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三维质子波谱在人脑成像中的可重复性研究

Reproducibility of 3D proton spectroscopy in the human brain.

作者信息

Li Belinda S Y, Babb James S, Soher Brian J, Maudsley Andrew A, Gonen Oded

机构信息

Department of Radiology, New York University School of Medicine, New York, New York 10016, USA.

出版信息

Magn Reson Med. 2002 Mar;47(3):439-46. doi: 10.1002/mrm.10081.

Abstract

The inter- and intrasubject reproducibility of the metabolite levels of N-acetylaspartate (NAA), creatine (Cr), and choline (Cho), obtained with three-dimensional (3D) multivoxel proton spectroscopy (1H-MRS), was analyzed in eight healthy volunteers. Serial, back-to-back measurements on a phantom showed the methodology and instrumentation to be highly reproducible, with a median coefficient of variation (CV) of 3.8%. In the human brain, the metabolite levels' variability was larger, with intrasubject median CVs for a total of 1876 signal voxels of 13.8%, 18.5%, and 20.1% for NAA, Cr, and Cho, respectively. These variations possibly arise from small, unavoidable, +/-1-2 mm volume-of-interest (VOI) repositioning uncertainties, which vary each 0.75-cm(3) voxel's partial fluid/gray/white-matter fractions. Comparing the CVs between eight subjects in a total of 324 selected voxels gave total interindividual CVs of 15.6%, 23.3%, and 24.4%, compared with intraindividual CVs in the same voxels of 14.4%, 14.8%, and 15.3%, for NAA, Cr, and Cho, respectively. Replacing the signal(s) from each voxel by the average of itself with its six canonical neighbors reduces the intrasubject median CVs to 8.3%, 9.5%, and 9.7%. The measurement uncertainties can be reduced at a cost of either spatial resolution (by using larger voxels) or time (by performing serial follow-ups).

摘要

在八名健康志愿者中,分析了通过三维(3D)多体素质子磁共振波谱(1H-MRS)获得的N-乙酰天门冬氨酸(NAA)、肌酸(Cr)和胆碱(Cho)代谢物水平的受试者间和受试者内重复性。对体模进行连续的、背对背测量显示该方法和仪器具有高度可重复性,变异系数(CV)中位数为3.8%。在人脑当中,代谢物水平的变异性更大,对于总共1876个信号体素,受试者内NAA、Cr和Cho的CV中位数分别为13.8%、18.5%和20.1%。这些变异可能源于不可避免的小的感兴趣区(VOI)重新定位不确定性(±1-2 mm),这会使每个0.75 cm3体素的部分液体/灰质/白质比例发生变化。比较八名受试者在总共324个选定体素之间的CV,得出NAA、Cr和Cho的个体间总CV分别为15.6%、23.3%和24.4%,而相同体素内的个体内CV分别为14.4%、14.8%和15.3%。用每个体素自身及其六个标准相邻体素的平均值代替每个体素的信号,可将受试者内CV中位数降低至8.3%、9.5%和9.7%。测量不确定性可以通过牺牲空间分辨率(使用更大的体素)或时间(进行连续随访)来降低。

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