Short noncoding RNAs as predictive biomarkers for the development from inflammatory bowel disease unclassified to Crohn’s disease or ulcerative colitis

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Standard

Short noncoding RNAs as predictive biomarkers for the development from inflammatory bowel disease unclassified to Crohn’s disease or ulcerative colitis. / James, Jaslin P.; Riis, Lene Buhl; Søkilde, Rolf; Malham, Mikkel; Høgdall, Estrid; Langholz, Ebbe; Nielsen, Boye Schnack.

I: PLoS ONE, Bind 19, Nr. 2 February, e0297353, 2024.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

James, JP, Riis, LB, Søkilde, R, Malham, M, Høgdall, E, Langholz, E & Nielsen, BS 2024, 'Short noncoding RNAs as predictive biomarkers for the development from inflammatory bowel disease unclassified to Crohn’s disease or ulcerative colitis', PLoS ONE, bind 19, nr. 2 February, e0297353. https://doi.org/10.1371/journal.pone.0297353

APA

James, J. P., Riis, L. B., Søkilde, R., Malham, M., Høgdall, E., Langholz, E., & Nielsen, B. S. (2024). Short noncoding RNAs as predictive biomarkers for the development from inflammatory bowel disease unclassified to Crohn’s disease or ulcerative colitis. PLoS ONE, 19(2 February), [e0297353]. https://doi.org/10.1371/journal.pone.0297353

Vancouver

James JP, Riis LB, Søkilde R, Malham M, Høgdall E, Langholz E o.a. Short noncoding RNAs as predictive biomarkers for the development from inflammatory bowel disease unclassified to Crohn’s disease or ulcerative colitis. PLoS ONE. 2024;19(2 February). e0297353. https://doi.org/10.1371/journal.pone.0297353

Author

James, Jaslin P. ; Riis, Lene Buhl ; Søkilde, Rolf ; Malham, Mikkel ; Høgdall, Estrid ; Langholz, Ebbe ; Nielsen, Boye Schnack. / Short noncoding RNAs as predictive biomarkers for the development from inflammatory bowel disease unclassified to Crohn’s disease or ulcerative colitis. I: PLoS ONE. 2024 ; Bind 19, Nr. 2 February.

Bibtex

@article{834e743d6a7b435890f8009308582e06,
title = "Short noncoding RNAs as predictive biomarkers for the development from inflammatory bowel disease unclassified to Crohn{\textquoteright}s disease or ulcerative colitis",
abstract = "Numerous pathogenic processes are mediated by short noncoding RNAs (sncRNA). Twenty percent of inflammatory bowel disease (IBD) patients are labelled as IBD unclassified (IBDU) at disease onset. Most IBDU patients are reclassified as Crohn{\textquoteright}s disease (CD) or ulcerative colitis (UC) within few years. Since the therapeutic methods for CD and UC differ, biomarkers that can forecast the categorization of IBDU into CD or UC are highly desired. Here, we investigated whether sncRNAs can predict CD or UC among IBDU patients. 35 IBDU patients who were initially diagnosed with IBDU were included in this retrospective investigation; of them, 12, 15, and 8 were reclassified into CD (IBDU-CD), UC (IBDU-UC), or remained as IBDU (IBDU-IBDU), respectively. Eight IBD patients, were included as references. SncRNA profiling on RNA from mucosal biopsies were performed using Affymetrix miRNA 4.0 array. Selected probe sets were validated using RT-qPCR. Among all patients and only adults, 306 and 499 probe sets respectively were differentially expressed between IBDU-CD and IBDU-UC. Six of the probe sets were evaluated by RT-qPCR, of which miR-182-5p, miR-451a and ENSG00000239080 (snoU13) together with age and sex resulted in an AUC of 78.6% (95% CI: 60–97) in discriminating IBDU-CD from IBDU-UC. Based on the three sncRNAs profile it is possible to predict if IBDU patients within 3 years will be reclassified as CD or UC. We showed that the expression profile of IBDU patients differ from that of definite CD or UC, suggesting that a subgroup of IBDU patients may compose a third unique IBD subtype.",
author = "James, {Jaslin P.} and Riis, {Lene Buhl} and Rolf S{\o}kilde and Mikkel Malham and Estrid H{\o}gdall and Ebbe Langholz and Nielsen, {Boye Schnack}",
note = "Publisher Copyright: {\textcopyright} 2024 James et al. This is an open access article distributed under the terms of the Creative Commons Attribution License,",
year = "2024",
doi = "10.1371/journal.pone.0297353",
language = "English",
volume = "19",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "2 February",

}

RIS

TY - JOUR

T1 - Short noncoding RNAs as predictive biomarkers for the development from inflammatory bowel disease unclassified to Crohn’s disease or ulcerative colitis

AU - James, Jaslin P.

