Evidence map›Paper›PMID 41963831›Full record

ArticleBMC medical imaging2026

Nano-radiomics of molecular MRI for early amyloid associated patterns in an Alzheimer's disease mouse model via an automatic pipeline.

Esther Ngan, Prajwal Bhandari, Parag A Parekh, Andrew A Badachhape, Ananth V Annapragada, Ketan B Ghaghada, Zbigniew A Starosolski

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Article in BMC medical imaging, 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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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

7 authors.

Esther NganDepartment of Radiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Prajwal BhandariDepartment of Radiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Parag A ParekhDepartment of Radiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Andrew A BadachhapeDepartment of Radiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Ananth V AnnapragadaDepartment of Radiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Ketan B GhaghadaDepartment of Radiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Zbigniew A StarosolskiDepartment of Radiology, Baylor College of Medicine, Houston, TX, 77030, USA. starosol@bcm.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe combination of nanoparticle contrast agents with advanced image analysis techniques like radiomics offers a powerful new approach for disease detection and characterization. This study presents a novel automated pipeline for segmentation and nano-radiomic analysis of nanoprobe-enhanced images. We demonstrate the effectiveness of this pipeline in an Alzheimer’s disease (AD) mouse model, showing improved detection of amyloid pathology compared to conventional methods.

methodsThe study used the magnetic resonance imaging (MRI) data collected from double transgenic (TG) AD mice, including 13 mice aged 6–8 month old with lower amyloid burden and 36 mice aged 11–18 month old with higher amyloid burden. Wild type (WT) mice served as controls. Three contrast doses were administered to older mice, while one dose was applied to younger mice. A UNet-based model was trained on mouse brain scans to automatically segment two specific regions, and the results were compared to those from semi-automatic segmentation (i.e. manual brain atlas registration to MRIs with automatic region extraction). 89 radiomic features (RFs) per region were computed, followed by genotype classification using machine learning and sensitivity analyses. Image-based conventional metric (percentage change between pre- and post-contrast MRI intensity signal) was compared to radiomics-based approaches.

resultsThe UNet-based model with SWIN transformer performed the best, achieving Dice coefficients between 0.80 and 0.95. Non-parametric statistical tests showed no significant difference in segmentation performance based on amyloid burden, nanoparticle contrast, or contrast doses. RF-based classification performance was similar between automatic and semi-automatic approaches. In older mice with good-quality segmentation, the automatic approach outperformed the semi-automatic method across all dose-specific test sets (all 1.0) but not the validation set (0.90 vs. 1.0). The top classifier from automatic approach also required 2x less RFs. In younger mice, classification performance varied with segmentation approach and inclusion of fair-quality segmentation. Yet the top classifiers typically required only one or two RFs.

conclusionsNano-radiomic analysis of targeted nanoparticle contrast-enhanced MRIs outperformed conventional imaging metrics for early detection of pathological amyloid deposition in an AD mouse model. Automated segmentation achieved performance comparable to the semi-automatic method, while improving efficiency.

Indexed as

Alzheimer DiseaseBrainMagnetic Resonance ImagingAnimalsContrast MediaDisease Models, AnimalMiceMice, TransgenicNanoparticlesRadiomicsContrast MediaAlzheimer’sAmyloid depositionClassificationMachine learningMolecular imagingMRINanoparticle contrast agentRadiomics

Identifiers

PMID41963831
PMCPMC13224451

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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.