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Cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis

BACKGROUND: Fingolimod is a sphingosine‐1‐phosphate receptor modulator for the treatment of relapsing–remitting multiple sclerosis (RRMS). Despite an established effect on heart rate, the effect of fingolimod on cardiac repolarization is not completely known. METHODS: Twenty‐seven patients with RRMS...

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Autores principales: Laiho, Aapo, Laitinen, Tiina M., Hartikainen, Päivi, Hartikainen, Juha E. K., Laitinen, Tomi P., Simula, Sakari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822581/
https://www.ncbi.nlm.nih.gov/pubmed/29484274
http://dx.doi.org/10.1002/brb3.925
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author Laiho, Aapo
Laitinen, Tiina M.
Hartikainen, Päivi
Hartikainen, Juha E. K.
Laitinen, Tomi P.
Simula, Sakari
author_facet Laiho, Aapo
Laitinen, Tiina M.
Hartikainen, Päivi
Hartikainen, Juha E. K.
Laitinen, Tomi P.
Simula, Sakari
author_sort Laiho, Aapo
collection PubMed
description BACKGROUND: Fingolimod is a sphingosine‐1‐phosphate receptor modulator for the treatment of relapsing–remitting multiple sclerosis (RRMS). Despite an established effect on heart rate, the effect of fingolimod on cardiac repolarization is not completely known. METHODS: Twenty‐seven patients with RRMS underwent 24‐hr ambulatory ECG before fingolimod (baseline), at the day of fingolimod initiation (1D) and after three‐month treatment (3M). The mean values of RR‐interval as well as QT‐interval corrected by Bazzet's (QTcBaz) and Fridericia's (QTcFri) formula were compared between baseline, 1D, and 3M over 24‐hr period as well as at daytime and nighttime. RESULTS: QTcBaz over 24‐hr was shorter at 1D (414 ± 20 ms, p < .001) and at 3M (414 ± 20 ms, p < .001) than at baseline (418 ± 20 ms). In contrast, QTcFri over 24‐hr was longer at 1D (410 ± 19 ms, p < .001) but similar at 3M (406 ± 19 ms, p = .355) compared to baseline (407 ± 19 ms). Daytime QTcBaz was shorter at 1D (p < .001) and at 3M (p = .007), whereas daytime QTcFri was longer at 1D (p < .05) but similar at 3M (p = ns) compared to baseline. During the night, changes were observed neither in QTcBaz nor in QTcFri between baseline, 1D, and 3M. CONCLUSIONS: Changes in cardiac repolarization after fingolimod initiation were mild and occurred at daytime. Ambiguously, QTcBaz demonstrated shortening, whereas QTcFri showed prolongation in cardiac repolarization after fingolimod initiation. The formula applied for QT‐interval correction needs to be taken carefully into account as evaluating pharmacovigilance issues related to fingolimod.
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spelling pubmed-58225812018-02-26 Cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis Laiho, Aapo Laitinen, Tiina M. Hartikainen, Päivi Hartikainen, Juha E. K. Laitinen, Tomi P. Simula, Sakari Brain Behav Original Research BACKGROUND: Fingolimod is a sphingosine‐1‐phosphate receptor modulator for the treatment of relapsing–remitting multiple sclerosis (RRMS). Despite an established effect on heart rate, the effect of fingolimod on cardiac repolarization is not completely known. METHODS: Twenty‐seven patients with RRMS underwent 24‐hr ambulatory ECG before fingolimod (baseline), at the day of fingolimod initiation (1D) and after three‐month treatment (3M). The mean values of RR‐interval as well as QT‐interval corrected by Bazzet's (QTcBaz) and Fridericia's (QTcFri) formula were compared between baseline, 1D, and 3M over 24‐hr period as well as at daytime and nighttime. RESULTS: QTcBaz over 24‐hr was shorter at 1D (414 ± 20 ms, p < .001) and at 3M (414 ± 20 ms, p < .001) than at baseline (418 ± 20 ms). In contrast, QTcFri over 24‐hr was longer at 1D (410 ± 19 ms, p < .001) but similar at 3M (406 ± 19 ms, p = .355) compared to baseline (407 ± 19 ms). Daytime QTcBaz was shorter at 1D (p < .001) and at 3M (p = .007), whereas daytime QTcFri was longer at 1D (p < .05) but similar at 3M (p = ns) compared to baseline. During the night, changes were observed neither in QTcBaz nor in QTcFri between baseline, 1D, and 3M. CONCLUSIONS: Changes in cardiac repolarization after fingolimod initiation were mild and occurred at daytime. Ambiguously, QTcBaz demonstrated shortening, whereas QTcFri showed prolongation in cardiac repolarization after fingolimod initiation. The formula applied for QT‐interval correction needs to be taken carefully into account as evaluating pharmacovigilance issues related to fingolimod. John Wiley and Sons Inc. 2018-01-30 /pmc/articles/PMC5822581/ /pubmed/29484274 http://dx.doi.org/10.1002/brb3.925 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Laiho, Aapo
Laitinen, Tiina M.
Hartikainen, Päivi
Hartikainen, Juha E. K.
Laitinen, Tomi P.
Simula, Sakari
Cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis
title Cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis
title_full Cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis
title_fullStr Cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis
title_full_unstemmed Cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis
title_short Cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis
title_sort cardiac repolarization during fingolimod treatment in patients with relapsing–remitting multiple sclerosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822581/
https://www.ncbi.nlm.nih.gov/pubmed/29484274
http://dx.doi.org/10.1002/brb3.925
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