Cargando…

Characterization of Myocardial Microstructure and Function in an Experimental Model of Isolated Subendocardial Damage

Subendocardial damage is among the first cardiac manifestations of hypertension and is already present in asymptomatic disease states. Accordingly, markers of subendocardial impairment may facilitate early detection of cardiac damages and risk stratification under these conditions. This study aimed...

Descripción completa

Detalles Bibliográficos
Autores principales: Beyhoff, Niklas, Lohr, David, Foryst-Ludwig, Anna, Klopfleisch, Robert, Brix, Sarah, Grune, Jana, Thiele, Arne, Erfinanda, Lasti, Tabuchi, Arata, Kuebler, Wolfgang M., Pieske, Burkert, Schreiber, Laura M., Kintscher, Ulrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott, Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635061/
https://www.ncbi.nlm.nih.gov/pubmed/31291149
http://dx.doi.org/10.1161/HYPERTENSIONAHA.119.12956
_version_ 1783435812781686784
author Beyhoff, Niklas
Lohr, David
Foryst-Ludwig, Anna
Klopfleisch, Robert
Brix, Sarah
Grune, Jana
Thiele, Arne
Erfinanda, Lasti
Tabuchi, Arata
Kuebler, Wolfgang M.
Pieske, Burkert
Schreiber, Laura M.
Kintscher, Ulrich
author_facet Beyhoff, Niklas
Lohr, David
Foryst-Ludwig, Anna
Klopfleisch, Robert
Brix, Sarah
Grune, Jana
Thiele, Arne
Erfinanda, Lasti
Tabuchi, Arata
Kuebler, Wolfgang M.
Pieske, Burkert
Schreiber, Laura M.
Kintscher, Ulrich
author_sort Beyhoff, Niklas
collection PubMed
description Subendocardial damage is among the first cardiac manifestations of hypertension and is already present in asymptomatic disease states. Accordingly, markers of subendocardial impairment may facilitate early detection of cardiac damages and risk stratification under these conditions. This study aimed to investigate the impact of subendocardial damage on myocardial microstructure and function to elucidate early pathophysiologic processes and to identify corresponding diagnostic measures. Mice (n=38) were injected with isoproterenol to induce isolated subendocardial scarring or saline as corresponding control. Cardiac function and myocardial deformation were determined by high-frequency echocardiography. The cardiac stress response was assessed in a graded exercise test and during dobutamine stress echocardiography. Myocardial microstructure was studied ex vivo by 7 T diffusion tensor magnetic resonance imaging at a spatial resolution of 100×100×100 µm(3). Results were correlated with histology and biomarker expression. Subendocardial fibrosis was accompanied by diastolic dysfunction, impaired longitudinal deformation (global peak longitudinal strain [LS]: −12.5±0.5% versus −15.6±0.5%; P<0.001) and elevated biomarker expression (ANP [atrial natriuretic peptide], Galectin-3, and ST2). Systolic function and cardiac stress response remained preserved. Diffusion tensor magnetic resonance imaging revealed a left-shift in helix angle towards lower values in isoproterenol-treated animals, which was mainly determined by subepicardial myofibers (mean helix angle: 2.2±0.8° versus 5.9±1.0°; P<0.01). Longitudinal strain and subepicardial helix angle were highly predictive for subendocardial fibrosis (sensitivity, 82%–92% and specificity, 89%–90%). The results indicate that circumscribed subendocardial damage alone can cause several hallmarks observed in cardiovascular high-risk patients. Microstructural remodeling under these conditions involves also remote regions, and corresponding changes in longitudinal strain and helix angle might serve as diagnostic markers.
format Online
Article
Text
id pubmed-6635061
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Lippincott, Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-66350612019-09-16 Characterization of Myocardial Microstructure and Function in an Experimental Model of Isolated Subendocardial Damage Beyhoff, Niklas Lohr, David Foryst-Ludwig, Anna Klopfleisch, Robert Brix, Sarah Grune, Jana Thiele, Arne Erfinanda, Lasti Tabuchi, Arata Kuebler, Wolfgang M. Pieske, Burkert Schreiber, Laura M. Kintscher, Ulrich Hypertension Original Articles Subendocardial damage is among the first cardiac manifestations of hypertension and is already present in asymptomatic disease states. Accordingly, markers of subendocardial impairment may facilitate early detection of cardiac damages and risk stratification under these conditions. This