Alemtuzumab induced hemodynamic change in relapsing multiple sclerosis occurs independent of corticosteroid premedication - a retrospective multicentre study.


Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 25 03 2022
revised: 03 04 2022
accepted: 15 04 2022
pubmed: 28 4 2022
medline: 29 6 2022
entrez: 27 4 2022
Statut: ppublish

Résumé

Background Alemtuzumab (ATZ), a highly effective disease modifying treatment for relapsing multiple sclerosis (MS), is associated with the rare risk of intracerebral hemorrhage. Increase of blood pressure (BP) was hypothesized to be causative, but prior administration of high-dose methylprednisolone (HDMP) is a potential confounder. Objective To analyze BP change in MS patients treated with ATZ and prior HDMP treatment compared to patients receiving HDMP only for acute relapse. Methods In this retrospective study, 30 patients treated with ATZ/HDMP and 60 age-, sex- and disability-matched controls treated with HDMP were included. Primary endpoint was the change of systolic BP (SBP) between before ATZ cycle and the maximum value measured during the treatment cycle; secondary endpoints were change in diastolic BP (DBP) and heart rate (HR). Results Change of SBP observed in ATZ/HDMP treated patients was significantly higher than in HDMP controls (mean maximal change of 12.8 vs. 8.1 mmHg, p = 0.033). An increase of SBP exceeding 20% from baseline was observed in 5 (16.7%) patients on ATZ/HDMP compared to 3 (5.0%) on HDMP (p = 0.078). The day after the 1st ATZ infusion, mean HR was higher in the ATZ/HDMP group compared to HDMP controls (82.5 vs. 73.2 bpm, p = 0.005), although there was no significant group difference over time. Conclusions ATZ treatment induced a slight, but significant increase in SBP independent of HDMP. Although hemodynamic alterations alone seem unlikely as putative mechanism for cerebral bleedings, strict cardiovascular monitoring is recommended to reduce rare, but severe cardiovascular side effects.

Identifiants

pubmed: 35477127
pii: S2211-0348(22)00322-4
doi: 10.1016/j.msard.2022.103810
pii:
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Alemtuzumab 3A189DH42V
Methylprednisolone X4W7ZR7023

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

103810

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier B.V. All rights reserved.

Auteurs

Franziska Di Pauli (F)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Katharina Riedl (K)

Department of Neurology, Medical University of Vienna, Vienna, Austria.

Harald Hegen (H)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Michael Auer (M)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Klaus Berek (K)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Nik Krajnc (N)

Department of Neurology, Medical University of Vienna, Vienna, Austria.

Fritz Leutmezer (F)

Department of Neurology, Medical University of Vienna, Vienna, Austria.

Anne Zinganell (A)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Thomas Berger (T)

Department of Neurology, Medical University of Vienna, Vienna, Austria.

Florian Deisenhammer (F)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Gabriel Bsteh (G)

Department of Neurology, Medical University of Vienna, Vienna, Austria.

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Classifications MeSH