Heart and health behavior responses to GLP-1 receptor agonists: a 12-wk study using wearable technology and causal inference.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS American journal of physiology. Heart and circulatory physiology Pub Date : 2025-02-01 Epub Date: 2024-12-20 DOI:10.1152/ajpheart.00809.2024
Gregory J Grosicki, Jeongeun Kim, Finn Fielding, Summer R Jasinski, Christopher Chapman, William von Hippel, Kristen E Holmes
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Abstract

Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) were originally developed for the treatment of type 2 diabetes but have recently been approved for chronic weight management and reducing cardiovascular risk in individuals with overweight and obesity. Despite this approval, significant heterogeneity in the cardioprotective benefits and less desirable increases in resting heart rate (RHR) with GLP-1 RAs have been reported. To better understand cardiovascular responses to GLP-1 RAs and the potential role of health behaviors in influencing these responses, we leveraged wearable technology and causal inference analysis. We tracked RHR, heart rate variability (HRV), physical activity, and sleep in 66 individuals (42 ± 9 yr, body mass index: 30.0 ± 7 kg/m2) from the week before to 12 wk following the initiation of GLP-1 RA medication. Propensity score matching on a larger sample of wearable users identified a control group with similar anthropometric and cardiovascular characteristics (Ps > 0.26). After the 12-wk study period, GLP-1 users showed significant (Ps < 0.05) weight loss (-10.0%, 95% CI: -11.2% to -8.5%) and changes in RHR (3.2 ± 0.8 beats/min) that were mediated (P < 0.01) by changes in HRV (-6.2 ± 1.4 ms) compared with control. Trends (Ps < 0.10) suggested that increases in weekly physical activity were associated with GLP-1 RA medication (31.5 ± 13.2 min) and that higher physical activity levels accompanied an attenuation of RHR increases. Our real-world findings align with clinical trial data in showing rapid and significant weight loss with GLP-1 RAs, coinciding with increases in RHR that are mediated by changes in autonomic function (i.e., HRV). Physical activity may help to offset RHR increases, but further research is needed to confirm these effects.NEW & NOTEWORTHY These findings are among the first to provide daily insights into cardiovascular and behavioral responses following GLP-1 RA initiation. Substantial weight loss and significant increases in resting heart rate mediated by reductions in heart rate variability during the initial 12 wk of GLP-1 RA therapy were observed. In addition, trends suggest an increase in physical activity with GLP-1 therapy, and that physical activity may help to temper GLP-1 RA-associated increases in resting heart rate.

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心脏和健康行为对GLP-1受体激动剂的反应:使用可穿戴技术和因果推理的12周研究
胰高血糖素样肽-1 受体激动剂(GLP-1 RAs)最初是为治疗 2 型糖尿病而开发的,但最近已被批准用于超重和肥胖症患者的慢性体重管理和降低心血管风险。尽管获得了批准,但据报道,GLP-1 RAs 在保护心血管方面的益处存在明显的异质性,而且静息心率(RHR)的增加也不尽如人意。为了更好地了解心血管对 GLP-1 RAs 的反应,以及健康行为在影响这些反应中的潜在作用,我们利用了可穿戴技术和因果推理分析。我们跟踪了 66 名患者(42±9 岁,体重指数:30.0±7kg/m2)从开始服用 GLP-1 RA 药物前一周到服药后 12 周的 RHR、心率变异性 (HRV)、体力活动和睡眠情况。通过对更大样本的可穿戴设备用户进行倾向得分匹配,确定了具有相似人体测量和心血管特征的对照组(Ps>0.26)。在为期 12 周的研究后,GLP-1 使用者显示出显著的(PsPPs
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
期刊最新文献
The mechanisms of Chr.9p21.3 risk locus in coronary artery disease: where are we today? Ceramide toxicity in cardiomyocytes: from Farber disease to cardiovascular diseases. Heart and health behavior responses to GLP-1 receptor agonists: a 12-wk study using wearable technology and causal inference. Lab-grown, 3D extracellular matrix particles improve cardiac function and morphology in myocardial ischemia. A comment on the physiological basis for longitudinal motion of the arterial wall.
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