Evidence map›Paper›PMID 28946878›Full record

ArticleJournal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance2017

Extra-cellular expansion in the normal, non-infarcted myocardium is associated with worsening of regional myocardial function after acute myocardial infarction.

Pankaj Garg, David A Broadbent, Peter P Swoboda, James R J Foley, Graham J Fent, Tarique A Musa, David P Ripley, Bara Erhayiem, Laura E Dobson, Adam K McDiarmid and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Observational
  7. Article
  8. Review
  9. Article
  10. Article
  11. Emerging mRNA therapies for cardiac fibrosis.American journal of physiology. Cell physiology · 2024
    Article
  12. The role and mechanisms of microvascular damage in the ischemic myocardium.Cellular and molecular life sciences : CMLS · 2023
    Review
  13. Review
  14. Imaging of heart disease in women: review and case presentation.European journal of nuclear medicine and molecular imaging · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Cardiac fibrosis.Cardiovascular research · 2021
    Review
  19. Article
  20. Journal of Cardiovascular Magnetic Resonance: 2017/2018 in review.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance · 2019
    Review
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

17 authors at 2 institutions in 2 countries.

Pankaj GargDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0002-5483-169X
David A BroadbentDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Peter P SwobodaDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
James R J FoleyDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Graham J FentDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Tarique A MusaDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
David P RipleyDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Bara ErhayiemDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Laura E DobsonDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Adam K McDiarmidDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Philip HaafDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Ananth KidambiDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Saul CrandonDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Pei G ChewDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
R J van der GeestDivision of Image Processing, Leiden University Medical Centre, Leiden, The Netherlands.
John P GreenwoodDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK.
Sven PleinDivision of Biomedical Imaging, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) & Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, LS2 9JT, UK. S.Plein@leeds.ac.uk.
University of Leeds · GBLeiden University Medical Center · NL

Funding

British Heart Foundation FS/10/62/28409
6 · The paper itself

Abstract

backgroundExpansion of the myocardial extracellular volume (ECV) is a surrogate measure of focal/diffuse fibrosis and is an independent marker of prognosis in chronic heart disease. Changes in ECV may also occur after myocardial infarction, acutely because of oedema and in convalescence as part of ventricular remodelling. The objective of this study was to investigate changes in the pattern of distribution of regional (normal, infarcted and oedematous segments) and global left ventricular (LV) ECV using semi-automated methods early and late after reperfused ST-elevation myocardial infarction (STEMI).

methodsFifty patients underwent cardiovascular magnetic resonance (CMR) imaging acutely (24 h-72 h) and at convalescence (3 months). The CMR protocol included: cines, T2-weighted (T2 W) imaging, pre-/post-contrast T1-maps and LGE-imaging. Using T2 W and LGE imaging on acute scans, 16-segments of the LV were categorised as normal, oedema and infarct. 800 segments (16 per-patient) were analysed for changes in ECV and wall thickening (WT).

resultsFrom the acute studies, 325 (40.6%) segments were classified as normal, 246 (30.8%) segments as oedema and 229 (28.6%) segments as infarct. Segmental change in ECV between acute and follow-up studies (Δ ECV) was significantly different for normal, oedema and infarct segments (0.8 ± 6.5%, -1.78 ± 9%, -2.9 ± 10.9%, respectively; P < 0.001). Normal segments which demonstrated deterioration in wall thickening at follow-up showed significantly increased Δ ECV compared with normal segments with preserved wall thickening at follow up (1.82 ± 6.05% versus -0.10 ± 6.88%, P < 0.05).

conclusionFollowing reperfused STEMI, normal myocardium demonstrates subtle expansion of the extracellular volume at 3-month follow up. Segmental ECV expansion of normal myocardium is associated with worsening of contractile function.

Indexed as

EdemaFemaleFibrosisHeartHeart VentriclesHumansMagnetic Resonance ImagingMaleMiddle AgedMyocardial InfarctionMyocardiumProspective StudiesUnited KingdomVentricular Dysfunction, LeftAcute myocardial infarctionCardiovascular imaging agents/techniquesCT and MRIExtracellular matrix

Identifiers

PMID28946878
PMCPMC5613621
OpenAlexW2760127139

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.