@article{b1e3b178e75c459ba669bcee7bf474d3,
title = "7T MRI Differentiates Remyelinated from Demyelinated Multiple Sclerosis Lesions",
abstract = "Objective: To noninvasively assess myelin status in chronic white matter lesions of multiple sclerosis (MS), we developed and evaluated a simple classification scheme based on T1 relaxation time maps derived from 7-tesla postmortem and in vivo MRI. Methods: Using the MP2RAGE MRI sequence, we classified 36 lesions from 4 postmortem MS brains as “long-T1,” “short-T1,” and “mixed-T1” by visual comparison to neocortex. Within these groups, we compared T1 times to histologically derived measures of myelin and axons. We performed similar analysis of 235 chronic lesions with known date of onset in 25 MS cases in vivo and in a validation cohort of 222 lesions from 66 MS cases, investigating associations with clinical and radiological outcomes. Results: Postmortem, lesions classified qualitatively as long-T1, short-T1, and mixed-T1 corresponded to fully demyelinated, fully remyelinated, and mixed demyelinated/remyelinated lesions, respectively (p ≤ 0.001). Demyelination (rather than axon loss) dominantly contributed to initial T1 prolongation. We observed lesions with similar characteristics in vivo, allowing manual classification with substantial interrater and excellent intrarater reliability. Short-T1 lesions were most common in the deep white matter, whereas long-T1 and mixed-T1 lesions were prevalent in the juxtacortical and periventricular white matter (p = 0.02) and were much more likely to have paramagnetic rims suggesting chronic inflammation (p < 0.001). Older age at the time of lesion formation portended less remyelination (p = 0.007). Interpretation: 7-tesla T1 mapping with MP2RAGE, a clinically available MRI method, allows qualitative and quantitative classification of chronic MS lesions according to myelin content, rendering straightforward the tracking of lesional myelination changes over time. ANN NEUROL 2021;90:612–626.",
author = "Hadar Kolb and Martina Absinta and Beck, {Erin S.} and Ha, {Seung Kwon} and Yeajin Song and Gina Norato and Irene Cortese and Pascal Sati and Govind Nair and Reich, {Daniel S.}",
note = "Funding Information: We thank the staff and fellows of the NINDS Neuroimmunology Clinic for recruiting and evaluating study participants, Rose Cuento for protocol support, and the NIMH Functional Magnetic Resonance Facility for helping with MRI scanning. We thank Tobias Kober and Sunil Patil of Siemens Healthineers for assistance with implementation of the MP2RAGE sequence. The study was supported by Intramural Research Program of the National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH); the Myelin Repair Foundation; and the Adelson Medical Research Foundation. Martina Absinta is also supported by the Conrad N. Hilton Foundation (Marylin Hilton Bridging Award for Physician‐Scientists, grant #17313), the Roche Foundation for Independent Research, the Cariplo Foundation (grant #1677) and the FRRB Early Career Award (grant#1750327). Erin Beck is also supported by a Career Transition Fellowship from the National Multiple Sclerosis Society. Funding Information: We thank the staff and fellows of the NINDS Neuroimmunology Clinic for recruiting and evaluating study participants, Rose Cuento for protocol support, and the NIMH Functional Magnetic Resonance Facility for helping with MRI scanning. We thank Tobias Kober and Sunil Patil of Siemens Healthineers for assistance with implementation of the MP2RAGE sequence. The study was supported by Intramural Research Program of the National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH); the Myelin Repair Foundation; and the Adelson Medical Research Foundation. Martina Absinta is also supported by the Conrad N. Hilton Foundation (Marylin Hilton Bridging Award for Physician-Scientists, grant #17313), the Roche Foundation for Independent Research, the Cariplo Foundation (grant #1677) and the FRRB Early Career Award (grant#1750327). Erin Beck is also supported by a Career Transition Fellowship from the National Multiple Sclerosis Society. Publisher Copyright: Published 2021. This article is a U.S. Government work and is in the public domain in the USA. Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.",
year = "2021",
month = oct,
doi = "10.1002/ana.26194",
language = "English (US)",
volume = "90",
pages = "612--626",
journal = "Annals of Neurology",
issn = "0364-5134",
publisher = "John Wiley and Sons Inc.",
number = "4",
}