Evidence map›Paper›PMID 41604389›Full record

ArticlePloS one2026

A novel methodology to characterize beat-to-beat alternations in whole-cell calcium currents.

Xavier Marimon, Miguel Cerrolaza, Carmen Tarifa, Leif Hove-Madsen

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Xavier MarimonDepartment of Strength of Materials and Structural Engineering, Universitat Politècnica de Catalunya, (UPC- BarcelonaTECH), Barcelona, Spain.ORCID https://orcid.org/0000-0001-7653-6299
Miguel CerrolazaSchool of Engineering, Science and Technology, Universitat Internacional de Valencia (VIU), Valencia, Spain.
Carmen TarifaSpanish National Center for Cardiovascular Research (CNIC), Madrid, Spain.
Leif Hove-MadsenInstituto de Investigaciones Biomédicas de Barcelona (IIBB-CSIC), Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An automated high-throughput procedure to quantify the degree of electrical beat-to-beat alternants in human atrial myocytes from electrophysiological recordings of the transmembrane ion currents of calcium ions (Ca2+) is presented and discussed. The patch clamp technique in whole-cell mode was used to record the myocyte calcium signal. A database consisting of 24 patch clamp signals (N = 24) of which 13 had a uniform behaviour and 11 had an alternating behaviour, was created. Several features were computed to characterize the transmembrane ion currents: peak amplitude, time constants, and area under the ion current trace. The presented algorithm includes a feature detector whose accuracy has been validated using simulated calcium signals generated by an electrical model that accurately represents the cardiomyocyte behaviour in a patch clamp experiment. Among these calculated features, a new index measure, called the "alternation index", is proposed in this work to quantify the degree of electrical beat-to-beat alternants. The index has been shown to be a robust measure (p ≤ 0.01 **) for cell detection with an alternating pattern. Good agreement was observed with alternations in other calculated features like the measurement of the inactivation of L-type calcium current (Ica) or the tail current (ITail) generated by calcium extrusion upon repolarization.

Indexed as

CalciumCalcium SignalingMyocytes, CardiacPatch-Clamp TechniquesAction PotentialsAlgorithmsCalcium Channels, L-TypeHumansCalciumCalcium Channels, L-Type

Identifiers

PMID41604389
PMCPMC12851451

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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.