bibtype J - Journal Article
ARLID 0586485
utime 20240624155602.5
mtime 20240605235959.9
SCOPUS 85189001729
WOS 001226696000001
DOI 10.1016/j.mri.2024.03.019
title (primary) (eng) Blind deconvolution decreases requirements on temporal resolution of DCE-MRI: Application to 2nd generation pharmacokinetic modeling
specification
page_count 11 s.
media_type P
serial
ARLID cav_un_epca*0254220
ISSN 0730-725X
title Magnetic Resonance Imaging
volume_id 109
page_num 238-248
publisher
name Elsevier
keyword DCE-MRI
keyword Blind deconvolution
keyword 2nd generation pharmacokinetic model
keyword Temporal resolution
author (primary)
ARLID cav_un_auth*0306308
name1 Kratochvíla
name2 Jiří
institution UPT-D
department D3: Magnetická rezonance a Kryogenika
full_dept (cz) D3: Magnetická rezonance a Kryogenika
full_dept (eng) D3: Magnetic Resonance and Cryogenics
garant K
fullinstit Ústav přístrojové techniky AV ČR, v. v. i.
author
ARLID cav_un_auth*0277120
name1 Jiřík
name2 Radovan
institution UPT-D
department D3: Magnetická rezonance a Kryogenika
full_dept (cz) D3: Magnetická rezonance a Kryogenika
full_dept D3: Magnetic Resonance and Cryogenics
fullinstit Ústav přístrojové techniky AV ČR, v. v. i.
author
ARLID cav_un_auth*0312355
name1 Bartoš
name2 Michal
institution UTIA-B
department ZOI
full_dept (cz) Zpracování obrazové informace
full_dept Department of Image Processing
department (cz) ZOI
department ZOI
mrcb701-q Inst Informat Technol & Automation, Inst Informat Technol & Automat, Pod Vodarenskou Vezi 4, Prague, Czech Republic,
fullinstit Ústav teorie informace a automatizace AV ČR, v. v. i.
author
ARLID cav_un_auth*0278224
name1 Standara
name2 M.
country CZ
mrcb701-q Masaryk Mem Canc Inst, Dept Radiol, Zluty Kopec 7, Brno 65653, Czech Republic,
author
ARLID cav_un_auth*0101622
name1 Starčuk jr.
name2 Zenon
institution UPT-D
department D3: Magnetická rezonance a Kryogenika
full_dept (cz) D3: Magnetická rezonance a Kryogenika
full_dept D3: Magnetic Resonance and Cryogenics
fullinstit Ústav přístrojové techniky AV ČR, v. v. i.
author
ARLID cav_un_auth*0277119
name1 Taxt
name2 T.
country NO
mrcb701-q Univ Bergen, Dept Biomed, Jonas Lies Vei 91, Bergen, Norway,
source
url https://www.sciencedirect.com/science/article/pii/S0730725X24000754
cas_special
project
project_id GA22-10953S
agency GA ČR
country CZ
ARLID cav_un_auth*0438251
project
project_id LM2023050
agency GA MŠk
country CZ
ARLID cav_un_auth*0445613
abstract (eng) Purpose: Dynamic Contrast-Enhanced (DCE) MRI with 2nd generation pharmacokinetic models provides estimates of plasma flow and permeability surface-area product in contrast to the broadly used 1st generation models (e.g. the Tofts models). However, the use of 2nd generation models requires higher frequency with which the dynamic images are acquired (around 1.5 s per image). Blind deconvolution can decrease the demands on temporal resolution as shown previously for one of the 1st generation models. Here, the temporal-resolution requirements achievable for blind deconvolution with a 2nd generation model are studied. Methods: The 2nd generation model is formulated as the distributed-capillary adiabatic-tissue-homogeneity (DCATH) model. Blind deconvolution is based on Parker's model of the arterial input function. The accuracy and precision of the estimated arterial input functions and the perfusion parameters is evaluated on synthetic and real clinical datasets with different levels of the temporal resolution. Results: The estimated arterial input functions remained unchanged from their reference high-temporalresolution estimates (obtained with the sampling interval around 1 s) when increasing the sampling interval up to about 5 s for synthetic data and up to 3.6-4.8 s for real data. Further increasing of the sampling intervals led to systematic distortions, such as lowering and broadening of the 1st pass peak. The resulting perfusionparameter estimation error was below 10% for the sampling intervals up to 3 s (synthetic data), in line with the real data perfusion-parameter boxplots which remained unchanged up to the sampling interval 3.6 s. Conclusion: We show that use of blind deconvolution decreases the demands on temporal resolution in DCE-MRI from about 1.5 s (in case of measured arterial input functions) to 3-4 s. This can be exploited in increased spatial resolution or larger organ coverage.
result_subspec WOS
RIV FS
FORD0 20000
FORD1 20600
FORD2 20601
reportyear 2025
num_of_auth 6
mrcbC47 UTIA-B 10000 10200 10201
mrcbC52 4 A sml 4as 20240618125157.8
mrcbC55 UTIA-B JC
inst_support RVO:68081731
inst_support RVO:67985556
permalink https://hdl.handle.net/11104/0353995
cooperation
ARLID cav_un_auth*0313487
name Masarykův onkologický ústav, Brno
country CZ
cooperation
ARLID cav_un_auth*0301683
name University of Bergen
country NO
mrcbC91 C
mrcbT16-e RADIOLOGYNUCLEARMEDICINEMEDICALIMAGING
mrcbT16-j 0.677
mrcbT16-D Q3
arlyear 2024
mrcbTft \nSoubory v repozitáři: 0586485_Smlouva.pdf
mrcbU01 MAGNETIC RESONANCE IMAGING 0730-725X 2024 109
mrcbU14 85189001729 SCOPUS
mrcbU24 3850829 PUBMED
mrcbU34 001226696000001 WOS
mrcbU63 cav_un_epca*0254220 Magnetic Resonance Imaging Roč. 109 June 2024 238 248 0730-725X 1873-5894 Elsevier