Detecting Cellular Microstructural Changes of Liver Fibrosis with Time-Dependent Diffusion MRI.

IF 12.1 1区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Radiology Pub Date : 2024-10-01 DOI:10.1148/radiol.240343
Lijie Zhang, Xi Long, Leqing Chen, Xiaoyu Han, Xiaoxiao Zhang, Peng Sun, Yuhan Yang, Jun Fan, Jiazheng Wang, Ziqiao Lei, Bin Liang, Xiaoming Liu, Heshui Shi
{"title":"Detecting Cellular Microstructural Changes of Liver Fibrosis with Time-Dependent Diffusion MRI.","authors":"Lijie Zhang, Xi Long, Leqing Chen, Xiaoyu Han, Xiaoxiao Zhang, Peng Sun, Yuhan Yang, Jun Fan, Jiazheng Wang, Ziqiao Lei, Bin Liang, Xiaoming Liu, Heshui Shi","doi":"10.1148/radiol.240343","DOIUrl":null,"url":null,"abstract":"<p><p>Background The potential of time-dependent diffusion MRI in imaging the progression from liver fibrosis to cirrhosis has not been established. Purpose To assess the effectiveness of time-dependent diffusion MRI in mapping the microstructure and characterizing cellular attributes during the progression of liver fibrosis to cirrhosis and to investigate its potential in grading liver fibrosis. Materials and Methods This prospective study, performed between December 2022 and October 2023, used 60 rats to establish a liver fibrosis model by means of diethylnitrosamine administration, with five additional rats serving as control animals. Time-dependent diffusion MRI was performed with equivalent diffusion time of 5.4, 10.7, and 69.3 msec on a 3.0-T scanner. Time-dependent diffusion MRI-based microstructural parameters, including cell diameter, intracellular volume fraction (ICVF), cellularity, and extracellular diffusivity, were estimated with use of the imaging microstructural parameters using limited spectrally edited diffusion, or IMPULSED, model. The fitted microstructural parameters were validated with histopathologic measurements. Results All 60 rats developed liver fibrosis, with a noticeable decrease in cell diameter and an increase in ICVF and cellularity observed as liver fibrosis progressed. The diameter measured at pathologic examination ranged from 11.4 μm to 35.4 μm, aligning with the range of 12.4-33.4 μm observed in time-dependent diffusion MRI, which indicated a strong correlation (<i>r</i> = 0.84; <i>P</i> < .001). The quantified ICVF at pathologic examination ranged from 0.28 to 0.89 and varied from 0.23 to 0.85 at time-dependent diffusion MRI, showing a high correlation (<i>r</i> = 0.62; <i>P</i> < .001). The cellularity observed at pathologic examination increased from 0.74 to 5.85, while the cellularity measured at time-dependent diffusion MRI ranged from 0.77 to 3.70, showing a correlation (<i>r</i> = 0.44; <i>P</i> < .001). Conclusion This study revealed the changes in quantitative microstructural mapping across the spectrum from liver fibrosis to cirrhosis. Cell diameter, ICVF, and cellularity are reliable markers for liver fibrosis, with diameter and ICVF presenting good discrimination ability. © RSNA, 2024 <i>Supplemental material is available for this article.</i> See also the editorial by Matos and Metens in this issue.</p>","PeriodicalId":20896,"journal":{"name":"Radiology","volume":"313 1","pages":"e240343"},"PeriodicalIF":12.1000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1148/radiol.240343","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
引用次数: 0

