Evidence map›Paper›PMID 28752958›Full record

ArticleThe Journal of physiology2017

Increased Ca buffering underpins remodelling of Ca

Jessica D Clarke, Jessica L Caldwell, Charles M Pearman, David A Eisner, Andrew W Trafford, Katharine M Dibb

Open access · hybridAbstract read
In one paragraph

Article in The Journal of physiology, 2017. 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
1.6field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Time's imprint on the left atrium: aging and atrial myopathy.The journal of cardiovascular aging · 2025
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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

6 authors at 1 institution in 1 country.

Jessica D ClarkeUnit of Cardiac Physiology, Manchester Academic Health Sciences Centre, Central Manchester Foundation Trust, 3.14 Core Technology Facility, University of Manchester, Manchester, UK.ORCID 0000-0001-6514-2104
Jessica L CaldwellUnit of Cardiac Physiology, Manchester Academic Health Sciences Centre, Central Manchester Foundation Trust, 3.14 Core Technology Facility, University of Manchester, Manchester, UK.ORCID 0000-0002-8616-318X
Charles M PearmanUnit of Cardiac Physiology, Manchester Academic Health Sciences Centre, Central Manchester Foundation Trust, 3.14 Core Technology Facility, University of Manchester, Manchester, UK.ORCID 0000-0001-6743-9817
David A EisnerUnit of Cardiac Physiology, Manchester Academic Health Sciences Centre, Central Manchester Foundation Trust, 3.14 Core Technology Facility, University of Manchester, Manchester, UK.ORCID 0000-0002-7002-3748
Andrew W TraffordUnit of Cardiac Physiology, Manchester Academic Health Sciences Centre, Central Manchester Foundation Trust, 3.14 Core Technology Facility, University of Manchester, Manchester, UK.ORCID 0000-0002-2770-445X
Katharine M DibbUnit of Cardiac Physiology, Manchester Academic Health Sciences Centre, Central Manchester Foundation Trust, 3.14 Core Technology Facility, University of Manchester, Manchester, UK.ORCID 0000-0002-9309-3853
Manchester Academic Health Science Centre · GB

Funding

British Heart Foundation FS/09/002/26487British Heart Foundation FS/12/34/29565British Heart Foundation FS/12/57/29717British Heart Foundation FS/14/4/30532British Heart Foundation PG/09/062British Heart Foundation PG/12/89/29970British Heart Foundation PG/15/70/31724
6 · The paper itself

Abstract

key pointsAgeing is associated with an increased risk of cardiovascular disease and arrhythmias, with the most common arrhythmia being found in the atria of the heart. Little is known about how the normal atria of the heart remodel with age and thus why dysfunction might occur. We report alterations to the atrial systolic Ca ABSTRACT: Many cardiovascular diseases, including those affecting the atria, are associated with advancing age. Arrhythmias, including those in the atria, can arise as a result of electrical remodelling or alterations in Ca

Indexed as

Calcium SignalingAnimalsCalcium Channels, L-TypeCells, CulturedHeart AtriaMyocardial ContractionMyocytes, CardiacRyanodine Receptor Calcium Release ChannelSarcoplasmic Reticulum Calcium-Transporting ATPasesSheepCalcium Channels, L-TypeRyanodine Receptor Calcium Release ChannelSarcoplasmic Reticulum Calcium-Transporting ATPasesageatriabufferingcalcium

Identifiers

PMID28752958
PMCPMC5621500
OpenAlexW2741766149

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.