JIRIK, Radovan, Torfinn TAXT, Ondrej MACICEK, Michal BARTOS, Jiri KRATOCHVILA, Karel SOUČEK, Eva DRAZANOVA, Lucie KRATKA, Aleš HAMPL and Zenon, Jr. STARCUK. Blind deconvolution estimation of an arterial input function for small animal DCE-MRI. MAGNETIC RESONANCE IMAGING. NEW YORK: ELSEVIER SCIENCE INC, 2019, vol. 62, OCT 2019, p. 46-56. ISSN 0730-725X. Available from: https://dx.doi.org/10.1016/j.mri.2019.05.024.
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Basic information
Original name Blind deconvolution estimation of an arterial input function for small animal DCE-MRI
Authors JIRIK, Radovan (203 Czech Republic, guarantor), Torfinn TAXT (578 Norway), Ondrej MACICEK (203 Czech Republic), Michal BARTOS (203 Czech Republic), Jiri KRATOCHVILA (203 Czech Republic), Karel SOUČEK (203 Czech Republic, belonging to the institution), Eva DRAZANOVA (203 Czech Republic), Lucie KRATKA (203 Czech Republic), Aleš HAMPL (203 Czech Republic, belonging to the institution) and Zenon, Jr. STARCUK (203 Czech Republic).
Edition MAGNETIC RESONANCE IMAGING, NEW YORK, ELSEVIER SCIENCE INC, 2019, 0730-725X.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30224 Radiology, nuclear medicine and medical imaging
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.053
RIV identification code RIV/00216224:14110/19:00112960
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1016/j.mri.2019.05.024
UT WoS 000481725200006
Keywords in English DCE-MRI; Blind deconvolution; Arterial input function
Tags 14110517, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 1/4/2020 14:15.
Abstract
Purpose: One of the main obstacles for reliable quantitative dynamic contrast-enhanced (DCE) MRI is the need for accurate knowledge of the arterial input function (AIF). This is a special challenge for preclinical small animal applications where it is very difficult to measure the AIF without partial volume and flow artifacts. Furthermore, using advanced pharmacokinetic models (allowing estimation of blood flow and permeability surface area product in addition to the classical perfusion parameters) poses stricter requirements on the accuracy and precision of AIF estimation. This paper addresses small animal DCE-MRI with advanced pharmacokinetic models and presents a method for estimation of the AIF based on blind deconvolution. Methods: A parametric AIF model designed for small animal physiology and use of advanced pharmacokinetic models is proposed. The parameters of the AIF are estimated using multichannel blind deconvolution. Results: Evaluation on simulated data show that for realistic signal to noise ratios blind deconvolution AIF estimation leads to comparable results as the use of the true AIF. Evaluation on real data based on DCE-MRI with two contrast agents of different molecular weights showed a consistence with the known effects of the molecular weight. Conclusion: Multi-channel blind deconvolution using the proposed AIF model specific for small animal DCE-MRI provides reliable perfusion parameter estimates under realistic signal to noise conditions.
Links
EE2.3.20.0185, research and development projectName: Centrum analýz a modelování tkání a orgánů
EF16_013/0001775, research and development projectName: Modernizace a podpora výzkumných aktivit národní infrastruktury pro biologické a medicínské zobrazování Czech-BioImaging
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