Evidence map›Paper›PMID 38995488›Full record

ArticleBiomechanics and modeling in mechanobiology2024

Modeling cardiac microcirculation for the simulation of coronary flow and 3D myocardial perfusion.

Giovanni Montino Pelagi, Francesco Regazzoni, Jacques M Huyghe, Andrea Baggiano, Marco Alì, Silvia Bertoluzza, Giovanni Valbusa, Gianluca Pontone, Christian Vergara

Abstract read
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Article in Biomechanics and modeling in mechanobiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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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

9 authors.

Giovanni Montino PelagiLABS, Dipartimento di Chimica, Materiali e Ingegneria Chimica Giulio Natta, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milan, 20133, Italy. giovanni.montino@polimi.it.
Francesco RegazzoniMOX, Dipartimento di Matematica, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milan, 20133, Italy.
Jacques M HuygheSchool of Engineering, University of Limerick, Limerick, V94 T9PX, Ireland.
Andrea BaggianoPerioperative Cardiology and Cardiovascular Imaging Department, Centro Cardiologico Monzino IRCCS, Via Carlo Parea 4, Milan, 20138, Italy.
Marco AlìBracco Imaging S.p.A., Via Caduti di Marcinelle 13, Milan, 20134, Italy.
Silvia BertoluzzaIMATI, CNR, Pavia, Italy.
Giovanni ValbusaBracco Imaging S.p.A., Via Caduti di Marcinelle 13, Milan, 20134, Italy.
Gianluca PontonePerioperative Cardiology and Cardiovascular Imaging Department, Centro Cardiologico Monzino IRCCS, Via Carlo Parea 4, Milan, 20138, Italy.
Christian VergaraLABS, Dipartimento di Chimica, Materiali e Ingegneria Chimica Giulio Natta, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milan, 20133, Italy.

Funding

PNRR Italian Research Funding Missione 4, DM226/2021
6 · The paper itself

Abstract

Accurate modeling of blood dynamics in the coronary microcirculation is a crucial step toward the clinical application of in silico methods for the diagnosis of coronary artery disease. In this work, we present a new mathematical model of microcirculatory hemodynamics accounting for microvasculature compliance and cardiac contraction; we also present its application to a full simulation of hyperemic coronary blood flow and 3D myocardial perfusion in real clinical cases. Microvasculature hemodynamics is modeled with a compliant multi-compartment Darcy formulation, with the new compliance terms depending on the local intramyocardial pressure generated by cardiac contraction. Nonlinear analytical relationships for vessels distensibility are included based on experimental data, and all the parameters of the model are reformulated based on histologically relevant quantities, allowing a deeper model personalization. Phasic flow patterns of high arterial inflow in diastole and venous outflow in systole are obtained, with flow waveforms morphology and pressure distribution along the microcirculation reproduced in accordance with experimental and in vivo measures. Phasic diameter change for arterioles and capillaries is also obtained with relevant differences depending on the depth location. Coronary blood dynamics exhibits a disturbed flow at the systolic onset, while the obtained 3D perfusion maps reproduce the systolic impediment effect and show relevant regional and transmural heterogeneities in myocardial blood flow (MBF). The proposed model successfully reproduces microvasculature hemodynamics over the whole heartbeat and along the entire intramural vessels. Quantification of phasic flow patterns, diameter changes, regional and transmural heterogeneities in MBF represent key steps ahead in the direction of the predictive simulation of cardiac perfusion.

Indexed as

Computer SimulationCoronary CirculationMicrocirculationModels, CardiovascularCoronary VesselsHeartHemodynamicsHumansImaging, Three-DimensionalMyocardiumComputational modelingCoronary artery diseaseCoronary pressureFractional flow reserveMyocardial blood flowMyocardial perfusion

Identifiers

PMID38995488
PMCPMC11554812

What Socratic 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 Socratic graph.