西马鲁肽治疗和老年2型糖尿病患者肌肉减少加速:一项24个月的回顾性队列研究。

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-07-03 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S531778
Qingjuan Ren, Lei Zhi, Hongfang Liu
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引用次数: 0

摘要

目的:本研究旨在调查接受西马鲁肽治疗的老年2型糖尿病患者肌肉质量和力量的变化。方法:这是一项回顾性队列研究,比较接受西马鲁肽治疗的老年2型糖尿病患者与匹配的对照组。评估24个月内肌肉质量和功能的变化。采用阑尾骨骼肌质量指数(ASMI)测量肌肉质量,通过握力和步态速度测量评估肌肉功能。采用t检验分析两组间差异及治疗前后变化。此外,构建了多变量线性回归模型,以确定Semaglutide治疗期间加速肌肉损失的临床预测因素。结果:该研究纳入了220例接受Semaglutide治疗的患者和212例对照受试者。参与者中肌肉减少症的患病率为27.7%。与对照组相比,Semaglutide治疗显著降低了体重指数和肌肉质量。值得注意的是,在功能测量中出现了不同的模式。男性的握力起初有所提高,但随后下降,而女性的握力继续下降。男女的步态速度都显著降低。多变量分析确定了Semaglutide剂量、基线ASMI和步态速度是肌肉损失的独立预测因子。结论:使用Semaglutide与老年2型糖尿病患者的肌肉损失和功能下降有关,特别是在高剂量时。这种效果在肌肉减少症患者中尤为显著。因此,对每位老年患者单独评估风险和益处并实施适当的监测和干预是至关重要的。潜在的营养补充和有针对性的运动方案,以抵消semaglu肽相关的肌肉衰退值得系统的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Semaglutide Therapy and Accelerated Sarcopenia in Older Adults with Type 2 Diabetes: A 24-Month Retrospective Cohort Study.

Purpose: This study aimed to investigate changes in muscle mass and strength among older adults with type 2 diabetes who were treated with Semaglutide.

Methods: This was a retrospective cohort study comparing elderly patients with type 2 diabetes receiving Semaglutide to a matched control group. Changes in muscle mass and function over 24 months were assessed. Muscle mass was measured using the appendicular skeletal muscle mass index (ASMI), while muscle function was evaluated through grip strength and gait speed measurements. Differences between the two groups and changes before and after treatment were analyzed using the t-test. Additionally, multivariable linear regression models were constructed to identify clinical predictors of accelerated muscle loss during Semaglutide treatment.

Results: The study involved 220 patients treated with Semaglutide and 212 control subjects. The prevalence of sarcopenia among participants was 27.7%. Semaglutide treatment significantly reduced both body mass index and muscle mass compared to controls. Notably, divergent patterns emerged in functional measures. Grip strength initially improved but then declined in men, while it continued to decrease in women. Gait speed significantly reduced in both genders. Multivariable analysis identified Semaglutide dosage, baseline ASMI, and gait speed as independent predictors of muscle loss.

Conclusion: The use of Semaglutide is associated with muscle loss and functional decline in older adults with type 2 diabetes, particularly at higher doses. This effect is especially significant in patients with sarcopenia. Consequently, it is crucial to assess the risks and benefits for each elderly patient individually and to implement appropriate monitoring and interventions. The potential for nutritional supplementation and targeted exercise regimens to counteract semaglutide-associated muscle decline merits systematic investigation.

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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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