Evidence map›Paper›PMID 42852371›Full record

ArticleBJR artificial intelligence2026

Aligning brain tumor imaging: generating synthetic 3D FA maps from T1-weighted MRI using CycleGAN models.

Xin Du, Francesca M Cozzi, Stephen J Price, Rajesh Jena

Abstract read
In one paragraph

Article in BJR artificial intelligence, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xin DuThe Cavendish Laboratory, University of Cambridge, Cambridge, CB3 0HE, United Kingdom.ORCID https://orcid.org/0000-0002-7948-4081
Francesca M CozziCambridge Brain Tumor Imaging Lab, University of Cambridge, Cambridge, CB2 1TN, United Kingdom.
Stephen J PriceDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, CB2 1TN, United Kingdom.ORCID https://orcid.org/0000-0002-7535-3009
Rajesh JenaDepartment of Oncology, University of Cambridge, Cambridge, CB2 1TN, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This study addresses the issue of spatial misalignment between fractional anisotropy (FA) maps and tractography atlases in neuroimaging. We propose a CycleGAN-based method to generate FA and directionally encoded color (DEC) maps directly from T1-weighted MRI scans, applicable to both healthy and tumor-affected cases. Methods: A CycleGAN model was developed and trained using unpaired data to convert T1-weighted MRI images into FA and DEC maps. The quality of the generated maps was assessed using Structural Similarity Index (SSIM) and Peak Signal-to-Noise Ratio (PSNR) metrics. Special emphasis was placed on evaluating performance in tumor regions. Radiological assessments were also conducted to determine the clinical applicability of the generated maps. Results: The CycleGAN-based model effectively generated high-fidelity FA and DEC maps, with robust SSIM and PSNR values, particularly in tumor regions. Radiological evaluations highlighted the potential of this approach to enhance clinical workflows, offering a reliable AI-driven alternative to traditional image processing methods. Conclusions: This CycleGAN-based approach successfully mitigates the problem of spatial misalignment by generating accurate FA and DEC maps from T1-weighted MRI scans. The method offers a promising pathway for integrating assessments of white matter integrity into predictive models without requiring additional imaging. Advances in knowledge: This study introduces the first use of CycleGAN for generating FA and DEC maps from T1-weighted images for tumor-affected cases, presenting a method that could enhance neuroimaging procedures by reducing the need for additional scans and improving efficiency in clinical settings.

Indexed as

CycleGAN modelFA mapsT1-weighted MRItumor-affected

Identifiers

PMID42852371
PMCPMC13648209

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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.