Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Division of Gastroenterology, Hepatology and Nutrition, Nationwide Children's Hospital, Columbus, OH.
Inflamm Bowel Dis. 2021 Jun 15;27(7):1045-1051. doi: 10.1093/ibd/izaa241.
The neutrophil fecal biomarkers, calprotectin (FCP) and lactoferrin (LCT), and peripheral blood neutrophil CD64 surface receptor (nCD64) are biomarkers for mucosal inflammation in inflammatory bowel disease (IBD). Although FCP has been evaluated as a biomarker for mucosal healing, cut points for LCT and nCD64 are less known. We aimed to identify the cut points for LCT and nCD64 that were associated with FCP remission, with a secondary aim to evaluate the relationship between biochemical outcomes and infliximab (IFX) trough concentrations.
We analyzed FCP, LCT, and nCD64 before and after IFX induction in a pediatric Crohn's disease (CD) cohort study. Week-14 FCP biomarker remission was defined as FCP <250 µg/g, with clinical response defined as a weighted Pediatric Crohn's Disease Activity Index <12.5 or Δ>17.5 improvement. Predictive outcomes were calculated by receiver operating characteristics (ROCs).
Among 56 CD patients, ROC analysis identified an infusion 4 LCT <8.06 (area under the receiver operator characteristics [AUROC], 0.934, P < 0.001) and nCD64 <6.12 (AUROC, 0.76, P = 0.02) as the ideal cut points for week-14 FCP biomarker remission. End of induction IFX-trough of >9.4 µg/mL (AUROC, 0.799, P = 0.002) and >11.5 µg/mL (AUROC, 0.835, P = 0.003) were associated with a FCP <250 and FCP <100, respectively. We found patients achieving end of induction trough >5 µg/mL had a median FCP improvement (dose 1 to dose 4) of 90% compared with a median of 35% with levels <5 µg/mL (P = 0.024) with a similar median reduction in nCD64 (48% vs 20%, P = 0.031).
This study establishes cut points in neutrophil stool and blood biomarkers for both biochemical remission and therapeutic trough levels following induction therapy. Further studies that evaluate pharmacodynamic biomarker targets for endoscopic and histologic healing are warranted.
中性粒细胞粪便生物标志物钙卫蛋白(FCP)和乳铁蛋白(LCT)以及外周血中性粒细胞 CD64 表面受体(nCD64)是炎症性肠病(IBD)黏膜炎症的生物标志物。虽然 FCP 已被评估为黏膜愈合的生物标志物,但 LCT 和 nCD64 的切点知之甚少。我们旨在确定与 FCP 缓解相关的 LCT 和 nCD64 的切点,次要目的是评估生化结果与英夫利昔单抗(IFX)谷浓度之间的关系。
我们在小儿克罗恩病(CD)队列研究中分析了 IFX 诱导前后的 FCP、LCT 和 nCD64。第 14 周时 FCP 生物标志物缓解定义为 FCP<250μg/g,临床反应定义为加权小儿克罗恩病活动指数<12.5 或 Δ>17.5 改善。通过接受者操作特征(ROC)分析计算预测结果。
在 56 例 CD 患者中,ROC 分析确定输注后 4 小时 LCT<8.06(ROC 下面积 [AUROC],0.934,P<0.001)和 nCD64<6.12(AUROC,0.76,P=0.02)是第 14 周 FCP 生物标志物缓解的理想切点。诱导结束时 IFX 谷浓度>9.4μg/mL(AUROC,0.799,P=0.002)和>11.5μg/mL(AUROC,0.835,P=0.003)分别与 FCP<250 和 FCP<100 相关。我们发现,达到诱导结束时谷浓度>5μg/mL 的患者与浓度<5μg/mL 的患者相比,FCP 的中位数改善(剂量 1 到剂量 4)为 90%,中位数为 35%(P=0.024),nCD64 的中位数也相似降低(48%比 20%,P=0.031)。
本研究确定了诱导治疗后生化缓解和治疗谷水平的中性粒细胞粪便和血液生物标志物的切点。需要进一步研究评估内镜和组织学愈合的药效学生物标志物靶标。