TY - JOUR
T1 - Integrated serum proteins and fatty acids analysis for putative biomarker discovery in inflammatory bowel disease
AU - Manfredi, Marcello
AU - Conte, Eleonora
AU - Barberis, Elettra
AU - Buzzi, Arianna
AU - Robotti, Elisa
AU - Caneparo, Valeria
AU - Cecconi, Daniela
AU - Brandi, Jessica
AU - Vanni, Ester
AU - Finocchiaro, Marco
AU - Astegiano, Marco
AU - Gariglio, Marisa
AU - Marengo, Emilio
AU - De Andrea, Marco
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/3/20
Y1 - 2019/3/20
N2 - The diagnosis and management of Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), is still challenging. There is no definitive gold standard diagnostic test, which is made on patient history and with endoscopic and histological findings. This study analyzed serum proteins and fatty acids using mass spectrometry-based techniques. Quantitation of serum proteins was performed by depleting 14 high-abundance proteins, followed by tryptic digestion and LC–MS analysis, while fatty acids were analyzed using GC–MS. Bioinformatic tools were used to identify several new potential biomarkers for an early and non-invasive diagnosis of IBD, and to differentiate CD from UC. Moreover, the diagnostic power of the MS-identified biomarkers was also corroborated by Western Blot and ELISA assays. Hence, we identified the biological functions and pathways involved in the various subsets of IBD. Coagulation, fibrinolysis and acute phase response processes were found to be strongly involved in the condition. The involvement of several fatty acids, such as anti-inflammatory mediators, was also identified. Finally, proteomic and lipidomic data were integrated by using combinatorial and multivariate analyses to discover new combined biomarkers and to study the molecular pathways involved in IBD.
AB - The diagnosis and management of Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), is still challenging. There is no definitive gold standard diagnostic test, which is made on patient history and with endoscopic and histological findings. This study analyzed serum proteins and fatty acids using mass spectrometry-based techniques. Quantitation of serum proteins was performed by depleting 14 high-abundance proteins, followed by tryptic digestion and LC–MS analysis, while fatty acids were analyzed using GC–MS. Bioinformatic tools were used to identify several new potential biomarkers for an early and non-invasive diagnosis of IBD, and to differentiate CD from UC. Moreover, the diagnostic power of the MS-identified biomarkers was also corroborated by Western Blot and ELISA assays. Hence, we identified the biological functions and pathways involved in the various subsets of IBD. Coagulation, fibrinolysis and acute phase response processes were found to be strongly involved in the condition. The involvement of several fatty acids, such as anti-inflammatory mediators, was also identified. Finally, proteomic and lipidomic data were integrated by using combinatorial and multivariate analyses to discover new combined biomarkers and to study the molecular pathways involved in IBD.
KW - Biomarkers
KW - Inflammatory bowel disease
KW - Lipidomics
KW - Proteomics
UR - http://www.scopus.com/inward/record.url?scp=85056243249&partnerID=8YFLogxK
U2 - 10.1016/j.jprot.2018.10.017
DO - 10.1016/j.jprot.2018.10.017
M3 - Article
SN - 1874-3919
VL - 195
SP - 138
EP - 149
JO - Journal of Proteomics
JF - Journal of Proteomics
ER -