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Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD

OBJECTIVE: Iron deficiency is a common complication in patients with IBD and oral iron therapy is suggested to exacerbate IBD symptoms. We performed an open-labelled clinical trial to compare the effects of per oral (PO) versus intravenous (IV) iron replacement therapy (IRT). DESIGN: The study popul...

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Autores principales: Lee, Thomas, Clavel, Thomas, Smirnov, Kirill, Schmidt, Annemarie, Lagkouvardos, Ilias, Walker, Alesia, Lucio, Marianna, Michalke, Bernhard, Schmitt-Kopplin, Philippe, Fedorak, Richard, Haller, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531225/
https://www.ncbi.nlm.nih.gov/pubmed/26848182
http://dx.doi.org/10.1136/gutjnl-2015-309940
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author Lee, Thomas
Clavel, Thomas
Smirnov, Kirill
Schmidt, Annemarie
Lagkouvardos, Ilias
Walker, Alesia
Lucio, Marianna
Michalke, Bernhard
Schmitt-Kopplin, Philippe
Fedorak, Richard
Haller, Dirk
author_facet Lee, Thomas
Clavel, Thomas
Smirnov, Kirill
Schmidt, Annemarie
Lagkouvardos, Ilias
Walker, Alesia
Lucio, Marianna
Michalke, Bernhard
Schmitt-Kopplin, Philippe
Fedorak, Richard
Haller, Dirk
author_sort Lee, Thomas
collection PubMed
description OBJECTIVE: Iron deficiency is a common complication in patients with IBD and oral iron therapy is suggested to exacerbate IBD symptoms. We performed an open-labelled clinical trial to compare the effects of per oral (PO) versus intravenous (IV) iron replacement therapy (IRT). DESIGN: The study population included patients with Crohn's disease (CD; N=31), UC (N=22) and control subjects with iron deficiency (non-inflamed, NI=19). After randomisation, participants received iron sulfate (PO) or iron sucrose (IV) over 3 months. Clinical parameters, faecal bacterial communities and metabolomes were assessed before and after intervention. RESULTS: Both PO and IV treatments ameliorated iron deficiency, but higher ferritin levels were observed with IV. Changes in disease activity were independent of iron treatment types. Faecal samples in IBD were characterised by marked interindividual differences, lower phylotype richness and proportions of Clostridiales. Metabolite analysis also showed separation of both UC and CD from control anaemic participants. Major shifts in bacterial diversity occurred in approximately half of all participants after IRT, but patients with CD were most susceptible. Despite individual-specific changes in phylotypes due to IRT, PO treatment was associated with decreased abundances of operational taxonomic units assigned to the species Faecalibacterium prausnitzii, Ruminococcus bromii, Dorea sp. and Collinsella aerofaciens. Clear IV-specific and PO-specific fingerprints were evident at the level of metabolomes, with changes affecting cholesterol-derived host substrates. CONCLUSIONS: Shifts in gut bacterial diversity and composition associated with iron treatment are pronounced in IBD participants. Despite similar clinical outcome, oral administration differentially affects bacterial phylotypes and faecal metabolites compared with IV therapy. TRIAL REGISTRATION NUMBER: clinicaltrial.gov (NCT01067547).
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spelling pubmed-55312252017-07-31 Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD Lee, Thomas Clavel, Thomas Smirnov, Kirill Schmidt, Annemarie Lagkouvardos, Ilias Walker, Alesia Lucio, Marianna Michalke, Bernhard Schmitt-Kopplin, Philippe Fedorak, Richard Haller, Dirk Gut Inflammatory Bowel Disease OBJECTIVE: Iron deficiency is a common complication in patients with IBD and oral iron therapy is suggested to exacerbate IBD symptoms. We performed an open-labelled clinical trial to compare the effects of per oral (PO) versus intravenous (IV) iron replacement therapy (IRT). DESIGN: The study population included patients with Crohn's disease (CD; N=31), UC (N=22) and control subjects with iron deficiency (non-inflamed, NI=19). After randomisation, participants received iron sulfate (PO) or iron sucrose (IV) over 3 months. Clinical parameters, faecal bacterial communities and metabolomes were assessed before and after intervention. RESULTS: Both PO and IV treatments ameliorated iron deficiency, but higher ferritin levels were observed with IV. Changes in disease activity were independent of iron treatment types. Faecal samples in IBD were characterised by marked interindividual differences, lower phylotype richness and proportions of Clostridiales. Metabolite analysis also showed separation of both UC and CD from control anaemic participants. Major shifts in bacterial diversity occurred in approximately half of all participants after IRT, but patients with CD were most susceptible. Despite individual-specific changes in phylotypes due to IRT, PO treatment was associated with decreased abundances of operational taxonomic units assigned to the species Faecalibacterium prausnitzii, Ruminococcus bromii, Dorea sp. and Collinsella aerofaciens. Clear IV-specific and PO-specific fingerprints were evident at the level of metabolomes, with changes affecting cholesterol-derived host substrates. CONCLUSIONS: Shifts in gut bacterial diversity and composition associated with iron treatment are pronounced in IBD participants. Despite similar clinical outcome, oral administration differentially affects bacterial phylotypes and faecal metabolites compared with IV therapy. TRIAL REGISTRATION NUMBER: clinicaltrial.gov (NCT01067547). BMJ Publishing Group 2017-05 2016-02-04 /pmc/articles/PMC5531225/ /pubmed/26848182 http://dx.doi.org/10.1136/gutjnl-2015-309940 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Inflammatory Bowel Disease
Lee, Thomas
Clavel, Thomas
Smirnov, Kirill
Schmidt, Annemarie
Lagkouvardos, Ilias
Walker, Alesia
Lucio, Marianna
Michalke, Bernhard
Schmitt-Kopplin, Philippe
Fedorak, Richard
Haller, Dirk
Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD
title Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD
title_full Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD
title_fullStr Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD
title_full_unstemmed Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD
title_short Oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with IBD
title_sort oral versus intravenous iron replacement therapy distinctly alters the gut microbiota and metabolome in patients with ibd
topic Inflammatory Bowel Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531225/
https://www.ncbi.nlm.nih.gov/pubmed/26848182
http://dx.doi.org/10.1136/gutjnl-2015-309940
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