Why the study?
Does carvedilol 25 mg daily improve oxidative stress markers and lipid profiles in patients with mild to moderate essential hypertension?
Does carvedilol 25 mg daily improve oxidative stress markers and lipid profiles in patients with mild to moderate essential hypertension?
Carvedilol may offer beneficial metabolic and antioxidant effects in hypertensive patients by augmenting HDL and PON1 activity.
May support antioxidant effects in hypertension; hypothesis-generating and requires RCT confirmation before practice change.
OBJECTIVE: Carvedilol is a nonselective third generation β-blocker that does not display the negative effects of traditional β-blockers. Regarding the antioxidant, anti-inflammatory and distinct metabolic properties of carvedilol which are similar to that of high-density lipoprotein (HDL) and paraoxonase 1 (PON1), the present study intends to investigate the effects of carvedilol treatment on malondialdehyde (MDA) and soluble lectin-like ox-low-density lipoprotein (LDL) receptor (sLOX-1) as markers of oxidative stress in association to lipid profiles, apolipoproteins (apo), and PON1 activity in hypertensive patients. PATIENTS AND METHODS: This clinical trial study was performed on forty patients with mild to moderate essential hypertension. Subjects were studied before and after 2 months treatment with carvedilol, 25 mg daily. Lipids and lipoproteins were measured using a biochemistry analyzer. PON and arylesterase activity were assayed using paraoxon and phenyl acetate as substrates, respectively. MDA was quantified using a chemical colorimetric assay. ELISA was used to measure sLOX-1. RESULTS: < 0.05), but the levels of triglyceride, LDL, apo A-I, and apo B did not significantly change. There was an inverse correlation between serum PON1 activity and serum MDA. CONCLUSION: This study confirmed the antihypertensive effect of the drug and its beneficial metabolic effects through augmenting HDL and PON1 activity. We propose that the antioxidant effects of carvedilol can be partially attributed to increased PON-1 activity.
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Yaghooti et al. (2016) studied this question.