Fundamental image quality limits for microcomputed tomography in small animals

被引:160
作者
Ford, NL [1 ]
Thornton, MM
Holdsworth, DW
机构
[1] John P Robarts Res Inst, Imaging Res Labs, London, ON N6A 5K8, Canada
[2] Univ Western Ontario, Dept Med Biophys, London, ON N6A 5B8, Canada
[3] GE Co, Med Syst Genom & Mol Imaging, London, ON N6A 4X8, Canada
[4] Univ Western Ontario, Dept Diagnost Radiol, London, ON N6A 5B8, Canada
关键词
high-resolution imaging; image quality; linear attenuation coefficients; small-animal imaging; micro computed tomography;
D O I
10.1118/1.1617353
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Small-animal imaging has become increasingly more important as transgenic and knockout mice are produced to model human diseases. One imaging technique that has emerged is microcomputed tomography (micro-CT). For live-animal imaging, the precision in the images will be determined by the x-ray dose given to the animal. As a result, we propose a simple method to predict the noise performance of an x-ray micro-CT system as a function of dose and image resolution. An ideal, quantum-noise limited micro-CT scanner, assumed to have perfect resolution and ideal efficiency, was modeled. Using a simplified model, the coefficient of variation (COV) of the linear attenuation coefficient was calculated for a range of entrance doses and isotropic voxel sizes. COV calculations were performed for the ideal case and with simulated imperfections in efficiency and resolution. Our model was validated in phantom studies and mouse images were acquired with a specimen scanner to illustrate the results. A simplified model of noise propagation in the case of isotropic resolution indicates that the COV in the linear attenuation coefficient is proportional to (dose)(-1/2) and to the (isotropic voxel size)(-2) in the reconstructed volume. Therefore an improvement in the precision can be achieved only by increasing the isotropic voxel size (thereby decreasing the resolution of the image) or by increasing the x-ray dose. For the ideal scanner, a COV of 1% in the linear attenuation coefficient for an image of a mouse exposed to 0.25 Gy is obtained with a minimum isotropic voxel size of 135 mum. However, the same COV is achieved at a dose of 5.0 Gy with a 65 mum isotropic voxel size. Conversely, for a 68 mm diameter rat, a COV of 1% obtained from an image at 5.0 Gy would require an isotropic voxel size of 100 mum. These results indicate that short-term, potentially lethal, effects of ionizing radiation will limit high-resolution live animal imaging. As improvements in detector technology allow the resolution to improve, by decreasing the detector element size to tens of microns or less, high quality images will be limited by the x-ray dose administered. For the highest quality images, these doses will approach the lethal dose or LD50 for the animals. Approaching the lethal dose will affect the way experiments are planned, and may reduce opportunities for experiments involving imaging the same animal over time. Dose considerations will become much more important for live small-animal imaging as the limits of resolution are tested. (C) 2003 American Association of Physicists in Medicine.
引用
收藏
页码:2869 / 2877
页数:9
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