Eva Štokelj, Urban Simončič, For The Alzheimer's Disease Neuroimaging Initiative
{"title":"Data-Driven Image-Based Protocol for Brain PET Image Harmonization.","authors":"Eva Štokelj, Urban Simončič, For The Alzheimer's Disease Neuroimaging Initiative","doi":"10.3390/s25134230","DOIUrl":null,"url":null,"abstract":"<p><p>Quantitative FDG-PET brain imaging across multiple centers is challenged by inter-scanner variability, impacting the comparability of neuroimaging data. This study proposes a data-driven image-based harmonization protocol to address these discrepancies without relying on traditional phantom scans. The protocol uses spatially normalized FDG-PET brain images to estimate scanner-specific Gaussian smoothing filters, optimizing parameters via the structural similarity index (SSIM). Validation was performed using images from cognitively normal individuals and Alzheimer's disease patients from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Results demonstrated robust harmonization at moderate target resolutions (8 and 10 mm FWHM), with filter estimates consistently within 1.2 mm of phantom-derived ground truths. However, at higher resolutions (6 mm FWHM), discrepancies reached up to 3 mm, reflecting reduced accuracy. These deviations were particularly evident for high-resolution scanners like HRRT, likely due to elevated noise levels and smaller sample sizes. The presented harmonization method effectively reduces inter-scanner variability in retrospective FDG-PET studies, especially valuable when phantom scans are unavailable. Nonetheless, the current limitations at finer resolutions underline the necessity for methodological refinements to meet the demands of evolving high-resolution PET imaging technologies.</p>","PeriodicalId":21698,"journal":{"name":"Sensors","volume":"25 13","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2025-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12252437/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sensors","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.3390/s25134230","RegionNum":3,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Quantitative FDG-PET brain imaging across multiple centers is challenged by inter-scanner variability, impacting the comparability of neuroimaging data. This study proposes a data-driven image-based harmonization protocol to address these discrepancies without relying on traditional phantom scans. The protocol uses spatially normalized FDG-PET brain images to estimate scanner-specific Gaussian smoothing filters, optimizing parameters via the structural similarity index (SSIM). Validation was performed using images from cognitively normal individuals and Alzheimer's disease patients from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Results demonstrated robust harmonization at moderate target resolutions (8 and 10 mm FWHM), with filter estimates consistently within 1.2 mm of phantom-derived ground truths. However, at higher resolutions (6 mm FWHM), discrepancies reached up to 3 mm, reflecting reduced accuracy. These deviations were particularly evident for high-resolution scanners like HRRT, likely due to elevated noise levels and smaller sample sizes. The presented harmonization method effectively reduces inter-scanner variability in retrospective FDG-PET studies, especially valuable when phantom scans are unavailable. Nonetheless, the current limitations at finer resolutions underline the necessity for methodological refinements to meet the demands of evolving high-resolution PET imaging technologies.
期刊介绍:
Sensors (ISSN 1424-8220) provides an advanced forum for the science and technology of sensors and biosensors. It publishes reviews (including comprehensive reviews on the complete sensors products), regular research papers and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.