Abstract

Background The potential of time-dependent diffusion MRI in imaging the progression from liver fibrosis to cirrhosis has not been established. Purpose To assess the effectiveness of time-dependent diffusion MRI in mapping the microstructure and characterizing cellular attributes during the progression of liver fibrosis to cirrhosis and to investigate its potential in grading liver fibrosis. Materials and Methods This prospective study, performed between December 2022 and October 2023, used 60 rats to establish a liver fibrosis model by means of diethylnitrosamine administration, with five additional rats serving as control animals. Time-dependent diffusion MRI was performed with equivalent diffusion time of 5.4, 10.7, and 69.3 msec on a 3.0-T scanner. Time-dependent diffusion MRI-based microstructural parameters, including cell diameter, intracellular volume fraction (ICVF), cellularity, and extracellular diffusivity, were estimated with use of the imaging microstructural parameters using limited spectrally edited diffusion, or IMPULSED, model. The fitted microstructural parameters were validated with histopathologic measurements. Results All 60 rats developed liver fibrosis, with a noticeable decrease in cell diameter and an increase in ICVF and cellularity observed as liver fibrosis progressed. The diameter measured at pathologic examination ranged from 11.4 μm to 35.4 μm, aligning with the range of 12.4-33.4 μm observed in time-dependent diffusion MRI, which indicated a strong correlation (r = 0.84; P < .001). The quantified ICVF at pathologic examination ranged from 0.28 to 0.89 and varied from 0.23 to 0.85 at time-dependent diffusion MRI, showing a high correlation (r = 0.62; P < .001). The cellularity observed at pathologic examination increased from 0.74 to 5.85, while the cellularity measured at time-dependent diffusion MRI ranged from 0.77 to 3.70, showing a correlation (r = 0.44; P < .001). Conclusion This study revealed the changes in quantitative microstructural mapping across the spectrum from liver fibrosis to cirrhosis. Cell diameter, ICVF, and cellularity are reliable markers for liver fibrosis, with diameter and ICVF presenting good discrimination ability. © RSNA, 2024 Supplemental material is available for this article. See also the editorial by Matos and Metens in this issue.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用随时间变化的弥散核磁共振成像检测肝纤维化的细胞微结构变化
背景 时间依赖性弥散核磁共振成像在肝纤维化进展到肝硬化过程中的成像潜力尚未确定。目的 评估时间依赖性弥散核磁共振成像在绘制肝纤维化进展到肝硬化过程中的微观结构和细胞属性特征方面的有效性,并研究其在肝纤维化分级方面的潜力。材料与方法 这项前瞻性研究于 2022 年 12 月至 2023 年 10 月间进行,通过给大鼠注射二乙基亚硝胺,用 60 只大鼠建立肝纤维化模型,另外 5 只大鼠作为对照动物。在 3.0-T 扫描仪上以 5.4、10.7 和 69.3 毫秒的等效扩散时间进行了时间依赖性扩散核磁共振成像。通过使用有限光谱编辑扩散模型或 IMPULSED,利用成像微结构参数估算了基于时间依赖性扩散 MRI 的微结构参数,包括细胞直径、细胞内体积分数 (ICVF)、细胞度和细胞外扩散率。拟合的微结构参数与组织病理学测量结果进行了验证。结果 所有 60 只大鼠都出现了肝纤维化,随着肝纤维化的发展,细胞直径明显减小,ICVF 和细胞度增加。病理检查时测得的直径范围为 11.4 μm 至 35.4 μm,与时间依赖性弥散核磁共振成像中观察到的 12.4-33.4 μm 范围一致,两者显示出很强的相关性(r = 0.84;P < .001)。病理检查的量化 ICVF 为 0.28 至 0.89,而时间依赖性弥散 MRI 的量化 ICVF 为 0.23 至 0.85,显示出高度相关性(r = 0.62;P < .001)。病理检查观察到的细胞度从 0.74 增加到 5.85,而时间依赖性弥散核磁共振成像测量到的细胞度从 0.77 增加到 3.70,显示出相关性(r = 0.44;P < .001)。结论 本研究揭示了从肝纤维化到肝硬化整个过程中定量微结构图谱的变化。细胞直径、ICVF 和细胞度是肝纤维化的可靠标记,其中直径和 ICVF 具有良好的鉴别能力。RSNA, 2024 这篇文章有补充材料。另请参阅本期 Matos 和 Metens 的社论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Radiology
Radiology 医学-核医学
CiteScore
35.20
自引率
3.00%
发文量
596
审稿时长
3.6 months
期刊介绍: Published regularly since 1923 by the Radiological Society of North America (RSNA), Radiology has long been recognized as the authoritative reference for the most current, clinically relevant and highest quality research in the field of radiology. Each month the journal publishes approximately 240 pages of peer-reviewed original research, authoritative reviews, well-balanced commentary on significant articles, and expert opinion on new techniques and technologies. Radiology publishes cutting edge and impactful imaging research articles in radiology and medical imaging in order to help improve human health.
期刊最新文献
Risk Factors for Pneumothorax Following Lung Biopsy: Another Peek at Air Leak. Sex-specific Associations between Left Ventricular Remodeling at MRI and Long-term Cardiovascular Risk. The Clinical Weight of Left Ventricular Mass and Shape. Assessment of Nonmass Lesions Detected with Screening Breast US Based on Mammographic Findings. CT-guided Coaxial Lung Biopsy: Number of Cores and Association with Complications.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1