Campione Elena, Artosi Fabio, Shumak Ruslana Gaeta, Giunta Alessandro, Argenziano Giuseppe, Assorgi Chiara, Balato Anna, Bernardini Nicoletta, Brunasso Alexandra Maria Giovanna, Burlando Martina, Caldarola Giacomo, Campanati Anna, Carugno Andrea, Castelli Franco, Conti Andrea, Costanzo Antonio, Cuccia Aldo, Dapavo Paolo, Dattola Annunziata, De Simone Clara, Di Lernia Vito, Dini Valentina, Donini Massimo, Errichetti Enzo, Esposito Maria, Fargnoli Maria Concetta, Foti Antonio, Fiorella Carmen, Gargiulo Luigi, Gisondi Paolo, Guarneri Claudio, Legori Agostina, Lembo Serena, Loconsole Francesco, Malagoli Piergiorigio, Marzano Angelo Valerio, Mercuri Santo Raffaele, Megna Matteo, Micali Giuseppe, Mortato Edoardo, Musumeci Maria Letizia, Narcisi Alessandra, Offidani Anna Maria, Orsini Diego, Paolino Giovanni, Pellacani Giovanni, Peris Ketty, Potenza Concetta, Prignano Francesca, Quaglino Pietro, Ribero Simone, Richetta Antonio Giovanni, Romanelli Marco, Rossi Antonio, Strippoli Davide, Trovato Emanuele, Venturini Marina, Bianchi Luca
Dermatology Unit, Department of Systems Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.
Dermatology Unit, University of Campania L. Vanvitelli, 80131 Naples, Italy.
Pharmaceuticals (Basel). 2024 Oct 16;17(10):1378. doi: 10.3390/ph17101378.
(1) Background/Objectives: Nail psoriasis (NP) is a chronic and difficult-to-treat disease, which causes significant social stigma and impairs the patients' quality of life. Moreover, nail psoriasis is a true therapeutic challenge for clinicians. The presence of nail psoriasis can be part of a severe form of psoriasis and can have predictive value for the development of psoriatic arthritis. Our real-world-evidence multicenter study aims to evaluate the efficacy of bimekizumab in nail psoriasis. (2) Methods: A retrospective analysis of a multicenter observational study included 834 patients affected by moderate-to-severe psoriasis, in 33 Dermatologic Units in Italy, treated with bimekizumab from December 2022 to September 2023. Clinimetric assessments were based on Psoriasis Area and Severity Index (PASI), Dermatology Life Quality Index (DLQI), and Physician's Global Assessment of Fingernail Psoriasis (PGA-F) for the severity of nail psoriasis at 0, 12, 24, and 36 weeks. (3) Results: Psoriatic nail involvement was present in 27.95% of patients. The percentage of patients who achieved a complete clearance of NP in terms of PGA-F 0 was 31.7%, 57%, and 88.5% at week 4, 16, and 36, respectively. PASI 100 was achieved by 32.03% of patients at week 4, by 61.8% at week 16, and by 78.92% of patients at week 36. The mean baseline PASI was 16.24. The mean DLQI values for the entire group of patients at baseline, at week 4, at week 16, and at week 36 were 14.62, 3.02, 0.83, and 0.5, respectively. (4) Conclusions: Therapies that promote the healing of both the skin and nails in a short time can also ensure a lower risk of subsequently developing arthritis which is disabling over time. Bimekizumab proved to be particularly effective to treat NP, with a fast response in terms of complete clearance, with over 88.5% of patients free from NP after 36 weeks. The findings of our real-world study showed that patients with moderate-to-severe PsO and concomitant NP had significantly faster and more substantial improvements in NP up to 36 weeks with respect to previous research findings. Considering the rapid healing of the nail, the dual inhibition of IL17 A and F might have a great value in re-establishing the dysregulation of keratin 17 at the nail level.
(1) 背景/目的:甲银屑病(NP)是一种慢性且难以治疗的疾病,会造成严重的社会污名化并损害患者的生活质量。此外,甲银屑病对临床医生来说是一个真正的治疗挑战。甲银屑病的存在可能是严重银屑病的一部分,并且对银屑病关节炎的发展具有预测价值。我们的真实世界证据多中心研究旨在评估比美吉珠单抗治疗甲银屑病的疗效。(2) 方法:对一项多中心观察性研究进行回顾性分析,该研究纳入了意大利33个皮肤科单位的834例中重度银屑病患者,这些患者在2022年12月至2023年9月期间接受了比美吉珠单抗治疗。临床测量评估基于银屑病面积和严重程度指数(PASI)、皮肤病生活质量指数(DLQI)以及医生对指甲银屑病严重程度的整体评估(PGA - F),分别在第0、12、24和36周进行评估。(3) 结果:27.95%的患者存在银屑病甲受累。就PGA - F 0而言,在第4周、16周和36周时,实现甲银屑病完全清除的患者百分比分别为31.7%、57%和88.5%。在第4周时,32.03%的患者达到PASI 100,在第16周时为61.8%,在第36周时为78.92%。基线时PASI的平均值为16.24。整个患者组在基线、第4周、第16周和第36周时的DLQI平均值分别为14.62、3.02、0.83和0.5。(4) 结论:能在短时间内促进皮肤和指甲愈合的疗法也可确保降低随后发生随时间推移会导致残疾的关节炎的风险。比美吉珠单抗被证明在治疗甲银屑病方面特别有效,在完全清除方面反应迅速,36周后超过88.5%的患者无甲银屑病。我们的真实世界研究结果表明,与先前的研究结果相比,中重度银屑病(PsO)合并甲银屑病的患者在36周内甲银屑病的改善明显更快且更显著。考虑到指甲的快速愈合,白细胞介素17A和F的双重抑制可能在恢复指甲水平角蛋白17的失调方面具有重要价值。