Cortese Andrea, Gargiulo Luigi, Ibba Luciano, Fiorillo Giovanni, Toso Francesco, Vignoli Carlo Alberto, Narcisi Alessandra, Costanzo Antonio, Valenti Mario
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele.
Dermatology Unit, Humanitas IRCCS Research Hospital, Rozzano, Italy.
Dermatol Reports. 2023 May 19;15(3):9692. doi: 10.4081/dr.2023.9692. eCollection 2023 Sep 12.
Genital psoriasis affects 3-33% of patients with psoriasis during the course of the disease, usually leading to a severe reduction in the patient's quality of life. This study aims to retrospectively assess the effectiveness of interleukin (IL)-23 and IL-17 inhibitors in a real-life population affected by moderate-to-severe plaque psoriasis with genital involvement coming from our dermatology department. A total of 86 patients with a diagnosis of moderate-tosevere plaque psoriasis with severe genital involvement were enrolled. Patient characteristics, psoriasis area and severity index (PASI), and static physician global assessment of genitalia (sPGAG) at each visit were recorded. During the treatment, the mean PASI decreased from 12.8 to 0.63 at week 52; a PGA of 0/1 was reached by 97.40% at week 52 and by 100% of patients (37/37) at week 104. No significant differences between IL-23 and IL-17 inhibitors were observed; indeed, the bio-naïve group of patients demonstrated a superior response compared to the group of bioexperienced patients.Our findings confirmed that IL-23 and IL-17 inhibitors are safe and effective therapeutic options for the treatment of genital psoriasis.
在银屑病病程中,生殖器银屑病影响3%-33%的银屑病患者,通常会导致患者生活质量严重下降。本研究旨在回顾性评估白细胞介素(IL)-23和IL-17抑制剂对来自我们皮肤科的中度至重度斑块状银屑病伴生殖器受累的现实人群的疗效。共纳入86例诊断为中度至重度斑块状银屑病且生殖器严重受累的患者。记录每次就诊时的患者特征、银屑病面积和严重程度指数(PASI)以及生殖器静态医师整体评估(sPGAG)。治疗期间,第52周时平均PASI从12.8降至0.63;第52周时97.40%的患者达到0/1的医师整体评估(PGA),第104周时100%的患者(37/37)达到该评估。未观察到IL-23和IL-17抑制剂之间存在显著差异;事实上,初治生物制剂组患者的反应优于接受过生物制剂治疗的患者组。我们的研究结果证实,IL-23和IL-17抑制剂是治疗生殖器银屑病的安全有效的治疗选择。