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1.
Biochem Pharmacol ; 165: 221-229, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-30904473

RESUMO

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.


Assuntos
Polimialgia Reumática/tratamento farmacológico , Glucocorticoides/uso terapêutico , Humanos , Janus Quinases/antagonistas & inibidores , Metotrexato/uso terapêutico , Polimialgia Reumática/complicações , Polimialgia Reumática/diagnóstico , Polimialgia Reumática/etiologia , Receptores de Interleucina-6/antagonistas & inibidores
2.
Expert Opin Biol Ther ; 19(4): 273-286, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30827128

RESUMO

INTRODUCTION: Adult-onset Still´s disease (AOSD) is a systemic inflammatory condition that affects mainly young people. The clinical course consists of two distinctive patterns: one with a predominance of systemic symptoms and another manifested by progressive chronic polyarthritis. Glucocorticoids remain the mainstay in the treatment of AOSD. However, biologic therapies are often required to achieve clinical remission and allow glucocorticoid discontinuation. Areas covered: The review summarizes the main retrospective and prospective studies, and case series on the use of the anti-interleukin (IL)-6 receptor tocilizumab in AOSD. Expert opinion: Since IL-6 serum levels are highly increased in both active systemic and polyarticular phenotypes, IL-6 blockade was considered to be a plausible therapeutic option for the management of AOSD. Tocilizumab, the only anti-IL-6-receptor antagonist currently available for AOSD, has proved to be effective for the management of refractory AOSD patients, including those with life-threatening complications. Nevertheless, there are some reports describing patients who are refractory to any therapy. Future research should focus on the identification of prognostic biomarkers that help us to tailor an individualized treatment for each type of patient and in the search of new disease activity indices that help us to monitor the response to the therapy more closely.


Assuntos
Anticorpos Monoclonais Humanizados/uso terapêutico , Doença de Still de Início Tardio/tratamento farmacológico , Adulto , Anticorpos Monoclonais Humanizados/farmacocinética , Ensaios Clínicos como Assunto , Glucocorticoides/uso terapêutico , Meia-Vida , Humanos , Receptores de Interleucina-6/imunologia , Receptores de Interleucina-6/metabolismo , Doença de Still de Início Tardio/diagnóstico , Resultado do Tratamento
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