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粪便乳铁蛋白预测炎症性肠病对生物制剂的原发性无应答。

Fecal Lactoferrin Predicts Primary Nonresponse to Biologic Agents in Inflammatory Bowel Disease.

机构信息

IBD Center, Division of Gastroenterology, Virginia Tech Carilion School of Medicine, Roanoke, Virginia, USA.

Department of Clinical and Experimental Medical Sciences, University of Udine School of Medicine, Udine, Italy.

出版信息

Dig Dis. 2021;39(6):626-633. doi: 10.1159/000515432. Epub 2021 Feb 25.

Abstract

INTRODUCTION

Fecal lactoferrin (FL) is a timely and accurate marker of inflammation in ulcerative colitis (UC) and Crohn's disease (CD). The aim of this study was to verify whether FL can predict primary nonresponse (PNR) to biologic agents during induction.

METHODS

Retrospective outcome review in 27 patients (13 with CD and 14 with UC) tested for baseline FL and retested within a week after the first and second induction doses. Clinical/biochemical outcomes were evaluated at end of induction and at follow-up (3-24 months).

RESULTS

Compared to baseline, changes of the Harvey-Bradshaw (CD) and Partial Mayo Scoring (UC) indices at end of induction separated responders (18/27 or 67%) from nonresponders (9/17 or 33%). In all patients, the initial FL value at induction decreased compared to baseline, continuing to decrease after the following dose in clinical responders while bouncing back in the others. Models targeting the 2 consecutively decreased FL values or the second FL value compared to baseline or the second FL value compared to the first were able to accurately predict response at end of induction. Follow-up assessment confirmed clinical remission in initial responders (with FL values reduced on the average by 94 ± 10% compared to baseline).

CONCLUSIONS

In CD and UC patients during induction with biologic agents, early FL measurements accurately separate clinical responders from those experiencing PNR. The method described here offers several potential advantages over other strategies to assess and manage these patients.

摘要

简介

粪便乳铁蛋白(FL)是溃疡性结肠炎(UC)和克罗恩病(CD)炎症的及时、准确标志物。本研究旨在验证 FL 是否可预测诱导期生物制剂的原发性无应答(PNR)。

方法

回顾性分析 27 例患者(13 例 CD 和 14 例 UC)的基线 FL 检测结果,在首次和第二次诱导剂量后一周内进行复测。在诱导结束时和随访(3-24 个月)时评估临床/生化结局。

结果

与基线相比,诱导结束时的 Harvey-Bradshaw(CD)和部分 Mayo 评分(UC)指数变化将应答者(27 例中的 18 例或 67%)与无应答者(17 例中的 9 例或 33%)区分开来。在所有患者中,诱导时的初始 FL 值与基线相比降低,在临床应答者中,在接受下一次剂量后继续降低,而在其他患者中则反弹。针对连续两次降低的 FL 值或与基线相比的第二次 FL 值或与第一次 FL 值相比的第二次 FL 值的模型能够准确预测诱导结束时的反应。随访评估证实了初始应答者的临床缓解(与基线相比,FL 值平均降低 94 ± 10%)。

结论

在接受生物制剂诱导治疗的 CD 和 UC 患者中,早期 FL 测量可准确区分临床应答者和 PNR 者。与其他评估和管理这些患者的策略相比,这里描述的方法具有几个潜在优势。

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