Evidence map›Paper›PMID 37305211›Full record

ArticleNature cardiovascular research2022

Blood flow modeling reveals improved collateral artery performance during the regenerative period in mammalian hearts.

Suhaas Anbazhakan, Pamela E Rios Coronado, Ana Natalia L Sy-Quia, Lek Wei Seow, Aubrey M Hands, Mingming Zhao, Melody L Dong, Martin R Pfaller, Zhainib A Amir, Brian C Raftrey and 10 more

Open access · greenAbstract read
In one paragraph

Article in Nature cardiovascular research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

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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

20 authors at 3 institutions in 1 country.

Suhaas AnbazhakanDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Pamela E Rios CoronadoDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Ana Natalia L Sy-QuiaDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Lek Wei SeowDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Aubrey M HandsDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Mingming ZhaoDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305.
Melody L DongDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Martin R PfallerDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Zhainib A AmirDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Brian C RaftreyDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Christopher K CookDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Gaetano D'AmatoDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Xiaochen FanDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Ian M WilliamsDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Sawan K JhaDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Daniel BernsteinDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305.
Koen NiemanDepartments of Cardiovascular Medicine and Radiology, School of Medicine, Stanford University, Stanford, CA, 94305, USA.
Anca M PașcaDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA, 94305.
Alison L MarsdenDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Kristy Red HorseDepartment of Biology, Stanford University, Stanford, CA 94305, USA.
Stanford University · USCardiovascular Institute of the South · USHoward Hughes Medical Institute · US

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Mechanotransduction and transcriptional regulation during artery developmentR01HL128503 · NHLBI · STANFORD UNIVERSITY · PI Mary Red-Horse · 2015 to 2026
$5.8M
Endothelial-pericyte interactions in the pathogenesis of pulmonary arterial hypertensionR01HL139664 · NHLBI · STANFORD UNIVERSITY · PI DE JESUS PEREZ, VINICIO A · 2018 to 2025
$4.7M
Comprehensive CT Guided Coronary Artery Bypass Graft SurgeryR01HL141712 · NHLBI · STANFORD UNIVERSITY · PI NIEMAN, KOEN · 2019 to 2023
$3.5M
International Consortium for Multimodality Phenotyping in Adults with Non-compactionR01HL146754 · NHLBI · STANFORD UNIVERSITY · PI NIEMAN, KOEN, TANG, WAI HONG WILSON · 2020 to 2023
$3.0M
Enabling reliable cardiovascular simulations via uncertainty quantificationR01EB018302 · NIBIB · STANFORD UNIVERSITY · PI MARSDEN, ALISON L · 2016 to 2019
$1.7M
Stanford Undergraduate URM Summer Cardiovascular Research ProgramR25HL147666 · NHLBI · STANFORD UNIVERSITY · PI VINICIO A DE JESUS PEREZ, Mary Red-Horse · 2019 to 2026
$1.0M
NHLBI NIH HHS R01 HL128503NHLBI NIH HHS R01 HL139664NHLBI NIH HHS R01 HL141712NHLBI NIH HHS R01 HL146754NHLBI NIH HHS R25 HL147666NIBIB NIH HHS R01 EB018302NIGMS NIH HHS T32 GM007276
6 · The paper itself

Abstract

Collateral arteries bridge opposing artery branches, forming a natural bypass that can deliver blood flow downstream of an occlusion. Inducing coronary collateral arteries could treat cardiac ischemia, but more knowledge on their developmental mechanisms and functional capabilities is required. Here we used whole-organ imaging and three-dimensional computational fluid dynamics modeling to define spatial architecture and predict blood flow through collaterals in neonate and adult mouse hearts. Neonate collaterals were more numerous, larger in diameter and more effective at restoring blood flow. Decreased blood flow restoration in adults arose because during postnatal growth coronary arteries expanded by adding branches rather than increasing diameters, altering pressure distributions. In humans, adult hearts with total coronary occlusions averaged 2 large collaterals, with predicted moderate function, while normal fetal hearts showed over 40 collaterals, likely too small to be functionally relevant. Thus, we quantify the functional impact of collateral arteries during heart regeneration and repair-a critical step toward realizing their therapeutic potential.

Identifiers

PMID37305211
PMCPMC10256232
OpenAlexW4290860520

What OpenQuestion holds

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Registered trials

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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.