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Clinical and Histopathological Features of Patients with Systemic Sclerosis Undergoing Endomyocardial Biopsy
BACKGROUND: Cardiac involvement in systemic sclerosis (SSc) is associated with a variable phenotype including heart failure, arrhythmias and pulmonary hypertension. The aim of the present study was to evaluate clinical characteristics, histopathological findings and outcome of patients with SSc and...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428754/ https://www.ncbi.nlm.nih.gov/pubmed/25966025 http://dx.doi.org/10.1371/journal.pone.0126707 |
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author | Mueller, Karin A. L. Mueller, Iris I. Eppler, David Zuern, Christine S. Seizer, Peter Kramer, Ulrich Koetter, Ina Roecken, Martin Kandolf, Reinhard Gawaz, Meinrad Geisler, Tobias Henes, Joerg C. Klingel, Karin |
author_facet | Mueller, Karin A. L. Mueller, Iris I. Eppler, David Zuern, Christine S. Seizer, Peter Kramer, Ulrich Koetter, Ina Roecken, Martin Kandolf, Reinhard Gawaz, Meinrad Geisler, Tobias Henes, Joerg C. Klingel, Karin |
author_sort | Mueller, Karin A. L. |
collection | PubMed |
description | BACKGROUND: Cardiac involvement in systemic sclerosis (SSc) is associated with a variable phenotype including heart failure, arrhythmias and pulmonary hypertension. The aim of the present study was to evaluate clinical characteristics, histopathological findings and outcome of patients with SSc and a clinical phenotype suggesting cardiac involvement. METHODS AND RESULTS: 25 patients with SSc and clinical signs of cardiac involvement were included between June 2007 and December 2010. They underwent routine clinical work-up including laboratory testing, echocardiography, left and right heart catheterization, holter recordings and endomyocardial biopsy. Primary endpoint (EP) was defined as the combination of cardiovascular death, arrhythmic endpoints (defined as appropriate discharge of implantable cardioverter defibrillator (ICD)) or rehospitalization due to heart failure. The majority of patients presented with slightly impaired left ventricular function (mean LVEF 54.1±9.0%, determined by echocardiography). Endomyocardial biopsies detected cardiac fibrosis in all patients with a variable area percentage of 8% to 32%. Cardiac inflammation was diagnosed as follows: No inflammation in 3.8%, isolated inflammatory cells in 38.5%, a few foci of inflammation in 30.8%, several foci of inflammation in 15.4%, and pronounced inflammation in 7.7% of patients. During follow up (FU) (22.5 months), seven (28%) patients reached the primary EP. Patients with subsequent events showed a higher degree of fibrosis and inflammation in the myocardium by trend. While patients with an inflammation grade 0 or 1 showed an event rate of 18.2%, the subgroup of patients with an inflammation grade 2 presented with an event rate of 25% versus an event rate of 50% in the subgroup of patients with an inflammation grade 3 and 4, respectively (p=0.193). Furthermore, the subgroup of patients with fibrosis grade 1 showed an event rate of 11%, patients with fibrosis grade 2 and 3 presented with an event rate of 33% and 42% respectively (p = 0.160). CONCLUSIONS: Patients with SSc and clinical signs of cardiac involvement presented with mildly impaired LVEF. Prognosis was poor with an event rate of 28% within 22.5 months FU and was associated with the degree of cardiac inflammation and fibrosis. |
format | Online Article Text |
id | pubmed-4428754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44287542015-05-21 Clinical and Histopathological Features of Patients with Systemic Sclerosis Undergoing Endomyocardial Biopsy Mueller, Karin A. L. Mueller, Iris I. Eppler, David Zuern, Christine S. Seizer, Peter Kramer, Ulrich Koetter, Ina Roecken, Martin Kandolf, Reinhard Gawaz, Meinrad Geisler, Tobias Henes, Joerg C. Klingel, Karin PLoS One Research Article BACKGROUND: Cardiac involvement in systemic sclerosis (SSc) is associated with a variable phenotype including heart failure, arrhythmias and pulmonary hypertension. The aim of the present study was to evaluate clinical characteristics, histopathological findings and outcome of patients with SSc and a clinical phenotype suggesting cardiac involvement. METHODS AND RESULTS: 25 patients with SSc and clinical signs of cardiac involvement were included between June 2007 and December 2010. They underwent routine clinical work-up including laboratory testing, echocardiography, left and right heart catheterization, holter recordings and endomyocardial biopsy. Primary endpoint (EP) was defined as the combination of cardiovascular death, arrhythmic endpoints (defined as appropriate discharge of implantable cardioverter defibrillator (ICD)) or rehospitalization due to heart failure. The majority of patients presented with slightly impaired left ventricular function (mean LVEF 54.1±9.0%, determined by echocardiography). Endomyocardial biopsies detected cardiac fibrosis in all patients with a variable area percentage of 8% to 32%. Cardiac inflammation was diagnosed as follows: No inflammation in 3.8%, isolated inflammatory cells in 38.5%, a few foci of inflammation in 30.8%, several foci of inflammation in 15.4%, and pronounced inflammation in 7.7% of patients. During follow up (FU) (22.5 months), seven (28%) patients reached the primary EP. Patients with subsequent events showed a higher degree of fibrosis and inflammation in the myocardium by trend. While patients with an inflammation grade 0 or 1 showed an event rate of 18.2%, the subgroup of patients with an inflammation grade 2 presented with an event rate of 25% versus an event rate of 50% in the subgroup of patients with an inflammation grade 3 and 4, respectively (p=0.193). Furthermore, the subgroup of patients with fibrosis grade 1 showed an event rate of 11%, patients with fibrosis grade 2 and 3 presented with an event rate of 33% and 42% respectively (p = 0.160). CONCLUSIONS: Patients with SSc and clinical signs of cardiac involvement presented with mildly impaired LVEF. Prognosis was poor with an event rate of 28% within 22.5 months FU and was associated with the degree of cardiac inflammation and fibrosis. Public Library of Science 2015-05-12 /pmc/articles/PMC4428754/ /pubmed/25966025 http://dx.doi.org/10.1371/journal.pone.0126707 Text en © 2015 Mueller et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Mueller, Karin A. L. Mueller, Iris I. Eppler, David Zuern, Christine S. Seizer, Peter Kramer, Ulrich Koetter, Ina Roecken, Martin Kandolf, Reinhard Gawaz, Meinrad Geisler, Tobias Henes, Joerg C. Klingel, Karin Clinical and Histopathological Features of Patients with Systemic Sclerosis Undergoing Endomyocardial Biopsy |
title | Clinical and Histopathological Features of Patients with Systemic Sclerosis Undergoing Endomyocardial Biopsy |
title_full | Clinical and Histopathological Features of Patients with Systemic Sclerosis Undergoing Endomyocardial Biopsy |
title_fullStr | Clinical and Histopathological Features of Patients with Systemic Sclerosis Undergoing Endomyocardial Biopsy |
title_full_unstemmed | Clinical and Histopathological Features of Patients with Systemic Sclerosis Undergoing Endomyocardial Biopsy |
title_short | Clinical and Histopathological Features of Patients with Systemic Sclerosis Undergoing Endomyocardial Biopsy |
title_sort | clinical and histopathological features of patients with systemic sclerosis undergoing endomyocardial biopsy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428754/ https://www.ncbi.nlm.nih.gov/pubmed/25966025 http://dx.doi.org/10.1371/journal.pone.0126707 |
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