Key result
Bezafibrate reduces resting heart rate by ~3 bpm alongside lower systolic BP in hypertriglyceridemia.
Why the study?
Hypertension frequently occurs in hypertriglyceridemic patients and may be associated with hyperinsulinemia and elevated plasma free fatty acids; the effects of bezafibrate on hemodynamics and related biochemical parameters were investigated.
Does bezafibrate reduce blood pressure and heart rate in hypertriglyceridemic patients?
RCT (n=17)
Double-blind
Randomized
Does bezafibrate reduce blood pressure and heart rate in hypertriglyceridemic patients?
Absolute Event Rate: 66% vs 69%
p-value: p=0.009
Bezafibrate reduces heart rate and blood pressure in hypertriglyceridemic patients, likely through improved endothelial function rather than changes in sympathetic activity or renal sodium absorption.
Bezafibrate modestly lowers BP and HR in hypertriglyceridemia; leaves open endothelial mechanism and clinical relevance pending larger trials.
Objective: In hypertriglyceridemic patients, hypertension occurs frequently and may be associated with hyperinsulinemia and elevated plasma levels of free fatty acids (FFA). Besides the lipid-lowering effects, fibrates have been shown to reduce blood pressure in hypertensive patients. The present study was undertaken to investigate the effects of bezafibrate on hemodynamics in relation to insulin, FFA, sympathetic activity, renal sodium absorption, cyclic-GMP (cGMP) and endothelin-1 in hypertriglyceridemic patients. Subjects and methods: Hypertriglyceridemic patients (17) were randomized to receive in a double-blind placebo-controlled study bezafibrate or placebo for 6 weeks. At the end of both treatment periods, blood pressure and heart rate were measured automatically. Plasma insulin, FFA, aldosterone, catecholamines, cGMP, endothelin-1 levels and 24 h urine catecholamines and sodium excretion were assessed. Results Bezafibrate therapy decreased serum triglycerides (-65%, P < 0.001) and hemodynamic parameters: heart rate decreased from 69 to 66/min (P = 0.009), systolic blood pressure from 137 to 132 mmHg (P = 0.01), diastolic blood pressure from 81 to 79 mmHg (P = 0.07) and mean blood pressure from 102 to 99 mmHg (P = 0.06). Bezafibrate therapy reduced FFA and insulin (-55 and -57% respectively, both P < 0.001), while sympathetic activity and renal sodium absorption were not affected, cGMP increased (+17%, P=0.008), whereas endothelin-1 levels tended to decrease upon bezafibrate therapy (-10%, P=0.077) Conclusion: Bezafibrate reduces heart rate, blood pressure, insulin and FFA in hypertriglyceridemic patients. The hemodynamic effects cannot be attributed to changes in sympathetic activity or renal sodium absorption. Instead, based on the increase in plasma cGMP levels, the bezafibrate-induced hemodynamic effects are most likely to be caused by bezafibrate-induced improvement of endothelial function.
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Jonkers et al. (2026) conducted an RCT in Hypertriglyceridemia (n=17). Bezafibrate vs. Placebo was evaluated on Heart rate (p=0.009). Bezafibrate therapy significantly reduced heart rate (69 to 66/min, P=0.009) and systolic blood pressure (137 to 132 mmHg, P=0.01) in hypertriglyceridemic patients.
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