Evidence map›Paper›PMID 33131149›Full record

ArticleHuman mutation2020

Relationship between sodium channel function and clinical phenotype in SCN5A variants associated with Brugada syndrome.

Charles M Pearman, Nathan C Denham, Robert W Mills, Wern Y Ding, Simon S Modi, Mark C S Hall, Derick M Todd, Saagar Mahida

Open access · hybridAbstract read
In one paragraph

Article in Human mutation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Functional Characterisation of the RareInternational journal of molecular sciences · 2023
    Article
  3. Case Report:Frontiers in cardiovascular medicine · 2023
    Article
  4. Review
  5. 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 at 2 institutions in 2 countries.

Charles M PearmanDepartment of Cardiac Electrophysiology and Inherited Cardiac Conditions, Liverpool Heart and Chest Hospital, Liverpool, UK.ORCID 0000-0001-6743-9817
Nathan C DenhamDepartment of Cardiac Electrophysiology and Inherited Cardiac Conditions, Liverpool Heart and Chest Hospital, Liverpool, UK.
Robert W MillsCardiovascular Research Center, Massachusetts General Hospital, Charlestown, Massachusetts, USA.
Wern Y DingDepartment of Cardiac Electrophysiology and Inherited Cardiac Conditions, Liverpool Heart and Chest Hospital, Liverpool, UK.
Simon S ModiDepartment of Cardiac Electrophysiology and Inherited Cardiac Conditions, Liverpool Heart and Chest Hospital, Liverpool, UK.
Mark C S HallDepartment of Cardiac Electrophysiology and Inherited Cardiac Conditions, Liverpool Heart and Chest Hospital, Liverpool, UK.
Derick M ToddDepartment of Cardiac Electrophysiology and Inherited Cardiac Conditions, Liverpool Heart and Chest Hospital, Liverpool, UK.
Saagar MahidaDepartment of Cardiac Electrophysiology and Inherited Cardiac Conditions, Liverpool Heart and Chest Hospital, Liverpool, UK.
University of Liverpool · GBHarvard University · US

Funding

British Heart Foundation FS/17/54/33126Department of Health
6 · The paper itself

Abstract

The identification of a pathogenic SCN5A variant confers an increased risk of conduction defects and ventricular arrhythmias (VA) in Brugada syndrome (BrS). However, specific aspects of sodium channel function that influence clinical phenotype have not been defined. A systematic literature search identified SCN5A variants associated with BrS. Sodium current (I

Indexed as

Arrhythmias, CardiacBrugada SyndromeElectrocardiographyHeart Conduction SystemHumansMutationNAV1.5 Voltage-Gated Sodium ChannelPhenotypeNAV1.5 Voltage-Gated Sodium ChannelSCN5A protein, humanBrugadapatch clamprisk stratificationsodium current

Identifiers

PMID33131149
PMCPMC7756571
OpenAlexW3095235543

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.