Accumulation of hypointense lesions (''black holes'') on T-1 spin-echo MRI correlates with disease progression in multiple sclerosis

被引:417
作者
Truyen, L
vanWaesberghe, JHTM
vanWalderveen, MAA
vanOosten, BW
Polman, CH
Hommes, OR
Ader, HJA
Barkhof, F
机构
[1] FREE UNIV AMSTERDAM HOSP,DEPT RADIOL,NL-1007 MB AMSTERDAM,NETHERLANDS
[2] FREE UNIV AMSTERDAM HOSP,DUTCH MR CTR MS RES,NL-1007 MB AMSTERDAM,NETHERLANDS
[3] UNIV NIJMEGEN ST RADBOUD HOSP,DEPT NEUROL,NL-6500 HB NIJMEGEN,NETHERLANDS
[4] FREE UNIV AMSTERDAM HOSP,DEPT BIOSTAT & EPIDEMIOL,AMSTERDAM,NETHERLANDS
关键词
D O I
10.1212/WNL.47.6.1469
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
MRI findings are increasingly used as outcome measures in therapeutic trials in MS. The discrepancy between the extent of the lesions on conventional T-2 images and the clinical condition of the patient is one of the problems encountered in such studies. This clinical-radiological paradox prevents the use of MRI data as surrogate markers of disability in MS. A recent pilot study suggested a relationship between hypointense lesions on T-1 MRI and disability. To assess in more detail the correlation of changes in hypointense lesion load on T-1-weighted spin-echo MR images (''black holes'') with changes in disability in MS, we studied 46 patients with clinically definite MS at baseline and after a median follow-up of 40 months. There was a significant correlation between baseline disability and hypointense lesion load (Spearman rank correlation coefficient [SRCC] = 0.46, p = 0.001). in secondary progressive patients, the rate of accumulation of these ''black holes'' was significantly related to progression rate (SRCC = 0.81, p < 0.0001). We speculate that the appearance of hypointense lesions is the MRI equivalent of a failure of remission. Overall, T-1 lesion load measurements correlated better with clinical assessments than T-2 lesion load measurements. Quantification of hypointense lesion load on T-1-weighted spin-echo MRI helps to resolve the clinical-radiological paradox between disability and MRI and has the potential to be a surrogate marker of disability in MS.
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页码:1469 / 1476
页数:8
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