This was a phase II, single-center, randomized controlled trial involving 137 adults aged 30-70 years with overweight or obesity and at least one feature of metabolic syndrome. Participants were randomized to receive either the epithelial sodium channel (ENAC) inhibitor amiloride at a low dose of 5 mg daily or a placebo for a follow-up period of 24 weeks. The primary outcome was not explicitly reported, but secondary outcomes included carotid-femoral pulse wave velocity (cfPWV), blood pressure, vascular function, serum potassium, fasting glucose, and brachial artery flow-mediated dilation.
The main results indicated that amiloride significantly reduced arterial stiffness, with decreases in cfPWV observed at both 12 and 24 weeks, while no changes were seen with placebo. Systolic blood pressure was reduced by a mean of 5.6 mmHg at 24 weeks in the amiloride group. The drug also lowered fasting glucose and increased serum potassium levels, but did not significantly affect brachial artery flow-mediated dilation. An exploratory analysis suggested that older age was associated with greater reductions in both cfPWV and systolic blood pressure.
Regarding safety, no severe adverse events were observed, though detailed adverse event, discontinuation, and tolerability data were not reported. Key limitations include the single-center design, the phase II nature of the trial, and the lack of reported specific effect sizes, p-values, or confidence intervals for most outcomes. The findings suggest a potential association between blood pressure lowering with amiloride and improved vascular stiffness in this population, but the evidence remains preliminary.
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Obesity and insulin resistance promote arterial stiffening and hypertension, increasing cardiovascular risk. Activation of the epithelial sodium channel (ENAC) contributes to vascular stiffening in preclinical models, but the vascular effects of ENAC inhibition in adults with obesity and insulin resistance are not well defined. In this phase II, 24-wk, randomized, double-blind, single-center, placebo-controlled trial, 137 adults aged 30-70 yr with overweight or obesity and at least one metabolic syndrome feature were randomized (2:1) to the ENAC inhibitor amiloride (5 mg daily) or placebo. Carotid-femoral pulse wave velocity (cfPWV), blood pressure, and vascular function were assessed at baseline, 12 wk, and 24 wk. Amiloride significantly reduced arterial stiffness, with decreases in cfPWV at 12 and 24 wk, whereas no changes were observed with placebo. Systolic blood pressure was also reduced, with a mean reduction of 5.6 mmHg at 24 wk. Older age was associated with greater reductions in cfPWV and systolic blood pressure. Amiloride increased serum potassium and lowered fasting glucose, but did not significantly affect brachial artery flow-mediated dilation. No severe adverse events were observed. In conclusion, low-dose amiloride improves blood pressure and arterial stiffness in adults with overweight or obesity and features of metabolic syndrome, without major safety concerns. These findings suggest that blood pressure lowering with amiloride is associated with favorable changes in vascular stiffness in this population. Obesity and insulin resistance accelerate arterial stiffening and hypertension, increasing cardiovascular risk. Activation of the epithelial sodium channel (ENAC) contributes to vascular stiffening in preclinical models, yet the vascular effects of ENAC inhibition in adults with obesity and insulin resistance remain poorly characterized. Here, we demonstrate that low-dose amiloride reduces blood pressure and improves arterial stiffness in adults with overweight or obesity and features of metabolic syndrome, without major safety concerns.