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Faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants

AIM: Very preterm birth is associated with a high risk of enteropathies. Diagnosis is challenging, especially in mild forms, leading to unnecessary periods of cessation of enteral feeding. This study aimed at establishing a prognosis score of enteropathy combining clinical parameters and faecal calp...

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Autores principales: Campeotto, Florence, Elie, Caroline, Rousseau, Clotilde, Giuseppi, Agnès, Hachem, Taymme, Gobalakichenane, Ponny, Le Touzey, Mathilde, de Stefano, Marie, Butel, Marie‐José, Kapel, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818215/
https://www.ncbi.nlm.nih.gov/pubmed/32418251
http://dx.doi.org/10.1111/apa.15354
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author Campeotto, Florence
Elie, Caroline
Rousseau, Clotilde
Giuseppi, Agnès
Hachem, Taymme
Gobalakichenane, Ponny
Le Touzey, Mathilde
de Stefano, Marie
Butel, Marie‐José
Kapel, Nathalie
author_facet Campeotto, Florence
Elie, Caroline
Rousseau, Clotilde
Giuseppi, Agnès
Hachem, Taymme
Gobalakichenane, Ponny
Le Touzey, Mathilde
de Stefano, Marie
Butel, Marie‐José
Kapel, Nathalie
author_sort Campeotto, Florence
collection PubMed
description AIM: Very preterm birth is associated with a high risk of enteropathies. Diagnosis is challenging, especially in mild forms, leading to unnecessary periods of cessation of enteral feeding. This study aimed at establishing a prognosis score of enteropathy combining clinical parameters and faecal calprotectin concentration. METHODS: This prospective multicentric study included preterm neonates born at a gestational age of 33 weeks or less. Stools were collected weekly until hospital discharge, and daily in case of digestive events for calprotectin measurement (ELISA and immunochromatography) and microbiota analyses (16S rRNA gene sequencing). RESULTS: Among the 121 neonates included, 21 experienced at least one episode of enteropathy, mainly mild forms. By ELISA testing, median faecal calprotectin was 88 (8‐798) µg/g faeces. No statistically significant association was found between the outset of enteropathy and maternal and neonatal characteristics, and calprotectin levels. The agreement between ELISA and immunochromatography assay was moderate (intra‐class correlation coefficient 0.58, 95%CI [0.47‐0.66]). Comparison of species diversity and relative bacterial abundance profiles between infants with or without enteropathy revealed no specific alterations associated with enteropathy. CONCLUSION: The study failed to propose a prognostic score of enteropathy, probably due the large inter‐ and intra‐individual variability of faecal calprotectin in very preterm neonates.
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spelling pubmed-78182152021-01-29 Faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants Campeotto, Florence Elie, Caroline Rousseau, Clotilde Giuseppi, Agnès Hachem, Taymme Gobalakichenane, Ponny Le Touzey, Mathilde de Stefano, Marie Butel, Marie‐José Kapel, Nathalie Acta Paediatr Regular Articles & Brief Reports AIM: Very preterm birth is associated with a high risk of enteropathies. Diagnosis is challenging, especially in mild forms, leading to unnecessary periods of cessation of enteral feeding. This study aimed at establishing a prognosis score of enteropathy combining clinical parameters and faecal calprotectin concentration. METHODS: This prospective multicentric study included preterm neonates born at a gestational age of 33 weeks or less. Stools were collected weekly until hospital discharge, and daily in case of digestive events for calprotectin measurement (ELISA and immunochromatography) and microbiota analyses (16S rRNA gene sequencing). RESULTS: Among the 121 neonates included, 21 experienced at least one episode of enteropathy, mainly mild forms. By ELISA testing, median faecal calprotectin was 88 (8‐798) µg/g faeces. No statistically significant association was found between the outset of enteropathy and maternal and neonatal characteristics, and calprotectin levels. The agreement between ELISA and immunochromatography assay was moderate (intra‐class correlation coefficient 0.58, 95%CI [0.47‐0.66]). Comparison of species diversity and relative bacterial abundance profiles between infants with or without enteropathy revealed no specific alterations associated with enteropathy. CONCLUSION: The study failed to propose a prognostic score of enteropathy, probably due the large inter‐ and intra‐individual variability of faecal calprotectin in very preterm neonates. John Wiley and Sons Inc. 2020-09-01 2021-01 /pmc/articles/PMC7818215/ /pubmed/32418251 http://dx.doi.org/10.1111/apa.15354 Text en © 2020 The Authors. Acta Paediatrica published by John Wiley & Sons Ltd on behalf of Foundation Acta Paediatrica This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Regular Articles & Brief Reports
Campeotto, Florence
Elie, Caroline
Rousseau, Clotilde
Giuseppi, Agnès
Hachem, Taymme
Gobalakichenane, Ponny
Le Touzey, Mathilde
de Stefano, Marie
Butel, Marie‐José
Kapel, Nathalie
Faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants
title Faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants
title_full Faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants
title_fullStr Faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants
title_full_unstemmed Faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants
title_short Faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants
title_sort faecal calprotectin and gut microbiota do not predict enteropathy in very preterm infants
topic Regular Articles & Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818215/
https://www.ncbi.nlm.nih.gov/pubmed/32418251
http://dx.doi.org/10.1111/apa.15354
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