Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, IL, USA.
Indiana University Health Southern Indiana Physicians, Bloomington, IN, USA.
Gut. 2021 Nov;70(11):2076-2084. doi: 10.1136/gutjnl-2020-321609. Epub 2020 Dec 17.
In treating patients with inflammatory bowel disease (IBD), how concomitant medications influence the response to infliximab is largely unexplored. We aim to evaluate whether proton pump inhibitors (PPIs) affect the response to infliximab therapy in patients with IBD.
Patient-level data of adult patients with moderate-to-severe IBD treated with infliximab were obtained from the Yale Open Data Access Framework. Multivariable analysis and propensity score-matched analysis were performed to assess week 30 remission rates, week 54 remission rates and hospitalisation rates in patients on infliximab therapy with and without PPI exposure.
Among the five randomised controlled studies, there were 147 and 889 patients on infliximab with and without PPI therapy, respectively. Patients on PPI were older, more likely to be Caucasian and were less likely to be on immunomodulator therapy. Patients on PPI were significantly less likely to achieve week 30 remission on multivariable analysis (OR 0.45, p<0.001). Following propensity score matching adjusting for baseline difference in patient characteristics, the week 30 remission rates were 30% and 49% in patients with and without PPI therapy, respectively (p<0.001). Analysing separately for disease, the findings remained statistically significant in Crohn's disease but did not reach significance in UC. Similar results were seen with week 54 remission rates. Patients on PPI were also more likely to be hospitalised (15% vs 8%, p=0.007). Rates of adverse events such as gastroenteritis were not different between the two groups.
In this patient-level meta-analysis of randomised controlled studies, we found that patients with IBD taking PPI were less likely to achieve remission while on infliximab therapy. The results of our study warrant further investigation into the effect of PPI on IBD outcomes and therapies.
在治疗炎症性肠病(IBD)患者时,伴随药物如何影响英夫利昔单抗的疗效在很大程度上尚未得到探索。我们旨在评估质子泵抑制剂(PPIs)是否会影响 IBD 患者对英夫利昔单抗治疗的反应。
从耶鲁大学开放数据访问框架中获取接受英夫利昔单抗治疗的中重度 IBD 成年患者的患者水平数据。进行多变量分析和倾向评分匹配分析,以评估接受和未接受 PPI 治疗的英夫利昔单抗治疗患者在第 30 周缓解率、第 54 周缓解率和住院率。
在五项随机对照研究中,分别有 147 例和 889 例接受英夫利昔单抗治疗且有或无 PPI 治疗的患者。接受 PPI 治疗的患者年龄更大,更可能为白种人,且更不可能接受免疫调节剂治疗。多变量分析显示,接受 PPI 治疗的患者第 30 周缓解的可能性显著降低(OR 0.45,p<0.001)。在调整患者特征基线差异的倾向评分匹配后,分别有 30%和 49%的患者接受 PPI 治疗和未接受 PPI 治疗达到第 30 周缓解(p<0.001)。按疾病分别分析,在克罗恩病中发现的结果仍具有统计学意义,但在溃疡性结肠炎中未达到统计学意义。第 54 周缓解率也有类似结果。接受 PPI 治疗的患者更有可能住院(15% vs 8%,p=0.007)。两组之间的胃肠炎等不良事件发生率没有差异。
在这项针对随机对照研究的患者水平荟萃分析中,我们发现接受 PPI 治疗的 IBD 患者在接受英夫利昔单抗治疗时更不可能达到缓解。我们的研究结果表明需要进一步研究 PPI 对 IBD 结局和治疗的影响。