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The clinical potential of GDF15 as a “ready-to-feed indicator” for critically ill adults

BACKGROUND: Circulating growth-differentiation factor-15 (GDF15), a cellular stress marker, abruptly increases during critical illness, but its later time course remains unclear. GDF15 physiologically controls oral intake by driving aversive responses to nutrition. Early parenteral nutrition (PN) in...

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Autores principales: Van Dyck, Lisa, Gunst, Jan, Casaer, Michaël P., Peeters, Bram, Derese, Inge, Wouters, Pieter J., de Zegher, Francis, Vanhorebeek, Ilse, Van den Berghe, Greet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488998/
https://www.ncbi.nlm.nih.gov/pubmed/32928255
http://dx.doi.org/10.1186/s13054-020-03254-1
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author Van Dyck, Lisa
Gunst, Jan
Casaer, Michaël P.
Peeters, Bram
Derese, Inge
Wouters, Pieter J.
de Zegher, Francis
Vanhorebeek, Ilse
Van den Berghe, Greet
author_facet Van Dyck, Lisa
Gunst, Jan
Casaer, Michaël P.
Peeters, Bram
Derese, Inge
Wouters, Pieter J.
de Zegher, Francis
Vanhorebeek, Ilse
Van den Berghe, Greet
author_sort Van Dyck, Lisa
collection PubMed
description BACKGROUND: Circulating growth-differentiation factor-15 (GDF15), a cellular stress marker, abruptly increases during critical illness, but its later time course remains unclear. GDF15 physiologically controls oral intake by driving aversive responses to nutrition. Early parenteral nutrition (PN) in ICU patients has overall been shown not beneficial. We hypothesized that low GDF15 can identify patients who benefit from early PN, tolerate enteral nutrition (EN), and resume spontaneous oral intake. METHODS: In secondary analyses of the EPaNIC-RCT on timing of PN initiation (early PN versus late PN) and the prospective observational DAS study, we documented the time course of circulating GDF15 in ICU (N = 1128) and 1 week post-ICU (N = 72), compared with healthy subjects (N = 65), and the impact hereon of randomization to early PN versus late PN in propensity score-matched groups (N = 564/group). Interaction between upon-admission GDF15 and randomization for its outcome effects was investigated (N = 4393). Finally, association between GDF15 and EN tolerance in ICU (N = 1383) and oral intake beyond ICU discharge (N = 72) was studied. RESULTS: GDF15 was elevated throughout ICU stay, similarly in early PN and late PN patients, and remained high beyond ICU discharge (p < 0.0001). Upon-admission GDF15 did not interact with randomization to early PN versus late PN for its outcome effects, but higher GDF15 independently related to worse outcomes (p ≤ 0.002). Lower GDF15 was only weakly related to gastrointestinal tolerance (p < 0.0001) and a steeper drop in GDF15 with more oral intake after ICU discharge (p = 0.05). CONCLUSION: In critically ill patients, high GDF15 reflected poor prognosis and may contribute to aversive responses to nutrition. However, the potential of GDF15 as “ready-to-feed indicator” appears limited. TRIAL REGISTRATION: ClinicalTrials.gov, NCT00512122, registered 31 July 2007, https://www.clinicaltrials.gov/ct2/show/NCT00512122 (EPaNIC trial) and ISRCTN, ISRCTN 98806770, registered 11 November 2014, http://www.isrctn.com/ISRCTN98806770 (DAS trial)
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spelling pubmed-74889982020-09-16 The clinical potential of GDF15 as a “ready-to-feed indicator” for critically ill adults Van Dyck, Lisa Gunst, Jan Casaer, Michaël P. Peeters, Bram Derese, Inge Wouters, Pieter J. de Zegher, Francis Vanhorebeek, Ilse Van den Berghe, Greet Crit Care Research BACKGROUND: Circulating growth-differentiation factor-15 (GDF15), a cellular stress marker, abruptly increases during critical illness, but its later time course remains unclear. GDF15 physiologically controls oral intake by driving aversive responses to nutrition. Early parenteral nutrition (PN) in ICU patients has overall been shown not beneficial. We hypothesized that low GDF15 can identify patients who benefit from early PN, tolerate enteral nutrition (EN), and resume spontaneous oral intake. METHODS: In secondary analyses of the EPaNIC-RCT on timing of PN initiation (early PN versus late PN) and the prospective observational DAS study, we documented the time course of circulating GDF15 in ICU (N = 1128) and 1 week post-ICU (N = 72), compared with healthy subjects (N = 65), and the impact hereon of randomization to early PN versus late PN in propensity score-matched groups (N = 564/group). Interaction between upon-admission GDF15 and randomization for its outcome effects was investigated (N = 4393). Finally, association between GDF15 and EN tolerance in ICU (N = 1383) and oral intake beyond ICU discharge (N = 72) was studied. RESULTS: GDF15 was elevated throughout ICU stay, similarly in early PN and late PN patients, and remained high beyond ICU discharge (p < 0.0001). Upon-admission GDF15 did not interact with randomization to early PN versus late PN for its outcome effects, but higher GDF15 independently related to worse outcomes (p ≤ 0.002). Lower GDF15 was only weakly related to gastrointestinal tolerance (p < 0.0001) and a steeper drop in GDF15 with more oral intake after ICU discharge (p = 0.05). CONCLUSION: In critically ill patients, high GDF15 reflected poor prognosis and may contribute to aversive responses to nutrition. However, the potential of GDF15 as “ready-to-feed indicator” appears limited. TRIAL REGISTRATION: ClinicalTrials.gov, NCT00512122, registered 31 July 2007, https://www.clinicaltrials.gov/ct2/show/NCT00512122 (EPaNIC trial) and ISRCTN, ISRCTN 98806770, registered 11 November 2014, http://www.isrctn.com/ISRCTN98806770 (DAS trial) BioMed Central 2020-09-14 /pmc/articles/PMC7488998/ /pubmed/32928255 http://dx.doi.org/10.1186/s13054-020-03254-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Van Dyck, Lisa
Gunst, Jan
Casaer, Michaël P.
Peeters, Bram
Derese, Inge
Wouters, Pieter J.
de Zegher, Francis
Vanhorebeek, Ilse
Van den Berghe, Greet
The clinical potential of GDF15 as a “ready-to-feed indicator” for critically ill adults
title The clinical potential of GDF15 as a “ready-to-feed indicator” for critically ill adults
title_full The clinical potential of GDF15 as a “ready-to-feed indicator” for critically ill adults
title_fullStr The clinical potential of GDF15 as a “ready-to-feed indicator” for critically ill adults
title_full_unstemmed The clinical potential of GDF15 as a “ready-to-feed indicator” for critically ill adults
title_short The clinical potential of GDF15 as a “ready-to-feed indicator” for critically ill adults
title_sort clinical potential of gdf15 as a “ready-to-feed indicator” for critically ill adults
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488998/
https://www.ncbi.nlm.nih.gov/pubmed/32928255
http://dx.doi.org/10.1186/s13054-020-03254-1
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