Kirsten M Lynch, Ryan P Cabeen, Andreia Lopes de Morais, Xuyan Jin, Erendiz Tarakci, Jessica Lamb, Basavaraju G Sanganahalli, Jelena M Mihailovic, Yamileck Olivas-Garcia, David B Berry, Marcio A Diniz, Joseph Mandeville, Fahmeed Hyder, Daniel R Thedens, Ali Arbab, Shuning Huang, Adnan Bibic, Wyatt Austin, Bingren Hu, Mohammad B Khan, Pradip K Kamat, Arthur W Toga, Patrick Lyden, Cenk Ayata
{"title":"A robust and reproducible automated MRI pipeline for quantifying tissue outcomes after experimental stroke in multi-center preclinical networks.","authors":"Kirsten M Lynch, Ryan P Cabeen, Andreia Lopes de Morais, Xuyan Jin, Erendiz Tarakci, Jessica Lamb, Basavaraju G Sanganahalli, Jelena M Mihailovic, Yamileck Olivas-Garcia, David B Berry, Marcio A Diniz, Joseph Mandeville, Fahmeed Hyder, Daniel R Thedens, Ali Arbab, Shuning Huang, Adnan Bibic, Wyatt Austin, Bingren Hu, Mohammad B Khan, Pradip K Kamat, Arthur W Toga, Patrick Lyden, Cenk Ayata","doi":"10.1162/IMAG.a.1328","DOIUrl":null,"url":null,"abstract":"<p><p>The failure to translate promising preclinical stroke therapies into clinical success is a multi-faceted problem; however, a critical contributing factor is the lack of rigorous, reproducible preclinical outcome measures. While magnetic resonance imaging (MRI) offers a translational alternative to traditional histology, its use in large, multi-site trials is challenged by data heterogeneity and the need for scalable analysis. To address this, we developed and validated a fully automated, open-source image analysis pipeline for the Stroke Preclinical Assessment Network (SPAN), a six-center preclinical trial network. The pipeline processed T2-weighted and apparent diffusion coefficient (ADC) maps from over 2,000 mice and rats, incorporating steps for cross-site data harmonization, deep learning-based brain extraction, and rule-based segmentation to quantify infarct volume, brain swelling, and atrophy. The pipeline demonstrated high accuracy, as automated lesion volumes strongly correlated with manual expert tracing on both MRI (R = 0.96) and 2,3,5-triphenyl-tetrazolium chloride (TTC)-stained tissue (R = 0.86). The U-net model for brain extraction achieved a Dice score of 0.96, and our harmonization method successfully reduced inter-site variability in quantitative MRI parameters. This robust and reproducible pipeline provides a scalable framework for standardizing tissue outcome assessment, enhancing the rigor of multi-site preclinical studies.</p>","PeriodicalId":73341,"journal":{"name":"Imaging neuroscience (Cambridge, Mass.)","volume":"4 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13455521/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Imaging neuroscience (Cambridge, Mass.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1162/IMAG.a.1328","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
The failure to translate promising preclinical stroke therapies into clinical success is a multi-faceted problem; however, a critical contributing factor is the lack of rigorous, reproducible preclinical outcome measures. While magnetic resonance imaging (MRI) offers a translational alternative to traditional histology, its use in large, multi-site trials is challenged by data heterogeneity and the need for scalable analysis. To address this, we developed and validated a fully automated, open-source image analysis pipeline for the Stroke Preclinical Assessment Network (SPAN), a six-center preclinical trial network. The pipeline processed T2-weighted and apparent diffusion coefficient (ADC) maps from over 2,000 mice and rats, incorporating steps for cross-site data harmonization, deep learning-based brain extraction, and rule-based segmentation to quantify infarct volume, brain swelling, and atrophy. The pipeline demonstrated high accuracy, as automated lesion volumes strongly correlated with manual expert tracing on both MRI (R = 0.96) and 2,3,5-triphenyl-tetrazolium chloride (TTC)-stained tissue (R = 0.86). The U-net model for brain extraction achieved a Dice score of 0.96, and our harmonization method successfully reduced inter-site variability in quantitative MRI parameters. This robust and reproducible pipeline provides a scalable framework for standardizing tissue outcome assessment, enhancing the rigor of multi-site preclinical studies.