AU - Riis, Lene Buhl

AU - Søkilde, Rolf

AU - Malham, Mikkel

AU - Høgdall, Estrid

AU - Langholz, Ebbe

AU - Nielsen, Boye Schnack

N1 - Publisher Copyright: © 2024 James et al. This is an open access article distributed under the terms of the Creative Commons Attribution License,

PY - 2024

Y1 - 2024

N2 - Numerous pathogenic processes are mediated by short noncoding RNAs (sncRNA). Twenty percent of inflammatory bowel disease (IBD) patients are labelled as IBD unclassified (IBDU) at disease onset. Most IBDU patients are reclassified as Crohn’s disease (CD) or ulcerative colitis (UC) within few years. Since the therapeutic methods for CD and UC differ, biomarkers that can forecast the categorization of IBDU into CD or UC are highly desired. Here, we investigated whether sncRNAs can predict CD or UC among IBDU patients. 35 IBDU patients who were initially diagnosed with IBDU were included in this retrospective investigation; of them, 12, 15, and 8 were reclassified into CD (IBDU-CD), UC (IBDU-UC), or remained as IBDU (IBDU-IBDU), respectively. Eight IBD patients, were included as references. SncRNA profiling on RNA from mucosal biopsies were performed using Affymetrix miRNA 4.0 array. Selected probe sets were validated using RT-qPCR. Among all patients and only adults, 306 and 499 probe sets respectively were differentially expressed between IBDU-CD and IBDU-UC. Six of the probe sets were evaluated by RT-qPCR, of which miR-182-5p, miR-451a and ENSG00000239080 (snoU13) together with age and sex resulted in an AUC of 78.6% (95% CI: 60–97) in discriminating IBDU-CD from IBDU-UC. Based on the three sncRNAs profile it is possible to predict if IBDU patients within 3 years will be reclassified as CD or UC. We showed that the expression profile of IBDU patients differ from that of definite CD or UC, suggesting that a subgroup of IBDU patients may compose a third unique IBD subtype.

AB - Numerous pathogenic processes are mediated by short noncoding RNAs (sncRNA). Twenty percent of inflammatory bowel disease (IBD) patients are labelled as IBD unclassified (IBDU) at disease onset. Most IBDU patients are reclassified as Crohn’s disease (CD) or ulcerative colitis (UC) within few years. Since the therapeutic methods for CD and UC differ, biomarkers that can forecast the categorization of IBDU into CD or UC are highly desired. Here, we investigated whether sncRNAs can predict CD or UC among IBDU patients. 35 IBDU patients who were initially diagnosed with IBDU were included in this retrospective investigation; of them, 12, 15, and 8 were reclassified into CD (IBDU-CD), UC (IBDU-UC), or remained as IBDU (IBDU-IBDU), respectively. Eight IBD patients, were included as references. SncRNA profiling on RNA from mucosal biopsies were performed using Affymetrix miRNA 4.0 array. Selected probe sets were validated using RT-qPCR. Among all patients and only adults, 306 and 499 probe sets respectively were differentially expressed between IBDU-CD and IBDU-UC. Six of the probe sets were evaluated by RT-qPCR, of which miR-182-5p, miR-451a and ENSG00000239080 (snoU13) together with age and sex resulted in an AUC of 78.6% (95% CI: 60–97) in discriminating IBDU-CD from IBDU-UC. Based on the three sncRNAs profile it is possible to predict if IBDU patients within 3 years will be reclassified as CD or UC. We showed that the expression profile of IBDU patients differ from that of definite CD or UC, suggesting that a subgroup of IBDU patients may compose a third unique IBD subtype.

U2 - 10.1371/journal.pone.0297353

DO - 10.1371/journal.pone.0297353

M3 - Journal article

C2 - 38408066

AN - SCOPUS:85186076716

VL - 19

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 2 February

M1 - e0297353

ER -

ID: 385009691