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Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease
BACKGROUND: Fingolimod is the first oral immunomodulatory therapy approved for highly active relapsing remitting multiple sclerosis. Based on the distribution pattern of fingolimod interacting sphingosine-1-phosphat receptors in organism including immune system and cardiovascular system clinical mon...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055797/ https://www.ncbi.nlm.nih.gov/pubmed/24906818 http://dx.doi.org/10.1186/1471-2377-14-126 |
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author | Thomas, Katja Schrötter, Hagen Halank, Michael Ziemssen, Tjalf |
author_facet | Thomas, Katja Schrötter, Hagen Halank, Michael Ziemssen, Tjalf |
author_sort | Thomas, Katja |
collection | PubMed |
description | BACKGROUND: Fingolimod is the first oral immunomodulatory therapy approved for highly active relapsing remitting multiple sclerosis. Based on the distribution pattern of fingolimod interacting sphingosine-1-phosphat receptors in organism including immune system and cardiovascular system clinical monitoring of patients and evaluation of adverse events are recommended. Despite extensive data on cardiovascular safety, experience with fingolimod in patients with concomitant cardiological disease, especially within the pulmonary circulation, is rare. CASE PRESENTATION: We report the case of a 46-year-old woman presented with relapsing remitting multiple sclerosis and severe idiopathic pulmonary arterial hypertension. Fingolimod was initiated because of disease activity of multiple sclerosis with two relapses and gadolinium-enhancing lesions in MRI. The patient demonstrated stable disease course of idiopathic pulmonary arterial hypertension when fingolimod was started. Fingolimod therapy did not alter or even worsen the pulmonary or cardiovascular conditions during first dose application as well as follow up of nine months. CONCLUSION: In this report, we present the first case of fingolimod treatment in a patient with highly active multiple sclerosis and severe idiopathic pulmonary arterial hypertension. We suggest an interdisciplinary approach with detailed cardiopulmonary monitoring for safety in such patients. |
format | Online Article Text |
id | pubmed-4055797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40557972014-06-14 Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease Thomas, Katja Schrötter, Hagen Halank, Michael Ziemssen, Tjalf BMC Neurol Case Report BACKGROUND: Fingolimod is the first oral immunomodulatory therapy approved for highly active relapsing remitting multiple sclerosis. Based on the distribution pattern of fingolimod interacting sphingosine-1-phosphat receptors in organism including immune system and cardiovascular system clinical monitoring of patients and evaluation of adverse events are recommended. Despite extensive data on cardiovascular safety, experience with fingolimod in patients with concomitant cardiological disease, especially within the pulmonary circulation, is rare. CASE PRESENTATION: We report the case of a 46-year-old woman presented with relapsing remitting multiple sclerosis and severe idiopathic pulmonary arterial hypertension. Fingolimod was initiated because of disease activity of multiple sclerosis with two relapses and gadolinium-enhancing lesions in MRI. The patient demonstrated stable disease course of idiopathic pulmonary arterial hypertension when fingolimod was started. Fingolimod therapy did not alter or even worsen the pulmonary or cardiovascular conditions during first dose application as well as follow up of nine months. CONCLUSION: In this report, we present the first case of fingolimod treatment in a patient with highly active multiple sclerosis and severe idiopathic pulmonary arterial hypertension. We suggest an interdisciplinary approach with detailed cardiopulmonary monitoring for safety in such patients. BioMed Central 2014-06-07 /pmc/articles/PMC4055797/ /pubmed/24906818 http://dx.doi.org/10.1186/1471-2377-14-126 Text en Copyright © 2014 Thomas et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Thomas, Katja Schrötter, Hagen Halank, Michael Ziemssen, Tjalf Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease |
title | Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease |
title_full | Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease |
title_fullStr | Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease |
title_full_unstemmed | Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease |
title_short | Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease |
title_sort | fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055797/ https://www.ncbi.nlm.nih.gov/pubmed/24906818 http://dx.doi.org/10.1186/1471-2377-14-126 |
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