Evidence map›Paper›PMID 29745425›Full record

ArticleBritish journal of pharmacology2018

Arrhythmic hazard map for a 3D whole-ventricle model under multiple ion channel block.

Jun-Ichi Okada, Takashi Yoshinaga, Junko Kurokawa, Takumi Washio, Tetsushi Furukawa, Kohei Sawada, Seiryo Sugiura, Toshiaki Hisada

Abstract read
In one paragraph

Article in British journal of pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. APL bioengineering · 2020
    Review
  8. Clinical and pharmacological application of multiscale multiphysics heart simulator, UT-Heart.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2019
    Review
  9. Digital heart for life.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2019
    Article
  10. Article
  11. 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

8 authors.

Jun-Ichi OkadaGraduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Japan.ORCID 0000-0003-0040-2432
Takashi YoshinagaGlobal CV Assessment, Eisai Co., Ltd., Ibaraki, Japan.
Junko KurokawaSchool of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Takumi WashioGraduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Japan.ORCID 0000-0001-5240-2050
Tetsushi FurukawaDepartment of Bio-informational Pharmacology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Kohei SawadaGlobal CV Assessment, Eisai Co., Ltd., Ibaraki, Japan.
Seiryo SugiuraGraduate School of Frontier Sciences, The University of Tokyo, Kashiwa, Japan.
Toshiaki HisadaUT-Heart Inc., Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeTo date, proposed in silico models for preclinical cardiac safety testing are limited in their predictability and usability. We previously reported a multi-scale heart simulation that accurately predicts arrhythmogenic risk for benchmark drugs. EXPERIMENTAL APPROACH: We created a comprehensive hazard map of drug-induced arrhythmia based on the electrocardiogram (ECG) waveforms simulated under wide range of drug effects using the multi-scale heart simulator described here, implemented with cell models of human cardiac electrophysiology. KEY

resultsA total of 9075 electrocardiograms constitute the five-dimensional hazard map, with coordinates representing the extent of the block of each of the five ionic currents (rapid delayed rectifier potassium current (I CONCLUSION AND IMPLICATIONS: Because concentration-dependent effects on electrocardiograms of any drug can be traced on this map based on in vitro current assay data, its arrhythmogenic risk can be evaluated without performing costly and potentially risky human electrophysiological assays. Hence, the map serves as a novel tool for use in pharmaceutical research and development.

Indexed as

Models, BiologicalAdultArrhythmias, CardiacDrug-Related Side Effects and Adverse ReactionsElectrocardiographyFinite Element AnalysisHeart VentriclesHumansIon ChannelsIon Channels

Identifiers

PMID29745425
PMCPMC6086978

What OpenQuestion holds

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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.