Comparison of the performance of tracer kinetic model-driven registration for dynamic contrast enhanced MRI using different models of contrast enhancement

被引:32
|
作者
Buonaccorsi, Giovanni A.
Roberts, Caleb
Cheung, Sue
Watson, Yvonne
O'Connor, James P. B.
Davies, Karen
Jackson, Alan
Jayson, Gordon C.
Parker, Geoff J. M.
机构
[1] Univ Manchester, Dept Imaging Sci & Biomed Engn, Manchester M13 9PT, Lancs, England
[2] Christie Hosp NHS Trust, Dept Med Oncol, Canc Res UK, Manchester M20 4BX, Lancs, England
基金
英国医学研究理事会;
关键词
MRI; Gd-DTPA; image processing; computer-assisted; angiogenesis inhibitors; image registration;
D O I
10.1016/j.acra.2006.05.016
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
Rationale and Objectives. The quantitative analysis of dynamic contrast-enhanced (DCE) magnetic resonance imaging (MRI) data is subject to model fitting errors caused by motion during the time-series data acquisition. However, the time-varying features that occur as a result of contrast enhancement can confound motion correction techniques based on conventional registration similarity measures. We have therefore developed a heuristic, locally controlled tracer kinetic model-driven registration procedure, in which the model accounts for contrast enhancement, and applied it to the registration of abdominal DCE-MRI data at high temporal resolution. Materials and Methods. Using severely motion-corrupted data sets that had been excluded from analysis in a clinical trial of an antiangiogenic agent, we compared the results obtained when using different models to drive the tracer kinetic model-driven registration with those obtained when using a conventional registration against the time series mean image volume. Results. Using tracer kinetic model-driven registration, it was possible to improve model fitting by reducing the sum of squared errors but the improvement was only realized when using a model that adequately described the features of the time series data. The registration against the time series mean significantly distorted the time series data, as did tracer kinetic model-driven registration using a simpler model of contrast enhancement. Conclusion. When an appropriate model is used, tracer kinetic model-driven registration influences motion-corrupted model fit parameter estimates and provides significant improvements in localization in three-dimensional parameter maps. This has positive implications for the use of quantitative DCE-MRl for example in clinical trials of antiangiogenic or antivascular agents.
引用
收藏
页码:1112 / 1123
页数:12
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