Novel parameter estimation methods for /sup 11/C-acetate dual-input liver model with dynamic PET

The successful investigation of 11C-acetate in positron emission tomography (PET) imaging for marking hepatocellular carcinoma (HCC) has been validated by both clinical and quantitative modeling studies. In the previous quantitative studies, all the individual model parameters were estimated by the weighted nonlinear least squares (NLS) algorithm. However, five parameters need to be estimated simultaneously, therefore, the computational time-complexity is high and some estimates are not quite reliable, which limits its application in clinical environment. In addition, liver system modeling with dual-input function is very different from the widespread single-input system modeling. Therefore, most of the currently developed estimation techniques are not applicable. In this paper, two parameter estimation techniques: graphed NLS (GNLS) and graphed dual-input generalized linear least squares (GDGLLS) algorithms were presented for 11C-acetate dual-input liver model. Clinical and simulated data were utilized to test the proposed algorithms by a systematic statistical analysis. Compared to NLS fitting, these two novel methods achieve better estimation reliability and are computationally efficient, and they are extremely powerful for the estimation of the two potential HCC indicators: local hepatic metabolic rate-constant of acetate and relative portal venous contribution to the hepatic blood flow

[1]  鳥塚 達郎,et al.  Value of fluorine-18-FDG-PET to monitor hepatocellular carcinoma after interventional therapy , 1995 .

[2]  Chi-Lai Ho,et al.  11C-acetate PET imaging in hepatocellular carcinoma and other liver masses. , 2003, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[3]  David Dagan Feng,et al.  Noninvasive quantification of the differential portal and arterial contribution to the liver blood supply from PET measurements using the 11C-acetate kinetic model , 2004, IEEE Trans. Biomed. Eng..

[4]  H. Akaike A new look at the statistical model identification , 1974 .

[5]  G. Schwarz Estimating the Dimension of a Model , 1978 .

[6]  S. Huang,et al.  Weighted Integration Method for Local Cerebral Blood Flow Measurements with Positron Emission Tomography , 1986, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[7]  Dagan Feng,et al.  An unbiased parametric imaging algorithm for nonuniformly sampled biomedical system parameter estimation , 1996, IEEE Trans. Medical Imaging.

[8]  M E Phelps,et al.  Measurement of Local Blood Flow and Distribution Volume with Short-Lived Isotopes: A General Input Technique , 1982, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[9]  L. Bass,et al.  Liver kinetics of glucose analogs measured in pigs by PET: importance of dual-input blood sampling. , 2001, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[10]  M. Ozaki,et al.  Evaluation of liver tumors using fluorine-18-fluorodeoxyglucose PET: characterization of tumor and assessment of effect of treatment. , 1992, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[11]  C S Patlak,et al.  Graphical Evaluation of Blood-to-Brain Transfer Constants from Multiple-Time Uptake Data , 1983, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[12]  Zheru Chi,et al.  Tracer kinetic modeling of /sup 11/C-acetate applied in the liver with positron emission tomography , 2004, IEEE Transactions on Medical Imaging.