• search hit 6 of 7
Back to Result List

Sarcopenia

  • Sarcopenia represents a muscle-wasting syndrome characterized by progressive and generalized degenerative loss of skeletal muscle mass, quality, and strength occurring during normal aging. Sarcopenia patients are mainly suffering from the loss in muscle strength and are faced with mobility disorders reducing their quality of life and are, therefore, at higher risk for morbidity (falls, bone fracture, metabolic diseases) and mortality. <br /> Several molecular mechanisms have been described as causes for sarcopenia that refer to very different levels of muscle physiology. These mechanisms cover e. g. function of hormones (e. g. IGF-1 and Insulin), muscle fiber composition and neuromuscular drive, myo-satellite cell potential to differentiate and proliferate, inflammatory pathways as well as intracellular mechanisms in the processes of proteostasis and mitochondrial function. <br /> In this review, we describe sarcopenia as a muscle-wasting syndrome distinct from other atrophic diseases and summarize the current view on molecular causesSarcopenia represents a muscle-wasting syndrome characterized by progressive and generalized degenerative loss of skeletal muscle mass, quality, and strength occurring during normal aging. Sarcopenia patients are mainly suffering from the loss in muscle strength and are faced with mobility disorders reducing their quality of life and are, therefore, at higher risk for morbidity (falls, bone fracture, metabolic diseases) and mortality. <br /> Several molecular mechanisms have been described as causes for sarcopenia that refer to very different levels of muscle physiology. These mechanisms cover e. g. function of hormones (e. g. IGF-1 and Insulin), muscle fiber composition and neuromuscular drive, myo-satellite cell potential to differentiate and proliferate, inflammatory pathways as well as intracellular mechanisms in the processes of proteostasis and mitochondrial function. <br /> In this review, we describe sarcopenia as a muscle-wasting syndrome distinct from other atrophic diseases and summarize the current view on molecular causes of sarcopenia development as well as open questions provoking further research efforts for establishing efficient lifestyle and therapeutic interventions.show moreshow less

Export metadata

Additional Services

Search Google Scholar Statistics
Metadaten
Author details:Petra WiedmerORCiDGND, Tobias JungORCiDGND, Jose Pedro CastroORCiD, Laura C. D. Pomatto, Patrick Y. Sun, Kelvin J. A. Davies, Tilman GruneORCiDGND
DOI:https://doi.org/10.1016/j.arr.2020.101200
ISSN:1568-1637
ISSN:1872-9649
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/33130247
Title of parent work (English):Ageing research reviews : ARR
Subtitle (English):molecular mechanisms and open questions
Publisher:Elsevier
Place of publishing:Clare
Publication type:Article
Language:English
Date of first publication:2020/10/29
Publication year:2020
Release date:2023/03/24
Tag:autophagy; mitochondria,; molecular pathways; muscle fibre composition; proteasome; proteostasis
Volume:65
Article number:101200
Number of pages:17
Funding institution:National Institute of Environmental Health Sciences of the US National Institutes of HealthUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Environmental Health Sciences (NIEHS) [ES003598]; National Institute on Aging of the US National Institutes of Health [AG052374]; Deutsche Forschungsgemeinschaft (DFG)German Research Foundation (DFG) [GR1240/20-1, GR 1240/22-1]
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Ernährungswissenschaft
DDC classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer review:Referiert
Publishing method:Open Access / Hybrid Open-Access
License (German):License LogoCC-BY-NC-ND - Namensnennung, nicht kommerziell, keine Bearbeitungen 4.0 International
Accept ✔
This website uses technically necessary session cookies. By continuing to use the website, you agree to this. You can find our privacy policy here.