ArticleBiomedical optics express2025
Learning-enhanced 3D fiber orientation mapping in thick cardiac tissues.
Article in Biomedical optics express, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Learning-enhanced 3D fiber orientation mapping in thick cardiac tissues.Biomedical optics express · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Fibrous proteins, such as elastin and collagen, are crucial for the structural integrity of the cardiovascular system. For thin tissue-engineered heart valves and surgical patches, the two-dimensional mapping of fiber orientation is well-established. However, for three-dimensional (3D) thick tissue samples, e.g., the embryonic whole heart, robust 3D fiber analysis tools are not available. This information is essential for computational vascular modeling and tissue microstructure characterization. Therefore, this study employs machine learning (ML) and deep learning (DL) techniques to analyze the 3D cardiovascular fiber structures in thick samples of porcine pericardium and embryonic whole hearts. It is hypothesized that ML/DL-based fiber orientation analysis will outperform traditional Fourier transform and directional filter methods by offering higher spatial accuracy and reduced dependency on manual preprocessing. We trained our ML/DL models on both synthetic and real-world cardiovascular datasets obtained from confocal imaging. The evaluation used a mixed dataset of 1200 samples and a porcine/bovine dataset of 400 samples. Support vector regression (SVR) demonstrated the highest accuracy, achieving a normalized mean absolute error (nMAE) of 5.0% on the mixed dataset and 13.0% on the biological dataset. Among DL models, convolutional neural network (CNN) and residual network-50 (ResNet50) had an nMAE of 12.0% and 11.0% on the mixed dataset and 23.0% and 22.0% on the biological dataset, respectively. Attention mechanisms improved performance further, with the channel attention ResNet50 achieving an nMAE of 5.8% on the mixed dataset and 21.0% on the biological dataset. These findings highlight the potential of ML and DL techniques in improving 3D fiber orientation detection, enabling detailed cardiovascular microstructural assessment.
Identifiers
What OpenQuestion holds
Registered trials
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.