Metabolic and inflammatory faecal markers in collagenous colitis

被引:72
|
作者
Wildt, Signe [1 ]
Nordgaard-Lassen, Inge [1 ]
Bendtsen, Flemming [1 ]
Rumessen, Juri J. [2 ]
机构
[1] Univ Copenhagen, Dept Med Gastroenterology, Hvidovre Hosp, DK-2650 Copenhagen, Denmark
[2] Univ Copenhagen, Dept Med Gastroentrology, Gentofte Hosp, DK-2650 Copenhagen, Denmark
关键词
calprotectin; collagenous colitis; lactoferrin; short-chain fatty acids;
D O I
10.1097/MEG.0b013e328058ed76
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives To evaluate the excretion of the inflammatory and metabolic faecal markers calprotectin, lactoferrin, and short-chain fatty acids in symptomatic and quiescent collagenous colitis. Methods Faecal samples from 21 patients with active collagenous colitis, 12 patients retested in remission, and 13 controls were analysed. Calprotectin was determined using an enzyme-linked immunosorbent assay. Lactoferrin was estimated by a latex agglutination test. Short-chain fatty acids were determined by steam distillation followed by gas-liquid chromatography. Results Calprotectin was increased in patients with active collagenous colitis [80 mu g/g (6.25-1899)] (median and range) compared with patients with quiescent collagenous colitis [26 mu g/g (6.25-340)], P=0.025 and controls [6.25 mu g/g (6.25-99)], P=0.002. Eight patients (38%) with active collagenous colitis had normal levels of calprotectin. Lactoferrin was detected in one patient only. Concentrations of total short-chain fatty acids did not differ in patients with active collagenous colitis compared with quiescent collagenous colitis or controls (P=0.75), whereas concentrations of the branched-chain fatty acids were decreased in patients with active collagenous colitis versus controls (P<0.005). In-vitro incubations demonstrated increased ratios of acetate in patients with active and quiescent collagenous colitis compared with controls (P<0.05), with a corresponding decrease in branched-chain fatty acids ratios (P<0.05). Conclusion Faecal calprotectin was increased in collagenous colitis; however, increased excretion was not a universal finding limiting the use of calprotectin as an inflammatory marker in collagenous colitis. Faecal lactoferrin was almost undetectable. Luminal fermentative conditions are altered in collagenous colitis. Fermentative alterations could be secondary to changes in substrate availability and intestinal transit time.
引用
收藏
页码:567 / 574
页数:8
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