@article{10.37349/ent.2025.1004133,
abstract = {Age-related neurological disorders such as ALS (Lou Gehrig's disease), Parkinson's disease, and Alzheimer's disease have few truly effective treatment options. At best, these may slow the inexorable disease progression without providing a cure. Part of the problem with therapeutic approaches may arise due to the stage at which these diseases are detected, particularly the sporadic forms. In most cases, early signs and symptoms may be insidious, thus hiding the significant damage done to the areas of the nervous system impacted prior to any firm clinical diagnosis. This situation appears to necessitate the development of earlier detection methods for "biomarkers" that might allow for much earlier phase disease state treatments that might serve to significantly slow or even halt disease progression. Currently, most biomarkers in use serve primarily as aids to disease diagnosis, at which point there are no successful treatment options. In contrast, a search for more effective early treatment options would need to identify characteristic and specific molecular signatures of disease onset and progression using methods that are simple, such as blood-based analytical assays, relatively cheap, and crucially minimally invasive.},
author = {Shaw, Christopher A. and Beck, Ceilidh and Marakoff, Leal},
doi = {10.37349/ent.2025.1004133},
journal = {Exploration of Neuroprotective Therapy},
elocation-id = {1004133},
title = {Can we find early phase biomarkers for ALS: What are the prospects and challenges?},
url = {https://www.explorationpub.com/Journals/ent/Article/1004133},
volume = {5},
year = {2025}
}