Fingolimod in a patient with heart failure on the background of pulmonary arterial hypertension and coronary artery disease

被引:5
作者
Thomas, Katja [1 ]
Schroetter, Hagen [2 ]
Halank, Michael [3 ]
Ziemssen, Tjalf [1 ]
机构
[1] Tech Univ Dresden, Univ Clin Carl Gustav Carus Dresden, Neurol Univ Clin Dresden, Dept Neurol,Ctr Clin Neurosci, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Univ Clin Carl Gustav Carus Dresden, Dresden Heart Ctr, D-01307 Dresden, Germany
[3] Tech Univ Dresden, Univ Clin Carl Gustav Carus Dresden, Dept Internal Med 1, D-01307 Dresden, Germany
关键词
Multiple sclerosis; Fingolimod; Pulmonary arterial hypertension; MULTIPLE-SCLEROSIS; FTY720; CONTRACTION; MECHANISM;
D O I
10.1186/1471-2377-14-126
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页数:4
相关论文
共 14 条
[1]   Sphingolipid signalling in the cardiovascular system: Good, bad or both? [J].
Alewijnse, Astrid E. ;
Peters, Stephan L. M. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2008, 585 (2-3) :292-302
[2]   FTY720, an immunomodulatory sphingolipid mimetic: translation of a novel mechanism into clinical benefit in multiple sclerosis [J].
Baumruker, Thomas ;
Billich, Andreas ;
Brinkmann, Volker .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2007, 16 (03) :283-289
[3]   Sphingosine-1-phosphate augments agonist-mediated contraction in the bronchial smooth muscles of mice [J].
Chiba, Yoshihiko ;
Takeuchi, Hiroki ;
Sakai, Hiroyasu ;
Misawa, Miwa .
PHARMACOLOGICAL REPORTS, 2011, 63 (02) :544-547
[4]   Mechanism of Action of Oral Fingolimod (FTY720) in Multiple Sclerosis [J].
Chun, Jerold ;
Hartung, Hans-Peter .
CLINICAL NEUROPHARMACOLOGY, 2010, 33 (02) :91-101
[5]   Delayed fingolimod-associated asystole [J].
Espinosa, Patricio S. ;
Berger, Joseph R. .
MULTIPLE SCLEROSIS JOURNAL, 2011, 17 (11) :1387-1389
[6]   Prolonged and symptomatic bradycardia following a single dose of fingolimod [J].
Faber, Hans ;
Fischer, Hans-Joerg ;
Weber, Frank .
MULTIPLE SCLEROSIS JOURNAL, 2013, 19 (01) :126-128
[7]   Guidelines for the diagnosis and treatment of pulmonary hypertension [J].
Galie, N. ;
Hoeper, M. M. ;
Humbert, M. ;
Torbicki, A. ;
Vachiery, J-L. ;
Barbera, J. A. ;
Beghetti, M. ;
Corris, P. ;
Gaine, S. ;
Gibbs, J. S. ;
Gomez-Sanchez, M. A. ;
Jondeau, G. ;
Klepetko, W. ;
Opitz, C. ;
Peacock, A. ;
Rubin, L. ;
Zellweger, M. ;
Simonneau, G. .
EUROPEAN RESPIRATORY JOURNAL, 2009, 34 (06) :1219-1263
[8]   Fingolimod in a patient with Wolff-Parkinson-White syndrome [J].
Huys, Anne-Catherine M. L. ;
Lalive, Patrice H. ;
Sekoranja, Lucka .
MULTIPLE SCLEROSIS JOURNAL, 2014, 20 (05) :636-637
[9]   Sudden unexpected death on fingolimod [J].
Lindsey, J. W. ;
Haden-Pinneri, K. ;
Memon, N. B. ;
Buja, L. M. .
MULTIPLE SCLEROSIS JOURNAL, 2012, 18 (10) :1507-1508
[10]   Sphingosine 1-phosphate induces contraction of coronary artery smooth muscle cells via SS1P2 [J].
Ohmori, T ;
Yatomi, Y ;
Osada, M ;
Kazama, F ;
Takafuta, T ;
Ikeda, H ;
Ozaki, Y .
CARDIOVASCULAR RESEARCH, 2003, 58 (01) :170-177