Original Article
Copyright ©2012 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Radiol. Jul 28, 2012; 4(7): 291-301
Published online Jul 28, 2012. doi: 10.4329/wjr.v4.i7.291
Impact of the arterial input function on microvascularization parameter measurements using dynamic contrast-enhanced ultrasonography
Marianne Gauthier, Stéphanie Pitre-Champagnat, Farid Tabarout, Ingrid Leguerney, Mélanie Polrot, Nathalie Lassau
Marianne Gauthier, Stéphanie Pitre-Champagnat, Farid Tabarout, Ingrid Leguerney, Nathalie Lassau, IR4M-UMR 8081, Institut Gustave Roussy, 94805 Villejuif cedex, France
Mélanie Polrot, Service Commun d’Expérimentation Animale, Institut Gustave Roussy, 94805 Villejuif cedex, France
Nathalie Lassau, Institut de recherche en cancérologie à Villejuif, Institut Gustave Roussy, 94805 Villejuif cedex, France
Author contributions: Gauthier M performed the majority of experiments, designed the study and wrote the manuscript; Pitre-Champagnat S and Polrot M provided substantial contributions to conception, design, acquisition, analysis and interpretation of the data; Tabarout F provided substantial contributions to conception and design; Leguerney I was involved in analyzing results and editing the manuscript; and Lassau N managed each step of the study, provided contribution to data analyses and was involved in editing the manuscript.
Correspondence to: Marianne Gauthier, PhD, IR4M-UMR 8081, Institut Gustave Roussy, Pavillon de recherche I, 39 rue Camille Desmoulins, 94805 Villejuif cedex, France. gauthier.marianne@gmail.com
Telephone: +33-1-42116215 Fax: +33-1-42115495
Received: April 22, 2012
Revised: June 5, 2012
Accepted: June 12, 2012
Published online: July 28, 2012
Abstract

AIM: To evaluate the sources of variation influencing the microvascularization parameters measured by dynamic contrast-enhanced ultrasonography (DCE-US).

METHODS: Firstly, we evaluated, in vitro, the impact of the manual repositioning of the ultrasound probe and the variations in flow rates. Experiments were conducted using a custom-made phantom setup simulating a tumor and its associated arterial input. Secondly, we evaluated, in vivo, the impact of multiple contrast agent injections and of examination day, as well as the influence of the size of region of interest (ROI) associated with the arterial input function (AIF). Experiments were conducted on xenografted B16F10 female nude mice. For all of the experiments, an ultrasound scanner along with a linear transducer was used to perform pulse inversion imaging based on linear raw data throughout the experiments. Semi-quantitative and quantitative analyses were performed using two signal-processing methods.

RESULTS: In vitro, no microvascularization parameters, whether semi-quantitative or quantitative, were significantly correlated (P values from 0.059 to 0.860) with the repositioning of the probe. In addition, all semi-quantitative microvascularization parameters were correlated with the flow variation while only one quantitative parameter, the tumor blood flow, exhibited P value lower than 0.05 (P = 0.004). In vivo, multiple contrast agent injections had no significant impact (P values from 0.060 to 0.885) on microvascularization parameters. In addition, it was demonstrated that semi-quantitative microvascularization parameters were correlated with the tumor growth while among the quantitative parameters, only the tissue blood flow exhibited P value lower than 0.05 (P = 0.015). Based on these results, it was demonstrated that the ROI size of the AIF had significant influence on microvascularization parameters: in the context of larger arterial ROI (from 1.17 ± 0.6 mm3 to 3.65 ± 0.3 mm3), tumor blood flow and tumor blood volume were correlated with the tumor growth, exhibiting P values lower than 0.001.

CONCLUSION: AIF selection is an essential aspect of the deconvolution process to validate the quantitative DCE-US method.

Keywords: Dynamic contrast-enhanced ultrasonography; Angiogenesis; Linear raw data; Arterial input function; Functional imaging