Literature DB >> 27093951

Effects of Carvedilol Compared to Nebivolol on Insulin Resistance and Lipid Profile in Patients With Essential Hypertension.

Ali Gokhan Ozyıldız1, Serpil Eroglu1, Ugur Bal1, Ilyas Atar1, Kaan Okyay1, Haldun Muderrisoglu1.   

Abstract

BACKGROUND AND AIM:: Beta-blockers have unfavorable effects on metabolic parameters in hypertensive treatment. New generation beta-blockers with vasodilatory capabilities are superior to traditional beta-blockers, but studies examining their effects on metabolic parameters are still lacking. This study aimed to compare the effects of 2 new generation beta-blockers, carvedilol and nebivolol, on insulin resistance (IR) and lipid profiles in patients with essential hypertension.
METHODS: : This was a prospective, randomized, open-label, single-center clinical trial. A total of 80 patients were randomized into 2 groups: the carvedilol group (n = 40, 25 mg of carvedilol daily) and the nebivolol group (n = 40, 5 mg of nebivolol daily). Follow-up was performed for 4 months. Fasting plasma glucose, insulin levels, and the lipid profile (high-density lipoprotein [HDL], low-density lipoprotein [LDL], total cholesterol, triglyceride, apolipoprotein AI, and apolipoprotein B levels) were measured and IR was calculated by the homeostasis model assessment (HOMA) index. These variables were compared before and 4 months after treatment.
RESULTS: : Blood pressure and heart rate were significantly and similarly reduced in the carvedilol and nebivolol groups after treatment compared to those before treatment (both P < .001). Serum glucose ( P < .001), insulin ( P < .01), HOMA-IR (P < .01), HDL ( P < .001), LDL ( P < .001), total cholesterol ( P < .001), and apolipoprotein B ( P < .05) levels decreased in a similar manner in the carvedilol and nebivolol groups after treatment compared to those before treatment. Serum triglyceride and apolipoprotein AI levels did not change after treatment with both drugs.
CONCLUSION: : New generation beta-blockers, carvedilol and nebivolol, efficiently and similarly decrease blood pressure. They have similar favorable effects on glucose, insulin, IR, and the lipid profile.

Entities:  

Keywords:  carvedilol; dyslipidemia; hypertension; insulin resistance; nebivolol

Year:  2016        PMID: 27093951     DOI: 10.1177/1074248416644987

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol Ther        ISSN: 1074-2484            Impact factor:   2.457


  5 in total

1.  Efficacy and Safety of Nebivolol and Rosuvastatin Combination Treatment in Patients with Concomitant Hypertension and Hyperlipidemia.

Authors:  Moo-Yong Rhee; Cheol Ho Kim; Youngkeun Ahn; Joon-Han Shin; Seung Hwan Han; Hyun-Jae Kang; Soon Jun Hong; Hae-Young Kim
Journal:  Drug Des Devel Ther       Date:  2020-11-17       Impact factor: 4.162

Review 2.  Differential Metabolic Effects of Beta-Blockers: an Updated Systematic Review of Nebivolol.

Authors:  Maria Marketou; Yashaswi Gupta; Shashank Jain; Panos Vardas
Journal:  Curr Hypertens Rep       Date:  2017-03       Impact factor: 5.369

Review 3.  Perivascular adipose tissue as a regulator of vascular disease pathogenesis: identifying novel therapeutic targets.

Authors:  Ioannis Akoumianakis; Akansha Tarun; Charalambos Antoniades
Journal:  Br J Pharmacol       Date:  2016-12-14       Impact factor: 8.739

4.  Treatment with β-blocker nebivolol ameliorates oxidative stress and endothelial dysfunction in tenofovir-induced nephrotoxicity in rats.

Authors:  Mariana Moura Nascimento; Desiree Rita Denelle Bernardo; Ana Carolina de Bragança; Maria Heloisa Massola Shimizu; Antonio Carlos Seguro; Rildo Aparecido Volpini; Daniele Canale
Journal:  Front Med (Lausanne)       Date:  2022-08-04

5.  Potential off-target effects of beta-blockers on gut hormone receptors: In silico study including GUT-DOCK-A web service for small-molecule docking.

Authors:  Pawel Pasznik; Ewelina Rutkowska; Szymon Niewieczerzal; Judyta Cielecka-Piontek; Dorota Latek
Journal:  PLoS One       Date:  2019-01-25       Impact factor: 3.240

  5 in total

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