Crohn's disease;
stool tests;
fecal biomarkers;
Crohn's disease index of severity;
tumor necrosis factor alpha;
mucosal healing;
D O I:
10.1002/ibd.20490
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Background: Fecal calprotectin and lactoferrin are promising noninvasive biomarkers for intestinal inflammation. In Crohn's disease (CD, during anti-TNF-alpha (TNF-alpha) treatment. the clinical significance of these markers has, however, been insufficient explored. Methods: Among CD patients receiving anti-TNF-alpha therapy we assessed the role of fecal calprotectin and lactoferrin as surrogate markers for mucosal healing. Before and 3 months after the beginning of anti-TNF-alpha induction, 15 patients underwent ileocolonoscopy with scoring of the Crohn's Disease Index oh Severity (CDEIS). Fecal samples for calprotectin and for lactoferrin measurements were collected and the Crohn's Disease Activity Index (CDAI) was calculated aft the time of the endoscopies and 2 and 8 weeks after the first treatment. Results: The median CDEIS fell from 13.0 to 4.8 (P = 0.002) and CDAI from 158 to 68 (P = 0.005). Accordingly. the median fecal calprotectin concentration fell from 1173 mu g/g to 130 mu g/g (P = 0.001) and fecal lactoferrin from 105.0 mu g/g to 2.7 mu g/g (P = 0.001). Of the 15 patients, 11 (73%) showed an endoscopic response to treatment and 5 of these achieved endoscopic remission (CDEIS < 3). In those 5 patients the fecal calprotectin concentration declined from 1891 mu g/g (range 813-2434) to 27 mu g/g (13-130) and lactoferrin from 92.4 mu g/g (35.5-235.6) to 1.9 mu g/g (0.0-2.1). Conclusions: Compared to pretreatment values. concentrations of focal calprotectin and lactoferrin after the anti-TNF-alpha treatment were significantly lower. During anti-TNF-alpha therapy these fecal neurophil-derived proteins may thus be useful surrogate markers for mucosal healing. (Inflamm Bowel Dis 2008; 14:1392-1398)
机构:
Univ Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Univ Clermont Auvergne, Serv dHepatogastro Enterol, 3iHP, CHU Clermont Ferrand,Inserm, Clermont Ferrand, France
Dept Med Univ Clermont Auvergne, M2iSH, Inserm U1071, 3iHP,USC INRA 2018, F-63000 Clermont Ferrand, FranceUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Buisson, Anthony
Mak, Wing Yan
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Univ Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Queen Elizabeth Hosp, Hong Kong, Peoples R ChinaUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Mak, Wing Yan
Andersen, Michael J.
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Univ Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USAUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Andersen, Michael J.
Lei, Donald
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Univ Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USAUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Lei, Donald
Pekow, Joel
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Univ Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USAUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Pekow, Joel
Cohen, Russell D.
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Univ Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USAUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Cohen, Russell D.
Kahn, Stacy A.
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Harvard Med Sch, Inflammatory Bowel Dis Ctr, Boston Childrens Hosp, Boston, MA USAUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Kahn, Stacy A.
Pereira, Bruno
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Univ Clermont Auvergne, Unite Biostat, DRCI, CHU Clermont Ferrand, Clermont Ferrand, FranceUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA
Pereira, Bruno
Rubin, David T.
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Univ Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USAUniv Chicago, Med Inflammatory Bowel Dis Ctr, Chicago, IL USA