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Myopenia and precision (P4) medicine

Precision (P4) medicine represents a new medical paradigm that focuses on Personalized, Predictive, Preventive and Participatory approaches. The P4 paradigm is particularly appropriate for moving the care of persons with myopenia forward. Muscular dystrophies are clearly a set of genetically differe...

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Detalles Bibliográficos
Autores principales: Morley, John E., Anker, Stefan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700444/
https://www.ncbi.nlm.nih.gov/pubmed/28944582
http://dx.doi.org/10.1002/jcsm.12231
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author Morley, John E.
Anker, Stefan D.
author_facet Morley, John E.
Anker, Stefan D.
author_sort Morley, John E.
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description Precision (P4) medicine represents a new medical paradigm that focuses on Personalized, Predictive, Preventive and Participatory approaches. The P4 paradigm is particularly appropriate for moving the care of persons with myopenia forward. Muscular dystrophies are clearly a set of genetically different diseases where genomics are the basis of diagnosis, and genetic modulation via DNA, oligonucleotides and clustered regularly interspaced short palendronic repeats hold great potential for a cure. The utility of personalized genomics for sarcopenia coupled with utilizing a predictive approach for the diagnosis with early preventive strategies is a key to improving sarcopenic outcomes. The importance of understanding different levels of patient enthusiasm and different responses to exercise should guide the participatory phase of sarcopenic treatment. In the case of cachexia, understanding the effects of the different therapies now available through the P4 approach on muscle wasting is a key to management strategies.
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spelling pubmed-57004442017-12-01 Myopenia and precision (P4) medicine Morley, John E. Anker, Stefan D. J Cachexia Sarcopenia Muscle Editorials Precision (P4) medicine represents a new medical paradigm that focuses on Personalized, Predictive, Preventive and Participatory approaches. The P4 paradigm is particularly appropriate for moving the care of persons with myopenia forward. Muscular dystrophies are clearly a set of genetically different diseases where genomics are the basis of diagnosis, and genetic modulation via DNA, oligonucleotides and clustered regularly interspaced short palendronic repeats hold great potential for a cure. The utility of personalized genomics for sarcopenia coupled with utilizing a predictive approach for the diagnosis with early preventive strategies is a key to improving sarcopenic outcomes. The importance of understanding different levels of patient enthusiasm and different responses to exercise should guide the participatory phase of sarcopenic treatment. In the case of cachexia, understanding the effects of the different therapies now available through the P4 approach on muscle wasting is a key to management strategies. John Wiley and Sons Inc. 2017-09-24 2017-12 /pmc/articles/PMC5700444/ /pubmed/28944582 http://dx.doi.org/10.1002/jcsm.12231 Text en © 2017 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of the Society on Sarcopenia, Cachexia and Wasting Disorders This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Editorials
Morley, John E.
Anker, Stefan D.
Myopenia and precision (P4) medicine
title Myopenia and precision (P4) medicine
title_full Myopenia and precision (P4) medicine
title_fullStr Myopenia and precision (P4) medicine
title_full_unstemmed Myopenia and precision (P4) medicine
title_short Myopenia and precision (P4) medicine
title_sort myopenia and precision (p4) medicine
topic Editorials
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700444/
https://www.ncbi.nlm.nih.gov/pubmed/28944582
http://dx.doi.org/10.1002/jcsm.12231
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