Evidence map›Paper›PMID 41573820›Full record

ArticlebioRxiv : the preprint server for biology2025

A Microstructurally-Motivated Framework to Study Autoregulation in the Coronary Circulation.

Matthew J Eden, Hamidreza Gharahi, Victoria E Sturgess, Domingo E Uceda, Seungik Baek, Daniel A Beard, Johnathan D Tune, C Alberto Figueroa

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Matthew J EdenDepartment of Surgery, Section of Vascular Surgery, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-9409-8974
Hamidreza GharahiDepartment of Surgery, Section of Vascular Surgery, University of Michigan, Ann Arbor, MI, USA.
Victoria E SturgessDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-7413-8657
Domingo E UcedaDepartment of Surgery, Section of Vascular Surgery, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-9916-8898
Seungik BaekDepartment of Mechanical Engineering, Michigan State University, East Lansing, MI, USA.ORCID 0000-0003-2007-339X
Daniel A BeardDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID 0000-0003-0974-2353
Johnathan D TuneDepartment of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX, USA.ORCID 0000-0003-2959-0801
C Alberto FigueroaDepartment of Surgery, Section of Vascular Surgery, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-3934-6506

Funding

Disentangling the Mechanisms of Coronary Blood Flow Regulation through Multi-scale ModelingR01HL158723 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BEARD, DANIEL A, FIGUEROA, CARLOS ALBERTO · 2022 to 2025
$2.7M
Image-based Multi-scale Modeling Framework of the Cardiopulmonary System: Longitudinal Calibration and Assessment of Therapies in Pediatric Pulmonary HypertensionU01HL135842 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BAEK, SEUNGIK, DORFMAN, ADAM LEE · 2017 to 2020
$2.3M
Multi-scale systems analysis of blood pressure control and hypertensionR01HL139813 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BEARD, DANIEL A · 2018 to 2021
$2.0M
NHLBI NIH HHS R01 HL139813NHLBI NIH HHS R01 HL158723NHLBI NIH HHS U01 HL135842
6 · The paper itself

Abstract

Coronary autoregulation maintains relatively constant myocardial flow over a wide range of perfusion pressures through myogenic, shear-dependent, and metabolic control mechanisms. Understanding this phenomenon is challenging due to the coupled nature of these mechanisms and their heterogeneous effects throughout the coronary tree. In this study we developed a novel microstructurally-motivated model of coronary autoregulation based on constrained mixture theory, with anatomical and structural parameters calibrated through a homeostatic optimization framework. Autoregulation was simulated at three myocardial depths (subepicardium, midwall, and subendocardium), with the calibrated model accurately reproducing baseline hemodynamics and autoregulatory responses. For changes in epicardial pressure, our model reproduced experimentally measured subendocardium-to-subepicardium flow ratios (ENDO/EPI) and changes in vessel diameter, demonstrating its predictive capability. Furthermore, we extended Womersley's theory to simulate phasic coronary hemodynamics with a time-varying intramyocardial pressure. This microstructurally-motivated framework provides a mechanistic foundation for investigating coronary autoregulation and long-term vascular growth and remodeling in pathphysiological conditions.

Identifiers

PMID41573820
PMCPMC12822814

What Socratic holds

Textmetadata
LicenceCC BY-ND
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.