FLAIR☆: A Combined MR Contrast Technique for Visualizing White Matter Lesions and Parenchymal Veins
FLAIR☆: A Combined MR Contrast Technique for Visualizing White Matter Lesions and Parenchymal Veins
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DOI:
10.1148/radiol.12120208
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发表时间:
2012-12-01
期刊:
影响因子:
19.7
通讯作者:
Reich, Daniel S.
中科院分区:
文献类型:
--
作者:
Sati, Pascal;George, Ilena C.;Reich, Daniel S.
Purpose: To evaluate a magnetic resonance (MR) imaging contrast technique, called FLAIR(star), that combines the advantages of T2-weighted fluid-attenuated inversion recovery (FLAIR) contrast and T2(star)-weighted contrast on a single image for assessment of white matter (WM) diseases such as multiple sclerosis (MS).Materials and Methods: This prospective pilot study was HIPAA compliant and institutional review board approved. Ten patients with clinically definite MS (eight men, two women; mean age, 41 years) provided informed consent and underwent 3.0-T MR imaging. Images from a T2-weighted FLAIR sequence were combined with images from a T2(star)-weighted segmented echo-planar imaging sequence performed during contrast material injection, yielding high-isotropic-resolution (0.55 x 0.55 x 0.55 mm(3)) FLAIR(star) images. Qualitative assessment was performed for image quality, lesion conspicuity, and vein conspicuity. Contrast-to-noise ratio (CNR) was calculated to compare normal-appearing WM (NAWM) with cerebrospinal fluid, lesions, and veins. To evaluate the differences in CNR among imaging modalities, a bootstrap procedure clustered on subjects was used, together with paired t tests.Results: High-quality FLAIR(star) images of the brain were produced at 3.0 T, yielding conspicuous lesions and veins. Lesion-to-NAWM and NAWM-to-vein CNR values were significantly higher for FLAIR(star) images than for T2-weighted FLAIR images (P < .0001). Findings on FLAIR(star) images included intralesional veins for lesions located throughout the brain and a hypointense rim around some WM lesions.Conclusion: High-isotropic-resolution FLAIR(star) images obtained at 3.0 T yield high contrast for WM lesions and parenchymal veins, making it well suited to investigate the relationship between WM abnormalities and veins in a clinical setting. (C) RSNA, 2012