Evidence map›Paper›PMID 41694667›Full record

ArticleBiochemistry and biophysics reports2026

Microstructural analysis of the human ventricular myocardium in subjects with Type-II Diabetes.

Haritha Keerthi, Salma P Ramirez, Mario M Corral, Ivana Hernandez de Estrada, Zayra N Dorado, C Gobinath, Aibhlin E Esparza, Wilson Poon, Binata Joddar

Abstract read
In one paragraph

Article in Biochemistry and biophysics 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

9 authors.

Haritha KeerthiEnvironmental Science and Engineering, University of Texas at El Paso (UTEP), El Paso, TX, 79902, USA.
Salma P RamirezBiomedical Engineering Program, Department of Metallurgical, Materials, and Biomedical Engineering, UTEP, El Paso, TX, 79902, USA.
Mario M CorralBiomedical Engineering Program, Department of Metallurgical, Materials, and Biomedical Engineering, UTEP, El Paso, TX, 79902, USA.
Ivana Hernandez de EstradaInspired Materials & Stem-Cell Based Tissue Engineering Laboratory, Chemical, Biological and Environmental Engineering, Oregon State University (OSU), 308 Gleeson Hall, 2115 SW Campus Way, Corvallis, OR, 97331, USA.
Zayra N DoradoMetallurgical and Materials Engineering, Department of Metallurgical, Materials, and Biomedical Engineering, UTEP, El Paso, TX, 79902, USA.
C GobinathInspired Materials & Stem-Cell Based Tissue Engineering Laboratory, Chemical, Biological and Environmental Engineering, Oregon State University (OSU), 308 Gleeson Hall, 2115 SW Campus Way, Corvallis, OR, 97331, USA.
Aibhlin E EsparzaBiomedical Engineering Program, Department of Metallurgical, Materials, and Biomedical Engineering, UTEP, El Paso, TX, 79902, USA.
Wilson PoonBiomedical Engineering Program, Department of Metallurgical, Materials, and Biomedical Engineering, UTEP, El Paso, TX, 79902, USA.
Binata JoddarInspired Materials & Stem-Cell Based Tissue Engineering Laboratory, Chemical, Biological and Environmental Engineering, Oregon State University (OSU), 308 Gleeson Hall, 2115 SW Campus Way, Corvallis, OR, 97331, USA.

Funding

Development and validation of a novel bioprinted, human-diabetic cardiac organoid modelSC1HL154511 · NHLBI · UNIVERSITY OF TEXAS EL PASO · PI HAN, KYUNG-AN · 2020 to 2023
$1.2M
NHLBI NIH HHS SC1 HL154511
6 · The paper itself

Abstract

Prolonged onset of Type-II Diabetes is known to induce structural and mechanical remodeling in the ventricular myocardium or heart wall. This study aimed to compare the microarchitecture, fiber organization, and stiffness of left ventricular heart tissues from diabetic vs non-diabetic donor myocardium tissues. Myocardial tissue samples were obtained from six human donors (three diabetic, three non-diabetic) and processed using cryotome sectioning, tissue clearing, and staining protocols. Light sheet fluorescence microscopy was employed to visualize vascular and extracellular matrix components using lectin, propidium iodide, and fast-green staining. Scanning electron microscopy (SEM) was used to assess fibril morphology, and rheological testing was conducted to determine tissue stiffness. Light sheet microscopy revealed disrupted and reduced vascular networks in diabetic tissue samples, accompanied by decreased cellularity and increased fiber content. SEM analysis showed that fibrils in diabetic myocardium were generally longer and more variable in length, suggesting altered extracellular matrix remodeling. Rheological testing demonstrated that diabetic tissues had higher elastic modulus, and complex viscosity, implying increased stiffness and reduced compliance. Collectively, these substantial changes in myocardial architecture include excessive fiber deposition, disrupted vasculature, and enhanced tissue stiffness. These alterations are consistent with features of cardiac disease pathologies and underscore the potential of imaging and mechanical profiling as diagnostic tools for early detection and therapeutic targeting of diabetic cardiac remodeling. This pilot study is limited by its small sample size (n = 3 per group) and is intended as a feasibility assessment, providing a roadmap for high-throughput screening of larger sample sets. Findings represent preliminary trends rather than definitive conclusions, and larger-scale studies will be required to validate these observations.

Indexed as

Diabetic cardiac remodelingFibrous depositionMicroscopyStiffnessVentricular myocardium

Identifiers

PMID41694667
PMCPMC12905775

What OpenQuestion 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 OpenQuestion graph.