univ, Dept Neurol, New York, NY USA
[5] Rush Univ, Med Ctr, Dept Neurosci, Chicago, IL 60612 USA
[6] Telemed & Adv Technol Res Ctr, Ft Detrick, MD USA
[7] Univ Toronto, Dept Med, Div Neurol, Toronto, ON, Canada
[8] Inst Neurodegenerat Disorders, New Haven, CT USA
[9] Parkinsons Dis Fdn, New York, NY USA
关键词
Parkinson's disease; progression; biomarker; MONTREAL COGNITIVE ASSESSMENT; RATING-SCALE; CLINICAL-DIAGNOSIS; SCREENING TOOL; HUMAN PLASMA; ACCURACY; RELIABILITY; IMPAIRMENT;
D O I
10.1002/mds.22690
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Long-term follow up is necessary to understand the natural history of treated Parkinson's disease (PD). The Longitudinal and Biomarker Study in PD (LABS-PD) is an observational study designed to prospectively measure the evolution of motor and non-motor features of PD and sample promising biomarkers from early to late stage illness. LABS-PD is organized on the premise that cohorts from completed clinical trials can be re-recruited for long-term follow up. LABS-PD will eventually contain multiple cohorts, but to test the feasibility of the strategy, we examined enrollment and biomarker sampling in the initial cohorts. The first PD cohort (PostCEPT) comes from the de novo clinical trial of a mixed lineage kinase inhibitor (PRECEPT). We assessed the recruitment from PRECEPT to PostCEPT, the ability to link data from the two studies, and sample collection for a variety of biomarkers. A total of 537 of 709 eligible PRECEPT subjects (76%) enrolled in PostCEPT; 509 (95%) had repeat dopamine transporter imaging. PRECEPT clinical and imaging data were successfully linked to PostCEPT, to provide 3 to 4 year follow-up. A biomarker sub-study enrolled over 100 PD cases from PostCEPT and 100 controls to measure olfaction and blood markers of gene expression, alpha-synuclein, and proteomic profiles. We were also successful in linking clinical and biomarker data to DNA samples that have been collected in the publicly accessible Coriell repository. The PostCEPT cohort and associated studies strongly Support the feasibility of the LABS-PD approach of retaining and repurposing clinical trial cohorts to collect longitudinal clinical and biomarker data. (C) 2009 Movement Disorder Society
引用
收藏
页码:2081 / 2090
页数:10
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