Treatment of polymyalgia rheumatica.
Anti-interleukin-6 receptor tocilizumab
Biologic therapies
DMARD
Glucocorticoids
Methotrexate
Polymyalgia rheumatic
Journal
Biochemical pharmacology
ISSN: 1873-2968
Titre abrégé: Biochem Pharmacol
Pays: England
ID NLM: 0101032
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
received:
02
02
2019
accepted:
18
03
2019
pubmed:
25
3
2019
medline:
15
2
2020
entrez:
25
3
2019
Statut:
ppublish
Résumé
Polymyalgia rheumatica (PMR) is an inflammatory disease characterized by bilateral pain involving predominantly the shoulders and proximal aspects of the arms and less commonly the neck and the pelvic girdle. This review discusses briefly the main epidemiological data and clinical features of this condition. Especial attention is paid in the management of the disease. For this reason, both the classic management and the impact of new therapies are discussed in depth. In general, patients with PMR experience a rapid response to 12.5-25 mg/prednisone/day in less than a week. Patients with poor response to glucocorticoids or with relapsing disease require other therapies aimed mainly to spare glucocorticoids. Among them, methotrexate is the most commonly used. Nevertheless, different studies indicate that this agent yields only a modest effect. Biologic therapies against the main cytokines involved in the pathogenesis of the disease have been used in refractory patients. However, randomized controlled trials do not support the use of anti-tumor necrosis factor agents in PMR. In contrast, several case series and retrospective studies highlight the efficacy of the anti-interleukin-6 receptor tocilizumab in PMR. Nonetheless, controlled trials are needed to fully establish the beneficial effect of this agent. The potential favorable effect of the Janus-kinase inhibitors and new anti-interleukin-6 antagonists remains to be determined.
Identifiants
pubmed: 30904473
pii: S0006-2952(19)30113-3
doi: 10.1016/j.bcp.2019.03.027
pii:
doi:
Substances chimiques
Glucocorticoids
0
Receptors, Interleukin-6
0
Janus Kinases
EC 2.7.10.2
Methotrexate
YL5FZ2Y5U1
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
221-229Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.