Mucosal expression of PI3, ANXA1, and VDR discriminates Crohn’s disease from ulcerative colitis

Author:

James Jaslin Pallikkunnath,Nielsen Boye Schnack,Christensen Ib Jarle,Langholz Ebbe,Malham Mikkel,Poulsen Tim Svenstrup,Holmstrøm Kim,Riis Lene Buhl,Høgdall Estrid

Abstract

AbstractDifferential diagnosis of inflammatory bowel disease (IBD) to Crohn’s disease (CD) or ulcerative colitis (UC) is crucial for treatment decision making. With the aim of generating a clinically applicable molecular-based tool to classify IBD patients, we assessed whole transcriptome analysis on endoscopy samples. A total of 408 patient samples were included covering both internal and external samples cohorts. Whole transcriptome analysis was performed on an internal cohort of FFPE IBD samples (CD, n = 16 and UC, n = 17). The 100 most significantly differentially expressed genes (DEG) were tested in two external cohorts. Ten of the DEG were further processed by functional enrichment analysis from which seven were found to show consistent significant performance in discriminating CD from UC: PI3, ANXA1, VDR, MTCL1, SH3PXD2A-AS1, CLCF1, and CD180. Differential expression of PI3, ANXA1, and VDR was reproduced by RT-qPCR, which was performed on an independent sample cohort of 97 patient samples (CD, n = 44 and UC, n = 53). Gene expression levels of the three-gene profile, resulted in an area under the curve of 0.84 (P = 0.02) in discriminating CD from UC, and therefore appear as an attractive molecular-based diagnostic tool for clinicians to distinguish CD from UC.

Funder

Aage og Johanne Louis-Hansens Fond

Herlev Hospital

Colitis-Crohn Foreningen

Torben og Alice Frimodts Fond

Aase og Ejnar Danielsens Fond

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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