Heart and Health Behavior Responses to GLP-1 Receptor Agonists: A 12-Week Study Using Wearable Technology and Causal Inference.

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±9yrs, BMI:30.0±7kg/m) from the week before to 12 weeks 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 (>0.26). After the 12-week study period, GLP-1 users showed significant (<0.05) weight loss (-10.0%, 95%CI: -11.2 to -8.5%) and changes in RHR (3.2±0.8bpm) that were mediated (<0.01) by changes in HRV (-6.2±1.4ms) compared with control. Trends (<0.10) suggested that increases in weekly physical activity were associated with GLP-1 RA medication (31.5±13.2min), 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.