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银屑病与非酒精性脂肪性肝病

Psoriasis and Nonalcoholic Fatty Liver Disease.

作者信息

Carrascosa J M, Bonanad C, Dauden E, Botella R, Olveira-Martín A

机构信息

Servicio de Dermatologia, Hospital Universitari Germans Trias i Pujol. Universitat Autònoma de Barcelona, Badadalona, España.

Servicio de Cardiología, Hospital Clínico Universitario, Valencia, España.

出版信息

Actas Dermosifiliogr. 2017 Jul-Aug;108(6):506-514. doi: 10.1016/j.ad.2016.12.017. Epub 2017 Mar 16.

Abstract

Nonalcoholic fatty liver disease (NAFLD) is the most prevalent liver condition in the West. The prevalence and severity of NAFLD is higher and the prognosis worse in patients with psoriasis. The pathogenic link between psoriasis and NAFLD is chronic inflammation and peripheral insulin resistance, a common finding in diseases associated with psoriasis. NAFLD should therefore be ruled out during the initial evaluation of patients with psoriasis, in particular if they show signs of metabolic syndrome and require systemic treatment. Concomitant psoriasis and NAFLD and the likelihood of synergy between them place limitations on general recommendations and treatment for these patients given the potential for liver toxicity. As hepatotoxic risk is associated with some of the conventional drugs used in this setting (e.g., acitretin, methotrexate, and ciclosporin), patients prescribed these treatments should be monitored as appropriate. Anti-tumor necrosis factor agents hold the promise of potential benefits based on their effects on the inflammatory process and improving peripheral insulin resistance. However, cases of liver toxicity have also been reported in relation to these biologics. No evidence has emerged to suggest that anti-p40 or anti-interleukin 17 agents provide benefits or have adverse effects.

摘要

非酒精性脂肪性肝病(NAFLD)是西方最常见的肝脏疾病。银屑病患者中NAFLD的患病率和严重程度更高,预后更差。银屑病与NAFLD之间的致病联系是慢性炎症和外周胰岛素抵抗,这在与银屑病相关的疾病中很常见。因此,在对银屑病患者进行初始评估时应排除NAFLD,特别是如果他们表现出代谢综合征的迹象并需要全身治疗。银屑病和NAFLD同时存在以及它们之间协同作用的可能性,鉴于存在肝毒性的可能性,对这些患者的一般建议和治疗造成了限制。由于肝毒性风险与该情况下使用的一些传统药物(如阿维A、甲氨蝶呤和环孢素)有关,因此应适当监测接受这些治疗的患者。抗肿瘤坏死因子药物基于其对炎症过程的影响和改善外周胰岛素抵抗,有望带来潜在益处。然而,也有关于这些生物制剂导致肝毒性的报道。没有证据表明抗p40或抗白细胞介素17药物有好处或有不良反应。

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