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The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort
OBJECTIVE: The Parkinson's Progression Markers Initiative (PPMI) is an observational, international study designed to establish biomarker‐defined cohorts and identify clinical, imaging, genetic, and biospecimen Parkinson's disease (PD) progression markers to accelerate disease‐modifying th...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292383/ https://www.ncbi.nlm.nih.gov/pubmed/30564614 http://dx.doi.org/10.1002/acn3.644 |
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author | Marek, Kenneth Chowdhury, Sohini Siderowf, Andrew Lasch, Shirley Coffey, Christopher S. Caspell‐Garcia, Chelsea Simuni, Tanya Jennings, Danna Tanner, Caroline M. Trojanowski, John Q. Shaw, Leslie M. Seibyl, John Schuff, Norbert Singleton, Andrew Kieburtz, Karl Toga, Arthur W. Mollenhauer, Brit Galasko, Doug Chahine, Lana M. Weintraub, Daniel Foroud, Tatiana Tosun‐Turgut, Duygu Poston, Kathleen Arnedo, Vanessa Frasier, Mark Sherer, Todd |
author_facet | Marek, Kenneth Chowdhury, Sohini Siderowf, Andrew Lasch, Shirley Coffey, Christopher S. Caspell‐Garcia, Chelsea Simuni, Tanya Jennings, Danna Tanner, Caroline M. Trojanowski, John Q. Shaw, Leslie M. Seibyl, John Schuff, Norbert Singleton, Andrew Kieburtz, Karl Toga, Arthur W. Mollenhauer, Brit Galasko, Doug Chahine, Lana M. Weintraub, Daniel Foroud, Tatiana Tosun‐Turgut, Duygu Poston, Kathleen Arnedo, Vanessa Frasier, Mark Sherer, Todd |
author_sort | Marek, Kenneth |
collection | PubMed |
description | OBJECTIVE: The Parkinson's Progression Markers Initiative (PPMI) is an observational, international study designed to establish biomarker‐defined cohorts and identify clinical, imaging, genetic, and biospecimen Parkinson's disease (PD) progression markers to accelerate disease‐modifying therapeutic trials. METHODS: A total of 423 untreated PD, 196 Healthy Control (HC) and 64 SWEDD (scans without evidence of dopaminergic deficit) subjects were enrolled at 24 sites. To enroll PD subjects as early as possible following diagnosis, subjects were eligible with only asymmetric bradykinesia or tremor plus a dopamine transporter (DAT) binding deficit on SPECT imaging. Acquisition of data was standardized as detailed at www.ppmi-info.org. RESULTS: Approximately 9% of enrolled subjects had a single PD sign at baseline. DAT imaging excluded 16% of potential PD subjects with SWEDD. The total MDS‐UPDRS for PD was 32.4 compared to 4.6 for HC and 28.2 for SWEDD. On average, PD subjects demonstrated 45% and 68% reduction in mean striatal and contralateral putamen Specific Binding Ratios (SBR), respectively. Cerebrospinal fluid (CSF) was acquired from >97% of all subjects. CSF (PD/HC/SWEDD pg/mL) α‐synuclein (1845/2204/2141) was reduced in PD vs HC or SWEDD (P < 0.03). Similarly, t‐tau (45/53) and p‐tau (16/18) were reduced in PD versus HC (P < 0.01), INTERPRETATION: PPMI has detailed the biomarker signature for an early PD cohort defined by clinical features and imaging biomarkers. This strategy provides the framework to establish biomarker cohorts and to define longitudinal progression biomarkers to support future PD treatment trials. |
format | Online Article Text |
id | pubmed-6292383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62923832018-12-18 The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort Marek, Kenneth Chowdhury, Sohini Siderowf, Andrew Lasch, Shirley Coffey, Christopher S. Caspell‐Garcia, Chelsea Simuni, Tanya Jennings, Danna Tanner, Caroline M. Trojanowski, John Q. Shaw, Leslie M. Seibyl, John Schuff, Norbert Singleton, Andrew Kieburtz, Karl Toga, Arthur W. Mollenhauer, Brit Galasko, Doug Chahine, Lana M. Weintraub, Daniel Foroud, Tatiana Tosun‐Turgut, Duygu Poston, Kathleen Arnedo, Vanessa Frasier, Mark Sherer, Todd Ann Clin Transl Neurol Research Articles OBJECTIVE: The Parkinson's Progression Markers Initiative (PPMI) is an observational, international study designed to establish biomarker‐defined cohorts and identify clinical, imaging, genetic, and biospecimen Parkinson's disease (PD) progression markers to accelerate disease‐modifying therapeutic trials. METHODS: A total of 423 untreated PD, 196 Healthy Control (HC) and 64 SWEDD (scans without evidence of dopaminergic deficit) subjects were enrolled at 24 sites. To enroll PD subjects as early as possible following diagnosis, subjects were eligible with only asymmetric bradykinesia or tremor plus a dopamine transporter (DAT) binding deficit on SPECT imaging. Acquisition of data was standardized as detailed at www.ppmi-info.org. RESULTS: Approximately 9% of enrolled subjects had a single PD sign at baseline. DAT imaging excluded 16% of potential PD subjects with SWEDD. The total MDS‐UPDRS for PD was 32.4 compared to 4.6 for HC and 28.2 for SWEDD. On average, PD subjects demonstrated 45% and 68% reduction in mean striatal and contralateral putamen Specific Binding Ratios (SBR), respectively. Cerebrospinal fluid (CSF) was acquired from >97% of all subjects. CSF (PD/HC/SWEDD pg/mL) α‐synuclein (1845/2204/2141) was reduced in PD vs HC or SWEDD (P < 0.03). Similarly, t‐tau (45/53) and p‐tau (16/18) were reduced in PD versus HC (P < 0.01), INTERPRETATION: PPMI has detailed the biomarker signature for an early PD cohort defined by clinical features and imaging biomarkers. This strategy provides the framework to establish biomarker cohorts and to define longitudinal progression biomarkers to support future PD treatment trials. John Wiley and Sons Inc. 2018-10-31 /pmc/articles/PMC6292383/ /pubmed/30564614 http://dx.doi.org/10.1002/acn3.644 Text en © 2018 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Marek, Kenneth Chowdhury, Sohini Siderowf, Andrew Lasch, Shirley Coffey, Christopher S. Caspell‐Garcia, Chelsea Simuni, Tanya Jennings, Danna Tanner, Caroline M. Trojanowski, John Q. Shaw, Leslie M. Seibyl, John Schuff, Norbert Singleton, Andrew Kieburtz, Karl Toga, Arthur W. Mollenhauer, Brit Galasko, Doug Chahine, Lana M. Weintraub, Daniel Foroud, Tatiana Tosun‐Turgut, Duygu Poston, Kathleen Arnedo, Vanessa Frasier, Mark Sherer, Todd The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort |
title | The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort |
title_full | The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort |
title_fullStr | The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort |
title_full_unstemmed | The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort |
title_short | The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort |
title_sort | parkinson's progression markers initiative (ppmi) – establishing a pd biomarker cohort |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292383/ https://www.ncbi.nlm.nih.gov/pubmed/30564614 http://dx.doi.org/10.1002/acn3.644 |
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