Grosicki Gregory J, Kim Jeongeun, Fielding Finn, Jasinski Summer R, Chapman Christopher, Hippel William von, Holmes Kristen E
Scienceye, Bluffton, South Carolina, United States.
Performance Science, WHOOP Inc., Boston, Massachusetts, United States.
Am J Physiol Heart Circ Physiol. 2025 Feb 1;328(2):H235-H241. doi: 10.1152/ajpheart.00809.2024. Epub 2024 Dec 20.
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/m) 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 (s > 0.26). After the 12-wk study period, GLP-1 users showed significant (s < 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 ( < 0.01) by changes in HRV (-6.2 ± 1.4 ms) compared with control. Trends (s < 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. 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.
胰高血糖素样肽-1受体激动剂(GLP-1 RAs)最初是为治疗2型糖尿病而研发的,但最近已被批准用于慢性体重管理以及降低超重和肥胖个体的心血管风险。尽管获得了批准,但有报告称GLP-1 RAs在心脏保护益处方面存在显著异质性,且静息心率(RHR)出现了不太理想的升高。为了更好地理解对GLP-1 RAs的心血管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断分析。我们追踪了66名个体(42±9岁,体重指数:30.0±7 kg/m²)从开始使用GLP-1 RA药物前一周到用药后12周的RHR、心率变异性(HRV)、身体活动和睡眠情况。在更大样本的可穿戴设备用户中进行倾向得分匹配,确定了一个具有相似人体测量和心血管特征的对照组(s>0.26)。在为期12周的研究期结束后,与对照组相比,使用GLP-1的用户体重显著下降(-10.0%,95%CI:-11.2%至-8.5%),RHR变化(3.2±0.8次/分钟)由HRV变化(-6.2±1.4毫秒)介导(<0.01)。趋势(s<0.10)表明,每周身体活动的增加与GLP-1 RA药物治疗有关(31.5±13.2分钟),且较高的身体活动水平伴随着RHR升高的减弱。我们的实际研究结果与临床试验数据一致,表明GLP-1 RAs能快速显著减重,同时伴随着自主神经功能变化(即HRV)介导的RHR升高。身体活动可能有助于抵消RHR的升高,但需要进一步研究来证实这些影响。这些发现是首批提供GLP-1 RA起始治疗后心血管和行为反应每日见解的研究之一。在GLP-1 RA治疗的最初12周内,观察到体重显著下降以及心率变异性降低介导的静息心率显著升高。此外,趋势表明GLP-1治疗会使身体活动增加,且身体活动可能有助于缓和GLP-1 RA相关的静息心率升高。