在PIONEER I和II试验中,用阿达木单抗治疗化脓性扁桃体炎可降低全身炎症指数,而这些指数是公认的心血管疾病风险因素。

IF 3.7 4区 医学 Q1 DERMATOLOGY
Niamh Kearney, Xin Chen, Yingtao Bi, Kinjal Hew, Kathleen M Smith, Brian Kirby
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引用次数: 0

摘要

背景:化脓性扁平湿疹(HS)与心血管疾病(CVD)风险增加有关。全身免疫炎症指数(SII)、中性粒细胞/淋巴细胞(NLR)、血小板/淋巴细胞(PLR)和单核细胞/淋巴细胞比率(MLR)是全身炎症和心血管疾病的生物标志物。一项小型研究发现,接受阿达木单抗治疗的患者NLR和PLR较低:我们的目的是在一个更大的队列中评估SII、NLR、PLR和MLR的变化,并评估它们与疾病严重程度和治疗反应的关系:这是对PIONEER I和PIONEER II两项阿达木单抗治疗HS的3期随机安慰剂对照临床试验进行的事后分析。对SII、NLR、PLR和MLR进行对数10转换,并使用线性混合模型估计治疗效果:结果:阿达木单抗治疗到第12周(评估主要反应终点)时,SII、NLR、PLR和MLR从基线水平降低。显著变化首次出现在第4周,并持续到第36周。相比之下,安慰剂治疗的患者则没有观察到明显变化。在第12周从安慰剂重新随机接受阿达木单抗治疗的患者中,SII、NLR、PLR和MLR在4周内也有所下降。在从阿达木单抗重新随机到安慰剂的患者中,这些生物标志物在第36周时恢复到基线水平。此外,SII、NLR和PLR与引流瘘计数相关(r=0.26-0.43,p结论:用阿达木单抗治疗HS患者可快速、持续地降低全身炎症反应,如SII、NLR、PLR和MLR,这些指标与心血管疾病风险相关。SII、NLR和PLR可预测阿达木单抗的反应,但取决于它们与引流瘘管数量的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of hidradenitis suppurativa with adalimumab in the PIONEER I and II randomized controlled trials reduced indices of systemic inflammation, recognized risk factors for cardiovascular disease.

Background: Hidradenitis suppurativa (HS) is associated with increased cardiovascular disease (CVD) risk. Systemic immune inflammation index (SII), neutrophil/lymphocyte ratio (NLR), platelet/lymphocyte ratio (PLR) and monocyte/lymphocyte ratio (MLR) are biomarkers of systemic inflammation and CVD. One small study identified a lower NLR and PLR in patients treated with adalimumab (ADA).

Objectives: To assess changes in SII, NLR, PLR and MLR in a larger cohort and to evaluate their association with disease severity and treatment response.

Methods: This was a post hoc analysis of PIONEER I (ClinicalTrials.gov ID: NCT01468207) and PIONEER II (ClinicalTrials.gov ID: NCT01468233), two phase III randomized placebo-controlled clinical trials of ADA for HS. SII, NLR, PLR and MLR were log10-transformed and a linear mixed model was used to estimate the treatment effect.

Results: SII, NLR, PLR and MLR decreased from baseline levels with ADA treatment by week 12, when the primary response endpoint was assessed. Significant changes first appeared at week 4 and were maintained to week 36. In contrast, no significant changes were observed in placebo-treated patients. In patients re-randomized at week 12 from placebo to ADA, SII, NLR, PLR and MLR also reduced within 4 weeks. In patients re-randomized from ADA to placebo, these biomarkers returned to baseline by week 36. In addition, SII, NLR and PLR correlated with draining fistula count (r = 0.26-0.43, P < 0.001). ADA nonresponders in PIONEER I had a higher SII, NLR and PLR at baseline and week 12, but this change did not achieve statistical significance when draining fistulae were adjusted for.

Conclusions: Treatment of patients with HS with ADA resulted in rapid sustained reduction in systemic inflammation, measured by the biomarkers SII, NLR, PLR and MLR, which correlate with CVD risk. SII, NLR and PLR may predict ADA response, although this may be dependent on their interaction with the number of draining fistulae.

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来源期刊
CiteScore
3.20
自引率
2.40%
发文量
389
审稿时长
3-8 weeks
期刊介绍: Clinical and Experimental Dermatology (CED) is a unique provider of relevant and educational material for practising clinicians and dermatological researchers. We support continuing professional development (CPD) of dermatology specialists to advance the understanding, management and treatment of skin disease in order to improve patient outcomes.
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