Evidence map›Paper›PMID 41892098›Full record

ArticleBiomimetics (Basel, Switzerland)2026

GAN-Based Cross-Modality Brain MRI Synthesis: Paired Versus Unpaired Training and Comparison with Diffusion and Transformer Models.

Behnam Kiani Kalejahi, Sebelan Danishvar, Mohammad Javad Rajabi

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Article in Biomimetics (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Behnam Kiani KalejahiDepartment of Computer Science, School of Engineering, Central Asian University, Tashkent 111211, Uzbekistan.ORCID 0000-0002-7118-0382
Sebelan DanishvarDepartment of Electronic and Computer Engineering, Brunel University, Uxbridge UB83PH, UK.ORCID 0000-0002-8258-0437
Mohammad Javad RajabiFaculty of Data Science and Information Technology, INTI International University, Persiaran Perdana BBN Putra Nilai, Nilai 71800, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Incomplete or faulty MRI sequences are common in clinical practice and can impair AI-based analyses that rely on complete multi-contrast data. The relative effectiveness of classical generative adversarial networks (GANs) versus modern diffusion and transformer-based models for clinically usable MRI synthesis remains unclear. This study evaluates cross-modality MRI synthesis using the BraTS 2019 brain tumour dataset, focusing on T1-to-T2 translation. We assess paired and unpaired CycleGAN models and compare them with two stronger but computationally intensive baselines, a conditional denoising diffusion probabilistic model (DDPM) and a transformer-enhanced GAN, using identical data splits and preprocessing pipelines. Inter-modality correlation was evaluated to estimate the achievable similarity between modalities. Conceptually, modality synthesis may be viewed as a representation-learning approach that compensates for missing imaging information by reconstructing clinically relevant features from available contrasts. Paired CycleGAN achieved correlations of r≈0.92-0.93 and SSIM ≈0.90-0.92, approaching natural T1-T2 correlation (r≈0.95) while maintaining very fast inference (<50 ms/slice). Unpaired CycleGAN achieved r≈0.74-0.78 and SSIM ≈0.82-0.85, producing clinically interpretable reconstructions without voxel-level supervision. DDPM achieved the highest fidelity (SSIM ≈0.93-0.95, r≈0.94) but required substantially greater computational resources, while transformer-enhanced GAN performance was intermediate. Qualitative analysis showed that CycleGAN and DDPM best preserved tumour and tissue boundaries, whereas unpaired CycleGAN occasionally over-smoothed subtle lesions. These findings highlight the trade-off between fidelity and efficiency in cross-modality MRI synthesis, suggesting paired CycleGAN for time-sensitive clinical workflows and diffusion models as a computationally expensive accuracy upper bound.

Indexed as

brain tumourCycleGANdiffusion modelsgenerative adversarial networkshuman health

Identifiers

PMID41892098
PMCPMC13024612

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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.