Accéder au contenu
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
RÉSUMÉ

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.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Acide sulfurique, ACS reagent, 95.0-98.0%
Sigma-Aldrich
Sulfate de sodium, ACS reagent, ≥99.0%, anhydrous, granular
Sigma-Aldrich
Sulfate de sodium, ACS reagent, ≥99.0%, anhydrous, powder
Sigma-Aldrich
Acide sulfurique, 99.999%
Sigma-Aldrich
Acide sulfurique, puriss. p.a., for determination of Hg, ACS reagent, reag. ISO, reag. Ph. Eur., 95.0-97.0%
Sigma-Aldrich
Sulfate de sodium, ReagentPlus®, ≥99.0%
Sigma-Aldrich
Sulfate de sodium, puriss., meets analytical specification of Ph. Eur., BP, USP, anhydrous, 99.0-100.5% (calc. to the dried substance)
Sigma-Aldrich
Sulfate de sodium, anhydrous, free-flowing, Redi-Dri, ACS reagent, ≥99%
Sigma-Aldrich
Acide sulfurique, puriss., meets analytical specification of Ph. Eur., BP, 95-97%
Sigma-Aldrich
Acide sulfurique solution, puriss. p.a., ≥25% (T)
Supelco
Acide sulfurique solution, 0.1 M H2SO4 in water (0.2N), eluent concentrate for IC
Sigma-Aldrich
Sulfate de sodium, anhydrous, free-flowing, Redi-Dri, ReagentPlus®, ≥99%
Sigma-Aldrich
2-Ethylbutyric acid, 99%
Sigma-Aldrich
Sulfate de sodium, ≥99.99% trace metals basis
Sigma-Aldrich
Sulfate de sodium, BioUltra, anhydrous, ≥99.0% (T)
Sigma-Aldrich
Sulfate de sodium, BioXtra, ≥99.0%
Supelco
Acide sulfurique, for the determination of nitrogen, ≥97.0%
Sigma-Aldrich
Acide sulfurique, puriss., meets analytical specification of Ph. Eur., BP, 95-97%
Sigma-Aldrich
2-Ethylbutyric acid, ≥98%, FCC, FG
Sigma-Aldrich
Sulfate de sodium, ≥99.0%, suitable for plant cell culture
Sigma-Aldrich
Sulfate de sodium, tested according to Ph. Eur., anhydrous