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Finding good biomarkers for sarcopenia

The term sarcopenia describes the age-related loss of skeletal muscle mass and function. While this process, in principal, occurs in every adult person and already starts around the age of 40, it is associated with disability, morbidity, and increased mortality in some individuals. In the absence of...

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Detalles Bibliográficos
Autores principales: Scharf, Gesine, Heineke, Joerg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424189/
https://www.ncbi.nlm.nih.gov/pubmed/22911244
http://dx.doi.org/10.1007/s13539-012-0081-7
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author Scharf, Gesine
Heineke, Joerg
author_facet Scharf, Gesine
Heineke, Joerg
author_sort Scharf, Gesine
collection PubMed
description The term sarcopenia describes the age-related loss of skeletal muscle mass and function. While this process, in principal, occurs in every adult person and already starts around the age of 40, it is associated with disability, morbidity, and increased mortality in some individuals. In the absence of clear clinical manifestation, we today lack the ability to differentiate between physiological and pathological sarcopenia. In this regard, we need good biomarkers that can be quantified in a reliable, cost-effective manner and that guide diagnosis and therapy of pathological sarcopenia in routine clinical practice and clinical trials. We suggest that a combination of serum markers, diagnostic imaging, and functional tests of muscle function would constitute an ideal biomarker panel. Importantly, sarcopenia biomarkers will have to be tested and validated in clinical trials.
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spelling pubmed-34241892012-09-01 Finding good biomarkers for sarcopenia Scharf, Gesine Heineke, Joerg J Cachexia Sarcopenia Muscle Editorial The term sarcopenia describes the age-related loss of skeletal muscle mass and function. While this process, in principal, occurs in every adult person and already starts around the age of 40, it is associated with disability, morbidity, and increased mortality in some individuals. In the absence of clear clinical manifestation, we today lack the ability to differentiate between physiological and pathological sarcopenia. In this regard, we need good biomarkers that can be quantified in a reliable, cost-effective manner and that guide diagnosis and therapy of pathological sarcopenia in routine clinical practice and clinical trials. We suggest that a combination of serum markers, diagnostic imaging, and functional tests of muscle function would constitute an ideal biomarker panel. Importantly, sarcopenia biomarkers will have to be tested and validated in clinical trials. Springer-Verlag 2012-08-02 2012-09 /pmc/articles/PMC3424189/ /pubmed/22911244 http://dx.doi.org/10.1007/s13539-012-0081-7 Text en © Springer-Verlag 2012
spellingShingle Editorial
Scharf, Gesine
Heineke, Joerg
Finding good biomarkers for sarcopenia
title Finding good biomarkers for sarcopenia
title_full Finding good biomarkers for sarcopenia
title_fullStr Finding good biomarkers for sarcopenia
title_full_unstemmed Finding good biomarkers for sarcopenia
title_short Finding good biomarkers for sarcopenia
title_sort finding good biomarkers for sarcopenia
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424189/
https://www.ncbi.nlm.nih.gov/pubmed/22911244
http://dx.doi.org/10.1007/s13539-012-0081-7
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