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Serum Bile Acids Profiling in Inflammatory Bowel Disease Patients Treated with Anti-TNFs

Authors :
Alexandros Skamnelos
Konstantinos H. Katsanos
Emanuele Porru
Gionata Fiorino
Giulia Roda
Aldo Roda
Silvio Danese
Dimitrios K. Christodoulou
Kallirroi Kyriakidi
Roda, G
Porru, E
Katsanos, K
Skamnelos, A
Kyriakidi, K
Fiorino, G
Christodoulou, D
Danese, S
Roda, A
Source :
Cells, Vol 8, Iss 8, p 817 (2019), Cells, Volume 8, Issue 8
Publication Year :
2019
Publisher :
MDPI AG, 2019.

Abstract

Background: Inflammatory bowel diseases (IBD), ulcerative colitis (UC), and Crohn&rsquo<br />s disease (CD), represent systematic chronic conditions with a deficient intestinal absorption. We first attempt to investigate the serum bile acids (sBAs) profile in a large cohort of IBD patients to evaluate changes under anti-TNF alpha treatment. Methods: Forty CD and 40 UC patients were enrolled and BAs were quantified by high-pressure liquid chromatography-electrospray-tandem mass spectrometry (HPLC-ES-MS/MS). Up to 15 different sBAs concentrations and clinical biomarkers where added to a Principal Component Analysis (PCA) to discriminate IBD from healthy conditions and treatment. Results: PCA allowed a separation into two clusters within CD (biologic-free patients and patients treated with anti-TNF alpha drugs and healthy subjects) but not UC. The first included CD. CD patients receiving anti-TNF alpha have an increase in total sBAs (4.11 1.23 &mu<br />M) compared to patients not exposed. Secondary BAs significantly increase after anti-TNF alpha treatment (1.54 0.83 &mu<br />M). Furthermore, multivariate analysis based on sBA concentration highlighted a different qualitative sBAs profile for UC and CD patients treated with conventional therapy. Conclusion: According to our results, anti-TNF alpha in CD restores the sBA profile by re-establishing the physiological levels. These findings indicate that, secondary BAs might serve as an indirect biomarker of the healing process.

Details

Language :
English
ISSN :
20734409
Volume :
8
Issue :
8
Database :
OpenAIRE
Journal :
Cells
Accession number :
edsair.doi.dedup.....513550b11ea5cf37b61b2eba6c8a3b82