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Parkinson’s disease prognostic scores for progression of cognitive decline
Clinical and biochemical diversity of Parkinson’s disease (PD) presents a major challenge for accurate diagnosis and prediction of its progression. We propose, develop and optimize PD clinical scores as efficient integrated progression biomarkers for prediction of the likely rate of cognitive declin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877592/ https://www.ncbi.nlm.nih.gov/pubmed/31767922 http://dx.doi.org/10.1038/s41598-019-54029-w |
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author | Gramotnev, Galina Gramotnev, Dmitri K. Gramotnev, Alexandra |
author_facet | Gramotnev, Galina Gramotnev, Dmitri K. Gramotnev, Alexandra |
author_sort | Gramotnev, Galina |
collection | PubMed |
description | Clinical and biochemical diversity of Parkinson’s disease (PD) presents a major challenge for accurate diagnosis and prediction of its progression. We propose, develop and optimize PD clinical scores as efficient integrated progression biomarkers for prediction of the likely rate of cognitive decline in PD patients. We considered 269 drug-naïve participants from the Parkinson’s Progression Marker Initiative database, diagnosed with idiopathic PD and observed between 4 and 6 years. Nineteen baseline clinical and pathological measures were systematically considered. Relative variable importance and logistic regressions were used to optimize combinations of significant baseline measures as integrated biomarkers. Parkinson’s disease cognitive decline scores were designed as new clinical biomarkers using optimally categorized baseline measures. Specificities and sensitivities of the biomarkers reached ~93% for prediction of severe rate of cognitive decline (with more than 5 points decline in 4 years on the Montreal Cognitive Assessment scale), and up to ~73% for mild-to-moderate decline (between 1 and 5 points decline). The developed biomarkers and clinical scores could resolve the long-standing clinical problem about reliable prediction of PD progression into cognitive deterioration. The outcomes also provide insights into the contributions of individual clinical and pathological measures to PD progression, and will assist with better-targeted treatment regiments, stratification of clinical trial and their evaluation. |
format | Online Article Text |
id | pubmed-6877592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68775922019-12-05 Parkinson’s disease prognostic scores for progression of cognitive decline Gramotnev, Galina Gramotnev, Dmitri K. Gramotnev, Alexandra Sci Rep Article Clinical and biochemical diversity of Parkinson’s disease (PD) presents a major challenge for accurate diagnosis and prediction of its progression. We propose, develop and optimize PD clinical scores as efficient integrated progression biomarkers for prediction of the likely rate of cognitive decline in PD patients. We considered 269 drug-naïve participants from the Parkinson’s Progression Marker Initiative database, diagnosed with idiopathic PD and observed between 4 and 6 years. Nineteen baseline clinical and pathological measures were systematically considered. Relative variable importance and logistic regressions were used to optimize combinations of significant baseline measures as integrated biomarkers. Parkinson’s disease cognitive decline scores were designed as new clinical biomarkers using optimally categorized baseline measures. Specificities and sensitivities of the biomarkers reached ~93% for prediction of severe rate of cognitive decline (with more than 5 points decline in 4 years on the Montreal Cognitive Assessment scale), and up to ~73% for mild-to-moderate decline (between 1 and 5 points decline). The developed biomarkers and clinical scores could resolve the long-standing clinical problem about reliable prediction of PD progression into cognitive deterioration. The outcomes also provide insights into the contributions of individual clinical and pathological measures to PD progression, and will assist with better-targeted treatment regiments, stratification of clinical trial and their evaluation. Nature Publishing Group UK 2019-11-25 /pmc/articles/PMC6877592/ /pubmed/31767922 http://dx.doi.org/10.1038/s41598-019-54029-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gramotnev, Galina Gramotnev, Dmitri K. Gramotnev, Alexandra Parkinson’s disease prognostic scores for progression of cognitive decline |
title | Parkinson’s disease prognostic scores for progression of cognitive decline |
title_full | Parkinson’s disease prognostic scores for progression of cognitive decline |
title_fullStr | Parkinson’s disease prognostic scores for progression of cognitive decline |
title_full_unstemmed | Parkinson’s disease prognostic scores for progression of cognitive decline |
title_short | Parkinson’s disease prognostic scores for progression of cognitive decline |
title_sort | parkinson’s disease prognostic scores for progression of cognitive decline |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877592/ https://www.ncbi.nlm.nih.gov/pubmed/31767922 http://dx.doi.org/10.1038/s41598-019-54029-w |
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