TY - JOUR
T1 - Normalizing Flow-Based Distribution Estimation of Pharmacokinetic Parameters in Dynamic Contrast-Enhanced Magnetic Resonance Imaging
AU - Fang, Ke
AU - Wang, Zejun
AU - Xia, Qi
AU - Liu, Yingchao
AU - Wang, Bao
AU - Cheng, Zhaowei
AU - Cheng, Jian
AU - Jin, Xinyu
AU - Bai, Ruiliang
AU - Li, Lanjuan
N1 - Publisher Copyright:
© 1964-2012 IEEE.
PY - 2024/3/1
Y1 - 2024/3/1
N2 - Objective: The pharmacokinetic (PK) parameters estimated from dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) provide valuable information for clinical research and diagnosis. However, these estimated PK parameters suffer from many sources of variability. Thus, the estimation of the posterior distributions of these PK parameters could provide a way to simultaneously quantify the values and uncertainties of the PK parameters. Our objective is to develop an efficient and flexible method to more closely approximate and estimate the underlying posterior distributions of the PK parameters. Methods: The normalizing flow model-based parameters distribution estimation neural network (FPDEN) is proposed to adaptively learn and estimate the posterior distributions of the PK parameters. The maximum likelihood estimation (MLE) loss is directly constructed based on the parameter distributions learned by the normalizing flow model, rather than pre-defined distributions. Results: Experimental analysis shows that the proposed method can improve parameter estimation accuracy. Moreover, the uncertainty derived from the parameter distribution constitutes an effective indicator to exclude unreliable parametric results. A successful demonstration is the improved classification performance of the glioma World Health Organization (WHO) grading task, specifically in terms of distinguishing between low and high grades, as well as between Grade III and Grade IV. Conclusion: The FPDEN method offers improved accuracy for estimation of PK parameters and boosts the performance of the glioma grading task. Significance: By enhancing the precision and reliability of DCE-MRI, the proposed method promotes its further applications in clinical practice.
AB - Objective: The pharmacokinetic (PK) parameters estimated from dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) provide valuable information for clinical research and diagnosis. However, these estimated PK parameters suffer from many sources of variability. Thus, the estimation of the posterior distributions of these PK parameters could provide a way to simultaneously quantify the values and uncertainties of the PK parameters. Our objective is to develop an efficient and flexible method to more closely approximate and estimate the underlying posterior distributions of the PK parameters. Methods: The normalizing flow model-based parameters distribution estimation neural network (FPDEN) is proposed to adaptively learn and estimate the posterior distributions of the PK parameters. The maximum likelihood estimation (MLE) loss is directly constructed based on the parameter distributions learned by the normalizing flow model, rather than pre-defined distributions. Results: Experimental analysis shows that the proposed method can improve parameter estimation accuracy. Moreover, the uncertainty derived from the parameter distribution constitutes an effective indicator to exclude unreliable parametric results. A successful demonstration is the improved classification performance of the glioma World Health Organization (WHO) grading task, specifically in terms of distinguishing between low and high grades, as well as between Grade III and Grade IV. Conclusion: The FPDEN method offers improved accuracy for estimation of PK parameters and boosts the performance of the glioma grading task. Significance: By enhancing the precision and reliability of DCE-MRI, the proposed method promotes its further applications in clinical practice.
KW - DCE-MRI
KW - deep learning
KW - maximum likelihood estimation
KW - normalizing flow model
KW - posterior distribution estimation
UR - https://www.scopus.com/pages/publications/85173031319
U2 - 10.1109/TBME.2023.3318087
DO - 10.1109/TBME.2023.3318087
M3 - 文章
C2 - 37738180
AN - SCOPUS:85173031319
SN - 0018-9294
VL - 71
SP - 780
EP - 791
JO - IEEE Transactions on Biomedical Engineering
JF - IEEE Transactions on Biomedical Engineering
IS - 3
ER -