Saltar al contenido
Merck

Faecal metabolite profiling identifies medium-chain fatty acids as discriminating compounds in IBD.

Gut (2014-05-09)
Vicky De Preter, Kathleen Machiels, Marie Joossens, Ingrid Arijs, Christophe Matthys, Severine Vermeire, Paul Rutgeerts, Kristin Verbeke
RESUMEN

Bacteria play a role in the onset and perpetuation of intestinal inflammation in IBD. Compositional alterations may also change the metabolic capacities of the gut bacteria. To examine the metabolic activity of the microbiota of patients with Crohn's disease (CD), UC or pouchitis compared with healthy controls (HC) and determine whether eventual differences might be related to the pathogenesis of the disease. Faecal samples were obtained from 40 HC, 83 patients with CD, 68 with UC and 13 with pouchitis. Disease activity was assessed in CD using the Harvey-Bradshaw Index, in UC using the UC Disease Activity Index and in pouchitis using the Pouchitis Disease Activity Index. Metabolite profiles were analysed using gas chromatography-mass spectrometry. The number of metabolites identified in HC (54) was significantly higher than in patients with CD (44, p<0.001), UC (47, p=0.042) and pouchitis (43, p=0.036). Multivariate discriminant analysis predicted HC, CD, UC and pouchitis group membership with high sensitivity and specificity. The levels of medium-chain fatty acids (MCFAs: pentanoate, hexanoate, heptanoate, octanoate and nonanoate), and of some protein fermentation metabolites, were significantly decreased in patients with CD, UC and pouchitis. Hexanoate levels were inversely correlated to disease activity in CD (correlation coefficient=-0.157, p=0.046), whereas a significant positive correlation was found between styrene levels and disease activity in UC (correlation coefficient=0.338, p=0.001). Faecal metabolic profiling in patients with IBD relative to healthy controls identified MCFAs as important metabolic biomarkers of disease-related changes. NCT 01666717.

MATERIALES
Referencia del producto
Marca
Descripción del producto

Sigma-Aldrich
Ácido sulfúrico, ACS reagent, 95.0-98.0%
Sigma-Aldrich
Sulfato de sodio, ACS reagent, ≥99.0%, anhydrous, granular
Sigma-Aldrich
Sulfato de sodio, ACS reagent, ≥99.0%, anhydrous, powder
Sigma-Aldrich
Ácido sulfúrico, 99.999%
Sigma-Aldrich
Ácido sulfúrico, puriss. p.a., for determination of Hg, ACS reagent, reag. ISO, reag. Ph. Eur., 95.0-97.0%
Sigma-Aldrich
Sulfato de sodio, ReagentPlus®, ≥99.0%
Sigma-Aldrich
Sulfato de sodio, puriss., meets analytical specification of Ph. Eur., BP, USP, anhydrous, 99.0-100.5% (calc. to the dried substance)
Sigma-Aldrich
Sulfato de sodio, anhydrous, free-flowing, Redi-Dri, ACS reagent, ≥99%
Sigma-Aldrich
Sulfuric acid solution, puriss. p.a., ≥25% (T)
Sigma-Aldrich
Sulfato de sodio, anhydrous, free-flowing, Redi-Dri, ReagentPlus®, ≥99%
Sigma-Aldrich
2-Ethylbutyric acid, 99%
Supelco
Sulfuric acid concentrate, 0.1 M H2SO4 in water (0.2N), eluent concentrate for IC
Sigma-Aldrich
Sulfato de sodio, ≥99.99% trace metals basis
Sigma-Aldrich
Sulfato de sodio, BioUltra, anhydrous, ≥99.0% (T)
Sigma-Aldrich
Sulfato de sodio, BioXtra, ≥99.0%
Sigma-Aldrich
2-Ethylbutyric acid, ≥98%, FCC, FG
Sigma-Aldrich
Sulfato de sodio, ≥99.0%, suitable for plant cell culture
Sigma-Aldrich
Sulfato de sodio, tested according to Ph. Eur., anhydrous