Beatrice Lena, Francesco Padormo, Rui Pedro A G Teixeira, Carly Bennallick, James Gholam, Ruben van den Broek, Samson Lecurieux Lafayette, Irene Vavasour, Mara Cercignani, Derek K Jones, Shannon Kolind, Jo Hajnal, Niall Bourke, Yiming Dong, William J Hollander, Todor Karaulanov, Sean C L Deoni, Steven C R Williams, Pia C Sundgren, Andrew G Webb, Emil Ljungberg
{"title":"64 mT脑组织快速T1成像的可重复性和再现性:一项多中心研究。","authors":"Beatrice Lena, Francesco Padormo, Rui Pedro A G Teixeira, Carly Bennallick, James Gholam, Ruben van den Broek, Samson Lecurieux Lafayette, Irene Vavasour, Mara Cercignani, Derek K Jones, Shannon Kolind, Jo Hajnal, Niall Bourke, Yiming Dong, William J Hollander, Todor Karaulanov, Sean C L Deoni, Steven C R Williams, Pia C Sundgren, Andrew G Webb, Emil Ljungberg","doi":"10.1162/IMAG.a.916","DOIUrl":null,"url":null,"abstract":"<p><p>Very-low-field MRI (<100 mT) holds promise for Point-of-Care brain imaging applications, including stroke and multiple sclerosis, with T<sub>1</sub> mapping emerging as a key biomarker for brain development and pathology. However, current low-field T<sub>1</sub> mapping protocols suffer from long acquisition times and limited multi-site repeatability. This study aimed to improve T<sub>1</sub> mapping at 64 mT using a clinically feasible 10-minute protocol and assess repeatability and reproducibility across sites. We present an analysis of the repeatability and reproducibility of rapid T<sub>1</sub> measurements in a commercially available phantom and in 60 volunteers, scanned with a portable 64 mT MRI systems at six sites. T<sub>1</sub> mapping was performed using an undersampled 3D inversion-recovery turbo spin-echo sequence with a 10.8-minute scan time, and reconstructed with a locally low-rank approach. Our results in phantom demonstrated high reproducibility in T<sub>1</sub> measurements (below 3% differences from the average), with non-significant differences between sites. Longitudinal measurements demonstrated high repeatability over time both in vivo and in phantom settings in one site, with minimal variability (average Coefficient of Variation of 0.6%). Average in vivo T<sub>1</sub> values for white matter and cortex were 290 ± 6 ms and 332 ± 8 ms, respectively and the values demonstrated high reproducibility, with differences of less than 4% from the average across sites. Our results demonstrate the feasibility of multi-site in vivo T<sub>1</sub> mapping at 64 mT, providing normative T<sub>1</sub> values at this field strength and supporting its use as a quantitative biomarker in clinical applications.</p>","PeriodicalId":73341,"journal":{"name":"Imaging neuroscience (Cambridge, Mass.)","volume":"3 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12508772/pdf/","citationCount":"0","resultStr":"{\"title\":\"Repeatability and reproducibility of rapid T<sub>1</sub> mapping of brain tissues at 64 mT: A multicentre study.\",\"authors\":\"Beatrice Lena, Francesco Padormo, Rui Pedro A G Teixeira, Carly Bennallick, James Gholam, Ruben van den Broek, Samson Lecurieux Lafayette, Irene Vavasour, Mara Cercignani, Derek K Jones, Shannon Kolind, Jo Hajnal, Niall Bourke, Yiming Dong, William J Hollander, Todor Karaulanov, Sean C L Deoni, Steven C R Williams, Pia C Sundgren, Andrew G Webb, Emil Ljungberg\",\"doi\":\"10.1162/IMAG.a.916\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Very-low-field MRI (<100 mT) holds promise for Point-of-Care brain imaging applications, including stroke and multiple sclerosis, with T<sub>1</sub> mapping emerging as a key biomarker for brain development and pathology. However, current low-field T<sub>1</sub> mapping protocols suffer from long acquisition times and limited multi-site repeatability. This study aimed to improve T<sub>1</sub> mapping at 64 mT using a clinically feasible 10-minute protocol and assess repeatability and reproducibility across sites. We present an analysis of the repeatability and reproducibility of rapid T<sub>1</sub> measurements in a commercially available phantom and in 60 volunteers, scanned with a portable 64 mT MRI systems at six sites. T<sub>1</sub> mapping was performed using an undersampled 3D inversion-recovery turbo spin-echo sequence with a 10.8-minute scan time, and reconstructed with a locally low-rank approach. Our results in phantom demonstrated high reproducibility in T<sub>1</sub> measurements (below 3% differences from the average), with non-significant differences between sites. Longitudinal measurements demonstrated high repeatability over time both in vivo and in phantom settings in one site, with minimal variability (average Coefficient of Variation of 0.6%). Average in vivo T<sub>1</sub> values for white matter and cortex were 290 ± 6 ms and 332 ± 8 ms, respectively and the values demonstrated high reproducibility, with differences of less than 4% from the average across sites. Our results demonstrate the feasibility of multi-site in vivo T<sub>1</sub> mapping at 64 mT, providing normative T<sub>1</sub> values at this field strength and supporting its use as a quantitative biomarker in clinical applications.</p>\",\"PeriodicalId\":73341,\"journal\":{\"name\":\"Imaging neuroscience (Cambridge, Mass.)\",\"volume\":\"3 \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-10-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12508772/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Imaging neuroscience (Cambridge, Mass.)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1162/IMAG.a.916\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Imaging neuroscience (Cambridge, Mass.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1162/IMAG.a.916","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
Repeatability and reproducibility of rapid T1 mapping of brain tissues at 64 mT: A multicentre study.
Very-low-field MRI (<100 mT) holds promise for Point-of-Care brain imaging applications, including stroke and multiple sclerosis, with T1 mapping emerging as a key biomarker for brain development and pathology. However, current low-field T1 mapping protocols suffer from long acquisition times and limited multi-site repeatability. This study aimed to improve T1 mapping at 64 mT using a clinically feasible 10-minute protocol and assess repeatability and reproducibility across sites. We present an analysis of the repeatability and reproducibility of rapid T1 measurements in a commercially available phantom and in 60 volunteers, scanned with a portable 64 mT MRI systems at six sites. T1 mapping was performed using an undersampled 3D inversion-recovery turbo spin-echo sequence with a 10.8-minute scan time, and reconstructed with a locally low-rank approach. Our results in phantom demonstrated high reproducibility in T1 measurements (below 3% differences from the average), with non-significant differences between sites. Longitudinal measurements demonstrated high repeatability over time both in vivo and in phantom settings in one site, with minimal variability (average Coefficient of Variation of 0.6%). Average in vivo T1 values for white matter and cortex were 290 ± 6 ms and 332 ± 8 ms, respectively and the values demonstrated high reproducibility, with differences of less than 4% from the average across sites. Our results demonstrate the feasibility of multi-site in vivo T1 mapping at 64 mT, providing normative T1 values at this field strength and supporting its use as a quantitative biomarker in clinical applications.