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Stojanov, D. Hybrid Method for Automated MRI Prostate Segmentation. Encyclopedia. Available online: https://encyclopedia.pub/entry/58566 (accessed on 05 December 2025).
Stojanov D. Hybrid Method for Automated MRI Prostate Segmentation. Encyclopedia. Available at: https://encyclopedia.pub/entry/58566. Accessed December 05, 2025.
Stojanov, Done. "Hybrid Method for Automated MRI Prostate Segmentation" Encyclopedia, https://encyclopedia.pub/entry/58566 (accessed December 05, 2025).
Stojanov, D. (2025, June 30). Hybrid Method for Automated MRI Prostate Segmentation. In Encyclopedia. https://encyclopedia.pub/entry/58566
Stojanov, Done. "Hybrid Method for Automated MRI Prostate Segmentation." Encyclopedia. Web. 30 June, 2025.
Hybrid Method for Automated MRI Prostate Segmentation
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The paper aims to advance automated prostate segmentation on T2‑weighted MRI by introducing a hybrid topological atlas‑based method. It leverages a collection of pre‑labeled MRI atlas images to capture anatomical variability and produce accurate prostate segmentations. The approach was evaluated on 30 T2‑weighted MRI scans. Automated contours were compared with manual expert segmentations using the Dice Similarity Coefficient (DSC). The method achieved high DSC values, indicating that it closely approximates expert-defined prostate boundaries. This research demonstrated good overlap between automated and manual segmentations, proving that the hybrid approach is effective and offered a quantitative performance benchmark: consistently solid DSC scores across the 30-case dataset.

MRI T2 image segmentation prostate image segmentation atlas hybrid method medical informatics

1. Objective & Motivation

The method introduces a hybrid topological atlas-based algorithm for fully automatic prostate segmentation using T2-weighted MRI, designed to address limitations in time and accuracy of manual delineation. It uses a set of pre-labeled atlas images, aiming to deliver robust contours across patients with diverse prostate shapes.

2. Atlas-Based & Topological Approach

Atlas Preparation

  • A small but diverse cohort of prostate MRIs are manually segmented to create labeled atlas images.

  • The atlas captures variations in size, shape, and orientation across prostates.

Matching & Registration

  1. A new MRI (target) is aligned spatially to each atlas via image registration.

  2. The topological similarity (contour shape, directional edges, intensity gradient) between atlases is computed.

  3. This determines which atlas (or weighted combination) best matches the target’s topology.

Contour Estimation

  • Leveraging the union of compatible contours from selected atlases, a composite “inferred prostate region” is built.

  • The method then maps these contours precisely to the target image, granting an automated prostate outline.

3. Performance & Evaluation

  • Tested on 30 T2-weighted prostate MRI scans, with segmentations compared to expert manual delineations.

  • Evaluated via Dice Similarity Coefficient (DSC): results indicated high overlap, demonstrating strong segmentation accuracy.

  • The algorithm exhibited fast execution; typically, only a small region of interest is processed, reducing computational load.

4. Strengths & Constraints

Strengths

  • Topologically driven matching ensures segmentation respects prostate shape and contour direction.

  • It’s conceptually straightforward and easier to implement than complex deep learning methods.

  • Computationally efficient, as only relevant subregions are processed.

Limitations

  • Relies heavily on the atlas database: new prostate shapes not represented may be missed.

  • If the target’s unique anatomy (e.g., due to severe hypertrophy) lies outside the atlas union, segmentation may fail.

5. Broader Context & Follow-up Methods

Atlas vs. Deep Learning Today

  • Modern approaches (e.g., U-Net, 3D CNNs, transformers) achieve DSC ≈ 0.9+ for whole gland; zonal segmentation lags slightly behind (DSC ≈ 0.79–0.87).

  • Data robustness is key: domain adaptation and boundary-aware losses help compensate for MRI variance and boundary uncertainty.

Technical Evolution

  • 3D multi-planar CNNs (axial + sagittal scans) improved accuracy near prostate apex/base.

  • Transformer-based models now use cross-slice attention to better capture structural continuity.

6. Summary Comparison Table

Aspect Topological Atlas Method Modern Deep Learning Models
Data 30 manually segmented MRIs Hundreds to thousands of annotated MRIs
Approach Atlas registration + contour union CNNs (e.g., U-Net, V-Net), Transformers
Performance Good DSC; efficient contours Higher DSC (≈0.90 W.G., ≈0.79–0.87 zonal)
Speed Quick due to ROI focus Varies; commonly fast with GPU acceleration
Scalability Atlas-limited; manual atlas prep Scalable; needs large annotated datasets
Robustness Sensitive to anatomy not seen in atlas Generally robust with data augmentation
  • Suite for resource-limited environments: reproducible without massive datasets or specialized hardware.

  • Good fit for institutions with a small atlas archive aiming for quick deployment.

  • Ideal as a baseline or teaching tool to understand topological segmentation before transitioning to neural methods.

8. Future Directions

To enhance the topological method, one could:

  1. Expand atlas diversity – more cases, including atypical anatomy.

  2. Integrate ML-derived shape priors to handle contour variability absent in atlas.

  3. Use hybrid pipelines: topological outputs guide or refine deep learning segmenters.

  4. Blend active contour techniques to adapt atlas contours dynamically rather than fixed mapping.

9. In Summary

The topological atlas-based method (2014) offers a fast, interpretable, and implementation-friendly approach for segmenting the prostate on T2 MRI. While deep learning now dominates—with higher accuracy, scalability, and anatomical generalizability—this method remains relevant for small-scale environments and algorithmic education. It underscores the persistent value of topology-driven segmentation, and provides foundational insights for modern hybrid systems that blend atlas priors with data-driven learning [1][2].

References

  1. Daniela Hristov; Done Stojanov; In silico report on five high-risk Protein C pathogenic variants: G403R, P405S, S421N, C238S, and I243T. Mutat. Res. Mol. Mech. Mutagen.. 2025, 831, 111907.
  2. Daniela Hristov; Done Stojanov; Exploring Regulatory Properties of Genes Associated with Nonsyndromic Male Infertility. Reprod. Med.. 2024, 5, 136-153.
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