Key result
Carvedilol and bisoprolol fail to reduce oxidative stress or endothelial damage markers in chronic HF.
Why the study?
Does carvedilol reduce oxidative stress and endothelial damage compared to bisoprolol in patients with chronic heart failure?
Cohort (n=68)
Does carvedilol reduce oxidative stress and endothelial damage compared to bisoprolol in patients with chronic heart failure?
Contrary to proposed antioxidative effects, neither carvedilol nor bisoprolol significantly reduces oxidative stress or endothelial damage in patients with chronic heart failure.
Neither beta-blocker reduced oxidative stress or endothelial damage markers; leaves open whether these agents exert clinically relevant antioxidative effects in chronic heart failure.
We hypothesized that abnormal oxidative stress in chronic heart failure (CHF) could be related to endothelial damage and platelet activation, and that the vasodilating beta-blocker carvedilol would have beneficial effects on these processes compared with a selective non-vasodilating cardioselective beta-blocker, bisoprolol. We therefore assessed the effects of introducing carvedilol and bisoprolol in a prospective manner on indices of oxidative stress [lipid hydroperoxides (LHP)], endothelial damage [von Willebrand factor (vWf)], platelet activation (soluble P-selectin) and coagulation (fibrinogen) and their inter-relationships in stable outpatients with CHF in sinus rhythm. We recruited 46 patients [23 male; age 64 +/- 13 years (mean +/- S.D.); range 38-85 years] with CHF. Baseline levels of serum LHP (P<0.002), plasma vWf (P<0.001) and soluble P-selectin (P=0.02), but not fibrinogen (P=0.16), were higher in CHF patients compared with 22 age- and sex-matched healthy controls. After treatment for 2 months, systolic blood pressure fell in both arms of the study (both P<0.01), but there were no statistically significant (defined as P<0.01) decreases in LHP, vWf, fibrinogen or soluble P-selectin levels with either carvedilol or bisoprolol. In conclusion, patients with CHF have increased levels of plasma LHP and vWf, indicating increased oxidative stress and endothelial damage respectively. Contrary to the proposed antioxidative effects of carvedilol, initiating and titrating such therapy did not result in a reduction in levels of LHP in CHF.
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Chin et al. (2003) conducted a cohort in chronic heart failure (n=68). Carvedilol vs. Bisoprolol was evaluated on indices of oxidative stress (lipid hydroperoxides), endothelial damage (von Willebrand factor), platelet activation (soluble P-selectin) and coagulation (fibrinogen). Treatment with maximally tolerated doses of carvedilol or bisoprolol for 2 months did not significantly reduce oxidative stress or endothelial damage markers in patients with chronic heart failure.
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