Serveur d'exploration sur les relations entre la France et l'Australie

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A rolling phenotype in Crohn's disease

Identifieur interne : 001264 ( Main/Exploration ); précédent : 001263; suivant : 001265

A rolling phenotype in Crohn's disease

Auteurs : James Irwin [Australie] ; Emma Ferguson [Australie] ; Lisa A. Simms [Australie] ; Katherine Hanigan [Australie] ; Franck Carbonnel [France] ; Graham Radford-Smith [Australie]

Source :

RBID : PMC:5383106

Descripteurs français

English descriptors

Abstract

Background and aim

The Montreal classification of disease behaviour in Crohn's disease describes progression of disease towards a stricturing and penetrating phenotype. In the present paper, we propose an alternative representation of the long-term course of Crohn’s disease complications, the rolling phenotype. As is commonly observed in clinical practice, this definition allows progression to a more severe phenotype (stricturing, penetrating) but also, regression to a less severe behaviour (inflammatory, or remission) over time.

Methods

All patients diagnosed with Crohn's Disease between 01/01/1994 and 01/03/2008, managed at a single centre and observed for a minimum of 5 years, had development and resolution of all complications recorded. A rolling phenotype was defined at each time point based on all observed complications in the three years prior to the time point. Phenotype was defined as B1, B2, B3, or B23 (penetrating and stenotic). The progression over time of the rolling phenotype was compared to that of the cumulative Montreal phenotype.

Results

305 patients were observed a median of 10.0 (Intraquartile range 7.3–13.7) years. Longitudinal progression of rolling phenotype demonstrated a consistent proportion of patients with B1 (70%), B2 (20%), B3 (5%) and B23 (5%) phenotypes. These proportions were observed regardless of initial phenotype. In contrast, the cumulative Montreal phenotype progressed towards a more severe phenotype with time (B1 (39%), B2 (26%), B3(35%) at 10 years).

Conclusion

A rolling phenotype provides an alternative view of the longitudinal burden of intra-abdominal complications in Crohn's disease. From this viewpoint, 70% of patients have durable freedom from complication over time (>3 years).


Url:
DOI: 10.1371/journal.pone.0174954
PubMed: 28384331
PubMed Central: 5383106


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<title>Background and aim</title>
<p>The Montreal classification of disease behaviour in Crohn's disease describes progression of disease towards a stricturing and penetrating phenotype. In the present paper, we propose an alternative representation of the long-term course of Crohn’s disease complications, the rolling phenotype. As is commonly observed in clinical practice, this definition allows progression to a more severe phenotype (stricturing, penetrating) but also, regression to a less severe behaviour (inflammatory, or remission) over time.</p>
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<title>Methods</title>
<p>All patients diagnosed with Crohn's Disease between 01/01/1994 and 01/03/2008, managed at a single centre and observed for a minimum of 5 years, had development and resolution of all complications recorded. A rolling phenotype was defined at each time point based on all observed complications in the three years prior to the time point. Phenotype was defined as B1, B2, B3, or B23 (penetrating and stenotic). The progression over time of the rolling phenotype was compared to that of the cumulative Montreal phenotype.</p>
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<title>Results</title>
<p>305 patients were observed a median of 10.0 (Intraquartile range 7.3–13.7) years. Longitudinal progression of rolling phenotype demonstrated a consistent proportion of patients with B1 (70%), B2 (20%), B3 (5%) and B23 (5%) phenotypes. These proportions were observed regardless of initial phenotype. In contrast, the cumulative Montreal phenotype progressed towards a more severe phenotype with time (B1 (39%), B2 (26%), B3(35%) at 10 years).</p>
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<title>Conclusion</title>
<p>A rolling phenotype provides an alternative view of the longitudinal burden of intra-abdominal complications in Crohn's disease. From this viewpoint, 70% of patients have durable freedom from complication over time (>3 years).</p>
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</back>
</TEI>
<affiliations>
<list>
<country>
<li>Australie</li>
<li>France</li>
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<name sortKey="Ferguson, Emma" sort="Ferguson, Emma" uniqKey="Ferguson E" first="Emma" last="Ferguson">Emma Ferguson</name>
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<name sortKey="Radford Smith, Graham" sort="Radford Smith, Graham" uniqKey="Radford Smith G" first="Graham" last="Radford-Smith">Graham Radford-Smith</name>
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<name sortKey="Simms, Lisa A" sort="Simms, Lisa A" uniqKey="Simms L" first="Lisa A." last="Simms">Lisa A. Simms</name>
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</record>

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