Key result
Simulated baroreflex activation therapy reduces MAP by ~15 mmHg in virtual obesity-induced hypertension.
Why the study?
The mechanisms by which baroreflex activation therapy lowers blood pressure are unclear, and it is uncertain which patients are most likely to receive clinical benefit.
Does baroreflex activation therapy reduce blood pressure in obesity-induced hypertension?
Does baroreflex activation therapy reduce blood pressure in obesity-induced hypertension?
Absolute Event Rate: 100% vs 115%
p-value: p=<0.05
In silico modeling suggests that suppression of renal sympathetic nerve activity and increased secretion of atrial natriuretic peptide are key mechanisms contributing to blood pressure lowering during baroreflex activation therapy in obesity-mediated hypertension.
Hypothesis-generating for baroreflex activation therapy in obesity hypertension models; leaves open human efficacy.
Clinical trials evaluating the efficacy of chronic electrical stimulation of the carotid baroreflex for the treatment of hypertension (HTN) are ongoing. However, the mechanisms by which this device lowers blood pressure (BP) are unclear, and it is uncertain which patients are most likely to receive clinical benefit. Mathematical modeling provides the ability to analyze complicated interrelated effects across multiple physiological systems. Our current model HumMod is a large physiological simulator that has been used previously to investigate mechanisms responsible for BP lowering during baroreflex activation therapy (BAT). First, we used HumMod to create a virtual population in which model parameters (n = 335) were randomly varied, resulting in unique models (n = 6092) that we define as a virtual population. This population was calibrated using data from hypertensive obese dogs (n = 6) subjected to BAT. The resultant calibrated virtual population (n = 60) was based on tuning model parameters to match the experimental population in 3 key variables: BP, glomerular filtration rate, and plasma renin activity, both before and after BAT. In the calibrated population, responses of these 3 key variables to chronic BAT were statistically similar to experimental findings. Moreover, blocking suppression of renal sympathetic nerve activity (RSNA) and/or increased secretion of atrial natriuretic peptide (ANP) during BAT markedly blunted the antihypertensive response in the virtual population. These data suggest that in obesity-mediated HTN, RSNA and ANP responses are key factors that contribute to BP lowering during BAT. This modeling approach may be of value in predicting BAT responses in future clinical studies.
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Clemmer et al. (2021) studied Obesity-induced hypertension (n=60). Baroreflex activation therapy (BAT) simulation vs. Baseline (pre-BAT) was evaluated on Mean arterial pressure (MAP) in mmHg (p=<0.05). In a virtual population of obesity-induced hypertension, simulated baroreflex activation therapy significantly reduced mean arterial pressure from 115 mmHg to 100 mmHg.
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