Infections in patients with multiple sclerosis: A national cohort study in Sweden.


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:
Oct 2020
Historique:
received: 29 04 2020
revised: 08 07 2020
accepted: 22 07 2020
pubmed: 1 8 2020
medline: 15 5 2021
entrez: 1 8 2020
Statut: ppublish

Résumé

Multiple sclerosis (MS) patients have an increased risk of infections, but few population-based studies have reported infections occurring in MS in the years immediately after diagnosis. To explore incident infections in MS, stratified by age and sex. In a Swedish population-based cohort study 6602 incident MS patients (aged ≥18 years), matched at diagnosis with 61,828 matched MS-free individuals were identified between 1st January 2008 and 31st December 2016, using national registers. Incidence rates (IR) and incidence rate ratios (IRR) with 95% CI were calculated for each outcome. The IRRs were 2.54 (95% CI 2.28-2.83) for first serious infection and 1.61 (1.52-1.71) for first non-serious infection. Compared with MS-free individuals, MS patients had higher IRs for skin, respiratory/throat infections, pneumonia/influenza, bacterial, viral, and fungal infections, with the highest IRR observed for urinary tract/kidney infections (2.44; 2.24-2.66). The cumulative incidence for most of these infections was higher among MS patients than MS-free individuals, both 0 to <5 and 5 to <9 years after index date. The burden of infections around the time of MS diagnosis and subsequent infection risk, underscore the need for careful considerations regarding the risk-benefit across different disease-modifying therapies.

Sections du résumé

BACKGROUND BACKGROUND
Multiple sclerosis (MS) patients have an increased risk of infections, but few population-based studies have reported infections occurring in MS in the years immediately after diagnosis.
OBJECTIVE OBJECTIVE
To explore incident infections in MS, stratified by age and sex.
METHODS METHODS
In a Swedish population-based cohort study 6602 incident MS patients (aged ≥18 years), matched at diagnosis with 61,828 matched MS-free individuals were identified between 1st January 2008 and 31st December 2016, using national registers. Incidence rates (IR) and incidence rate ratios (IRR) with 95% CI were calculated for each outcome.
RESULTS RESULTS
The IRRs were 2.54 (95% CI 2.28-2.83) for first serious infection and 1.61 (1.52-1.71) for first non-serious infection. Compared with MS-free individuals, MS patients had higher IRs for skin, respiratory/throat infections, pneumonia/influenza, bacterial, viral, and fungal infections, with the highest IRR observed for urinary tract/kidney infections (2.44; 2.24-2.66). The cumulative incidence for most of these infections was higher among MS patients than MS-free individuals, both 0 to <5 and 5 to <9 years after index date.
CONCLUSION CONCLUSIONS
The burden of infections around the time of MS diagnosis and subsequent infection risk, underscore the need for careful considerations regarding the risk-benefit across different disease-modifying therapies.

Identifiants

pubmed: 32736217
pii: S2211-0348(20)30495-8
doi: 10.1016/j.msard.2020.102420
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102420

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The author(s) declared the following potential conflicts of interest with respect to the research, authorship and/or publication of this article:SM has received research funding from Roche, Novartis and AstraZeneca, a speaker's fee from Teva and is a member of a study advisory board with IQVIA (this study). FP has received research grants from Genzyme, Merck KGaA and Novartis, and fees for serving as Chair of DMC in clinical trials with Parexel. SL, NM, SN and AL are employees of Celgene (now Bristol-Myer Squibb) and own company stock. ACB, SC, FC, MR and CB were consultants to Celgene through their employment at IQVIA at the time of the study.

Auteurs

Anna Castelo-Branco (A)

Real-world Insights, IQVIA Nordics, Pyramidvägen 7, 169 56 Solna, Sweden.

Flaminia Chiesa (F)

Real-world Insights, IQVIA Nordics, Pyramidvägen 7, 169 56 Solna, Sweden.

Simona Conte (S)

Real-world Insights, IQVIA Nordics, Pyramidvägen 7, 169 56 Solna, Sweden.

Camilla Bengtsson (C)

Real-world Insights, IQVIA Nordics, Pyramidvägen 7, 169 56 Solna, Sweden. Electronic address: cbengtsson@iqvia.com.

Sally Lee (S)

Celgene Corporation, 86 Morris Avenue, Summit, NJ 07901, United States.

Neil Minton (N)

Celgene Corporation, 86 Morris Avenue, Summit, NJ 07901, United States.

Steve Niemcryk (S)

Celgene Corporation, 86 Morris Avenue, Summit, NJ 07901, United States.

Anders Lindholm (A)

Celgene Corporation, 86 Morris Avenue, Summit, NJ 07901, United States.

Mats Rosenlund (M)

Department of Learning, Informatics, Management and Ethics (LIME), Tomtebodavägen 18a, 171 65 Solna, Karolinska Institutet, Stockholm, Sweden.

Fredrik Piehl (F)

Department of Clinical Neuroscience, Karolinska Institutet, Tomtebodavägen 18A, 171 77 Stockholm, Stockholm Sweden.

Scott Montgomery (S)

Clinical Epidemiology and Biostatistics, School of Medical Sciences, Örebro University Hospital and Örebro University, Fakultetsgatan 1, 701 82 Örebro, Sweden; Clinical Epidemiology Division, Karolinska Institutet, Stockholm, Sweden; Department of Epidemiology and Public Health, University College London, London, United Kingdom.

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