Department of Dermatology, Venereology and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India.
J Eur Acad Dermatol Venereol. 2013 Mar;27(3):e384-9. doi: 10.1111/jdv.12004. Epub 2012 Oct 16.
Palmoplantar psoriasis (PP) is a chronic, inflammatory and proliferative dermatosis of the palms and/or soles with significant morbidity. It is notoriously difficult to treat and unresponsive to traditional topical agents. MATERIAL AND METHODS This was a prospective, randomized study involving 111 patients of psoriasis with significant palmoplantar disease. Patients meeting the eligibility criteria were randomly assigned to one of the two treatment groups. Patients in Group I received methotrexate in doses of 0.4 mg/kg weekly, and patients in Group II received acitretin in doses of 0.5 mg/kg daily. Patients were evaluated by modified PPPASI (m-PPPASI) score for palm and sole involvement at baseline, at two weekly intervals for the first 4 weeks and then four weekly for next 8 weeks. Treatment protocol was continued for a period till patient achieved 75% reduction in m-PPPASI from baseline or 12 weeks whichever was earlier.
There was a statistically significant difference in reduction of m-PPPASI of patients on methotrexate at weeks 8 and 12. The mean m-PPPASI at week 8 was 15.38 ± 6.08 in methotrexate group and 17.23 ± 5.25 in acitretin group (P = 0.04). The mean m-PPPASI at week 12 was 10.30 ± 5.97 in methotrexate group and 12.40 ± 5.31 in acitretin group (P = 0.03). Marked improvement (m-PPPASI 75) was achieved in 12 (24%) patients in methotrexate group compared with 4 (8%) in acitretin group which was statistically significant (P = 0.029). Adverse events were generally mild and were seen in 14 patients in methotrexate group and 15 patients in acitretin group (P = 0.080).
Methotrexate is relatively inexpensive, safe and efficacious drug for the treatment of psoriasis patients with significant palmoplantar involvement. Acitretin can be used as an alternative therapy and with a good safety profile.
掌跖银屑病(PP)是一种慢性、炎症性和增生性皮肤病,手掌和/或脚底有明显的发病率。它的治疗非常困难,传统的局部治疗药物对其无效。
这是一项涉及 111 例银屑病伴明显掌跖疾病患者的前瞻性、随机研究。符合入选标准的患者被随机分配到两个治疗组之一。第 I 组患者接受每周 0.4mg/kg 的甲氨蝶呤治疗,第 II 组患者接受每天 0.5mg/kg 的阿维 A 治疗。患者在基线时、前 4 周每两周评估一次、之后每 4 周评估一次,使用改良的 PPPASI(m-PPPASI)评分评估手掌和足底受累情况。治疗方案持续到患者从基线水平获得 m-PPPASI 降低 75%或 12 周,以先达到者为准。
甲氨蝶呤组患者在第 8 周和第 12 周时 m-PPPASI 降低有统计学差异。第 8 周时,甲氨蝶呤组 m-PPPASI 平均值为 15.38 ± 6.08,阿维 A 组为 17.23 ± 5.25(P = 0.04)。第 12 周时,甲氨蝶呤组 m-PPPASI 平均值为 10.30 ± 5.97,阿维 A 组为 12.40 ± 5.31(P = 0.03)。在甲氨蝶呤组中,12 名(24%)患者达到了明显的改善(m-PPPASI 降低 75%),而阿维 A 组只有 4 名(8%)患者达到了这一标准,这具有统计学意义(P = 0.029)。甲氨蝶呤组有 14 名患者和阿维 A 组有 15 名患者出现了一般轻微的不良反应(P = 0.080)。
甲氨蝶呤是一种相对廉价、安全且有效的药物,可用于治疗伴有明显掌跖受累的银屑病患者。阿维 A 可作为替代治疗药物,且安全性良好。