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Magnetic Resonance Imaging of Myelin
Open accessAbstract
The ability to measure myelin in vivo has great consequences for furthering our knowledge of normal development, as well as for understanding a wide range of neurological disorders. The following review summarizes the current state of myelin imaging using MR. We consider five MR techniques that have been used to study myelin: 1) conventional MR, 2) MR spectroscopy, 3) diffusion, 4) magnetization transfer, and 5) T2 relaxation. Fundamental studies involving peripheral nerve and MR/histology comparisons have aided in the interpretation and validation of MR data. We highlight a number of important findings related to myelin development, damage, and repair, and we conclude with a critical summary of the current techniques available and their potential to image myelin in vivo.
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“a relatively abundant MAG level might indicate a relatively intact myelin-axon interface in the CD1 mice, albeit a damaged outer myelin sheath.”
From Strain differences in cuprizone induced demyelination (2017) · cites this paper as [37]
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Cites
Solving least squares problems
Björk, Ǎ., Lawson, C., & Hanson, R. (1976) · Classics in applied mathematics · doi:10.2307/2286501 · Cited by 7,171
Solving Least Squares Problems
Lawson, C. L., & Hanson, R. J. (1995) · doi:10.1137/1.9781611971217 · Cited by 7,103
The basis of anisotropic water diffusion in the nervous system—A technical review.
Beaulieu, C. (2002) · NMR in Biomedicine · doi:10.1002/nbm.782 · Cited by 4,628
Axonal transection in the lesions of multiple sclerosis
Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029
Dysmyelination revealed through MRI as increased radial (but unchanged axial) diffusion of water
Song, S.-K., Sun, S.-W., Ramsbottom, M. J., Chang, C., Russell, J., & Cross, A. H. (2002) · NeuroImage · doi:10.1006/nimg.2002.1267 · Cited by 2,582
Regional Development of the Brain in Early Life
(1968) · Archives of Disease in Childhood · doi:10.1136/adc.43.229.388 · Cited by 2,107
Song, S.-K., Sun, S.-W., Ju, W.-K., Lin, S.-J., Cross, A. H., & Neufeld, A. H. (2003) · NeuroImage · doi:10.1016/j.neuroimage.2003.07.005 · Cited by 1,738
A Method for the Combined Staining of Cells and Fibers in the Nervous System
Klüver, H., & Barrera, E. (1953) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-195312040-00008 · Cited by 1,724
Demyelination increases radial diffusivity in corpus callosum of mouse brain
Song, S.-K., Yoshino, J., Le, T. Q., Lin, S.-J., Sun, S.-W., Cross, A. H., & Armstrong, R. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.01.028 · Cited by 1,658
Magnetization transfer contrast (MTC) and tissue water proton relaxation in vivo
Wolff, S. D., & Balaban, R. S. (1989) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910100113 · Cited by 1,482
Research works printed but not linked: 5
- Yung, 2004, Measurements of myelin water in rat spinal cord in vivo, Int Soc Magn Reson Med, 1537
- Minty, 2002, Measurement of myelin water in human and bovine spinal cord, Int Soc Magn Reson Med Sci, 940
- Laule, 2003, Cervical cord abnormalities in primary progressive multiple sclerosis: atrophy and myelin water changes, Mult Scler, 9, S63
- Helms, 2000, Regression analysis of metabolite concentrations estimated from localized proton MR spectra of active and chronic multiple sclerosis lesions, Magn Reson Med, 43, 102, 10.1002/(SICI)1522-2594(200001)43:1<102::AID-MRM12>3.0.CO;2-I · DOI
- Leuzzi, 2007, The pathogenesis of the white matter abnormalities in phenylketonuria, J Inherit Metab Dis, 23, 23
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Stüber, C., Morawski, M., Schäfer, A., Labadie, C., Wähnert, M., Leuze, C., Streicher, M., Barapatre, N., Reimann, K., Geyer, S., et al. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.02.026 · Cited by 635
Rae, C. D. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1199-5 · Cited by 524
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Serag, A., Aljabar, P., Ball, G., Counsell, S. J., Boardman, J. P., Rutherford, M., Edwards, A. D., Hajnal, J. V., & Rueckert, D. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.062 · Cited by 316
Studying neuroanatomy using MRI
Lerch, J. P., van der Kouwe, A. J. W., Raznahan, A., Paus, T., Johansen‐Berg, H., Miller, K. L., Smith, S. M., Fischl, B. R., & Sotiropoulos, S. N. (2017) · Nature Neuroscience · doi:10.1038/nn.4501 · Cited by 330
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Self-citationMRI‐based myelin water imaging: A technical review
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Mezer, A., Yeatman, J. D., Stikov, N., Kay, K., Cho, N., Dougherty, R. F., Perry, L. M., Parvizi, J., Hua, L. H., Pauly, K. B., et al. (2013) · Nature Medicine · doi:10.1038/nm.3390 · Cited by 276
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Mondelli, V., Vernon, A. C., Turkheimer, F., Dazzan, P., & Pariante, C. M. (2017) · The Lancet Psychiatry · doi:10.1016/s2215-0366(17)30101-3 · Cited by 271
Wisnieff, C., Ramanan, S., Olesik, J., Gauthier, S., Wang, Y., & Pitt, D. (2015) · Magnetic Resonance in Medicine · doi:10.1002/mrm.25420 · Cited by 245
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Self-citationWhole brain myelin mapping using T1- and T2-weighted MR imaging data.
