Psoriasis comorbidities: complications and benefits of immunobiological treatment

被引:32
|
作者
Esteves de Carvalho, Andre Vicente [1 ]
Souza, Cacilda da Silva [2 ]
Milman, Laura de Mattos [1 ,2 ]
Romiti, Ricardo
Paschoal, Renato Soriani [3 ]
Meneghello, Luana Pizarro [1 ]
机构
[1] Santa Casa Misericordia Porto Alegre, Porto Alegre, RS, Brazil
[2] Univ Sao Paulo, Sao Paulo, SP, Brazil
[3] Private Clin, Sao Paulo, SP, Brazil
关键词
Comorbidity; Metabolic Syndrome X; Psoriasis; Tumor necrosis factor-alpha; TUMOR-NECROSIS-FACTOR; CHRONIC PLAQUE PSORIASIS; FACTOR-ALPHA THERAPY; BODY-MASS INDEX; ANTI-TNF-ALPHA; PLACEBO-CONTROLLED TRIAL; TO-SEVERE PSORIASIS; RHEUMATOID-ARTHRITIS; LIPID PROFILE; INSULIN-RESISTANCE;
D O I
10.1590/abd1806-4841.20165080
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
During the last decade, different studies have converged to evidence the high prevalence of comorbidities in subjects with psoriasis. Although a causal relation has not been fully elucidated, genetic relation, inflammatory pathways and/or common environmental factors appear to be underlying the development of psoriasis and the metabolic comorbidities. The concept of psoriasis as a systemic disease directed the attention of the scientific community in order to investigate the extent to which therapeutic interventions influence the onset and evolution of the most prevalent comorbidities in patients with psoriasis. This study presents scientific evidence of the influence of immunobiological treatments for psoriasis available in Brazil (infliximab, adalimumab, etanercept and ustekinumab) on the main comorbidities related to psoriasis. It highlights the importance of the inflammatory burden on the clinical outcome of patients, not only on disease activity, but also on the comorbidities. In this sense, systemic treatments, whether immunobiologicals or classic, can play a critical role to effectively control the inflammatory burden in psoriatic patients.
引用
收藏
页码:781 / 789
页数:9
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