Evidence map›Paper›PMID 31653449›Full record

ArticleBiophysical journal2019

Microstructurally Motivated Constitutive Modeling of Heart Failure Mechanics.

Abdallah I Hasaballa, Vicky Y Wang, Gregory B Sands, Alexander J Wilson, Alistair A Young, Ian J LeGrice, Martyn P Nash

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. The Heart by Numbers.Biophysical journal · 2019
    Article
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

7 authors at 4 institutions in 3 countries.

Abdallah I HasaballaAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Vicky Y WangAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Gregory B SandsAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand; Department of Physiology, University of Auckland, Auckland, New Zealand.
Alexander J WilsonRadiological Sciences Laboratory, School of Medicine, Stanford University, Stanford, California.
Alistair A YoungAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand; Department of Biomedical Engineering, King's College London, London, United Kingdom.
Ian J LeGriceAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand; Department of Physiology, University of Auckland, Auckland, New Zealand.
Martyn P NashAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand; Department of Engineering Science, University of Auckland, Auckland, New Zealand. Electronic address: martyn.nash@auckland.ac.nz.
University of Auckland · NZAuckland University of Technology · NZKing's College London · GBStanford University · US

Funding

The Cardiac Atlas ProjectR01HL121754 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MCCULLOCH, ANDREW D., OMENS, JEFFREY H. · 2014 to 2023
$5.0M
NHLBI NIH HHS R01 HL121754
6 · The paper itself

Abstract

Heart failure (HF) is one of the leading causes of death worldwide. HF is associated with substantial microstructural remodeling, which is linked to changes in left ventricular geometry and impaired cardiac function. The role of myocardial remodeling in altering the mechanics of failing hearts remains unclear. Structurally based constitutive modeling provides an approach to improve understanding of the relationship between biomechanical function and tissue organization in cardiac muscle during HF. In this study, we used cardiac magnetic resonance imaging and extended-volume confocal microscopy to quantify the remodeling of left ventricular geometry and myocardial microstructure of healthy and spontaneously hypertensive rat hearts at the ages of 12 and 24 months. Passive cardiac mechanical function was characterized using left ventricular pressure-volume compliance measurements. We have developed a, to our knowledge, new structurally based biomechanical constitutive equation built on parameters quantified directly from collagen distributions observed in confocal images of the myocardium. Three-dimensional left ventricular finite element models were constructed from subject-specific in vivo magnetic resonance imaging data. The structurally based constitutive equation was integrated into geometrically subject-specific finite element models of the hearts and used to investigate the underlying mechanisms of ventricular dysfunction during HF. Using a single pair of material parameters for all hearts, we were able to produce compliance curves that reproduced all of the experimental compliance measurements. The value of this study is not limited to reproducing the mechanical behavior of healthy and diseased hearts, but it also provides important insights into the structure-function relationship of diseased myocardium that will help pave the way toward more effective treatments for HF.

Indexed as

Models, CardiovascularAnimalsDisease ProgressionHeart FailureMyocardiumPressureRatsVentricular Dysfunction, Left

Identifiers

PMID31653449
PMCPMC6990375
OpenAlexW2979897691

What OpenQuestion holds

Textmetadata
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.