{"title":"Multi-scale Gaussian product-of-experts for missing sequence multiple sclerosis lesion segmentation.","authors":"Seung Hoon Lee, Lun Matthew Wong, Tiffany Y So","doi":"10.3389/fradi.2026.1868811","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To develop and evaluate a unified framework for multiple sclerosis (MS) white matter lesion segmentation that operates robustly under clinically prevalent missing sequence magnetic resonance imaging conditions.</p><p><strong>Methods: </strong>We propose a multi-scale Gaussian product-of-experts framework (MG-PoE) integrated into nnU-Net, where sequence-specific inputs are independently processed through a shared encoder and parameterized as Gaussian experts before combination through precision-weighted product-of-experts (PoE) fusion at each encoder scale. The unified fusion rule handles different sequence configurations without requiring subset-specific architectures. The framework was systematically evaluated under different sequence configurations on diverse datasets (MSSEG2016, MS3SEG, and MSLesSeg24).</p><p><strong>Results: </strong>On the five-sequence MSSEG2016, the proposed framework achieved the best overall performance compared to benchmark methods across all full-sequence and partially observed multisequence settings, with a mean Dice Similarity Coefficient (DSC) of 0.7029, a mean 95th percentile Hausdorff distance (HD95) of 22.4030, and a mean Composite Score (CS) of 0.7235 across the 26 sequence configurations. On MS3SEG, MG-PoE achieved the highest mean DSC and CS across the full sequence and missing-sequence settings, with significant improvements over competing methods, while HD95 performance was generally comparable. In zero-shot evaluation on MSLesSeg24, the method achieved the best overall DSC and HD95 in the full sequence setting (DSC, 0.5566; HD95, 27.3729) and the best mean DSC, HD95 and CS across the missing-sequence settings (DSC, 0.5096; HD95, 30.5054; CS, 0.5811).</p><p><strong>Conclusion: </strong>The MG-PoE framework provides a unified approach to missing-sequence MS lesion segmentation, achieving favorable performance on independent datasets and providing initial evidence of cross-dataset robustness.</p>","PeriodicalId":73101,"journal":{"name":"Frontiers in radiology","volume":"6 ","pages":"1868811"},"PeriodicalIF":4.0000,"publicationDate":"2026-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13658566/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fradi.2026.1868811","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To develop and evaluate a unified framework for multiple sclerosis (MS) white matter lesion segmentation that operates robustly under clinically prevalent missing sequence magnetic resonance imaging conditions.
Methods: We propose a multi-scale Gaussian product-of-experts framework (MG-PoE) integrated into nnU-Net, where sequence-specific inputs are independently processed through a shared encoder and parameterized as Gaussian experts before combination through precision-weighted product-of-experts (PoE) fusion at each encoder scale. The unified fusion rule handles different sequence configurations without requiring subset-specific architectures. The framework was systematically evaluated under different sequence configurations on diverse datasets (MSSEG2016, MS3SEG, and MSLesSeg24).
Results: On the five-sequence MSSEG2016, the proposed framework achieved the best overall performance compared to benchmark methods across all full-sequence and partially observed multisequence settings, with a mean Dice Similarity Coefficient (DSC) of 0.7029, a mean 95th percentile Hausdorff distance (HD95) of 22.4030, and a mean Composite Score (CS) of 0.7235 across the 26 sequence configurations. On MS3SEG, MG-PoE achieved the highest mean DSC and CS across the full sequence and missing-sequence settings, with significant improvements over competing methods, while HD95 performance was generally comparable. In zero-shot evaluation on MSLesSeg24, the method achieved the best overall DSC and HD95 in the full sequence setting (DSC, 0.5566; HD95, 27.3729) and the best mean DSC, HD95 and CS across the missing-sequence settings (DSC, 0.5096; HD95, 30.5054; CS, 0.5811).
Conclusion: The MG-PoE framework provides a unified approach to missing-sequence MS lesion segmentation, achieving favorable performance on independent datasets and providing initial evidence of cross-dataset robustness.