Evidence map›Paper›PMID 31415613›Full record

ArticlePloS one2019

A pharmacokinetic model including arrival time for two inputs and compensating for varying applied flip-angle in dynamic gadoxetic acid-enhanced MR imaging.

Tian Zhang, Jurgen H Runge, Cristina Lavini, Jaap Stoker, Thomas van Gulik, Kasia P Cieslak, Lucas J van Vliet, Frans M Vos

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Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Tian ZhangDepartment of Imaging Physics, Delft University of Technology, Delft, The Netherlands.ORCID 0000-0002-9091-2358
Jurgen H RungeDepartment of Radiology, Academic Medical Center, Amsterdam, The Netherlands.
Cristina LaviniDepartment of Radiology, Academic Medical Center, Amsterdam, The Netherlands.
Jaap StokerDepartment of Radiology, Academic Medical Center, Amsterdam, The Netherlands.
Thomas van GulikDepartment of Surgery, Academic Medical Center, Amsterdam, The Netherlands.
Kasia P CieslakDepartment of Surgery, Academic Medical Center, Amsterdam, The Netherlands.
Lucas J van VlietDepartment of Imaging Physics, Delft University of Technology, Delft, The Netherlands.
Frans M VosDepartment of Imaging Physics, Delft University of Technology, Delft, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePharmacokinetic models facilitate assessment of properties of the micro-vascularization based on DCE-MRI data. However, accurate pharmacokinetic modeling in the liver is challenging since it has two vascular inputs and it is subject to large deformation and displacement due to respiration.

methodsWe propose an improved pharmacokinetic model for the liver that (1) analytically models the arrival-time of the contrast agent for both inputs separately; (2) implicitly compensates for signal fluctuations that can be modeled by varying applied flip-angle e.g. due to B1-inhomogeneity. Orton's AIF model is used to analytically represent the vascular input functions. The inputs are independently embedded into the Sourbron model. B1-inhomogeneity-driven variations of flip-angles are accounted for to justify the voxel's displacement with respect to a pre-contrast image.

resultsThe new model was shown to yield lower root mean square error (RMSE) after fitting the model to all but a minority of voxels compared to Sourbron's approach. Furthermore, it outperformed this existing model in the majority of voxels according to three model-selection criteria.

conclusionOur work primarily targeted to improve pharmacokinetic modeling for DCE-MRI of the liver. However, other types of pharmacokinetic models may also benefit from our approaches, since the techniques are generally applicable.

Indexed as

AgedAlgorithmsContrast MediaFemaleGadolinium DTPAHumansImage EnhancementLiverLiver NeoplasmsMagnetic Resonance ImagingMaleMiddle AgedModels, BiologicalContrast MediaGadolinium DTPAgadolinium ethoxybenzyl DTPA

Identifiers

PMID31415613
PMCPMC6695151

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