High-Temporal-Resolution Lung Kinetic Modeling Using Total-Body Dynamic PET with Time-Delay and Dispersion Corrections

被引:9
|
作者
Wang, Yiran [1 ,2 ]
Spencer, Benjamin A. [1 ,2 ]
Schmall, Jeffrey [3 ]
Li, Elizabeth [2 ]
Badawi, Ramsey D. [1 ,2 ]
Jones, Terry [1 ]
Cherry, Simon R. [1 ,2 ]
Wang, Guobao [1 ]
机构
[1] Univ Calif Sacramento, Dept Radiol, Davis Med Ctr, Sacramento, CA 95819 USA
[2] Univ Calif Davis, Dept Biomed Engn, Davis, CA 95616 USA
[3] United Imaging Healthcare America Inc, Houston, TX USA
基金
美国国家卫生研究院;
关键词
total-body PET; kinetic modeling; dynamic PET; lung; high temporal resolution; POSITRON-EMISSION-TOMOGRAPHY; BLOOD-FLOW; F-18-FDG UPTAKE; QUANTIFICATION; CANCER; EXPRESSION; AGE;
D O I
10.2967/jnumed.122.264810
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
Tracer kinetic modeling in dynamic PET has the potential to improve the diagnosis, prognosis, and research of lung diseases. The advent of total body PET systems with much greater detection sensitivity enables high temporal-resolution (HTR) dynamic PET imaging of the lungs. However, existing models may become insufficient for modeling the HTR data. In this paper, we investigate the necessity of additional corrections to the input function for HTR lung kinetic modeling. Methods: Dynamic scans with HTR frames of as short as 1 s were performed on 13 healthy subjects with a bolus injection of about 370 MBq of 18F-FDG using the uEXPLORER total-body PET/CT system. Three kinetic models with and without time-delay and dispersion corrections were compared for the quality of lung time-activity curve fitting using the Akaike information criterion. The impact on quantification of 18F-FDG delivery rate K1, net influx rate Ki and fractional blood volume vb was assessed. Parameter identifiability analysis was also performed to evaluate the reliability of kinetic quantification with respect to noise. Correlation of kinetic parameters with age was investigated. Results: HTR dynamic imaging clearly revealed the rapid change in tracer concentration in the lungs and blood supply (i.e., the right ventricle). The uncorrected input function led to poor time-activity curve fitting and biased quantification in HTR kinetic modeling. The fitting was improved by time-delay and dispersion corrections. The proposed model resulted in an approximately 85% decrease in K1, an approximately 75% increase in Ki, and a more reasonable vb (-0.14) than the uncorrected model (-0.04). The identifiability analysis showed that the proposed models had good quantification stability for K1, Ki, and vb. The vb estimated by the proposed model with simultaneous time-delay and dispersion corrections correlated inversely with age, as would be expected. Conclusion: Corrections to the input function are important for accurate lung kinetic analysis of HTR dynamic PET data. The modeling of both delay and dispersion can improve model fitting and significantly impact quantification of K1, Ki, and vb.
引用
收藏
页码:1154 / 1161
页数:8
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