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Mucosal expression of PI3, ANXA1, and VDR discriminates Crohn's disease from ulcerative colitis.
James, Jaslin Pallikkunnath; Nielsen, Boye Schnack; Christensen, Ib Jarle; Langholz, Ebbe; Malham, Mikkel; Poulsen, Tim Svenstrup; Holmstrøm, Kim; Riis, Lene Buhl; Høgdall, Estrid.
Afiliação
  • James JP; Department of Pathology, Herlev University Hospital, Borgmester Ib Juuls Vej 73, 2730, Herlev, Denmark. jaslin.pallikkunnath.james@regionh.dk.
  • Nielsen BS; Bioneer A/S, Hørsholm, Kogle Allé 2, 2970, Hørsholm, Denmark.
  • Christensen IJ; Department of Pathology, Herlev University Hospital, Borgmester Ib Juuls Vej 73, 2730, Herlev, Denmark.
  • Langholz E; Gastroenheden D, Herlev University Hospital, 2730, Herlev, Denmark.
  • Malham M; Institute for Clinical Medicine, University of Copenhagen, 2200, Copenhagen, Denmark.
  • Poulsen TS; The Department of Pediatric and Adolescence Medicine, Copenhagen University Hospital-Amager and Hvidovre, 2650, Hvidovre, Denmark.
  • Holmstrøm K; Copenhagen Center for Inflammatory Bowel Disease in Children, Adolescents and Adults, Hvidovre Hospital, University of Copenhagen, 2650, Hvidovre, Denmark.
  • Riis LB; Department of Pathology, Herlev University Hospital, Borgmester Ib Juuls Vej 73, 2730, Herlev, Denmark.
  • Høgdall E; Bioneer A/S, Hørsholm, Kogle Allé 2, 2970, Hørsholm, Denmark.
Sci Rep ; 13(1): 18421, 2023 10 27.
Article em En | MEDLINE | ID: mdl-37891214
ABSTRACT
Differential 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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Inflamatórias Intestinais / Colite Ulcerativa / Doença de Crohn Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Inflamatórias Intestinais / Colite Ulcerativa / Doença de Crohn Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca
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