Rheumatology Unit, Department of Clinical Medicine and Surgery, University Federico II, Naples, Naples, Italy.
Rheumatology unit, Department of Medicine DIMED, University of Padova, Padova, Italy.
Clin Rheumatol. 2019 Sep;38(9):2355-2362. doi: 10.1007/s10067-019-04663-6. Epub 2019 Jun 28.
Patients with psoriatic arthritis (PsA) have an increased prevalence of obesity, but mechanisms underlying this association remain unknown and it is unclear if obesity is the cause or effect of PsA. For PsA patients, comorbid obesity may influence their clinical response to systemic treatment, and especially targeted immunomodulators such as anti-tumor necrosis factor (TNF)α. Weight gain has also been associated with anti-TNFα treatment. Consequently, modification of the therapeutic approach may be needed for patients with an inadequate response to TNFα inhibitors. In recent years, interleukin (IL)-12/IL-23 inhibitors have entered clinical practice as a new class of drug for the treatment of PsA, with some data suggesting a lower effect of body weight on their effectiveness. Recent findings demonstrate effective and sustained responses in patients with PsA to ustekinumab, an IL-12/IL-23 inhibitor. This narrative review critically discusses the link between PsA, obesity, and response to therapy. The current role of ustekinumab in this setting is also discussed.
患有银屑病关节炎(PsA)的患者肥胖症的患病率增加,但这种关联的潜在机制尚不清楚,也不清楚肥胖是导致 PsA 的原因还是结果。对于 PsA 患者,合并肥胖症可能会影响他们对全身治疗的临床反应,尤其是针对肿瘤坏死因子(TNF)α的靶向免疫调节剂。体重增加也与抗 TNFα 治疗有关。因此,对于对 TNFα 抑制剂反应不足的患者,可能需要修改治疗方法。近年来,白细胞介素(IL)-12/IL-23 抑制剂已作为治疗 PsA 的新药进入临床实践,有一些数据表明体重对其疗效的影响较小。最近的研究结果表明,IL-12/IL-23 抑制剂乌司奴单抗在治疗 PsA 患者方面具有有效且持久的反应。本叙述性综述批判性地讨论了 PsA、肥胖症和治疗反应之间的联系。还讨论了乌司奴单抗在这种情况下的作用。