Saied Schabnam, Prokopidis Konstantinos, Adenaya Adeoye, Isanejad Masoud, Sankaranarayanan Rajiv
School of Medicine, University of Liverpool, Liverpool, United Kingdom.
Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, United Kingdom.
Front Cardiovasc Med. 2024 Jan 25;11:1293537. doi: 10.3389/fcvm.2024.1293537. eCollection 2024.
There is controversy in relation to commonly used drugs in heart failure (HF) and their impact on muscle function. The aim of this study was to evaluate the odds of receiving specific medications often used in clinical practice by patients with HF and sarcopenia vs. without sarcopenia.
A systematic literature search of cohort studies via databases (PubMed, Web of Science, Scopus, and Cochrane Library) was conducted from inception until March 2023. To determine if sarcopenia is linked to a higher number of specific HF-related medications, a meta-analysis using a random-effects model was used to calculate the pooled effects.
Our main analyses showed no significant association of sarcopenia with administration of higher HF-related medication count vs. those without sarcopenia. Those with lower appendicular lean mass (ALM) had significantly lower odds of receiving angiotensin converting enzyme inhibitors (ACE-Is)/angiotensin receptor blockers (ARBs) (OR: 0.68, 95%CI 0.50-0.90, = 12%, < 0.01) vs. patients with higher ALM for which age could be an important confounder based on meta-regression. No statistically significant differences were found in relation to B-blockers OR: 0.84, 95%CI 0.63-1.12, = 7%, = 0.24) and loop diuretics (OR: 1.19, 95%CI 0.87-1.63, = 0%, = 0.27). Regarding handgrip strength, gait speed, and short physical performance battery, our narrative synthesis found mixed results.
This systematic review and meta-analysis did not find a relationship of specific medication count in sarcopenia vs. without sarcopenia in patients with HF, although increased odds of ACE-I/ARB was shown in those with higher ALM.
PROSPERO (CRD42023411137).
心力衰竭(HF)常用药物及其对肌肉功能的影响存在争议。本研究的目的是评估心力衰竭合并肌肉减少症患者与无肌肉减少症患者在临床实践中接受特定药物治疗的几率。
通过数据库(PubMed、Web of Science、Scopus和Cochrane图书馆)对队列研究进行系统文献检索,检索时间从开始至2023年3月。为了确定肌肉减少症是否与更多特定的心力衰竭相关药物有关,采用随机效应模型进行荟萃分析以计算合并效应。
我们的主要分析表明,与无肌肉减少症的患者相比,肌肉减少症与更高的心力衰竭相关药物使用数量之间无显著关联。根据荟萃回归分析,四肢瘦体重(ALM)较低的患者接受血管紧张素转换酶抑制剂(ACE-Is)/血管紧张素受体阻滞剂(ARBs)治疗的几率显著较低(OR:0.68,95%CI 0.50-0.90,P=12%,P<0.01),而ALM较高的患者中年龄可能是一个重要的混杂因素。在β受体阻滞剂(OR:0.84,95%CI 0.63-1.12,P=7%,P=0.24)和袢利尿剂(OR:1.19,95%CI 0.87-1.63,P=0%,P=0.27)方面未发现统计学显著差异。关于握力、步态速度和简短体能测试,我们的叙述性综合分析结果不一。
本系统评价和荟萃分析未发现心力衰竭患者中肌肉减少症患者与无肌肉减少症患者在特定药物使用数量上的关系,尽管ALM较高的患者使用ACE-I/ARB的几率增加。
PROSPERO(CRD42023411137)。