Laura C. Bell, Alexandre Fernandez Coimbra, Yixuan Zou, Colin Dimond, Jaime Mata, John Muglar, Yun Michael Shim, David Mummy, Bastiaan Driehuys, Yuh-Chin Huang, Peter Niedbalski, Mario Castro, Yonni Friedlander, Norm Konyer, Sarah Svenningsen, Parameswaran Nair, Terence Ho, Andrew Hahn, Sean Fain, Eric A. Hoffman, Guilhem J. Collier, Jim M. Wild, Robert Thormen, Talissa Altes, Paula Belloni
{"title":"多地点实施129Xe-MRI评估COPD疾病进展:XeCITE早期结果","authors":"Laura C. Bell, Alexandre Fernandez Coimbra, Yixuan Zou, Colin Dimond, Jaime Mata, John Muglar, Yun Michael Shim, David Mummy, Bastiaan Driehuys, Yuh-Chin Huang, Peter Niedbalski, Mario Castro, Yonni Friedlander, Norm Konyer, Sarah Svenningsen, Parameswaran Nair, Terence Ho, Andrew Hahn, Sean Fain, Eric A. Hoffman, Guilhem J. Collier, Jim M. Wild, Robert Thormen, Talissa Altes, Paula Belloni","doi":"10.1183/13993003.congress-2023.pa2283","DOIUrl":null,"url":null,"abstract":"<b>Background</b>: Sensitive markers of COPD progression are needed. Xe-MRI ventilation defect % (VDP) and gas-exchange metrics (membrane/gas (MDP), red-blood-cells/gas (RDP)) may be more sensitive to early progression than current clinical endpoints. <b>Objectives</b>: 1) Validate a harmonized Xe-MRI protocol in multicenter setting, and 2) Evaluate suitability of Xe-MRI metrics as measures of progression and predictors of acute exacerbations (AEx). <b>Methods</b>: Effectiveness of a Xe-MRI protocol for Siemens and GE MRI systems [1] was tested in healthy volunteers (HV) at 7 sites with a standardized quality check via a reproducibility assessment. Patient cohorts (n = 11 ongoing) included GOLD II-IV with history of AEx treated with SOC ± azithromycin, and GOLD I. Xe-MRI and PFTs were done at 0, 6, 12, 24, and 48 weeks. Quantitative CT exams at 0, 24 and 48 weeks for volume %normal, %emphysema, and %gas-trapping [2]. <b>Results</b>: In HVs homogeneous gas exchange and repeatability was observed (n = 5, r=0.98, p<.001). In COPD patients, baseline VDP correlated with FEV1 (-0.78, p<.05) and %normal CT (-0.72, p<.05). MDP correlated with %emphysema (0.81, p<.05). A GOLD III patient who experienced AExs and COVID during the 48 weeks showed an increase in MDP & RDP, and decrease in FEV1 (Fig1). <b>Conclusions</b>: A harmonized multicenter Xe-MRI protocol was successful. Early results in COPD patients show correlations between Xe-MRI, HRCT, and PFT.","PeriodicalId":34850,"journal":{"name":"Imaging","volume":"28 1","pages":"0"},"PeriodicalIF":0.7000,"publicationDate":"2023-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multisite implementation of 129Xe-MRI assessment of COPD disease progression: XeCITE early results\",\"authors\":\"Laura C. Bell, Alexandre Fernandez Coimbra, Yixuan Zou, Colin Dimond, Jaime Mata, John Muglar, Yun Michael Shim, David Mummy, Bastiaan Driehuys, Yuh-Chin Huang, Peter Niedbalski, Mario Castro, Yonni Friedlander, Norm Konyer, Sarah Svenningsen, Parameswaran Nair, Terence Ho, Andrew Hahn, Sean Fain, Eric A. Hoffman, Guilhem J. Collier, Jim M. Wild, Robert Thormen, Talissa Altes, Paula Belloni\",\"doi\":\"10.1183/13993003.congress-2023.pa2283\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<b>Background</b>: Sensitive markers of COPD progression are needed. Xe-MRI ventilation defect % (VDP) and gas-exchange metrics (membrane/gas (MDP), red-blood-cells/gas (RDP)) may be more sensitive to early progression than current clinical endpoints. <b>Objectives</b>: 1) Validate a harmonized Xe-MRI protocol in multicenter setting, and 2) Evaluate suitability of Xe-MRI metrics as measures of progression and predictors of acute exacerbations (AEx). <b>Methods</b>: Effectiveness of a Xe-MRI protocol for Siemens and GE MRI systems [1] was tested in healthy volunteers (HV) at 7 sites with a standardized quality check via a reproducibility assessment. Patient cohorts (n = 11 ongoing) included GOLD II-IV with history of AEx treated with SOC ± azithromycin, and GOLD I. Xe-MRI and PFTs were done at 0, 6, 12, 24, and 48 weeks. Quantitative CT exams at 0, 24 and 48 weeks for volume %normal, %emphysema, and %gas-trapping [2]. <b>Results</b>: In HVs homogeneous gas exchange and repeatability was observed (n = 5, r=0.98, p<.001). In COPD patients, baseline VDP correlated with FEV1 (-0.78, p<.05) and %normal CT (-0.72, p<.05). MDP correlated with %emphysema (0.81, p<.05). A GOLD III patient who experienced AExs and COVID during the 48 weeks showed an increase in MDP & RDP, and decrease in FEV1 (Fig1). <b>Conclusions</b>: A harmonized multicenter Xe-MRI protocol was successful. Early results in COPD patients show correlations between Xe-MRI, HRCT, and PFT.\",\"PeriodicalId\":34850,\"journal\":{\"name\":\"Imaging\",\"volume\":\"28 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2023-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Imaging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1183/13993003.congress-2023.pa2283\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1183/13993003.congress-2023.pa2283","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Multisite implementation of 129Xe-MRI assessment of COPD disease progression: XeCITE early results
Background: Sensitive markers of COPD progression are needed. Xe-MRI ventilation defect % (VDP) and gas-exchange metrics (membrane/gas (MDP), red-blood-cells/gas (RDP)) may be more sensitive to early progression than current clinical endpoints. Objectives: 1) Validate a harmonized Xe-MRI protocol in multicenter setting, and 2) Evaluate suitability of Xe-MRI metrics as measures of progression and predictors of acute exacerbations (AEx). Methods: Effectiveness of a Xe-MRI protocol for Siemens and GE MRI systems [1] was tested in healthy volunteers (HV) at 7 sites with a standardized quality check via a reproducibility assessment. Patient cohorts (n = 11 ongoing) included GOLD II-IV with history of AEx treated with SOC ± azithromycin, and GOLD I. Xe-MRI and PFTs were done at 0, 6, 12, 24, and 48 weeks. Quantitative CT exams at 0, 24 and 48 weeks for volume %normal, %emphysema, and %gas-trapping [2]. Results: In HVs homogeneous gas exchange and repeatability was observed (n = 5, r=0.98, p<.001). In COPD patients, baseline VDP correlated with FEV1 (-0.78, p<.05) and %normal CT (-0.72, p<.05). MDP correlated with %emphysema (0.81, p<.05). A GOLD III patient who experienced AExs and COVID during the 48 weeks showed an increase in MDP & RDP, and decrease in FEV1 (Fig1). Conclusions: A harmonized multicenter Xe-MRI protocol was successful. Early results in COPD patients show correlations between Xe-MRI, HRCT, and PFT.