Evidence map›Paper›PMID 40745225›Full record

ArticleCommunications medicine2025

Advanced 4-chamber echocardiography techniques enable clinically matched precise characterization of heart disease progression in mice.

Ege Kacira, Mariam F Oueis, Nawal H Tamimi, Sarah L Sturgill, Xianyao Xu, Thomas J Hund, Mark T Ziolo, Yuchi Han, Isabelle Deschênes, Ji-Dong Fu

Abstract read
In one paragraph

Article in Communications medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Ege KaciraDepartment of Physiology and Cell Biology, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, The Ohio State University, Columbus, OH, USA.
Mariam F OueisDepartment of Physiology and Cell Biology, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, The Ohio State University, Columbus, OH, USA.
Nawal H TamimiDepartment of Physiology and Cell Biology, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, The Ohio State University, Columbus, OH, USA.
Sarah L SturgillDepartment of Physiology and Cell Biology, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, The Ohio State University, Columbus, OH, USA.
Xianyao XuDepartments of Internal Medicine and Biomedical Engineering, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Thomas J HundDepartments of Internal Medicine and Biomedical Engineering, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Mark T ZioloDepartment of Physiology and Cell Biology, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, The Ohio State University, Columbus, OH, USA.
Yuchi HanCardiovascular Division, Department of Internal Medicine, The Dorothy M. Davis Heart and Lung Research Institute, Wexner Medical Center, The Ohio State University, Columbus, OH, USA.
Isabelle DeschênesDepartment of Physiology and Cell Biology, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, The Ohio State University, Columbus, OH, USA.
Ji-Dong FuDepartment of Physiology and Cell Biology, The Dorothy M. Davis Heart and Lung Research Institute, Frick Center for Heart Failure and Arrhythmia, The Ohio State University, Columbus, OH, USA. Jidong.fu@osumc.edu.ORCID http://orcid.org/0000-0003-2797-5193

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
Biophysical Modulation of Cardiac Ion Channels by MicroRNAR01HL139006 · NHLBI · OHIO STATE UNIVERSITY · PI Isabelle Deschenes, Jidong Fu · 2017 to 2026
$5.1M
BAT as a therapeutic for the metabolic and cardiac dysfunction with senescence.R01AG060542 · NIA · OHIO STATE UNIVERSITY · PI COEN, PAUL MARTIN, STANFORD, KRISTIN I · 2019 to 2023
$3.0M
Distinct Ion Channel Pools and Intercalated Disk Nanoscale Structure Regulate Cardiac ConductionR01HL165751 · NHLBI · OHIO STATE UNIVERSITY · PI Thomas Jeffrey Hund, Rengasayee Veeraraghavan · 2023 to 2026
$2.9M
Imaging-based Indentification of Premature Ventricular Contraction-mediatedR01HL148103 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI HAN, YUCHI · 2020 to 2025
$2.8M
Role of TREK-1 in modulating cardiac excitability and arrhythmiaR01HL156652 · NHLBI · OHIO STATE UNIVERSITY · PI HUND, THOMAS JEFFREY · 2021 to 2024
$1.7M
Novel role for the spectrin cytoskeleton in regulation of cardiac fibroblast activity, long-range communication and injury-induced fibrosisR01HL171689 · NHLBI · OHIO STATE UNIVERSITY · PI Thomas Jeffrey Hund · 2024 to 2026
$1.6M
A novel mouse model to distinguish the specific physiological significance of RNAi and biophysical mechanisms of microRNAR21OD031965 · OD · OHIO STATE UNIVERSITY · PI FU, JIDONG · 2022 to 2023
$433k
American Heart Association (American Heart Association, Inc.) 24IPA1267153NCI NIH HHS P30 CA016058NHLBI NIH HHS R01 HL139006NHLBI NIH HHS R01 HL148103NHLBI NIH HHS R01 HL156652NHLBI NIH HHS R01 HL165751NHLBI NIH HHS R01 HL171689NIA NIH HHS R01 AG060542NIH HHS R21 OD031965U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL139006
6 · The paper itself

Abstract

backgroundTransthoracic echocardiography remains the primary non-invasive method for assessing cardiac function in clinical practice. However, technical challenges in acquiring accurate apical 4-chamber-long-axis (A4CLAX) views have historically limited mouse studies to left ventricle (LV) assessment using parasternal short-axis (SAX) M-mode imaging.

methodsTo overcome this limitation, we developed an A4CLAX imaging approach for mice and performed a comparative analysis with established echocardiographic methods to assess cardiac function in healthy mouse hearts. To evaluate the utility of A4CLAX in detecting disease progression, we longitudinally monitored cardiac function of C57BL/6 N mice (male and female) following severe transverse aortic constriction (TAC), using both long-axis biplane (LAX-BP) and conventional SAX M-mode assays.

resultsHere we show that LAX-BP echocardiography demonstrates volumetric accuracy comparable to cardiac magnetic resonance (CMR) and detects significant LV functional decline within the first week post-TAC-changes that are not clearly captured by M-mode imaging. Importantly, A4CLAX further enables clinically relevant Doppler assessments, allowing detection of mitral valve regurgitation, restrictive filling patterns, and desynchronized valve motion. It also facilitates right ventricle (RV) functional evaluation and improved atrial visualization, revealing progressive enlargement of the left atrial (LA) and left atrial appendage (LAA) associated with worsening diastolic function.

conclusionsThe A4CLAX imaging approach provides clinically comparable, comprehensive echocardiographic evaluation in murine models and offers improved sensitivity for detecting subtle changes in cardiac performance during disease progression.

Identifiers

PMID40745225
PMCPMC12314085

What Socratic holds

Textmetadata
LicenceCC BY-NC-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.