Evidence map›Paper›PMID 24681351›Full record

ReviewCurrent opinion in pharmacology2014

Ligand bias prevents class equality among beta-blockers.

Vaidehi J Thanawala, Gloria S Forkuo, Wayne Stallaert, Paul Leff, Michel Bouvier, Richard Bond

Abstract readReview
In one paragraph

Review in Current opinion in pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Allosteric "beta-blocker" isolated from a DNA-encoded small molecule library.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Vaidehi J ThanawalaDepartment of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, USA.
Gloria S ForkuoDepartment of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, USA.
Wayne StallaertDepartment of Biochemistry, Université de Montréal, Montréal, Quebec, Canada; Institute for Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec, Canada.
Paul LeffConsultant in Pharmacology, Cheshire, UK.
Michel BouvierDepartment of Biochemistry, Université de Montréal, Montréal, Quebec, Canada; Institute for Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec, Canada.
Richard BondDepartment of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, USA. Electronic address: rabond@uh.edu.

Funding

Mechanisms of beta-blocker induced improvements in asthmaR01AI079236 · NIAID · UNIVERSITY OF HOUSTON · PI BOND, RICHARD AGUSTIN · 2009 to 2010
$1.0M
Mechanisms of Beta-blocker Induced Improvements in AsthmaR56AI079236 · NIAID · UNIVERSITY OF HOUSTON · PI BOND, RICHARD AGUSTIN, DICKEY, BURTON F · 2012 to 2013
$499k
NIAID NIH HHS R01 AI079236NIAID NIH HHS R56 AI079236
6 · The paper itself

Abstract

β-Blockers are used for a wide range of diseases from hypertension to glaucoma. In some diseases/conditions all β-blockers are effective, while in others only certain subgroups are therapeutically beneficial. The best-documented example for only a subset of β-blockers showing clinical efficacy is in heart failure, where members of the class have ranged from completely ineffective, to drugs of choice for treating the disease. Similarly, β-blockers were tested in murine asthma models and two pilot clinical studies. A different subset was found to be effective for this clinical indication. These findings call into question the current system of classifying these drugs. To consider 'β-blockers', as a single class is misleading when considering their rigorous pharmacological definition and their appropriate clinical application.

Indexed as

Adrenergic beta-AntagonistsAnimalsAsthmaHumansLigandsReceptors, Adrenergic, beta-2Signal TransductionAdrenergic beta-AntagonistsLigandsReceptors, Adrenergic, beta-2

Identifiers

PMID24681351
PMCPMC4065631

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.