Histopathologic correlate of hypointense lesions on T1-weighted spin-echo MRI in multiple sclerosis

被引:532
作者
van Walderveen, MAA
Kamphorst, W
Scheltens, P
van Waesberghe, JHTM
Ravid, R
Valk, J
Polman, CH
Barkhof, F
机构
[1] Vrije Univ Amsterdam, Acad Hosp, MR Ctr MS Res, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Acad Hosp, Dept Radiol, NL-1007 MB Amsterdam, Netherlands
[3] Netherlands Brain Bank, Amsterdam, Netherlands
关键词
D O I
10.1212/WNL.50.5.1282
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Postmortem unfixed whole brains from five multiple sclerosis (RIS) patients were examined by MRI using a T2- and T1-weighted spin-echo (SE) sequence and histology to investigate the histopathologic characteristics of hypointense lesions on T1-weighted SE MR images. The degree of hypointensity was scored semiquantitatively by two blinded observers in reference to normal-appearing white matter. Signal intensities of the lesions and the normal-appearing white matter were measured to obtain contrast ratios. Hematoxylin-eosin stain was used to assess degree of matrix destruction (decrease of density of the neuropil) and cellularity of a lesion, Kluver-Barrera stain for degree of demyelination, Bodian stain for axonal density, and immunostaining of glial fibrillary acid protein for reactive astrocytes and fibrillary gliosis. Nineteen lesions were selected for analysis. Nearly all lesions were compatible with the chronic MS plaque: hypocellularity, absence of myelinated axons, in the presence of reactive astrocytes. Contrast ratios of the lesions were highly correlated (R = -0.90; p < 0.01), with degree of hypointensity scored semiquantitatively. Degree of hypointensity on T1-weighted SE images did not correlate with degree of demyelination or number of reactive astrocytes, but was associated with axonal density (R = -0.71; p = 0.001). A trend was found with degree of matrix destruction (R = 0.45; p = 0.052). We conclude that, in our limited sample, hypointense lesions seen on T1-weighted SE MR images are associated histopathologically with severe tissue destruction, including axonal loss. Our results need to be substantiated in a larger study on more varied patient material to evaluate the use of hypointense lesions as a surrogate marker of persistent deficit in MS patients.
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页码:1282 / 1288
页数:7
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