Satoshi Kitagawa, Kenji Kufukihara, Haruhiko Motegi, Koji Sekiguchi, Yayoi Sato, Jin Nakahara
{"title":"q-Space 髓鞘图:用于多发性硬化症治疗监测的新型髓鞘特异性成像技术","authors":"Satoshi Kitagawa, Kenji Kufukihara, Haruhiko Motegi, Koji Sekiguchi, Yayoi Sato, Jin Nakahara","doi":"10.1111/cen3.12796","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objectives</h3>\n \n <p>In multiple sclerosis (MS) patients, hyperintense signals on T2-weighted images by magnetic resonance imaging are signs of demyelination; however, T2 signals lack specificity and fail to detect remyelination. For more precise monitoring of MS, a new magnetic resonance imaging technique, <i>q</i>-space Myelin Map (qMM), which specifically identifies myelin, has been developed. This study aimed to explore clinical factors associated with remyelination for different disease-modifying drugs, and to examine the utility and feasibility of qMM in clinical practice.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Data from sequential patients with relapsing–remitting MS initiating disease-modifying drugs at our center were collected. After treatment initiation, qMM was carried out at 6-month intervals and the resulting images analyzed for evidence of remyelination.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A total of 48 patients with relapsing–remitting MS were included: 22 with dimethyl fumarate, 14 with fingolimod, four with glatiramer acetate and eight with natalizumab. qMM showed qMM-remyelination in 22 patients (45.8%). In natalizumab patients, baseline ages were 33.6 ± 6.9 years (<i>n</i> = 5) and 47.3 ± 5.8 years (<i>n</i> = 3) in patients with or without qMM remyelination, respectively. In dimethyl fumarate patients, the proportion of women was 100% (<i>n</i> = 10) and 50% (<i>n</i> = 12) in patients with or without qMM myelination, respectively.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>This exploratory study suggested the potential clinical utility of qMM for visualizing remyelination in MS patients and fine-tuning their pharmacotherapy. Two potential clinical factors promoting qMM-remyelination were identified: female sex with dimethyl fumarate and younger baseline age with natalizumab; a larger prospective study is warranted to confirm these results.</p>\n </section>\n </div>","PeriodicalId":10193,"journal":{"name":"Clinical and Experimental Neuroimmunology","volume":"15 4","pages":"169-176"},"PeriodicalIF":0.0000,"publicationDate":"2024-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cen3.12796","citationCount":"0","resultStr":"{\"title\":\"q-Space Myelin Map: A new myelin-specific imaging technique for treatment monitoring of multiple sclerosis\",\"authors\":\"Satoshi Kitagawa, Kenji Kufukihara, Haruhiko Motegi, Koji Sekiguchi, Yayoi Sato, Jin Nakahara\",\"doi\":\"10.1111/cen3.12796\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Objectives</h3>\\n \\n <p>In multiple sclerosis (MS) patients, hyperintense signals on T2-weighted images by magnetic resonance imaging are signs of demyelination; however, T2 signals lack specificity and fail to detect remyelination. For more precise monitoring of MS, a new magnetic resonance imaging technique, <i>q</i>-space Myelin Map (qMM), which specifically identifies myelin, has been developed. This study aimed to explore clinical factors associated with remyelination for different disease-modifying drugs, and to examine the utility and feasibility of qMM in clinical practice.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Data from sequential patients with relapsing–remitting MS initiating disease-modifying drugs at our center were collected. After treatment initiation, qMM was carried out at 6-month intervals and the resulting images analyzed for evidence of remyelination.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>A total of 48 patients with relapsing–remitting MS were included: 22 with dimethyl fumarate, 14 with fingolimod, four with glatiramer acetate and eight with natalizumab. qMM showed qMM-remyelination in 22 patients (45.8%). In natalizumab patients, baseline ages were 33.6 ± 6.9 years (<i>n</i> = 5) and 47.3 ± 5.8 years (<i>n</i> = 3) in patients with or without qMM remyelination, respectively. In dimethyl fumarate patients, the proportion of women was 100% (<i>n</i> = 10) and 50% (<i>n</i> = 12) in patients with or without qMM myelination, respectively.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>This exploratory study suggested the potential clinical utility of qMM for visualizing remyelination in MS patients and fine-tuning their pharmacotherapy. Two potential clinical factors promoting qMM-remyelination were identified: female sex with dimethyl fumarate and younger baseline age with natalizumab; a larger prospective study is warranted to confirm these results.</p>\\n </section>\\n </div>\",\"PeriodicalId\":10193,\"journal\":{\"name\":\"Clinical and Experimental Neuroimmunology\",\"volume\":\"15 4\",\"pages\":\"169-176\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cen3.12796\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical and Experimental Neuroimmunology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/cen3.12796\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Immunology and Microbiology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Experimental Neuroimmunology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/cen3.12796","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
q-Space Myelin Map: A new myelin-specific imaging technique for treatment monitoring of multiple sclerosis
Objectives
In multiple sclerosis (MS) patients, hyperintense signals on T2-weighted images by magnetic resonance imaging are signs of demyelination; however, T2 signals lack specificity and fail to detect remyelination. For more precise monitoring of MS, a new magnetic resonance imaging technique, q-space Myelin Map (qMM), which specifically identifies myelin, has been developed. This study aimed to explore clinical factors associated with remyelination for different disease-modifying drugs, and to examine the utility and feasibility of qMM in clinical practice.
Methods
Data from sequential patients with relapsing–remitting MS initiating disease-modifying drugs at our center were collected. After treatment initiation, qMM was carried out at 6-month intervals and the resulting images analyzed for evidence of remyelination.
Results
A total of 48 patients with relapsing–remitting MS were included: 22 with dimethyl fumarate, 14 with fingolimod, four with glatiramer acetate and eight with natalizumab. qMM showed qMM-remyelination in 22 patients (45.8%). In natalizumab patients, baseline ages were 33.6 ± 6.9 years (n = 5) and 47.3 ± 5.8 years (n = 3) in patients with or without qMM remyelination, respectively. In dimethyl fumarate patients, the proportion of women was 100% (n = 10) and 50% (n = 12) in patients with or without qMM myelination, respectively.
Conclusions
This exploratory study suggested the potential clinical utility of qMM for visualizing remyelination in MS patients and fine-tuning their pharmacotherapy. Two potential clinical factors promoting qMM-remyelination were identified: female sex with dimethyl fumarate and younger baseline age with natalizumab; a larger prospective study is warranted to confirm these results.