TY - JOUR
T1 - Cervical cord myelin water imaging shows degenerative changes over one year in multiple sclerosis but not neuromyelitis optica spectrum disorder
AU - Combes, Anna J.E.
AU - Matthews, Lucy
AU - Lee, Jimmy S.
AU - Li, David K.B.
AU - Carruthers, Robert
AU - Traboulsee, Anthony L.
AU - Barker, Gareth J.
AU - Palace, Jacqueline
AU - Kolind, Shannon
N1 - Funding Information:
Special thanks go to the study participants who gave up their time for this research. The authors would also like to thank Eric Fu and Janet Lam for assistance with statistical analysis, as well as everyone involved in initial data collection; the NHS Highly Specialised Service for neuromyelitis optica; support staff at the John Radcliffe Hospital and Nuffield Department of Clinical Neurosciences, University of Oxford, including the radiographers and specialist nurses; and Prof Angela Vincent and Dr. Mark Woodhall for antibody testing the patient cohort. This work was funded by an MRC fellowship to Dr. Matthews (G0901996) and a postdoctoral fellowship from the MS Society of Canada to Prof Kolind (#1034). We are also grateful for support from the NIHR Oxford Biomedical Research Centre, the Milan & Maureen Ilich Foundation and the Diamond Family Foundation.
Publisher Copyright:
© 2017 The Authors
PY - 2017
Y1 - 2017
N2 - Spinal cord pathology is a feature of both neuromyelitis optica spectrum disorder (NMOSD) and relapsing-remitting multiple sclerosis (MS). While subclinical disease activity has been described in MS using quantitative magnetic resonance imaging measures, current evidence suggests that neurodegeneration is absent between relapses in NMOSD, although most evidence comes from brain studies. We aimed to assess cross-sectional differences and longitudinal changes in myelin integrity in relapse-free MS and NMOSD subjects over one year. 15 NMOSD, 15 MS subjects, and 17 healthy controls were scanned at 3 T using a cervical cord mcDESPOT protocol. A subset of 8 NMOSD, 11 MS subjects and 14 controls completed follow-up. Measures of the myelin water fraction (fM) within lesioned and non-lesioned cord segments were collected. At baseline, fM in lesioned and non-lesioned segments was significantly reduced in MS (lesioned: p = 0.002; non-lesioned: p = 0.03) and NMOSD (lesioned: p = 0.0007; non-lesioned: p = 0.002) compared to controls. Longitudinally, fM decreased within non-lesioned cord segments in the MS group (− 7.3%, p = 0.02), but not in NMOSD (+ 5.8%, p = 0.1), while change in lesioned segments fM did not differ from controls' in either patient group. These results suggest that degenerative changes outside of lesioned areas can be observed over a short time frame in MS, but not NMOSD, and support the use of longitudinal myelin water imaging for the assessment of pathological changes in the cervical cord in demyelinating diseases.
AB - Spinal cord pathology is a feature of both neuromyelitis optica spectrum disorder (NMOSD) and relapsing-remitting multiple sclerosis (MS). While subclinical disease activity has been described in MS using quantitative magnetic resonance imaging measures, current evidence suggests that neurodegeneration is absent between relapses in NMOSD, although most evidence comes from brain studies. We aimed to assess cross-sectional differences and longitudinal changes in myelin integrity in relapse-free MS and NMOSD subjects over one year. 15 NMOSD, 15 MS subjects, and 17 healthy controls were scanned at 3 T using a cervical cord mcDESPOT protocol. A subset of 8 NMOSD, 11 MS subjects and 14 controls completed follow-up. Measures of the myelin water fraction (fM) within lesioned and non-lesioned cord segments were collected. At baseline, fM in lesioned and non-lesioned segments was significantly reduced in MS (lesioned: p = 0.002; non-lesioned: p = 0.03) and NMOSD (lesioned: p = 0.0007; non-lesioned: p = 0.002) compared to controls. Longitudinally, fM decreased within non-lesioned cord segments in the MS group (− 7.3%, p = 0.02), but not in NMOSD (+ 5.8%, p = 0.1), while change in lesioned segments fM did not differ from controls' in either patient group. These results suggest that degenerative changes outside of lesioned areas can be observed over a short time frame in MS, but not NMOSD, and support the use of longitudinal myelin water imaging for the assessment of pathological changes in the cervical cord in demyelinating diseases.
KW - Longitudinal study
KW - Magnetic resonance imaging
KW - Multiple sclerosis
KW - Myelin water imaging
KW - Neuromyelitis optica
KW - Spinal cord
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U2 - 10.1016/j.nicl.2017.06.019
DO - 10.1016/j.nicl.2017.06.019
M3 - Article
C2 - 28725551
AN - SCOPUS:85021961560
SN - 2213-1582
VL - 16
SP - 17
EP - 22
JO - NeuroImage: Clinical
JF - NeuroImage: Clinical
ER -