Evidence map›Paper›PMID 42779418›Full record

ArticlePhysiological reports2026

Prospective echocardiographic characterization of postnatal cardiac development in C57BL/6 mice: Strain analysis between birth and adulthood.

Sehjin Jo, George Spyropoulos, Logan G Hart, Taylor A Covington, Arvind K Pandey, Thomas Michel, Fotios Spyropoulos

Abstract read
In one paragraph

Article in Physiological reports, 2026. 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

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

7 authors.

Sehjin JoDivision of Newborn Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
George SpyropoulosCardiac Critical Care Medicine Division, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Logan G HartDivision of Newborn Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Taylor A CovingtonCardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Harvard University Boston, Boston, Massachusetts, USA.
Arvind K PandeyCardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Harvard University Boston, Boston, Massachusetts, USA.
Thomas MichelCardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Harvard University Boston, Boston, Massachusetts, USA.
Fotios SpyropoulosDivision of Newborn Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-1663-9701

Funding

Hydrogen peroxide in endothelial function and dysfunctionR01HL152173 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHEL, THOMAS · 2021 to 2024
$2.2M
Dynamic tissue-specific modulation of redox stress using chemogeneticsR33HL157918 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHEL, THOMAS · 2021 to 2022
$1.0M
Oxidative Stress and Mitochondrial Dysfunction in Chemogenetic Heart FailureK08HL168240 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Fotios Spyropoulos · 2023 to 2026
$735k
Chemogenetic approaches to define the roles of redox dysfunction in the cardiomyopathy of agingR21AG063073 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHEL, THOMAS · 2019 to 2020
$480k
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) K08HL168240HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL152173HHS | NIH | National Institute on Aging (NIA) R21AG063073HHS | NIH | NHLBI | NHLBI Division of Intramural Research (DIR) R33HL157918NHLBI NIH HHS K08 HL168240NHLBI NIH HHS R01 HL152173NHLBI NIH HHS R33 HL157918NIA NIH HHS R21 AG063073
6 · The paper itself

Abstract

Echocardiography is critical for characterizing murine models of cardiovascular disease, yet normative data for the early postnatal period, particularly advanced functional metrics like myocardial strain, remain undefined. This developmental window features rapid cardiac maturation and is central to modeling congenital and neonatal heart disease. To establish normative, sex-specific trajectories of cardiac structure and function between birth and adulthood, we performed prospective high-frequency echocardiography in C57BL/6 mice at postnatal day 0 (P0), P8, P21, and week 8 (Wk8). Somatic growth and left ventricular structural dimensions increased progressively from P0 to Wk8. This structural maturation was accompanied by lower ejection fraction and fractional shortening, attributable to geometric remodeling. In contrast, speckle-tracking strain analysis revealed that intrinsic myocardial deformation, including global circumferential and radial strain, remained stable throughout postnatal development. Importantly, we identified sexual dimorphism emerging during late adolescence; by Wk8, males exhibited significantly greater longitudinal and radial strain magnitudes than females. This study provides the first prospective, myocardial strain-based echocardiographic characterization of murine cardiac development between birth and adulthood, identifying P21-Wk8 as a critical window for sex-specific cardiac mechanics. These normative trajectories provide a translational framework for interpreting cardiac phenotypes in preclinical models of congenital, pediatric, and developmental cardiovascular disease.

Indexed as

EchocardiographyHeartAnimalsAnimals, NewbornFemaleMaleMiceMice, Inbred C57BLSex CharacteristicsC57BL/6echocardiographymyocardial strainpostnatal developmentsex‐dependent differences

Identifiers

PMID42779418
PMCPMC13601988

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.