老年人肌肉减少症和功能障碍的治疗方法:4期临床试验综述

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-03-27 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S507033
Nasser M Alorfi, Fahad S Alshehri, Ahmed M Ashour
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引用次数: 0

摘要

背景:骨骼肌减少症显著导致老年人身体残疾和生活质量下降,从而导致残疾。用于控制肌肉减少症的治疗方法不仅可以改善肌肉健康,还可以改善有发展残疾风险的个体的整体功能能力。这篇综述的重点是在4期临床试验中评估的治疗干预措施,以解决老年人肌肉减少症及其相关残疾。目的:回顾和总结4期临床试验中用于治疗肌肉减少症的药物及其对减少老年人功能障碍的潜在影响。方法:对2024年11月6日进行的4期临床试验进行回顾,重点关注老年人肌肉减少症的干预措施。有关治疗药物、试验结果及其对肌肉质量、力量和残疾预防的影响的数据收集自clinicaltrials.gov数据库。结果:几种治疗药物,包括乳清蛋白粉、eldecalcitol、enanthate睾酮和Denosumab,已经在4期试验中测试了它们增强老年肌肉减少症患者肌肉质量和功能的能力。别嘌呤醇和吡格列酮也被研究了它们改善肌肉代谢的潜力,而甲卓尔(甲基强的松龙)和左甲状腺素在炎症和代谢紊乱加剧肌肉损失方面提供了支持作用。此外,联合疗法,如HMB和维生素D的营养补充,显示出改善肌肉功能的希望。这些干预措施在改善老年人肌肉力量、减少身体残疾和提高整体功能能力方面表现出不同程度的功效。结论:针对老年人肌肉减少症的治疗策略具有减少功能障碍和改善生活质量的潜力。4期临床试验为这些治疗的长期安全性和有效性提供了有价值的见解。继续研究和改进这些疗法对于充分解决肌肉减少症的致残影响和促进健康衰老至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutics for Sarcopenia and Functional Disabilities in Older Adults: A Review of Phase 4 Clinical Trials.

Background: Sarcopenia significantly contributes to physical disability and reduced quality of life in older adults, leading to disability. Therapeutics used to manage sarcopenia can improve not only muscle health but also the overall functional capacity of individuals at risk of developing disabilities. This review focuses on the therapeutic interventions evaluated in phase 4 clinical trials to address sarcopenia and its associated disabilities in older adults.

Objective: To review and summarize the therapeutic agents tested in phase 4 clinical trials for the management of sarcopenia and their potential impact on reducing functional disabilities in older adults.

Methods: A review of phase 4 clinical trials was conducted on 6th November 2024, focusing on interventions for sarcopenia in older adults. Data on therapeutic agents, trial outcomes, and their effects on muscle mass, strength, and disability prevention were collected from clinicaltrials.gov database.

Results: Several therapeutic agents, including whey protein powder, eldecalcitol, testosterone enanthate, and Denosumab, have been tested in Phase 4 trials for their ability to enhance muscle mass and function in older adults with sarcopenia. Allopurinol and Pioglitazone were also studied for their potential to improve muscle metabolism, while Medrol (Methylprednisolone) and Levothyroxine offered supportive effects in inflammatory and metabolic disorders that exacerbate muscle loss. Moreover, combination therapies, such as nutritional supplementation with HMB and vitamin D, showed promise in improving muscle function. These interventions demonstrated varying degrees of efficacy in improving muscle strength, reducing physical disability, and enhancing overall functional capacity in older adults.

Conclusion: Therapeutic strategies targeting sarcopenia in older adults have the potential to reduce functional disabilities and improve quality of life. Phase 4 clinical trials provide valuable insights into the long-term safety and effectiveness of these treatments. Continued research and refinement of these therapies are essential to fully address the disabling effects of sarcopenia and promote healthy aging.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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