Evidence map›Paper›PMID 40791328›Full record

ArticlebioRxiv : the preprint server for biology2025

Non-invasive Free-breathing Gating-free Extracellular Cellular Volume Quantification for Repetitive Myocardial Fibrosis Evaluation in Rodents.

Devin R E Cortes, Thomas Becker-Szurszewski, Sean Hartwick, Muhammad Wahab Amjad, Soheb Anwar Mohammed, Xucai Chen, John J Pacella, Anthony G Christodoulou, Yijen L Wu

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

9 authors.

Devin R E CortesDepartment of Pediatrics, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Thomas Becker-SzurszewskiDepartment of Pediatrics, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Sean HartwickDepartment of Pediatrics, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Muhammad Wahab AmjadCenter for Ultrasound Molecular Imaging and Therapeutics, Heart and Vascular Medicine Institute, University of Pittsburgh; Pittsburgh, PA, USA.
Soheb Anwar MohammedCenter for Ultrasound Molecular Imaging and Therapeutics, Heart and Vascular Medicine Institute, University of Pittsburgh; Pittsburgh, PA, USA.
Xucai ChenCenter for Ultrasound Molecular Imaging and Therapeutics, Heart and Vascular Medicine Institute, University of Pittsburgh; Pittsburgh, PA, USA.
John J PacellaCenter for Ultrasound Molecular Imaging and Therapeutics, Heart and Vascular Medicine Institute, University of Pittsburgh; Pittsburgh, PA, USA.
Anthony G ChristodoulouDepartment of Radiological Sciences, David Geffen School of Medicine, at UCLA, Los Angeles, CA, USA.
Yijen L WuDepartment of Pediatrics, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Funding

Gating-Free Ultra-Fast Fetal Cardiac MRI with Sub-Nyquist Sampling for Live in Utero Imaging and Cardiovascular Phenotyping of Fetal MiceR21EB023507 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WU, YIJEN LIN · 2019 to 2020
$452k
NIBIB NIH HHS R21 EB023507
6 · The paper itself

Abstract

Background: Interstitial myocardial fibrosis is a crucial pathological feature of many cardiovascular disorders. Myocardial fibrosis resulting in extracellular volume (ECV) expansion can be non-invasively quantified by cardiac MRI (CMR) with T Methods: To address these challenges, the objective of this study is to establish a fast, free-breathing, and gating-free ECV procedure with a non-invasive subcutaneous catheter for in-scanner Gd administration that can allow longitudinal repetitive ECV evaluations in rodent models. This is achieved by (1) IntraGate sequence for free-breathing gating-free cardiac imaging, (2) non-invasive subcutaneous in-scanner Gd administration, and (3) fast T Results: We have successfully established a non-invasive fast ECV quantification protocol to enable longitudinal repetitive ECV quantifications in rodents. Non-invasive subcutaneous Gd bolus administration induced reasonable dynamic contrast enhancement (DCE) time course reaching a steady state in ~ 20 min for stable T Conclusion: We have established a simple, fast, non-invasive, and robust CMR protocol in rodents that can enable longitudinal repetitive ECV quantifications for cardiovascular disease progression. It can be used to monitor disease regression with interventions.

Indexed as

Extracellular volume (ECV)fibrosisrodent

Identifiers

PMID40791328
PMCPMC12338535

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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.