Tamer Funda, Edek Yusuf Can, Aksakal Ahmet Burhan
Department of Dermatology, Gazi University School of Medicine, Ankara, Turkey.
Dermatol Pract Concept. 2024 Jan 1;14(1):e2024065. doi: 10.5826/dpc.1401a65.
Psoriasis is a chronic cutaneous disorder with underlying systemic inflammation. The systemic immune inflammation (SII) and systemic inflammation response indexes (SIRI) are novel biomarkers that indicate systemic inflammation.
We aimed to evaluate the effect of biological agent treatment on SII and SIRI in psoriasis patients.
Between April 2019 and October 2022, SII and SIRI were retrospectively evaluated in patients with psoriasis before and three months after the initiation of biological agents.
This study included 220 patients, 101 females and 119 males. SIRI was significantly higher in male patients compared to females (P < 0.001). Although not statistically significant, SII and SIRI were higher in obese patients, patients with severe psoriasis, longer disease duration, nail involvement and patients who received previous biological agent treatment. SII was also higher in patients with hypertension, diabetes, hepatic steatosis, depression and coronary artery disease (P = 0.801, P = 0.752, P = 0.706, P = 0.079, P = 0.861, respectively), whereas SIRI was higher in patients with diabetes and depression (P = 0.263, P = 0.777, respectively). Both SII and SIRI statistically significantly decreased after treatment with adalimumab, infliximab, ixekizumab, secukinumab, ustekinumab and risankizumab.
SII and SIRI may indicate the severity of psoriasis as well as SII may be associated with psoriatic arthritis, hypertension, hepatic steatosis and coronary artery disease in patients with psoriasis. There is no consensus on the biomarkers that can be used to create an optimized treatment strategy in psoriasis. Therefore, SII and SIRI may be helpful in making the choice of treatment and in the follow-up of patients with psoriasis treated with biological agents.
银屑病是一种伴有潜在全身炎症的慢性皮肤病。全身免疫炎症(SII)和全身炎症反应指数(SIRI)是指示全身炎症的新型生物标志物。
我们旨在评估生物制剂治疗对银屑病患者SII和SIRI的影响。
在2019年4月至2022年10月期间,对银屑病患者在开始使用生物制剂前及治疗三个月后进行SII和SIRI的回顾性评估。
本研究纳入220例患者,其中女性101例,男性119例。男性患者的SIRI显著高于女性(P<0.001)。虽然无统计学意义,但肥胖患者、重度银屑病患者、病程较长患者、有指甲受累患者以及曾接受过生物制剂治疗的患者的SII和SIRI更高。高血压、糖尿病、肝脂肪变性、抑郁症和冠状动脉疾病患者的SII也更高(分别为P = 0.801、P = 0.752、P = 0.706、P = 0.079、P = 0.861),而糖尿病和抑郁症患者的SIRI更高(分别为P = 0.263、P = 0.777)。使用阿达木单抗、英夫利昔单抗、司库奇尤单抗、苏金单抗、乌司奴单抗和瑞莎珠单抗治疗后,SII和SIRI均有统计学意义的显著下降。
SII和SIRI可能指示银屑病的严重程度,并且SII可能与银屑病关节炎、高血压、肝脂肪变性和银屑病患者的冠状动脉疾病相关。在可用于制定银屑病优化治疗策略的生物标志物方面尚无共识。因此,SII和SIRI可能有助于银屑病生物制剂治疗患者的治疗选择和随访。