Cargando…

Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool

BACKGROUND: In terms of cardiovascular magnetic resonance are haematocrit values required for calculation of extracellular volume fraction (ECV). Previously published studies have hypothesized that haematocrit could be calculated from T1 blood pool relaxation time, however only native T1 relaxation...

Descripción completa

Detalles Bibliográficos
Autores principales: Opatril, Lukas, Panovsky, Roman, Machal, Jan, Holecek, Tomas, Masarova, Lucia, Feitova, Vera, Kincl, Vladimir, Hodejovsky, Marek, Spinarova, Lenka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325220/
https://www.ncbi.nlm.nih.gov/pubmed/34330214
http://dx.doi.org/10.1186/s12872-021-02179-z
_version_ 1783731523170598912
author Opatril, Lukas
Panovsky, Roman
Machal, Jan
Holecek, Tomas
Masarova, Lucia
Feitova, Vera
Kincl, Vladimir
Hodejovsky, Marek
Spinarova, Lenka
author_facet Opatril, Lukas
Panovsky, Roman
Machal, Jan
Holecek, Tomas
Masarova, Lucia
Feitova, Vera
Kincl, Vladimir
Hodejovsky, Marek
Spinarova, Lenka
author_sort Opatril, Lukas
collection PubMed
description BACKGROUND: In terms of cardiovascular magnetic resonance are haematocrit values required for calculation of extracellular volume fraction (ECV). Previously published studies have hypothesized that haematocrit could be calculated from T1 blood pool relaxation time, however only native T1 relaxation time values have been used and the resulting formulae had been both in reciprocal and linear proportion. The aim of the study was to generate a synthetic haematocrit formula from only native relaxation time values first, calculate whether linear or reciprocal model is more precise in haematocrit estimation and then determine whether adding post-contrast values further improve its precision. METHODS: One hundred thirty-nine subjects underwent CMR examination. Haematocrit was measured using standard laboratory methods. Afterwards T1 relaxation times before and after the application of a contrast agent were measured and a statistical relationship between these values was calculated. RESULTS: Different linear and reciprocal models were created to estimate the value of synthetic haematocrit and ECV. The highest coefficient of determination was observed in the combined reciprocal model “− 0.047 + (779/ blood native) − (11.36/ blood post-contrast)”. CONCLUSIONS: This study provides more evidence that assessing synthetic haematocrit and synthetic ECV is feasible and statistically most accurate model to use is reciprocal. Adding post-contrast values to the calculation was proved to improve the precision of the formula statistically significantly.
format Online
Article
Text
id pubmed-8325220
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-83252202021-08-02 Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool Opatril, Lukas Panovsky, Roman Machal, Jan Holecek, Tomas Masarova, Lucia Feitova, Vera Kincl, Vladimir Hodejovsky, Marek Spinarova, Lenka BMC Cardiovasc Disord Research BACKGROUND: In terms of cardiovascular magnetic resonance are haematocrit values required for calculation of extracellular volume fraction (ECV). Previously published studies have hypothesized that haematocrit could be calculated from T1 blood pool relaxation time, however only native T1 relaxation time values have been used and the resulting formulae had been both in reciprocal and linear proportion. The aim of the study was to generate a synthetic haematocrit formula from only native relaxation time values first, calculate whether linear or reciprocal model is more precise in haematocrit estimation and then determine whether adding post-contrast values further improve its precision. METHODS: One hundred thirty-nine subjects underwent CMR examination. Haematocrit was measured using standard laboratory methods. Afterwards T1 relaxation times before and after the application of a contrast agent were measured and a statistical relationship between these values was calculated. RESULTS: Different linear and reciprocal models were created to estimate the value of synthetic haematocrit and ECV. The highest coefficient of determination was observed in the combined reciprocal model “− 0.047 + (779/ blood native) − (11.36/ blood post-contrast)”. CONCLUSIONS: This study provides more evidence that assessing synthetic haematocrit and synthetic ECV is feasible and statistically most accurate model to use is reciprocal. Adding post-contrast values to the calculation was proved to improve the precision of the formula statistically significantly. BioMed Central 2021-07-31 /pmc/articles/PMC8325220/ /pubmed/34330214 http://dx.doi.org/10.1186/s12872-021-02179-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Opatril, Lukas
Panovsky, Roman
Machal, Jan
Holecek, Tomas
Masarova, Lucia
Feitova, Vera
Kincl, Vladimir
Hodejovsky, Marek
Spinarova, Lenka
Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool
title Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool
title_full Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool
title_fullStr Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool
title_full_unstemmed Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool
title_short Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool
title_sort extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation t1 times of a blood pool
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325220/
https://www.ncbi.nlm.nih.gov/pubmed/34330214
http://dx.doi.org/10.1186/s12872-021-02179-z
work_keys_str_mv AT opatrillukas extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool
AT panovskyroman extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool
AT machaljan extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool
AT holecektomas extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool
AT masarovalucia extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool
AT feitovavera extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool
AT kinclvladimir extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool
AT hodejovskymarek extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool
AT spinarovalenka extracellularvolumequantificationusingsynthetichaematocritassessedfromnativeandpostcontrastlongitudinalrelaxationt1timesofabloodpool