Evidence map›Paper›PMID 22460122›Full record

ReviewNature reviews. Drug discovery2012

Novel molecular targets for atrial fibrillation therapy.

Dobromir Dobrev, Leif Carlsson, Stanley Nattel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
17.6field-weighted citation impact, top 1% of its field
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

84 citing papers in PubMed, 180 citations in OpenAlex.

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24 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 3 countries.

Dobromir DobrevDivision of Experimental Cardiology, Medical Faculty Mannheim, University of Heidelberg, 68167 Mannheim, Germany. dobromir.dobrev@medma.uni-heidelberg.de
Leif Carlsson
Stanley Nattel
AstraZeneca (Sweden) · SEMontreal Heart Institute · CAUniversity Medical Centre Mannheim · DE

Funding

Canadian Institutes of Health Research MGP-6957Canadian Institutes of Health Research MOP-44365
6 · The paper itself

Abstract

Atrial fibrillation is the most common type of cardiac arrhythmia, and is responsible for substantial morbidity and mortality in the general population. Current treatments have moderate efficacy and considerable risks, especially of pro-arrhythmia, highlighting the need for new therapeutic strategies. In recent years, substantial efforts have been invested in developing novel treatments that target the underlying molecular determinants of atrial fibrillation, and several new compounds are under development. This Review focuses on the mechanistic rationale for the development of new anti-atrial fibrillation drugs, on the molecular and structural motifs that they target and on the results obtained so far in experimental and clinical studies.

Indexed as

AnimalsAnti-Arrhythmia AgentsAtrial FibrillationHumansMolecular Targeted TherapyAnti-Arrhythmia Agents

Identifiers

PMID22460122
OpenAlexW2064757035

What OpenQuestion holds

Textmetadata
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.