Evidence map›Paper›PMID 34004185›Full record

ArticleJournal of molecular and cellular cardiology2021

Mechanisms of flecainide induced negative inotropy: An in silico study.

Pei-Chi Yang, Wayne R Giles, Luiz Belardinelli, Colleen E Clancy

Open access · bronzeAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Enhanced CaJACC. Clinical electrophysiology · 2024
    Article
  6. Review
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

4 authors at 3 institutions in 2 countries.

Pei-Chi YangDepartment of Physiology and Membrane Biology, School of Medicine, University of California, Davis, United States of America.
Wayne R GilesDepartment of Physiology & Pharmacology, University of Calgary, Canada.
Luiz BelardinelliInCarda Therapeutics, Newark, CA, United States of America.
Colleen E ClancyDepartment of Physiology and Membrane Biology, School of Medicine, University of California, Davis, United States of America. Electronic address: ceclancy@ucdavis.edu.
University of California, Davis · USAcorda Therapeutics (United States) · USUniversity of Calgary · CA

Funding

Development of the Predictive NeuroCardiovascular SimulatorOT2OD026580 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CLANCY, COLLEEN E, GRANDI, ELEONORA · 2018 to 2021
$5.7M
In silico Safety PharmacologyR01HL128537 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CLANCY, COLLEEN E, SANTANA, LUIS F · 2016 to 2024
$5.7M
Predictive multiscale in silico cardio-pharmacologyU01HL126273 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CLANCY, COLLEEN E · 2015 to 2019
$3.8M
A Systems Biology Approach to Study Cardiac Arrhythmias: iPS Cells and In Silico ModelingR01HL128170 · NHLBI · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO, CLANCY, COLLEEN E · 2015 to 2018
$3.0M
Multi-Scale Modeling of Vascular Signaling UnitsR01HL152681 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CLANCY, COLLEEN E, SANTANA, LUIS F · 2020 to 2023
$2.4M
NHLBI NIH HHS R01 HL128170NHLBI NIH HHS R01 HL128537NHLBI NIH HHS R01 HL152681NHLBI NIH HHS U01 HL126273NIH HHS OT2 OD026580
6 · The paper itself

Abstract

It is imperative to develop better approaches to predict how antiarrhythmic drugs with multiple interactions and targets may alter the overall electrical and/or mechanical function of the heart. Safety Pharmacology studies have provided new insights into the multi-target effects of many different classes of drugs and have been aided by the addition of robust new in vitro and in silico technology. The primary focus of Safety Pharmacology studies has been to determine the risk profile of drugs and drug candidates by assessing their effects on repolarization of the cardiac action potential. However, for decades experimental and clinical studies have described substantial and potentially detrimental effects of Na

Indexed as

Computer SimulationAction PotentialsAnti-Arrhythmia AgentsCalcium ChannelsFlecainideHeart RateHeart VentriclesHomeostasisHumansModels, CardiovascularMyocardial ContractionMyocytes, CardiacRyanodine Receptor Calcium Release ChannelSignal TransductionSodium ChannelsVoltage-Gated Sodium Channel BlockersAnti-Arrhythmia AgentsCalcium ChannelsFlecainideRyanodine Receptor Calcium Release ChannelSodium ChannelsVoltage-Gated Sodium Channel BlockersCardiac inotropyFlecainideIon channelPharmacologySafety pharmacology

Identifiers

PMID34004185
PMCPMC8772296
OpenAlexW3160712484

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.