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Disease Modification in Psoriasis Through Early IL-17 Inhibitor Intervention: A Retrospective Cohort Study

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Mendeley Data2026-04-09 收录
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This dataset contains seven supplementary tables enabling assessment of the disease-modifying effects of early IL-17A inhibitor intervention on psoriasis in a real-world cohort. Table 1 presents baseline laboratory parameters stratified by disease duration:USDD: Psoriasis duration≤1 year,LDD1:Psoriasis duration>1 year;SDD:Psoriasis duration≤2 year,LDD2:Psoriasis duration>2 year. Tables 2-3 identify predictors of PASI 100 achievement at 4 and 52 weeks via logistic regression, demonstrating that shorter disease duration significantly increases the likelihood of achieving PASI 100 at both timepoints. Table 4 compares baseline characteristics and discontinuation rates by recurrence status, showing significantly longer mean disease duration and higher discontinuation rates in the recurrence group. Table 5 establishes predictors of relapse through logistic regression, revealing that each additional year of disease duration increases relapse risk by 3% (OR=1.03, 95%CI=1.007-1.054, p=0.01). Table 6 examines relapse after IL-17A discontinuation in ultra-short disease duration (USDD: Psoriasis duration≤1 year) versus long duration (LDD1:Psoriasis duration>1 year): After adjusting for baseline PASI, BSA, and other confounders, USDD showed 78.8% lower relapse risk (OR=0.212, 95%CI=0.055-0.826, p=0.025). Table 7 compares short disease duration (SDD:Psoriasis duration≤2 year) versus long duration (LDD2:Psoriasis duration>2 year): SDD was associated with 70.5% reduced relapse risk (OR=0.295, 95%CI=0.099-0.874, p=0.028) after similar adjustments.

本数据集包含7份补充表格,可用于评估真实世界队列中早期白细胞介素-17A(Interleukin-17A,IL-17A)抑制剂干预对银屑病的疾病修饰效应。 表格1展示了按疾病时长分层的基线实验室指标:其中USDD指银屑病病程≤1年,LDD1指银屑病病程>1年;SDD指银屑病病程≤2年,LDD2指银屑病病程>2年。 表格2至表格3通过逻辑回归(logistic regression)分析了第4周与第52周的银屑病面积和严重程度指数100(Psoriasis Area and Severity Index 100,PASI 100)达标预测因素,结果表明更短的疾病时长可显著提升两个时间点下PASI 100的达标概率。 表格4按复发状态对比了基线特征与停药率,结果显示复发组的平均疾病时长显著更长,停药率也更高。 表格5通过逻辑回归确立了复发预测因素,结果显示每增加1年病程,复发风险升高3%(比值比(Odds Ratio,OR)=1.03,95%置信区间(95% Confidence Interval,95%CI)=1.007~1.054,p=0.01)。 表格6对比了超短病程(USDD:银屑病病程≤1年)与长病程(LDD1:银屑病病程>1年)患者在停用IL-17A抑制剂后的复发情况:在校正基线PASI、体表面积(Body Surface Area,BSA)及其他混杂因素后,USDD组的复发风险降低78.8%(OR=0.212,95%CI=0.055~0.826,p=0.025)。 表格7对比了短病程(SDD:银屑病病程≤2年)与长病程(LDD2:银屑病病程>2年)患者的复发情况:经类似校正后,SDD组的复发风险降低70.5%(OR=0.295,95%CI=0.099~0.874,p=0.028)。

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