英夫利昔单抗
医学
新喋呤
乳铁蛋白
溃疡性结肠炎
钙蛋白酶
炎症性肠病
内科学
胃肠病学
疾病
生物
生物化学
作者
Anne-Claire Frin,Jérôme Filippi,Gilles Boschetti,Bernard Flourié,Jocelyne Drai,P Ferrari,Xavier Hébuterne,Stéphane Nancey
标识
DOI:10.1016/j.dld.2016.09.001
摘要
Fecal markers might predict the response to anti-TNFα in ulcerative colitis (UC).To compare the performance of fecal calprotectin (fCal), lactoferrin (fLact), M2-PK (fM2-PK), neopterin (fNeo), and zonulin (fZon) to predict the response to therapy in active UC patients.Disease activity from 31 consecutive patients with an active UC, treated with infliximab (IFX) was assessed by the Mayo score at baseline and at week 14 and by the partial Mayo score at W52 and stool samples collected for fecal marker measurements at W0, W2, and W14.At W14, 19 patients (61%) were responders to IFX induction. The median levels of fCal, fLact and fM2-PK drop dramatically from baseline to W14 in clinical responders. At W2, fM2-PK, fLact and fCal levels predicted accurately the response to IFX induction. At W14, fLact, fCal, and fM2-PK were individually reliable markers to predict sustained response at W52. The performances of fNeo and fZon were weaker in this setting.The performance of fM2-PK at W2 to predict response to induction therapy with IFX was superior to that of fLact and fCal, whereas monitoring fLact was the best tool to predict adequately the course of the disease at one year under maintenance IFX in UC.
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