Evidence map›Paper›PMID 41953669›Full record

ArticleFrontiers in cardiovascular medicine2026

Biomechanical index for predicting the risk of acute coronary syndrome.

Michael J Johnson, Michael R A Abdelmalik, Gilwoo Choi, Shaolie S Hossain, Bon-Kwon Koo, Sabrina R Lynch, Kersten Petersen, Gregory J Rodin, Michiel Schaap, Charles A Taylor and 2 more

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Michael J JohnsonOden Institute, University of Texas, Austin, TX, United States.
Michael R A AbdelmalikDepartment of Mechanical Engineering, Eindhoven University of Technology, Eindhoven, Netherlands.
Gilwoo ChoiHeartFlow, Inc., Mountain View, CA, United States.
Shaolie S HossainOden Institute, University of Texas, Austin, TX, United States.
Bon-Kwon KooDepartment of Internal Medicine and Cardiovascular Center, Seoul National University Hospital, Seoul, Republic of Korea.
Sabrina R LynchHeartFlow, Inc., Mountain View, CA, United States.
Kersten PetersenHeartFlow, Inc., Mountain View, CA, United States.
Gregory J RodinOden Institute, University of Texas, Austin, TX, United States.
Michiel SchaapHeartFlow, Inc., Mountain View, CA, United States.
Charles A TaylorOden Institute, University of Texas, Austin, TX, United States.
Christopher K ZarinsHeartFlow, Inc., Mountain View, CA, United States.
Thomas J R HughesOden Institute, University of Texas, Austin, TX, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: A patient-specific biomechanical model for quantifying the stress state within coronary atherosclerotic lesions for the noninvasive prediction of acute coronary syndrome (ACS) has not been established. Methods: Sixty-nine patients with clearly documented ACS and available coronary computed tomographic angiography (cCTA) acquired between 1 month and 2 years before the development of ACS were included. In 63 culprit and 146 nonculprit lesions, lumen geometry, the presence of adverse plaque characteristics (APC), and hemodynamic parameters were evaluated using previously described methods. A novel biomechanical metric, denoted as the Cap Vulnerability Index (CVI), was calculated from cCTA data using computational solid and fluid mechanics and compared to anatomic, plaque and hemodynamics variables for the ability to discriminate culprit from nonculprit lesions. Results: Culprit lesions had a greater diameter stenosis, lesion length, more adverse plaque and hemodynamic characteristics and a greater CVI. Among all parameters evaluated, CVI had the highest AUC (0.75), was the strongest independent predictor for ACS and was comparable to previously described statistical models combining anatomy, plaque and hemodynamic variables. Conclusions: Noninvasive biomechanical assessment of coronary plaques using computational solid and fluid mechanics may improve identification of culprit lesions for ACS and simplify the interpretation of risk factors for individual lesions.

Indexed as

biomechanical modelcap vulnerability index (CVI)computational medicinecoronary artery diseasecoronary computed tomographic angiogram (CCTA)FFR-CTfinite element stress analysisvulnerable plaque

Identifiers

PMID41953669
PMCPMC13053513

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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.