study aimed to investigate the impact of subendocardial damage on myocardial microstructure and function to elucidate early pathophysiologic processes and to identify corresponding diagnostic measures. Mice (n=38) were injected with isoproterenol to induce isolated subendocardial scarring or saline as corresponding control. Cardiac function and myocardial deformation were determined by high-frequency echocardiography. The cardiac stress response was assessed in a graded exercise test and during dobutamine stress echocardiography. Myocardial microstructure was studied ex vivo by 7 T diffusion tensor magnetic resonance imaging at a spatial resolution of 100×100×100 µm(3). Results were correlated with histology and biomarker expression. Subendocardial fibrosis was accompanied by diastolic dysfunction, impaired longitudinal deformation (global peak longitudinal strain [LS]: −12.5±0.5% versus −15.6±0.5%; P<0.001) and elevated biomarker expression (ANP [atrial natriuretic peptide], Galectin-3, and ST2). Systolic function and cardiac stress response remained preserved. Diffusion tensor magnetic resonance imaging revealed a left-shift in helix angle towards lower values in isoproterenol-treated animals, which was mainly determined by subepicardial myofibers (mean helix angle: 2.2±0.8° versus 5.9±1.0°; P<0.01). Longitudinal strain and subepicardial helix angle were highly predictive for subendocardial fibrosis (sensitivity, 82%–92% and specificity, 89%–90%). The results indicate that circumscribed subendocardial damage alone can cause several hallmarks observed in cardiovascular high-risk patients. Microstructural remodeling under these conditions involves also remote regions, and corresponding changes in longitudinal strain and helix angle might serve as diagnostic markers. Lippincott, Williams & Wilkins 2019-08 2019-07-10 /pmc/articles/PMC6635061/ /pubmed/31291149 http://dx.doi.org/10.1161/HYPERTENSIONAHA.119.12956 Text en © 2019 The Authors. Hypertension is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
spellingShingle Original Articles
Beyhoff, Niklas
Lohr, David
Foryst-Ludwig, Anna
Klopfleisch, Robert
Brix, Sarah
Grune, Jana
Thiele, Arne
Erfinanda, Lasti
Tabuchi, Arata
Kuebler, Wolfgang M.
Pieske, Burkert
Schreiber, Laura M.
Kintscher, Ulrich
Characterization of Myocardial Microstructure and Function in an Experimental Model of Isolated Subendocardial Damage
title Characterization of Myocardial Microstructure and Function in an Experimental Model of Isolated Subendocardial Damage
title_full Characterization of Myocardial Microstructure and Function in an Experimental Model of Isolated Subendocardial Damage
title_fullStr Characterization of Myocardial Microstructure and Function in an Experimental Model of Isolated Subendocardial Damage
title_full_unstemmed Characterization of Myocardial Microstructure and Function in an Experimental Model of Isolated Subendocardial Damage
title_short Characterization of Myocardial Microstructure and Function in an Experimental Model of Isolated Subendocardial Damage
title_sort characterization of myocardial microstructure and function in an experimental model of isolated subendocardial damage
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635061/
https://www.ncbi.nlm.nih.gov/pubmed/31291149
http://dx.doi.org/10.1161/HYPERTENSIONAHA.119.12956
work_keys_str_mv AT beyhoffniklas characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT lohrdavid characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT forystludwiganna characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT klopfleischrobert characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT brixsarah characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT grunejana characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT thielearne characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT erfinandalasti characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT tabuchiarata characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT kueblerwolfgangm characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT pieskeburkert characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT schreiberlauram characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage
AT kintscherulrich characterizationofmyocardialmicrostructureandfunctioninanexperimentalmodelofisolatedsubendocardialdamage