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Samartzis, L., Dima, D., Fusar‐Poli, P., & Kyriakopoulos, M. (2014) · Journal of Neuroimaging · doi:10.1111/j.1552-6569.2012.00779.x · Cited by 236
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Nilsson, M., van Westen, D., Ståhlberg, F., Sundgren, P. C., & Lätt, J. (2013) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-013-0371-x · Cited by 163
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Stikov, N., Perry, L. M., Mezer, A., Rykhlevskaia, E. I., Wandell, B. A., Pauly, J. M., & Dougherty, R. F. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.068 · Cited by 145
Sacchet, M. D., & Gotlib, I. H. (2017) · Scientific Reports · doi:10.1038/s41598-017-02062-y · Cited by 153
Sepehrband, F., Clark, K. A., Ullmann, J. F. P., Kurniawan, N. D., Leanage, G., Reutens, D. C., & Yang, Z. (2015) · Human Brain Mapping · doi:10.1002/hbm.22872 · Cited by 143
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Bock, N. A., Kocharyan, A., Liu, J. V., & Silva, A. C. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.08.022 · Cited by 143
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Denk, C., Hernández‐Torres, E., MacKay, A. L., & Rauscher, A. (2010) · NMR in Biomedicine · doi:10.1002/nbm.1581 · Cited by 135
Self-citationPromise and pitfalls of g-ratio estimation with MRI
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Edwards, L., Kirilina, E. P., Mohammadi, S., & Weiskopf, N. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.02.055 · Cited by 122
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Billiet, T., Mädler, B., D'Arco, F., Peeters, R., Deprez, S., Plasschaert, E., Leemans, A., Zhang, H., den Bergh, B. V., Vandenbulcke, M., et al. (2014) · NeuroImage: Clinical · doi:10.1016/j.nicl.2014.04.005 · Cited by 101
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Girard, O. M., Prévost, V., Varma, G., Cozzone, P. J., Alsop, D. C., & Duhamel, G. (2014) · Magnetic Resonance in Medicine · doi:10.1002/mrm.25330 · Cited by 62
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Drori, E., Berman, S., & Mezer, A. (2022) · Science Advances · doi:10.1126/sciadv.abm1971 · Cited by 52
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Self-citationDrakesmith, M., Dutt, A., Fonville, L., Zammit, S., Reichenberg, A., Evans, J., Lewis, G., Jones, D. K., & David, A. S. (2016) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.3375 · Cited by 50
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Beljebbar, A., Amharref, N., Lévèques, A., Dukic, S., Ventéo, L., Schneider, L., Pluot, M., & Manfait, M. (2008) · Analytical Chemistry · doi:10.1021/ac800990y · Cited by 48
Advances in MRI of the myelin bilayer
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Understanding aqueous and non-aqueous proton T1 relaxation in brain
Manning, A. P., MacKay, A. L., & Michal, C. A. (2021) · Journal of Magnetic Resonance · doi:10.1016/j.jmr.2020.106909 · Cited by 47
Self-citationHypothyroidism and mood disorders: integrating novel insights from brain imaging techniques
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Self-citation
Metadata
- Authors
- Laule, C., Vavasour, I. M., Kolind, S. H., Li, D. K. B., Traboulsee, T. L., Moore, G. R. W., & MacKay, A. L.
- Affiliations
- University of British Columbia (CA)
- University of British Columbia Hospital (CA)
- Corresponding author
- Laule, Cornelia
- Venue
- Neurotherapeutics
- Publisher
- Elsevier BV
- Published
- 2007-07
- Volume
- 4
- Issue
- 3
- Pages
- 460-484
- ISSN
- 1878-7479 (ISSN-L)
- PMC
- PMC7479725
- OpenAlex
- W2080423736
- Cited by
- 334
- References
- 291
- Citations by year
- 2026: 9 · 2025: 17 · 2024: 20 · 2023: 19 · 2022: 17 · 2021: 28 · 2020: 32 · 2019: 28 · 2018: 23 · 2017: 27 · 2016: 16 · 2015: 17 · 2014: 18 · 2013: 15 · 2012: 8
- FWCI
- 1.15
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neurotherapeutics (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Multiple Sclerosis Society of Canada
- Multiple Sclerosis Society
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Keywords
- myelin imaging, myelin, myelination, myelin damage, remyelination, MR spectroscopy, diffusion MRI, magnetization transfer, T2 relaxation, peripheral nerves
- MeSH terms
- Animals, Humans, Magnetic Resonance Imaging, Myelin Sheath
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