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Combining datasets from multiple sites/scanners has been becoming increasingly more prevalent in modern neuroimaging studies. Despite numerous benefits from the growth in sample size, substantial technical variability associated with site/scanner-related effects exists which may inadvertently bias subsequent downstream analyses. Such a challenge calls for a data harmonization procedure which reduces the scanner effects and allows the scans to be combined for pooled analyses. In this work, we present MISPEL (Multi-scanner Image harmonization via Structure Preserving Embedding Learning), a multi-scanner harmonization framework. Unlike existing techniques, MISPEL does not assume a perfect coregistration across the scans, and the framework is naturally extendable to more than two scanners. Importantly, we incorporate our multi-scanner dataset where each subject is scanned on four different scanners. This unique paired dataset allows us to define and aim for an ideal harmonization (e.g., each subject with identical brain tissue volumes on all scanners). We extensively view scanner effects under varying metrics and demonstrate how MISPEL significantly improves them.
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http://dx.doi.org/10.1109/ICCVW54120.2021.00367 | DOI Listing |
Front Neurosci
June 2025
Department of Radiology, University Hospital Antwerp (UZA), Antwerp, Belgium.
The structural integrity of brain white matter is commonly assessed using quantitative diffusion metric maps derived from diffusion MRI (dMRI) data. However, in multi-site, multi-scanner studies, variability across and within scanners presents challenges in ensuring consistent and comparable diffusion evaluations. This study assesses the effectiveness of ComBat-based harmonization algorithms in reducing intra- and inter-scanner variability in diffusion metrics such as FA, MD, AD, RD, MK, AK, and RK.
View Article and Find Full Text PDFEJNMMI Phys
March 2025
Department of Radiology and Nuclear Medicine, University Medical Centre Utrecht, Heidelberglaan 100, 3584CX, Utrecht, The Netherlands.
Background: Reliable dosimetry based on SPECT/CT imaging is essential to achieve personalized Ho-radioembolization treatment planning and evaluation. This study quantitatively evaluates multiple acquisition and reconstruction protocols for Ho-SPECT imaging based on data from five Dutch hospitals. We aim to recommend an imaging protocol which harmonizes Ho-SPECT images for reproducible and accurate dosimetry in a multi-scanner and multi-center setting.
View Article and Find Full Text PDFLife (Basel)
January 2025
Institute for Diagnostic and Interventional Radiology, Faculty of Medicine and University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.
Kirsten Rat Sarcoma viral oncogene homolog (KRAS) is a frequently occurring mutation in non-small-cell lung cancer (NSCLC) and influences cancer treatment and disease progression. In this study, a machine learning (ML) pipeline was applied to radiomic features extracted from public and internal CT images to identify KRAS mutations in NSCLC patients. Both datasets were analyzed using parametric ( test) and non-parametric statistical tests (Mann-Whitney U test) and dimensionality reduction techniques.
View Article and Find Full Text PDFPLoS One
December 2024
ASU-Mayo Center for Innovative Imaging, Tempe, Arizona, United States of America.
Multicenter and multi-scanner imaging studies may be necessary to ensure sufficiently large sample sizes for developing accurate predictive models. However, multicenter studies, incorporating varying research participant characteristics, MRI scanners, and imaging acquisition protocols, may introduce confounding factors, potentially hindering the creation of generalizable machine learning models. Models developed using one dataset may not readily apply to another, emphasizing the importance of classification model generalizability in multi-scanner and multicenter studies for producing reproducible results.
View Article and Find Full Text PDFNeuroSci
November 2024
National Institute of Neurological Disorders and Strokes, National Institutes of Health, Bethesda, MD 20892, USA.
Classification of disease and healthy volunteer cohorts provides a useful clinical alternative to traditional group statistics due to individualized, personalized predictions. Classifiers for neurodegenerative disease can be trained on structural MRI morphometry, but require large multi-scanner datasets, introducing confounding batch effects. We test ComBat, a common harmonization model, in an example application to classify subjects with Parkinson's disease from healthy volunteers and identify common pitfalls, including data leakage.
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