Gisondi Paolo, Bellinato Francesco, Girolomoni Giampiero, Albanesi Cristina
Section of Dermatology and Venereology, Department of Medicine, University of Verona, Verona, Italy.
Laboratory of Experimental Immunology, Istituto Dermopatico dell'Immacolata, IDI-IRCCS, Rome, Italy.
Front Pharmacol. 2020 Feb 25;11:117. doi: 10.3389/fphar.2020.00117. eCollection 2020.
Psoriasis is a chronic, systemic immune-mediated disease characterized by development of erythematous, indurated, scaly, pruritic plaques on the skin. Psoriasis is frequently associated to comorbidities, including psoriatic arthritis, cardiovascular diseases, diabetes mellitus, obesity, non-alcoholic fatty liver disease, and inflammatory bowel diseases. In this review, we discuss the pathophysiological relationship between psoriasis and cardio-metabolic comorbidities and the importance of therapeutic strategies to reduce systemic inflammation in patients with moderate-to-severe psoriasis. Pathogenesis of psoriasis and its comorbidities share both genetic predisposition and inflammatory pathways, which include the TNFα and the IL-23/IL-17 pathways. These pathways are selectively addressed by biological treatments, which have substantially changed the outcomes of psoriasis therapy and affect positively comorbidities including reducing cardiovascular risk, allowing a more comprehensive approach to the patient.
银屑病是一种慢性全身性免疫介导性疾病,其特征是皮肤上出现红斑、硬结、鳞屑、瘙痒性斑块。银屑病常与多种合并症相关,包括银屑病关节炎、心血管疾病、糖尿病、肥胖症、非酒精性脂肪性肝病和炎症性肠病。在本综述中,我们讨论了银屑病与心血管代谢合并症之间的病理生理关系,以及减轻中重度银屑病患者全身炎症的治疗策略的重要性。银屑病及其合并症的发病机制既有遗传易感性又有炎症途径,其中包括TNFα和IL-23/IL-17途径。生物治疗可选择性地针对这些途径,这已极大地改变了银屑病治疗的结果,并对合并症产生积极影响,包括降低心血管风险,从而为患者提供更全面的治疗方法。