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Quantitative Susceptibility Mapping and R2*Measured Changes during White Matter Lesion Development in Multiple Sclerosis: Myelin Breakdown, Myelin Debris Degradation and Removal, and Iron Accumulation

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单位: [1]Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Radiol, Wuhan, Peoples R China [2]Weill Cornell Med Coll, Dept Radiol, 515 East 71th St, New York, NY 10021 USA [3]Weill Cornell Med Coll, Dept Neurol, New York, NY USA [4]Weill Cornell Med Coll, Dept Healthcare Policy & Res, New York, NY USA [5]Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06510 USA [6]Cornell Univ, Dept Biomed Engn, Ithaca, NY USA
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BACKGROUND BACKGROUND AND PURPOSE: Quantitative susceptibility mapping and R2* are sensitive to myelin and iron changes in multiple sclerosis lesions. This study was designed to characterize lesion changes on quantitative susceptibility mapping and R2* at various gadolinium enhancement stages. MATERIALS AND METHODS: This study included 64 patients with MS with different enhancing patterns in white matter lesions: nodular, shell-like, nonenhancing < 1 year old, and nonenhancing 1-3 years old. These represent acute, late acute, early chronic, and late chronic lesions, respectively. Susceptibility values measured on quantitative susceptibility mapping and R2* values were compared among the 4 lesion types. Their differences were assessed with a generalized estimating equation, controlling for Expanded Disability Status Scale score, age, and disease duration. RESULTS: We analyzed 203 lesions: 80 were nodular-enhancing, of which 77 (96.2%) were isointense on quantitative susceptibility mapping; 33 were shell-enhancing, of which 30 (90.9%) were hyperintense on quantitative susceptibility mapping; and 49 were nonenhancing lesions <1 year old and 41 were nonenhancing lesions 1-3 years old, all of which were hyperintense on quantitative susceptibility mapping. Their relative susceptibility/R2* values were 0.5 +/- 4.4 parts per billion/- 5.6 +/- 2.9 Hz,10.2 +/- 5.4 parts per billion/ -8.0 +/- 2.6 Hz, 20.2 +/- 7.8 parts per billion/-3.1 +/- 2.3 Hz, and 33.2 +/- 8.2 parts per billion/-2.0 +/- 2.6 Hz, respectively, and were significantly different (P < .005). CONCLUSIONS: Early active MS lesions with nodular enhancement show R2* decrease but no quantitative susceptibility mapping change, reflecting myelin breakdown; late active lesions with peripheral enhancement show R2* decrease and quantitative susceptibility mapping increase in the lesion center, reflecting further degradation and removal of myelin debris; and early or late chronic nonenhancing lesions show both quantitative susceptibility mapping and R2* increase, reflecting iron accumulation.

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出版当年[2015]版:
大类 | 3 区 医学
小类 | 2 区 核医学 3 区 临床神经病学 3 区 神经成像
最新[2025]版:
大类 | 2 区 医学
小类 | 2 区 核医学 3 区 临床神经病学 3 区 神经成像
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出版当年[2014]版:
Q1 CLINICAL NEUROLOGY Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Q2 NEUROIMAGING
最新[2023]版:
Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Q2 CLINICAL NEUROLOGY Q2 NEUROIMAGING

影响因子: 最新[2023版] 最新五年平均 出版当年[2014版] 出版当年五年平均 出版前一年[2013版] 出版后一年[2015版]

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第一作者单位: [1]Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Radiol, Wuhan, Peoples R China [2]Weill Cornell Med Coll, Dept Radiol, 515 East 71th St, New York, NY 10021 USA
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通讯机构: [2]Weill Cornell Med Coll, Dept Radiol, 515 East 71th St, New York, NY 10021 USA [6]Cornell Univ, Dept Biomed Engn, Ithaca, NY USA
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