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Unbiased Approaches to Biomarker Discovery in Neurodegenerative Diseases
Neurodegenerative diseases such as Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, and frontotemporal dementia have several important features in common. They are progressive, they affect a relatively inaccessible organ, and we have no disease-modifying therapies for them. F...
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Published in: | Neuron (Cambridge, Mass.) Mass.), 2014-11, Vol.84 (3), p.594-607 |
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Main Author: | |
Format: | Article |
Language: | English |
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Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Neurodegenerative diseases such as Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, and frontotemporal dementia have several important features in common. They are progressive, they affect a relatively inaccessible organ, and we have no disease-modifying therapies for them. For these brain-based diseases, current diagnosis and evaluation of disease severity rely almost entirely on clinical examination, which may be only a rough approximation of disease state. Thus, the development of biomarkers—objective, relatively easily measured, and precise indicators of pathogenic processes—could improve patient care and accelerate therapeutic discovery. Yet existing, rigorously tested neurodegenerative disease biomarkers are few, and even fewer biomarkers have translated into clinical use. To find new biomarkers for these diseases, an unbiased, high-throughput screening approach may be needed. In this review, I will describe the potential utility of such an approach to biomarker discovery, using Parkinson’s disease as a case example.
The development of novel biomarkers for neurodegenerative conditions could improve patient care and accelerate therapeutic discovery. In this Perspective, using Parkinson’s disease as a case study, Chen-Plotkin discusses why an unbiased, high-throughput screening approach for finding new biomarkers may be needed. |
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ISSN: | 0896-6273 1097-4199 |
DOI: | 10.1016/j.neuron.2014.10.031 |