首页> 外文期刊>International journal of dermatology >The efficacy of methotrexate plus pioglitazone vs. methotrexate alone in the management of patients with plaque-type psoriasis: a single-blinded randomized controlled trial
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The efficacy of methotrexate plus pioglitazone vs. methotrexate alone in the management of patients with plaque-type psoriasis: a single-blinded randomized controlled trial

机译:甲氨蝶呤加吡格列酮与单用甲氨蝶呤在斑块型牛皮癣患者管理中的疗效:单盲随机对照试验

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Recently, thiazolidinediones have shown to be efficacious with a favorable safety profile when used in the treatment of chronic plaque-type psoriasis. The aim of this study was to evaluate and compare the efficacy and safety of a combination of methotrexate plus pioglitazone and methotrexate alone in plaque-type psoriasis. A total of 44 adult patients with plaque-type psoriasis were included in the study. Patients were randomized to treatment with methotrexate alone (group A) or methotrexate plus pioglitazone (group B) for 16 weeks. The primary efficacy outcome measure was psoriasis area and severity index (PASI) score change between the study groups at week 16 relative to baseline. The secondary efficacy outcome measure was dermatology life quality index (DLQI) score change between the two groups at week 16 relative to baseline. The PASI 75 score was also measured. After 16 weeks of therapy, the percentage of reduction in the mean PASI score was 70.3% in group B and 60.2% in group A. PASI 75 was achieved in 14 patients (63.6%) in group B compared with two patients (9.1%) in group A within 16 weeks, which was significant (P < 0.001). At 16 weeks from the baseline, a 63.6% decrease in the mean DLQI score of group B was seen, while the decrease for group A was 56.9%. Pioglitazone enhances the therapeutic effect of methotrexate in plaque-type psoriasis, as demonstrated by a reduction in the mean PASI scores. In terms of DLQI, there was no extra benefit by the addition of pioglitazone to methotrexate therapy.
机译:近来,噻唑烷二酮已显示出当用于治疗慢性斑块型牛皮癣时具有良好的安全性和有效的安全性。这项研究的目的是评估和比较甲氨蝶呤加吡格列酮和甲氨蝶呤单独使用在斑块型牛皮癣中的疗效和安全性。该研究共纳入了44名成年斑块型牛皮癣患者。患者被随机分配单独接受甲氨蝶呤治疗(A组)或接受甲氨蝶呤加吡格列酮治疗(B组)16周。主要疗效结局指标是牛皮癣面积和研究组在第16周相对于基线的严重程度指数(PASI)得分变化。次要疗效指标是两组在第16周相对于基线的皮肤病学生活质量指数(DLQI)得分变化。还测量了PASI 75得分。治疗16周后,B组平均PASI得分降低的百分比为70.3%,A组为60.2%。B组的14位患者(63.6%)达到了PASI 75,而两名患者(9.1%) A组在16周内显着(P <0.001)。在距基线16周时,B组的平均DLQI得分下降了63.6%,而A组的下降为56.9%。吡格列酮可增强氨甲蝶呤在斑块型牛皮癣中的治疗效果,这可通过降低平均PASI得分来证明。就DLQI而言,在氨甲蝶呤治疗中添加吡格列酮并没有额外的益处。

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