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银屑病的生物治疗与带状疱疹风险:来自银屑病纵向评估和登记研究(PSOLAR)的结果。

Biological treatment for psoriasis and the risk of herpes zoster: results from the Psoriasis Longitudinal Assessment and Registry (PSOLAR).

机构信息

a Department of Dermatology and Venereology, Soroka Medical Center , Beer-Sheva , Israel.

b Department of Dermatology, Azienda Ospedaliera Papa Giovanni XXIII, Study Center of the Italian Group for Epidemiologic Research in Dermatology (GISED) , Bergamo , Italy.

出版信息

J Dermatolog Treat. 2019 Sep;30(6):534-539. doi: 10.1080/09546634.2018.1445193. Epub 2019 Jun 6.

Abstract

To describe the risk of herpes zoster (HZ) in patients with psoriasis and its relation to non-biologic systemic therapies or biologic treatment. Psoriasis Longitudinal Assessment and Registry (PSOLAR) is an international, prospective, registry that follows adult patients with psoriasis eligible to receive non-biologic systemic therapies or biologic therapies. Mutually exclusive therapy cohorts were defined. HZ incident rates were calculated for each therapy cohort and rates between cohorts were compared using hazard ratios (HR) adjusted for potential confounders, in new users and prevalent-exposure patients. A total of 55 HZ events were identified in 10,469 patients in PSOLAR. The adjusted hazard ratio in the overall study population (new user and prevalent-exposed patients) was 2.22 (95% CI: 0.82-5.97;  = .116) for tumor necrosis factor-α (TNF) inhibitors, 2.73 (0.98-7.58;  = .054) for ustekinumab, and 1.04 (0.20-5.41;  = .966) for methotrexate versus reference (combined phototherapy, systemic steroids, topical therapy, and immunomodulators other than methotrexate). Exposure to ustekinumab, TNF-α inhibitors, and methotrexate was not associated with a statistically significant increased risk of HZ. However, HRs were elevated for ustekinumab and TNF-α inhibitors; a larger number of HZ events would be needed to assess the presence or absence of risk.

摘要

描述银屑病患者患带状疱疹(HZ)的风险及其与非生物性全身治疗或生物治疗的关系。银屑病纵向评估和登记(PSOLAR)是一项国际性、前瞻性登记研究,跟踪符合接受非生物性全身治疗或生物治疗条件的成年银屑病患者。定义了相互排斥的治疗队列。为每个治疗队列计算 HZ 发生率,并使用调整后的风险比(HR)比较队列之间的发生率,该 HR 针对新使用者和既有暴露患者的潜在混杂因素进行了调整。在 PSOLAR 中,共有 10469 名患者中发现了 55 例 HZ 事件。在总体研究人群(新使用者和既有暴露患者)中,肿瘤坏死因子-α(TNF)抑制剂的调整后 HR 为 2.22(95%CI:0.82-5.97; = .116),乌司奴单抗为 2.73(0.98-7.58; = .054),甲氨蝶呤为 1.04(0.20-5.41; = .966),与参考值(联合光疗、全身皮质类固醇、局部治疗和除甲氨蝶呤以外的免疫调节剂)相比。乌司奴单抗、TNF-α 抑制剂和甲氨蝶呤的暴露与 HZ 风险的显著增加无关。然而,乌司奴单抗和 TNF-α 抑制剂的 HR 升高;需要更多的 HZ 事件来评估风险的存在或不存在。

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