TY - JOUR
T1 - The NINDS Parkinson's disease biomarkers program
AU - Rosenthal, Liana S.
AU - Drake, Daniel
AU - Alcalay, Roy N.
AU - Babcock, Debra
AU - Bowman, F. Dubois
AU - Chen-Plotkin, Alice
AU - Dawson, Ted M.
AU - Dewey, Richard B.
AU - German, Dwight C.
AU - Huang, Xuemei
AU - Landin, Barry
AU - Mcauliffe, Matthew
AU - Petyuk, Vladislav A.
AU - Scherzer, Clemens R.
AU - Hillaire-Clarke, Coryse St
AU - Sieber, Beth Anne
AU - Sutherland, Margaret
AU - Tarn, Chi
AU - West, Andrew
AU - Vaillancourt, David
AU - Zhang, Jing
AU - Gwinn, Katrina
N1 - Funding Information:
This study is funded by the National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland. Dr. Rosenthal is supported for this project by NIH/NINDS U01 NS082133 and P50NS38377. Dr. Drake is supported for this project by Emory University, Columbia University, and NIH/NINDS U18 NS082143. Dr. Alcalay is supported for this project by NIH/NINDS K02 NS080915. Dr. Bowman is supported for this project by Columbia University and NIH/NINDS U18 NS082143. Dr. Chen-Plotkin is supported for this project by NIH/NINDS U01 NS082134. Dr. Dawson is supported for this project by NIH/NINDS U01NS082133 and P50NS38377. Dr. Dewey is supported for this project by NINDS U01 NS082148. Dr. German is supported for this project by NINDS U01 NS082148. This project is supported by NINDS U01 NS082151. Dr. Huang's work related to the project is also supported in part by UL1 RR033184 and UL1 TR00012, the Pennsylvania Department of Health Tobacco CURE Funds and intramural program of PSU-HMC. Dr. Petyuk is supported for this project by NIH/NINDS U18 NS082140. Dr. Scherzer is supported for this project by NIH/NINDS U01 NS082157. Dr. West is supported for this research by NIH/NINDS U18NS082132-01. Dr. Vaillancourt is supported by this project by NINDS R01 NS075012. Dr. Zhang is supported for this project by NINDS U01 NS082137. Dr. Gwinn is an employee of the National Institutes of Health, which funded this project.
Publisher Copyright:
© 2015 International Parkinson and Movement Disorder Society.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Background: Neuroprotection for Parkinson's disease (PD) remains elusive. Biomarkers hold the promise of removing roadblocks to therapy development. The National Institute of Neurological Disorders and Stroke has therefore established the Parkinson's Disease Biomarkers Program to promote discovery of PD biomarkers for use in phase II and III clinical trials. Methods: Using a novel consortium design, the Parkinson's Disease Biomarker Program is focused on the development of clinical and laboratory-based biomarkers for PD diagnosis, progression, and prognosis. Standardized operating procedures and pooled reference samples were created to allow cross-project comparisons and assessment of batch effects. A web-based Data Management Resource facilitates rapid sharing of data and biosamples across the research community for additional biomarker projects. Results: Eleven consortium projects are ongoing, seven of which recruit participants and obtain biosamples. As of October 2014, 1,082 participants have enrolled (620 PD, 101 with other causes of parkinsonism, 23 essential tremor, and 338 controls), 1,040 of whom have at least one biosample. Six thousand eight hundred ninety-eight total biosamples are available from baseline, 6-, 12-, and 18-month visits: 1,006 DNA, 1,661 RNA, 1,419 whole blood, 1,382 plasma, 1,200 serum, and 230 cerebrospinal fluid (CSF). Quality control analysis of plasma, serum, and CSF samples indicates that almost all samples are high quality (24 of 2,812 samples exceed acceptable hemoglobin levels). Conclusions: By making samples and data widely available, using stringent operating procedures based on existing standards, hypothesis testing for biomarker discovery, and providing a resource that complements existing programs, the Parkinson's Disease Biomarker Program will accelerate the pace of PD biomarker research.
AB - Background: Neuroprotection for Parkinson's disease (PD) remains elusive. Biomarkers hold the promise of removing roadblocks to therapy development. The National Institute of Neurological Disorders and Stroke has therefore established the Parkinson's Disease Biomarkers Program to promote discovery of PD biomarkers for use in phase II and III clinical trials. Methods: Using a novel consortium design, the Parkinson's Disease Biomarker Program is focused on the development of clinical and laboratory-based biomarkers for PD diagnosis, progression, and prognosis. Standardized operating procedures and pooled reference samples were created to allow cross-project comparisons and assessment of batch effects. A web-based Data Management Resource facilitates rapid sharing of data and biosamples across the research community for additional biomarker projects. Results: Eleven consortium projects are ongoing, seven of which recruit participants and obtain biosamples. As of October 2014, 1,082 participants have enrolled (620 PD, 101 with other causes of parkinsonism, 23 essential tremor, and 338 controls), 1,040 of whom have at least one biosample. Six thousand eight hundred ninety-eight total biosamples are available from baseline, 6-, 12-, and 18-month visits: 1,006 DNA, 1,661 RNA, 1,419 whole blood, 1,382 plasma, 1,200 serum, and 230 cerebrospinal fluid (CSF). Quality control analysis of plasma, serum, and CSF samples indicates that almost all samples are high quality (24 of 2,812 samples exceed acceptable hemoglobin levels). Conclusions: By making samples and data widely available, using stringent operating procedures based on existing standards, hypothesis testing for biomarker discovery, and providing a resource that complements existing programs, the Parkinson's Disease Biomarker Program will accelerate the pace of PD biomarker research.
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U2 - 10.1002/mds.26438
DO - 10.1002/mds.26438
M3 - Article
C2 - 26442452
AN - SCOPUS:84949871151
SN - 0885-3185
VL - 31
SP - 915
EP - 923
JO - Movement Disorders
JF - Movement Disorders
IS - 6
ER -