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Beta-1-selectivity is not essential to achieve therapeutic efficacy with beta-blockade therapy for idiopathic dilated cardiomyopathy.

Abstract
This study investigated the therapeutic efficacy of two different beta-blockers, metoprolol (beta 1-selective) and nipradilol (nonselective) for the treatment of idiopathic dilated cardiomyopathy (DCM). The New York Heart Association functional class improved in the metoprolol group (n = 9) and the nipradilol group (n = 9), but not in the control group who received conventional therapy (n = 8). The left ventricular ejection fraction increased in both the beta-blocker groups (p < 0.01, p < 0.05). Lymphocyte beta-adrenoceptors were upregulated in the nipradilol group (p < 0.01). Cardiac events were less common in both the beta-blocker groups than in the control group (both p < 0.05). Thus, nipradilol improved symptoms and cardiac function with a favorable effect on sympathoneuronal activity as well as metoprolol in patients with DCM. Therefore, beta 1-selectivity is not essential to achieve therapeutic efficacy with beta-blockade therapy for DCM.
AuthorsT Yoshikawa, S Handa, M Akaishi, H Mitamura, S Ogawa
JournalCardiology (Cardiology) Vol. 86 Issue 3 Pg. 217-23 ( 1995) ISSN: 0008-6312 [Print] Switzerland
PMID7614494 (Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • Adrenergic beta-Antagonists
  • Propanolamines
  • Receptors, Adrenergic, beta
  • nipradilol
  • Metoprolol
Topics
  • Adrenergic beta-Antagonists (therapeutic use)
  • Adult
  • Aged
  • Cardiomyopathy, Dilated (diagnostic imaging, drug therapy, metabolism)
  • Confounding Factors, Epidemiologic
  • Coronary Angiography
  • Electrocardiography
  • Female
  • Humans
  • Lymphocytes (drug effects, metabolism)
  • Male
  • Metoprolol (therapeutic use)
  • Middle Aged
  • Propanolamines (therapeutic use)
  • Radionuclide Ventriculography
  • Receptors, Adrenergic, beta (drug effects)
  • Ventricular Function, Left (drug effects)

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