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Myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the Fontan circulation

INTRODUCTION: Single ventricle diastolic dysfunction and hepatic fibrosis are frequently observed in patients with a Fontan circulation. The relationship between adverse haemodynamics and end-organ fibrosis has not been investigated in adolescents and young adults with Fontan circulation. METHODS: P...

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Autores principales: Alsaied, Tarek, Moore, Ryan A, Lang, Sean M, Truong, Vien, Lubert, Adam M, Veldtman, Gruschen R, Averin, Konstantin, Dillman, Jonathan R, Trout, Andrew T, Mazur, Wojciech, Taylor, Michael D, He, Quan, Morales, David LS, Redington, Andrew N, Goldstein, Bryan H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7592252/
https://www.ncbi.nlm.nih.gov/pubmed/33109703
http://dx.doi.org/10.1136/openhrt-2020-001434
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author Alsaied, Tarek
Moore, Ryan A
Lang, Sean M
Truong, Vien
Lubert, Adam M
Veldtman, Gruschen R
Averin, Konstantin
Dillman, Jonathan R
Trout, Andrew T
Mazur, Wojciech
Taylor, Michael D
He, Quan
Morales, David LS
Redington, Andrew N
Goldstein, Bryan H
author_facet Alsaied, Tarek
Moore, Ryan A
Lang, Sean M
Truong, Vien
Lubert, Adam M
Veldtman, Gruschen R
Averin, Konstantin
Dillman, Jonathan R
Trout, Andrew T
Mazur, Wojciech
Taylor, Michael D
He, Quan
Morales, David LS
Redington, Andrew N
Goldstein, Bryan H
author_sort Alsaied, Tarek
collection PubMed
description INTRODUCTION: Single ventricle diastolic dysfunction and hepatic fibrosis are frequently observed in patients with a Fontan circulation. The relationship between adverse haemodynamics and end-organ fibrosis has not been investigated in adolescents and young adults with Fontan circulation. METHODS: Prospective observational study of Fontan patients who had a cardiac catheterisation. Cardiac MRI with T1 mapping was obtained to measure extracellular volume (ECV), a marker of myocardial fibrosis. Hepatic magnetic resonance elastography was performed to assess liver shear stiffness. Serum biomarkers of fibrosis including matrix metalloproteinases (MMPs) and tissue inhibitor of metalloproteinases (TIMPs) were measured. Very high ECV was defined as >30% and elevated serum biomarkers as >75th percentile for each biomarker. RESULTS: 25 Fontan patients (52% female) with mean age of 16.3±6.8 years were included. Mean ECV was 28%±5%. There was a significant correlation between ECV and systemic ventricular end-diastolic pressure (r=0.42, p=0.03) and between ECV and liver stiffness (r=0.45, p=0.05). Patients with elevated ECV demonstrated elevations in MMPs and TIMPs. Similarly, patients with elevated MMPs and TIMPs had greater liver stiffness compared with patients with normal levels of these biomarkers. CONCLUSIONS: In Fontan patients, cardiac magnetic resonance evidence of myocardial fibrosis is associated with diastolic dysfunction, increased liver stiffness and elevated circulating biomarkers of fibrosis. These findings suggest the presence of a profibrotic milieu, with end-organ implications, in some patients with Fontan circulation.
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spelling pubmed-75922522020-10-29 Myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the Fontan circulation Alsaied, Tarek Moore, Ryan A Lang, Sean M Truong, Vien Lubert, Adam M Veldtman, Gruschen R Averin, Konstantin Dillman, Jonathan R Trout, Andrew T Mazur, Wojciech Taylor, Michael D He, Quan Morales, David LS Redington, Andrew N Goldstein, Bryan H Open Heart Congenital Heart Disease INTRODUCTION: Single ventricle diastolic dysfunction and hepatic fibrosis are frequently observed in patients with a Fontan circulation. The relationship between adverse haemodynamics and end-organ fibrosis has not been investigated in adolescents and young adults with Fontan circulation. METHODS: Prospective observational study of Fontan patients who had a cardiac catheterisation. Cardiac MRI with T1 mapping was obtained to measure extracellular volume (ECV), a marker of myocardial fibrosis. Hepatic magnetic resonance elastography was performed to assess liver shear stiffness. Serum biomarkers of fibrosis including matrix metalloproteinases (MMPs) and tissue inhibitor of metalloproteinases (TIMPs) were measured. Very high ECV was defined as >30% and elevated serum biomarkers as >75th percentile for each biomarker. RESULTS: 25 Fontan patients (52% female) with mean age of 16.3±6.8 years were included. Mean ECV was 28%±5%. There was a significant correlation between ECV and systemic ventricular end-diastolic pressure (r=0.42, p=0.03) and between ECV and liver stiffness (r=0.45, p=0.05). Patients with elevated ECV demonstrated elevations in MMPs and TIMPs. Similarly, patients with elevated MMPs and TIMPs had greater liver stiffness compared with patients with normal levels of these biomarkers. CONCLUSIONS: In Fontan patients, cardiac magnetic resonance evidence of myocardial fibrosis is associated with diastolic dysfunction, increased liver stiffness and elevated circulating biomarkers of fibrosis. These findings suggest the presence of a profibrotic milieu, with end-organ implications, in some patients with Fontan circulation. BMJ Publishing Group 2020-10-27 /pmc/articles/PMC7592252/ /pubmed/33109703 http://dx.doi.org/10.1136/openhrt-2020-001434 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Congenital Heart Disease
Alsaied, Tarek
Moore, Ryan A
Lang, Sean M
Truong, Vien
Lubert, Adam M
Veldtman, Gruschen R
Averin, Konstantin
Dillman, Jonathan R
Trout, Andrew T
Mazur, Wojciech
Taylor, Michael D
He, Quan
Morales, David LS
Redington, Andrew N
Goldstein, Bryan H
Myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the Fontan circulation
title Myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the Fontan circulation
title_full Myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the Fontan circulation
title_fullStr Myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the Fontan circulation
title_full_unstemmed Myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the Fontan circulation
title_short Myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the Fontan circulation
title_sort myocardial fibrosis, diastolic dysfunction and elevated liver stiffness in the fontan circulation
topic Congenital Heart Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7592252/
https://www.ncbi.nlm.nih.gov/pubmed/33109703
http://dx.doi.org/10.1136/openhrt-2020-001434
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