Literature DB >> 1349791

The paradox of beta-adrenergic blockade for the management of congestive heart failure.

E J Eichhorn1.   

Abstract

PURPOSE: To review the current data regarding the use of beta-adrenergic blockers for the treatment of congestive heart failure.
MATERIAL AND METHODS: Relevant studies published between 1975 and 1991 were reviewed. Key data from each study were extracted. The significance of conclusions reached by each author(s) was identified.
RESULTS: beta-adrenergic blockade, although still considered an investigational therapy for the treatment of congestive heart failure, has been proven in several studies to improve ventricular function, including myocardial contractility and relaxation. In addition, since beta-blockade up-regulates myocardial beta-receptors, the myocardium becomes more responsive to graded doses of beta-agonists. Speculation regarding the possible mechanisms of these effects is presented. In addition, since beta-blockers have been shown to reduce neurohormonal activation, they may have a beneficial effect on survival. Although small pilot studies or subgroup analysis of larger studies suggest beta-blockade therapy improves survival in heart failure, this has yet to be proven. Large prospective trials are warranted to study this issue.
CONCLUSIONS: As current data suggest, beta-blockers improve ventricular function and reduce neurohormonal activation in heart failure. beta-blockers should be considered as adjunctive therapy in patients with congestive heart failure. In addition, future studies are warranted to better elucidate their effects on ventricular function and survival.

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Year:  1992        PMID: 1349791     DOI: 10.1016/0002-9343(92)90750-6

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  10 in total

1.  Beta-blocker timolol alleviates hyperglycemia-induced cardiac damage via inhibition of endoplasmic reticulum stress.

Authors:  Figen Amber Cicek; Aysegul Toy; Erkan Tuncay; Belgin Can; Belma Turan
Journal:  J Bioenerg Biomembr       Date:  2014-07-27       Impact factor: 2.945

Review 2.  Adrenergic and muscarinic receptor regulation and therapeutic implications in heart failure.

Authors:  W Schmitz; P Boknik; B Linck; F U Müller
Journal:  Mol Cell Biochem       Date:  1996 Apr 12-26       Impact factor: 3.396

3.  Quality of life on treatment with metoprolol in dilated cardiomyopathy: results from the MDC trial. Metoprolol in Dilated Cardiomyopathy trial.

Authors:  I Wiklund; F Waagstein; K Swedberg; A Hjalmarsson
Journal:  Cardiovasc Drugs Ther       Date:  1996-07       Impact factor: 3.727

Review 4.  Beta-adrenergic receptors in heart failure.

Authors:  P A Insel; H K Hammond
Journal:  J Clin Invest       Date:  1993-12       Impact factor: 14.808

Review 5.  Controversies surrounding the use of beta-blockers in older patients with cardiovascular disease.

Authors:  R W Jansen; J H Gurwitz
Journal:  Drugs Aging       Date:  1994-03       Impact factor: 3.923

6.  Initiation or maintenance of beta-blocker therapy in patients hospitalized for acute heart failure.

Authors:  Luiz Carlos Passos; Márcio Galvão Oliveira; Andre Rodrigues Duraes; Thiago Moreira Trindade; Andréa Cristina Costa Barbosa
Journal:  Int J Clin Pharm       Date:  2016-04-30

Review 7.  A risk-benefit assessment of carvedilol in the treatment of cardiovascular disorders.

Authors:  W J Louis; H Krum; E L Conway
Journal:  Drug Saf       Date:  1994-08       Impact factor: 5.606

8.  Clinical usefulness of 123I meta-iodobenzylguanidine imaging in predicting the effectiveness of beta blockers for patients with idiopathic dilated cardiomyopathy before and soon after treatment.

Authors:  H Kakuchi; T Sasaki; Y Ishida; K Komamura; K Miyatake
Journal:  Heart       Date:  1999-02       Impact factor: 5.994

Review 9.  Use of beta-adrenoceptor blockers in patients with congestive heart failure.

Authors:  V Panfilov; I Wahlqvist; G Olsson
Journal:  Cardiovasc Drugs Ther       Date:  1995-04       Impact factor: 3.727

10.  Myocardial MiR-30 downregulation triggered by doxorubicin drives alterations in β-adrenergic signaling and enhances apoptosis.

Authors:  L Roca-Alonso; L Castellano; A Mills; A F Dabrowska; M B Sikkel; L Pellegrino; J Jacob; A E Frampton; J Krell; R C Coombes; S E Harding; A R Lyon; J Stebbing
Journal:  Cell Death Dis       Date:  2015-05-07       Impact factor: 8.469

  10 in total

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