2005
DOI: 10.1001/archneur.62.9.1371
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Prediction of Longitudinal Brain Atrophy in Multiple Sclerosis by Gray Matter Magnetic Resonance Imaging T2 Hypointensity

Abstract: Background: Gray matter magnetic resonance imaging T2 hypointensity, a marker of iron deposition, is associated with clinical impairment and brain atrophy in cross-sectional studies of multiple sclerosis. Treatment with intramuscular interferon beta-1a limits brain atrophy in the second year of treatment. Objective: To test whether T2 hypointensity predicts brain atrophy and whether interferon affects this relationship.

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Cited by 97 publications

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“…SPMS showed left versus right differences in all these regions (caudate nucleus, P = 0.001; globus pallidus, P = 0.032; putamen, P = 0.019; thalamus, P = 0.036). For all significant differences, except the thalamus in BMS patients, we found more significant GM T2 hypointensity in the left side, consistent with findings shown in previous MRI studies in MS [7,26,43]. Because of these laterality differences, the GM T2 hypointensity for each hemisphere was retained as a variable in each statistical comparison.…”
Section: Results
supporting
confidence: 89%
“…Our findings are in agreement with previous studies showing that GM T2 hypointensity is linked to measures of disease severity [19][20][21][22][23][24][25][26][27]45]. In the present study, we found a moderate correlation with EDSS score in BMS patients.…”
Section: Discussion
supporting
confidence: 94%
“…The presence of MRI-based evidence of GM iron deposition in MS versus HC in our study is in agreement with several other studies, which have used T2 hypointensity [19][20][21][22]24], magnetic field correlation [23], or phase imaging [44]. Previous studies have raised the possibility that GM T2 hypointensity may be a clinically relevant biological marker of brain injury and brain dysfunction [19][20][21][22][23][24][25][26][27]45]. However, unlike previous studies [19][20][21] that have showed more prominent deep GM T2 hypointensity in SPMS when compared with RRMS, we found no differences in GM T2 hypointensity between BMS and SPMS.…”
Section: Discussion
supporting
confidence: 92%
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