» Articles » PMID: 37371730

Pathogenesis, Intervention, and Current Status of Drug Development for Sarcopenia: A Review

Overview
Journal Biomedicines
Date 2023 Jun 28
PMID 37371730
Authors
Affiliations
Soon will be listed here.
Abstract

Sarcopenia refers to the loss of muscle strength and mass in older individuals and is a major determinant of fall risk and impaired ability to perform activities of daily living, often leading to disability, loss of independence, and death. Owing to its impact on morbidity, mortality, and healthcare expenditure, sarcopenia in the elderly has become a major focus of research and public policy debates worldwide. Despite its clinical importance, sarcopenia remains under-recognized and poorly managed in routine clinical practice, partly owing to the lack of available diagnostic testing and uniform diagnostic criteria. Since the World Health Organization and the United States assigned a disease code for sarcopenia in 2016, countries worldwide have assigned their own disease codes for sarcopenia. However, there are currently no approved pharmacological agents for the treatment of sarcopenia; therefore, interventions for sarcopenia primarily focus on physical therapy for muscle strengthening and gait training as well as adequate protein intake. In this review, we aimed to examine the latest information on the epidemiology, molecular mechanisms, interventions, and possible treatments with new drugs for sarcopenia.

Citing Articles

Impact of Glucose Profile, Fasting Insulin, and Renal Function on Sarcopenia in Elderly at Single Centered Nursing Home: A Cross-Sectional Structural Equation Model Analysis.

Santoso A, Destra E, Firmansyah Y, Lontoh S J Multidiscip Healthc. 2025; 18:1393-1404.

PMID: 40066249 PMC: 11892493. DOI: 10.2147/JMDH.S486370.


Effect and mechanism of miRNA-144-5p-regulated autophagy in older adults with Sarcopenia.

Hu M, Zhang Y, Ding H, Chao R, Cao Z Immun Ageing. 2025; 22(1):7.

PMID: 39953589 PMC: 11827453. DOI: 10.1186/s12979-025-00499-8.


Ginsenoside Rc prevents dexamethasone-induced muscle atrophy and enhances muscle strength and motor function.

Kim A, Park S, Kim N, Park M, Cha S J Ginseng Res. 2025; 49(1):42-52.

PMID: 39872283 PMC: 11764205. DOI: 10.1016/j.jgr.2024.09.002.


Fermented antler extract attenuates muscle atrophy by regulating the PI3K/Akt pathway and inflammatory response in immobilization-treated C57BL/6J mice.

Yoo J, Kim C, Lee H, Ko B, Lee D, Hwang J Food Sci Biotechnol. 2024; 33(15):3617-3628.

PMID: 39493393 PMC: 11525372. DOI: 10.1007/s10068-024-01606-z.


Protective Effects of and Mixture (KGC01CE) on Muscle Loss and Function in Aged Rats.

Koo G, Kwon H, Kim J, Lee S, Shim S, Jang K Curr Issues Mol Biol. 2024; 46(10):11190-11206.

PMID: 39451544 PMC: 11506417. DOI: 10.3390/cimb46100664.


References
1.
Mendell J, Sahenk Z, Malik V, Gomez A, Flanigan K, Lowes L . A phase 1/2a follistatin gene therapy trial for becker muscular dystrophy. Mol Ther. 2014; 23(1):192-201. PMC: 4426808. DOI: 10.1038/mt.2014.200. View

2.
Coats A, Srinivasan V, Surendran J, Chiramana H, Vangipuram S, Bhatt N . The ACT-ONE trial, a multicentre, randomised, double-blind, placebo-controlled, dose-finding study of the anabolic/catabolic transforming agent, MT-102 in subjects with cachexia related to stage III and IV non-small cell lung cancer and colorectal.... J Cachexia Sarcopenia Muscle. 2011; 2(4):201-207. PMC: 3222831. DOI: 10.1007/s13539-011-0046-2. View

3.
Amato A, Hanna M, Machado P, Badrising U, Chinoy H, Benveniste O . Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis: Long-term Extension of RESILIENT. Neurology. 2021; 96(12):e1595-e1607. PMC: 8032371. DOI: 10.1212/WNL.0000000000011626. View

4.
Visnjic D, Lalic H, Dembitz V, Tomic B, Smoljo T . AICAr, a Widely Used AMPK Activator with Important AMPK-Independent Effects: A Systematic Review. Cells. 2021; 10(5). PMC: 8147799. DOI: 10.3390/cells10051095. View

5.
Sherlock S, Palmer J, Wagner K, Abdel-Hamid H, Bertini E, Tian C . Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumab. J Neurol. 2022; 269(8):4421-4435. PMC: 9294028. DOI: 10.1007/s00415-022-11084-0. View