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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1093/ecco-jcc/jjaa134</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">122237</subfield>
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    <subfield code="a">ART-2021-122237</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Kalla, R.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Whole Blood Profiling of T-cell-Derived microRNA Allows the Development of Prognostic models in Inflammatory Bowel Disease</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2021</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Background: MicroRNAs [miRNAs] are cell-specific small non-coding RNAs that can regulate gene expression and have been implicated in inflammatory bowel disease [IBD] pathogenesis. Here we define the cell-specific miRNA profiles and investigate its biomarker potential in IBD. 
Methods: In a two-stage prospective multi-centre case control study, next generation sequencing was performed on a discovery cohort of immunomagnetically separated leukocytes from 32 patients (nine Crohn''s disease [CD], 14 ulcerative colitis [UC], eight healthy controls) and differentially expressed signals were validated in whole blood in 294 patients [97 UC, 98 CD, 98 non-IBD, 1 IBDU] using quantitative PCR. Correlations were analysed with phenotype, including need for early treatment escalation as a marker of progressive disease using Cox proportional hazards. 
Results: In stage 1, each leukocyte subset [CD4+ and CD8+ T-cells and CD14+ monocytes] was analysed in IBD and controls. Three specific miRNAs differentiated IBD from controls in CD4+ T-cells, including miR-1307-3p [p = 0.01], miR-3615 [p = 0.02] and miR-4792 [p = 0.01]. In the extension cohort, in stage 2, miR-1307-3p was able to predict disease progression in IBD (hazard ratio [HR] 1.98, interquartile range [IQR]: 1.20-3.27; logrank p = 1.80 × 10-3), in particular CD [HR 2.81; IQR: 1.11-3.53, p = 6.50 × 10-4]. Using blood-based multimarker miRNA models, the estimated chance of escalation in CD was 83% if two or more criteria were met and 90% for UC if three or more criteria are met. 
Interpretation: We have identified and validated unique CD4+ T-cell miRNAs that are differentially regulated in IBD. These miRNAs may be able to predict treatment escalation and have the potential for clinical translation; further prospective evaluation is now indicated.</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">All rights reserved</subfield>
    <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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  <datafield tag="590" ind1=" " ind2=" ">
    <subfield code="a">10.02</subfield>
    <subfield code="b">2021</subfield>
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    <subfield code="a">GASTROENTEROLOGY &amp; HEPATOLOGY</subfield>
    <subfield code="b">12 / 92 = 0.13</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q1</subfield>
    <subfield code="e">T1</subfield>
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  <datafield tag="592" ind1=" " ind2=" ">
    <subfield code="a">2.429</subfield>
    <subfield code="b">2021</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Medicine (miscellaneous)</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q1</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Gastroenterology</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">12.4</subfield>
    <subfield code="b">2021</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Adams, A.T.</subfield>
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    <subfield code="a">Ventham, N.T.</subfield>
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    <subfield code="a">Kennedy, N.A.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">White, R.</subfield>
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    <subfield code="a">Clarke, C.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Ivens, A.</subfield>
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    <subfield code="a">Bergemalm, D.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Vatn, S.</subfield>
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    <subfield code="a">Lopez-Jimena, B.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Ricanek, P.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Vatn, M.H.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Söderholm, J.D.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Gomollón, F.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-0076-3529</subfield>
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    <subfield code="a">Nowak, J.K.</subfield>
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    <subfield code="a">Jahnsen, J.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Halfvarson, J.</subfield>
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    <subfield code="a">Mctaggart, S.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Ho, G.T.</subfield>
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    <subfield code="a">Buck, A.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Satsangi, J.</subfield>
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    <subfield code="1">1007</subfield>
    <subfield code="2">610</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">14, 12 (2021), 1724-1733</subfield>
    <subfield code="p">J. Crohns  Colitis</subfield>
    <subfield code="t">Journal of Crohn's &amp; colitis</subfield>
    <subfield code="x">1873-9946</subfield>
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    <subfield code="a">2023-05-18-15:19:47</subfield>
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