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Sarcopenia, Cachexia and Aging: Diagnosis, Mechanisms and Therapeutic Options - A Mini-Review
Open accessAbstract
By the year 2050, individuals over the age of 65 years will comprise 20% of the US population. Loss of muscle mass and strength is common in this age group and it is associated with increased dependence, frailty and mortality. Sarcopenia, defined as the loss of muscle mass and function associated with aging, and cachexia, defined as weight loss due to an underlying illness, are muscle wasting disorders of particular relevance in the aging population, but they go largely unrecognized. In this review we highlight the common pathophysiological mechanisms underlying muscle loss in sarcopenia and cachexia, the factors unique to each condition and means of diagnosing and differentiating them clinically. Therapeutic options including exercise, nutritional therapy, androgens and growth hormone as well as their practical limitations are discussed. We also shed light on newer agents being developed as potential therapeutic options for wasting diseases.
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“Protein synthesis is reduced under Os conditions [107, 108]”
From The critical role of oxidative stress in sarcopenic obesity (2021) · cites this paper as [107]
In the citing paper
“In sarcopenia, the loss of muscle mass and strength leads to reductions in physical activity and mobility, inducing Os, exacerbating sarcopenia, and generating an endless circle [107, 108, 110].”
From The critical role of oxidative stress in sarcopenic obesity (2021) · cites this paper as [107]
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“Moreover, in physiological conditions, PI-3K/Akt inhibits the forkhead box transcription factor O (Fox-O) (a potent inductor of the ubiquitin-proteasome system (UPS)), while mTOR decreases caspase activity. PI-3K/Akt/mTOR activity declines during aging, promoting the catabolic pathway.”
From The critical role of oxidative stress in sarcopenic obesity (2021) · cites this paper as [107]
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“Also, physical inactivity (a characteristic of obesity and sarcopenia in aging) indirectly inhibits the mTOR pathway through Fox-O stimulation [107, 108].”
From The critical role of oxidative stress in sarcopenic obesity (2021) · cites this paper as [107]
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Metadata
- Authors
- Ali, S., & Garcia, J. M.
- Affiliations
- Michael E. DeBakey VA Medical Center (US)
- Venue
- Gerontology
- Publisher
- S. Karger AG
- Published
- 2014
- Volume
- 60
- Issue
- 4
- Pages
- 294-305
- ISSN
- 0304-324X (ISSN-L)
- 1423-0003
- PMC
- PMC4112511
- OpenAlex
- W2124477946
- Cited by
- 462
- References
- 56
- Citations by year
- 2026: 22 · 2025: 40 · 2024: 39 · 2023: 51 · 2022: 48 · 2021: 60 · 2020: 51 · 2019: 38 · 2018: 46 · 2017: 30 · 2016: 17 · 2015: 18 · 2014: 2
- FWCI
- 2.61
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Gerontology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- U.S. Department of Veterans Affairs (I01 CX000174, I01 BX002807, I01-BX000507)
- National Institute on Aging (R03AG040583, AG040583, T32AG000183)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Keywords
- sarcopenia, cachexia, aging, muscle atrophy, muscle mass loss, frailty, pathophysiological mechanisms, diagnosis, exercise therapy, nutritional therapy, androgens, growth hormone
- MeSH terms
- Aged, Aging, Androgens, Cachexia, Dietary Proteins, Exercise Therapy, Humans, Muscle Proteins, Receptors, Androgen, Muscle, Skeletal, Appetite Stimulants, Human Growth Hormone, Ghrelin, Sarcopenia
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