TY - GEN
T1 - A fast reconstruction method for fluorescence molecular tomography based on improved iterated shrinkage
AU - Han, Dong
AU - Tian, Jie
AU - Qin, Chenghu
AU - Zhang, Bo
AU - Liu, Kai
AU - Ma, Xibo
PY - 2011
Y1 - 2011
N2 - Fluorescence molecular tomography (FMT) has become a promising imaging modality for in vivo small animal molecular imaging, and has many successful applications. This is partly due to the wealth of the fluorescent probes. By labeling the regions of interest with fluorescent probes, FMT can achieve non-invasive investigation of the biological process by localizing the targeted probes based on certain inverse mathematical models. However, FMT is usually an ill-posed problem, and some form of regularization should be included to stabilize the problem, which can be considered as the a priori information of the fluorescent probe bio-distribution. When FMT is used for the early detection of tumors, an important characteristic is the sparsity of the fluorescent sources. This is because tumors are usually very small and sparse at this stage. Considering this, general sparsity-promoting Lp-norm regularization is utilized in this paper. The iterated shrinkage based reconstruction method is adopted to solve the general Lp regularization problem. However, the original iterated shrinkage method is proved to have a linear convergence rate, and a large number of iterations are needed to obtain satisfactory results. In this paper, an improved iterated shrinkage based FMT reconstruction algorithm is proposed. By using the solutions from two previous iterations to determine the current solution, the convergence rate can be greatly increased. Heterogeneous simulation experiment shows that the proposed method can obtain comparable results with greatly reduced number of iterations compared with the original iterated shrinkage based method, which makes it a practical reconstruction algorithm.
AB - Fluorescence molecular tomography (FMT) has become a promising imaging modality for in vivo small animal molecular imaging, and has many successful applications. This is partly due to the wealth of the fluorescent probes. By labeling the regions of interest with fluorescent probes, FMT can achieve non-invasive investigation of the biological process by localizing the targeted probes based on certain inverse mathematical models. However, FMT is usually an ill-posed problem, and some form of regularization should be included to stabilize the problem, which can be considered as the a priori information of the fluorescent probe bio-distribution. When FMT is used for the early detection of tumors, an important characteristic is the sparsity of the fluorescent sources. This is because tumors are usually very small and sparse at this stage. Considering this, general sparsity-promoting Lp-norm regularization is utilized in this paper. The iterated shrinkage based reconstruction method is adopted to solve the general Lp regularization problem. However, the original iterated shrinkage method is proved to have a linear convergence rate, and a large number of iterations are needed to obtain satisfactory results. In this paper, an improved iterated shrinkage based FMT reconstruction algorithm is proposed. By using the solutions from two previous iterations to determine the current solution, the convergence rate can be greatly increased. Heterogeneous simulation experiment shows that the proposed method can obtain comparable results with greatly reduced number of iterations compared with the original iterated shrinkage based method, which makes it a practical reconstruction algorithm.
KW - Fluorescence molecular tomography (FMT)
KW - Iterated shrinkage
KW - Optical molecular imaging
UR - https://www.scopus.com/pages/publications/79955836503
U2 - 10.1117/12.878051
DO - 10.1117/12.878051
M3 - 会议稿件
AN - SCOPUS:79955836503
SN - 9780819485076
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Medical Imaging 2011
T2 - Medical Imaging 2011: Biomedical Applications in Molecular, Structural, and Functional Imaging
Y2 - 13 February 2011 through 16 February 2011
ER -