Evidence map›Paper›PMID 35579204›Full record

ArticleClinical and translational science2022

Cardiac sodium channel inhibition by lamotrigine: In vitro characterization and clinical implications.

Lindsey Ingleby-Talecki, Sven C van Dijkman, Sean P Oosterholt, Oscar Della Pasqua, Christina Winter, Marianne Cunnington, Linda Rebar, Sergio Forero-Schwanhaeuser, Vickas Patel, James A Cooper and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Treatment updates in myotonic disorders.Journal of neurology · 2026
    Review
  2. Lamotrigine Ameliorates Epilepsy during Pregnancy in Rats by Inhibiting Astrocyte Activation via the NLRP3/TXNIP Pathway.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Article
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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

12 authors at 6 institutions in 3 countries.

Lindsey Ingleby-TaleckiGSK Global Non-Clinical Safety, Collegeville, Pennsylvania, USA.
Sven C van DijkmanGSK Clinical Pharmacology Modelling and Simulation, Brentford, UK.
Sean P OosterholtGSK Clinical Pharmacology Modelling and Simulation, Brentford, UK.
Oscar Della PasquaGSK Clinical Pharmacology Modelling and Simulation, Brentford, UK.ORCID 0000-0002-6211-1430
Christina WinterGSK Clinical Safety and Pharmacovigilance, Brentford, UK.ORCID 0000-0002-3423-3422
Marianne CunningtonGSK Epidemiology, Value Evidence & Outcomes, Stevenage, UK.
Linda RebarGSK US Regulatory Affairs, Collegeville, Pennsylvania, USA.
Sergio Forero-SchwanhaeuserGSK, US Medical Affairs, Philadelphia, Pennsylvania, USA.
Vickas PatelFormer GSK Employee, Collegeville, Pennsylvania, USA.
James A CooperGSK General Medicines, Brentford, UK.
Anthony BahinskiGSK Global Non-Clinical Safety, Collegeville, Pennsylvania, USA.ORCID 0000-0002-2379-6027
Khuram W ChaudharyGSK Global Non-Clinical Safety, Collegeville, Pennsylvania, USA.ORCID 0000-0001-5693-0491
GlaxoSmithKline (United States) · USSystem Simulation (United Kingdom) · GBAge UK · GBGlaxoSmithKline (Germany) · DEHealth and Safety Executive · GBUnited States Nuclear Regulatory Commission · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lamotrigine, approved for use as an antiseizure medication as well as the treatment of bipolar disorder, inhibits sodium channels in the brain to reduce repetitive neuronal firing and pathological release of glutamate. The shared homology of sodium channels and lack of selectivity associated with channel blocking agents can cause slowing of cardiac conduction and increased proarrhythmic potential. The Vaughan-Williams classification system differentiates sodium channel blockers using biophysical properties of binding. As such, Class Ib inhibitors, including mexiletine, do not slow cardiac conduction as measured by the electrocardiogram, at therapeutically relevant exposure. Our goal was to characterize the biophysical properties of Na

Indexed as

MexiletineSodium ChannelsAnticonvulsantsFlecainideHEK293 CellsHumansLamotrigineSodium Channel BlockersAnticonvulsantsFlecainideLamotrigineMexiletineSodium Channel BlockersSodium Channels

Identifiers

PMID35579204
PMCPMC9372421
OpenAlexW4280586839

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.