T1-Dark Rim as a Marker of New and Chronic Active Multiple Sclerosis Lesions: A Serial Study With Frequent 7T MRI

IF 2.3 4区 医学 Q3 CLINICAL NEUROLOGY
Madeleine Marshall, Kingkarn Aphiwatthanasumet, Olivier Mougin, Christine Stadelmann, Paul S. Morgan, Rob A. Dineen, Penny Gowland, Nikos Evangelou, Margareta A. Clarke
{"title":"T1-Dark Rim as a Marker of New and Chronic Active Multiple Sclerosis Lesions: A Serial Study With Frequent 7T MRI","authors":"Madeleine Marshall,&nbsp;Kingkarn Aphiwatthanasumet,&nbsp;Olivier Mougin,&nbsp;Christine Stadelmann,&nbsp;Paul S. Morgan,&nbsp;Rob A. Dineen,&nbsp;Penny Gowland,&nbsp;Nikos Evangelou,&nbsp;Margareta A. Clarke","doi":"10.1111/jon.70044","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background and Purpose</h3>\n \n <p>Chronic active multiple sclerosis (MS) lesions represent a particularly destructive subset of lesions on pathology. However, their imaging correlates, including paramagnetic rim lesions (PRLs) detected on susceptibility-weighted imaging, lack sensitivity and are difficult to implement in clinical practice. This exploratory, longitudinal study investigates the prevalence and temporal dynamics of a novel imaging marker, T<sub>1</sub>-dark rims, and their relationship with PRLs observed on quantitative susceptibility mapping (QSM).</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Four untreated people with MS underwent 7-Tesla MRI scanning six times over a period of 36 weeks. New and pre-existing lesions were analyzed for the presence and temporal evolution of T<sub>1</sub>-dark and QSM rims. Quantitative T<sub>1</sub> values were derived using B<sub>1</sub> maps, and the relationship between rim status and lesion size was evaluated.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Of the 159 baseline lesions, 22 (14%) had T<sub>1</sub>-dark rims, 11 (7%) had QSM rims, and five lesions had both. T<sub>1</sub>-dark and QSM rims showed temporal changes, with T<sub>1</sub>-dark rims preceding new QSM rim appearance in three out of four (75%) lesions. Eleven out of 20 (55%) newly formed lesions had T<sub>1</sub>-dark rims, with a T<sub>1</sub>-dark rim present in all new lesions over 100 mm<sup>3</sup>. Small new lesions lacked discernible rims, but their overall T<sub>1</sub> values aligned with those of larger lesion T<sub>1</sub>-dark rims implying shared pathological processes.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>T<sub>1</sub>-dark rims were more common than QSM rims, with greater prevalence in newly formed lesions. We propose they represent edema and inflammation associated with early stages of chronic active lesion formation visible despite, not because of, iron accumulation.</p>\n </section>\n </div>","PeriodicalId":16399,"journal":{"name":"Journal of Neuroimaging","volume":"35 3","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jon.70044","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neuroimaging","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jon.70044","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background and Purpose

Chronic active multiple sclerosis (MS) lesions represent a particularly destructive subset of lesions on pathology. However, their imaging correlates, including paramagnetic rim lesions (PRLs) detected on susceptibility-weighted imaging, lack sensitivity and are difficult to implement in clinical practice. This exploratory, longitudinal study investigates the prevalence and temporal dynamics of a novel imaging marker, T1-dark rims, and their relationship with PRLs observed on quantitative susceptibility mapping (QSM).

Methods

Four untreated people with MS underwent 7-Tesla MRI scanning six times over a period of 36 weeks. New and pre-existing lesions were analyzed for the presence and temporal evolution of T1-dark and QSM rims. Quantitative T1 values were derived using B1 maps, and the relationship between rim status and lesion size was evaluated.

Results

Of the 159 baseline lesions, 22 (14%) had T1-dark rims, 11 (7%) had QSM rims, and five lesions had both. T1-dark and QSM rims showed temporal changes, with T1-dark rims preceding new QSM rim appearance in three out of four (75%) lesions. Eleven out of 20 (55%) newly formed lesions had T1-dark rims, with a T1-dark rim present in all new lesions over 100 mm3. Small new lesions lacked discernible rims, but their overall T1 values aligned with those of larger lesion T1-dark rims implying shared pathological processes.

Conclusions

T1-dark rims were more common than QSM rims, with greater prevalence in newly formed lesions. We propose they represent edema and inflammation associated with early stages of chronic active lesion formation visible despite, not because of, iron accumulation.

t1 -暗边缘作为新发和慢性活动性多发性硬化症病变的标志:一项频繁7T MRI的系列研究
背景和目的慢性活动性多发性硬化症(MS)病变在病理学上是一个特别具有破坏性的病变子集。然而,它们的成像相关性,包括在敏感性加权成像上检测到的顺磁边缘病变(prl),缺乏敏感性,难以在临床实践中实施。这项探索性的纵向研究调查了一种新的成像标记t1 -暗边缘的流行和时间动态,以及它们与定量敏感性图谱(QSM)观察到的prl的关系。方法对4例未经治疗的MS患者进行6次7特斯拉MRI扫描,时间为36周。分析新发病变和已有病变T1-dark和QSM边缘的存在和时间演变。利用B1图获得定量T1值,并评估边缘状态与病变大小之间的关系。结果在159个基线病变中,22个(14%)为t1 -暗边缘,11个(7%)为QSM边缘,5个病变两者兼有。t1 -深色和QSM边缘显示颞部变化,t1 -深色边缘先于新的QSM边缘出现在四分之三(75%)的病变中。20个新形成的病变中有11个(55%)有t1 -暗边缘,所有超过100 mm3的新病变都有t1 -暗边缘。小的新病变缺乏可识别的边缘,但它们的总体T1值与较大病变的T1-暗边缘一致,这意味着共同的病理过程。结论t1 -深色边缘比QSM边缘更常见,在新形成的病变中患病率更高。我们认为它们代表水肿和炎症与早期慢性活动性病变形成相关,尽管可见,而不是因为铁积累。
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 求助全文
来源期刊
Journal of Neuroimaging
Journal of Neuroimaging 医学-核医学
CiteScore
4.70
自引率
0.00%
发文量
117
审稿时长
6-12 weeks
期刊介绍: Start reading the Journal of Neuroimaging to learn the latest neurological imaging techniques. The peer-reviewed research is written in a practical clinical context, giving you the information you need on: MRI CT Carotid Ultrasound and TCD SPECT PET Endovascular Surgical Neuroradiology Functional MRI Xenon CT and other new and upcoming neuroscientific modalities.The Journal of Neuroimaging addresses the full spectrum of human nervous system disease, including stroke, neoplasia, degenerating and demyelinating disease, epilepsy, tumors, lesions, infectious disease, cerebral vascular arterial diseases, toxic-metabolic disease, psychoses, dementias, heredo-familial disease, and trauma.Offering original research, review articles, case reports, neuroimaging CPCs, and evaluations of instruments and technology relevant to the nervous system, the Journal of Neuroimaging focuses on useful clinical developments and applications, tested techniques and interpretations, patient care, diagnostics, and therapeutics. Start reading today!
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信