Biomarkers for Parkinson’s disease (PD) diagnosis, prognostication and clinical trial
cohort selection are an urgent need. While many promising markers have been
discovered through the National Institute of Neurological Disorders and Stroke
Parkinson’s Disease Biomarker Program (PDBP) and other mechanisms, no single PD
marker or set of markers are ready for clinical use. Here we discuss the current state of
biomarker discovery for platforms relevant to PDBP. We discuss the role of the PDBP
in PD biomarker identification and present guidelines to facilitate their development.
These guidelines include: harmonizing procedures for biofluid acquisition and
clinical assessments, replication of the most promising biomarkers, support and
encouragement of publications that report negative findings, longitudinal follow-up
of current cohorts including the PDBP, testing of wearable technologies to capture
readouts between study visits and development of recently diagnosed (de novo)
cohorts to foster identification of the earliest markers of disease onset.
Revised: February 11, 2020 |
Published: May 1, 2017
Citation
Gwinn K., K.K. David, C.R. Swanson-Fischer, R.L. Albin, C. Hillaire-Clarke, B. Sieber, and C. Lungu, et al. 2017.Parkinson’s disease biomarkers: perspective from the NINDS Parkinson’s Disease Biomarkers Program.Biomarkers in Medicine 11, no. 6:451-473.PNNL-SA-129861.doi:10.2217/bmm-2016-0370