Evidence map›Paper›PMID 29998358›Full record

ArticleJournal of cardiovascular translational research2018

Left Ventricular Diastolic Myocardial Stiffness and End-Diastolic Myofibre Stress in Human Heart Failure Using Personalised Biomechanical Analysis.

Zhinuo J Wang, Vicky Y Wang, Chris P Bradley, Martyn P Nash, Alistair A Young, J Jane Cao

Abstract read
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In one paragraph

Article in Journal of cardiovascular translational research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 53 citations in OpenAlex.

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  11. Effects of myocardial sheetlet sliding on left ventricular function.Biomechanics and modeling in mechanobiology · 2023
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  19. Human biventricular electromechanical simulations on the progression of electrocardiographic and mechanical abnormalities in post-myocardial infarction.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2021
    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

6 authors at 2 institutions in 2 countries.

Zhinuo J WangAuckland Bioengineering Institute, University of Auckland, Level 6 Reception, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.ORCID 0000-0001-5325-909X
Vicky Y WangAuckland Bioengineering Institute, University of Auckland, Level 6 Reception, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.
Chris P BradleyAuckland Bioengineering Institute, University of Auckland, Level 6 Reception, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.
Martyn P NashAuckland Bioengineering Institute, University of Auckland, Level 6 Reception, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand. martyn.nash@auckland.ac.nz.
Alistair A YoungAuckland Bioengineering Institute, University of Auckland, Level 6 Reception, 70 Symonds Street, Grafton, Auckland, 1010, New Zealand.
J Jane CaoThe Heart Center, St Francis Hospital, Roslyn, NY, USA.
University of Auckland · NZSt. Francis Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the aetiology of heart failure with preserved (HFpEF) and reduced (HFrEF) ejection fraction requires knowledge of biomechanical factors such as diastolic myocardial stiffness and stress. Cine CMR images and intra-ventricular pressure recordings were acquired in 8 HFrEF, 11 HFpEF and 5 control subjects. Diastolic myocardial stiffness was estimated using biomechanical models and found to be greater in HFrEF (6.4 ± 1.2 kPa) than HFpEF (2.7 ± 0.6 kPa, p < 0.05) and also greater than control (1.2 ± 0.4 kPa, p < 0.005). End-diastolic mid-ventricular myofibre stress derived from the personalised biomechanics model was higher in HFrEF (2.9 ± 0.3 kPa) than control (0.9 ± 0.3 kPa, p < 0.01). Chamber stiffness, measured from the slope of the diastolic pressure-volume relationship, is determined by the intrinsic tissue properties as well as the size and shape of the heart, and was unable to distinguish between any of the three groups (p > 0.05). Personalised biomechanical analysis may provide more specific information about myocardial mechanical behaviour than global chamber indices, which are confounded by variations in ventricular geometry.

Indexed as

AgedBiomechanical PhenomenaCardiac CatheterizationDiastoleFemaleHeart FailureHeart VentriclesHumansMagnetic Resonance Imaging, CineMaleMiddle AgedMyocardial ContractionProspective StudiesStroke VolumeSystoleVentricular Function, LeftBiomechanicsCatheterisationCine CMRHeart failureMyocardial tissue stiffnessMyofibre stress

Identifiers

PMID29998358
OpenAlexW2862312888

What OpenQuestion holds

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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.