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Suggested Citation:"Appendix B: Statement of Task." Institute of Medicine. 2013. Neurodegeneration: Exploring Commonalities Across Diseases: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/18341.
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Appendix B

Statement of Task

An ad hoc planning committee will plan and conduct a public workshop that will explore commonalities across neurodegenerative diseases such as Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, and frontotemporal dementia, and identify potential opportunities for collaboration across the respective research and development communities. Participants will be invited from academia; pharmaceutical and biotechnology industries; government agencies such as the National Institutes of Health, the National Science Foundation, and the Department of Veterans Affairs; and patient advocacy groups. Looking across the neurodegenerative diseases, workshop presentations and discussions will

 

•    Identify and discuss commonalities related to genetic and cellular mechanisms.

•    Identify areas of fundamental science needed to facilitate therapeutics development.

•    Explore areas of potential collaboration among the respective research communities and sponsors.

 

An individually authored workshop summary will be prepared based on the information gathered and the discussions held during the workshop in accordance with institutional policy and procedures.

Suggested Citation:"Appendix B: Statement of Task." Institute of Medicine. 2013. Neurodegeneration: Exploring Commonalities Across Diseases: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/18341.
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Suggested Citation:"Appendix B: Statement of Task." Institute of Medicine. 2013. Neurodegeneration: Exploring Commonalities Across Diseases: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/18341.
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Page 77
Suggested Citation:"Appendix B: Statement of Task." Institute of Medicine. 2013. Neurodegeneration: Exploring Commonalities Across Diseases: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/18341.
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Page 78
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Neurodegeneration: Exploring Commonalities Across Diseases is the summary of a workshop hosted by the Institute of Medicine's (IOM's) Forum on Neuroscience and Nervous System Disorders in Spring 2012 to explore commonalities across neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis (ALS), and frontotemporal dementia (FTD). Participants from academia; pharmaceutical and biotechnology industries; government agencies such as the National Institutes of Health and the U.S. Department of Veterans Affairs (VA); patient advocacy groups; and private foundations presented and identified potential opportunities for collaboration across the respective research and development communities. This report identifies and discusses commonalities related to genetic and cellular mechanisms, identifies areas of fundamental science needed to facilitate therapeutics development, and explores areas of potential collaboration among the respective research communities.

Neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, ALS, and FTD, are becoming increasingly prevalent in the United States due to an aging population. Implications are grave for quality of life and health care costs. Research on neurodegenerative diseases has expanded greatly over the past four decades. Nevertheless, fundamental questions remain about the biology of these diseases, and further insights into the mechanisms of these diseases would help to inform the development of effective means to prevent and to efficiently treat them. Recent findings have revealed certain commonalities in genetic and cellular mechanisms across neurodegenerative diseases. These findings suggest that it might be valuable - at least in some cases - to change the traditional way of studying these diseases by no longer seeing each as an independent entity, but rather as clinical variants of common cellular and molecular biological defects. This approach could help enhance basic scientific understanding of neurodegenerative disease, and could help with the development of biomarkers and new therapeutics.

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