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Quantitative Functional MR Imaging of the Visual Cortex at 1.5 T as a Function of Luminance Contrast in Healthy Volunteers and Patients with Multiple Sclerosis

机译:在健康志愿者和多发性硬化症患者中,视皮质的1.5 T定量功能性MR成像与亮度对比的函数

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BACKGROUND AND PURPOSE: In patients with multiple sclerosis (MS), a few preliminary functional MR (fMR) imaging studies of the visual cortex reveal information about magnitude differences between healthy individuals and patients with MS at only a single luminance level. We therefore investigated whether varying luminance contrast levels can help uncover subtle changes in fMR imaging characteristics of the visual cortex in healthy volunteers and patients with MS. METHODS: Blood oxygenation level–dependent fMR imaging signal changes in the primary visual cortex were examined as a function of luminance contrast at 1.5 T in 10 healthy volunteers and nine patients with MS. Ten axial sections through the calcarine fissure were obtained with an echo-planar T2*-weighted imaging sequence (4000/54/1 [TR/TE/excitation]; field of view, 220 mm; voxel size, 1.72 x 1.72 x 5 mm). The imaging series consisted of an alternating 20-second rest epoch (black screen) with a 20-second activation epoch (flickering checkerboard) repeated six times. Each imaging series used a graded increase of eight luminance contrast levels. A paired t test between rest and activation images was used to analyze significant (P < .001) contiguous voxels in the region of interest (primary visual cortex). RESULTS: A progressive increase in fMR imaging activation across all luminance contrast levels in healthy controls and patients with MS was shown. The patients with MS had a significantly lower magnitude in the number of fMR imaging activated voxels at all luminance contrast levels (P < .001). A statistically significant increase in fMR imaging activation (activation threshold) was seen at the second luminance contrast level in controls and at the seventh level in patients with MS. CONCLUSION: Quantifiable changes in blood oxygenation level-dependent signal and a progressive increase in activated voxels within the primary visual cortex with increasing luminance contrast were demonstrated at 1.5 T in controls. The patients with MS showed a significant decrease in the number of activated voxels and an increase in activation threshold compared with healthy controls.
机译:背景与目的:在多发性硬化症患者中,一些视觉皮层功能性MR(fMR)影像学初步研究 揭示了有关幅度差异的信息 < / sup>健康个体和MS患者之间,仅以 单个亮度级别。因此,我们调查了不同的亮度 对比度水平是否可以帮助揭示健康志愿者和MS患者的视皮层fMR成像特征的细微变化。 方法:检查初级视皮层中血液氧合水平依赖性的fMR成像 信号变化,作为 在10时1.5 T下亮度对比度的函数健康志愿者 和9例MS患者。通过回声平面T2 *加权成像 序列(4000/54/1 [TR / TE /激发],通过钙钛矿 裂缝获得了十个轴向剖面)。视图,220毫米; 体素尺寸,1.72 x 1.72 x 5毫米)。成像系列包括 交替的20秒休息时间(黑屏)和重复 六个的 20秒激活时间(闪烁的棋盘)次。每个成像系列都使用了八个 亮度对比度等级的分级增加。静止图像和 激活图像之间的配对t检验用于分析感兴趣区域中的显着(P <.001) 连续体素(主要视觉 所有亮度对比水平中的fMR成像激活逐渐增加。在所有亮度对比水平下,患有MS的MS患者的fMR成像激活体素的数量均显着降低(P <.001)。在患者的第二个亮度对比水平和患者的第七个水平,fMR成像激活(激活阈值) 的统计学 显着增加结论:血液氧合水平依赖性 信号的可量化变化以及 主视觉皮层内激活体素的逐渐增加,随着亮度的增加对比 在1.5 T的对照中得到证实。 MS 患者与健康的 对照相比,激活的体素 数量显着减少,激活阈值增加。 / sup>

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  • 来源
    《American Journal of Neuroradiology》 |2002年第1期|59-65|共7页
  • 作者单位

    Department of Radiological Sciences, MCP Hahnemann University, Philadelphia, PA|School of Biomedical Engineering and Health Sciences, Drexel University, Philadelphia, PA;

    Department of Radiological Sciences, MCP Hahnemann University, Philadelphia, PA|School of Biomedical Engineering and Health Sciences, Drexel University, Philadelphia, PA;

    Department of Neurology, Thomas Jefferson University, School of Medicine, Philadelphia, PA|School of Biomedical Engineering and Health Sciences, Drexel University, Philadelphia, PA;

    Department of Neurology, MCP Hahnemann University, Philadelphia, PA;

    Department of Radiological Sciences, MCP Hahnemann University, Philadelphia, PA|School of Biomedical Engineering and Health Sciences, Drexel University, Philadelphia, PA;

    Department of Neurology, Mount Sinai School of Medicine, New York, NY;

    Department of Radiological Sciences, MCP Hahnemann University, Philadelphia, PA;

    Tri-Service General Hospital and National Defense Medical Center, Taipei, Taiwan;

    Department of Radiological Sciences, University of California, Irvine, CA;

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