Evidence map›Paper›PMID 35295404›Full record

ArticleMathematics (Basel, Switzerland)2022

An Integrated Workflow for Building Digital Twins of Cardiac Electromechanics-A Multi-Fidelity Approach for Personalising Active Mechanics.

Alexander Jung, Matthias A F Gsell, Christoph M Augustin, Gernot Plank

Open access · goldAbstract read
In one paragraph

Article in Mathematics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
7.4field-weighted citation impact, top 2% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Enhancing randomized clinical trials with digital twins.NPJ systems biology and applications · 2025
    Review
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  15. Digital Twins of Biological Systems: A Narrative Review.IEEE open journal of engineering in medicine and biology · 2024
    Article
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  17. Review
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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

4 authors at 2 institutions in 1 country.

Alexander JungGottfried Schatz Research Center for Cell Signaling, Metabolism and Aging-Division of Biophysics, Medical University Graz, 8010 Graz, Austria.ORCID https://orcid.org/0000-0002-0723-4403
Matthias A F GsellGottfried Schatz Research Center for Cell Signaling, Metabolism and Aging-Division of Biophysics, Medical University Graz, 8010 Graz, Austria.ORCID https://orcid.org/0000-0001-7742-8193
Christoph M AugustinGottfried Schatz Research Center for Cell Signaling, Metabolism and Aging-Division of Biophysics, Medical University Graz, 8010 Graz, Austria.ORCID https://orcid.org/0000-0001-6341-4014
Gernot PlankGottfried Schatz Research Center for Cell Signaling, Metabolism and Aging-Division of Biophysics, Medical University Graz, 8010 Graz, Austria.ORCID https://orcid.org/0000-0002-7380-6908
Medical University of Graz · ATUniversity of Graz · AT

Funding

Austrian Science Fund FWF I 2760Austrian Science Fund FWF I 4652
6 · The paper itself

Abstract

Personalised computer models of cardiac function, referred to as cardiac digital twins, are envisioned to play an important role in clinical precision therapies of cardiovascular diseases. A major obstacle hampering clinical translation involves the significant computational costs involved in the personalisation of biophysically detailed mechanistic models that require the identification of high-dimensional parameter vectors. An important aspect to identify in electromechanics (EM) models are active mechanics parameters that govern cardiac contraction and relaxation. In this study, we present a novel, fully automated, and efficient approach for personalising biophysically detailed active mechanics models using a two-step multi-fidelity solution. In the first step, active mechanical behaviour in a given 3D EM model is represented by a purely phenomenological, low-fidelity model, which is personalised at the organ scale by calibration to clinical cavity pressure data. Then, in the second step, median traces of nodal cellular active stress, intracellular calcium concentration, and fibre stretch are generated and utilised to personalise the desired high-fidelity model at the cellular scale using a 0D model of cardiac EM. Our novel approach was tested on a cohort of seven human left ventricular (LV) EM models, created from patients treated for aortic coarctation (CoA). Goodness of fit, computational cost, and robustness of the algorithm against uncertainty in the clinical data and variations of initial guesses were evaluated. We demonstrate that our multi-fidelity approach facilitates the personalisation of a biophysically detailed active stress model within only a few (2 to 4) expensive 3D organ-scale simulations-a computational effort compatible with clinical model applications.

Indexed as

cardiac mechanicsglobal sensitivity analysishuman left ventricular functionparameter estimationpatient-specific modellingprecision medicine

Identifiers

PMID35295404
PMCPMC7612499
OpenAlexW4221063829

What OpenQuestion holds

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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.