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Inflammatory Mediators in Tracheal Aspirates of Preterm Infants Participating in a Randomized Trial of Permissive Hypercapnia

BACKGROUND: Ventilator-induced lung injury is considered to be a main factor in the pathogenesis of bronchopulmonary dysplasia (BPD). Optimizing ventilator strategies may reduce respiratory morbidities in preterm infants. Permissive hypercapnia has been suggested to attenuate lung injury. We aimed t...

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Autores principales: Gentner, Sarah, Laube, Mandy, Uhlig, Ulrike, Yang, Yang, Fuchs, Hans W., Dreyhaupt, Jens, Hummler, Helmut D., Uhlig, Stefan, Thome, Ulrich H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702441/
https://www.ncbi.nlm.nih.gov/pubmed/29209598
http://dx.doi.org/10.3389/fped.2017.00246
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author Gentner, Sarah
Laube, Mandy
Uhlig, Ulrike
Yang, Yang
Fuchs, Hans W.
Dreyhaupt, Jens
Hummler, Helmut D.
Uhlig, Stefan
Thome, Ulrich H.
author_facet Gentner, Sarah
Laube, Mandy
Uhlig, Ulrike
Yang, Yang
Fuchs, Hans W.
Dreyhaupt, Jens
Hummler, Helmut D.
Uhlig, Stefan
Thome, Ulrich H.
author_sort Gentner, Sarah
collection PubMed
description BACKGROUND: Ventilator-induced lung injury is considered to be a main factor in the pathogenesis of bronchopulmonary dysplasia (BPD). Optimizing ventilator strategies may reduce respiratory morbidities in preterm infants. Permissive hypercapnia has been suggested to attenuate lung injury. We aimed to determine if a higher PCO(2) target range results in less lung injury compared to the control target range and possibly reduces pro-inflammatory cytokines and acid sphingomyelinase (ASM) in tracheal aspirates (TA), which has not been addressed before. METHODS: During a multicenter trial of permissive hypercapnia in extremely low birthweight infants (PHELBI), preterm infants (birthweight 400–1,000 g, gestational age 23 0/7–28 6/7 weeks) requiring mechanical ventilation within 24 h of birth were randomly assigned to a high PCO(2) target or a control group. The high target group aimed at PCO(2) values of 55–65, 60–70, and 65–75 mmHg and the control group at PCO(2) values of 40–50, 45–55 and 50–60 mmHg on postnatal days 1–3, 4–6, and 7–14, respectively. TA was analyzed for pro-inflammatory cytokines from postnatal day 2–21. BPD was determined at a postmenstrual age of 36 weeks ± 2 days. MAIN FINDINGS: Levels of inflammatory cytokines and ASM were similar in both groups: interleukin (IL)-6 (p = 0.14), IL-8 (p = 0.43), IL-10 (p = 0.24), IL-1β (p = 0.11), macrophage inflammatory protein 1α (p = 0.44), albumin (p = 0.41), neuropeptide Y (p = 0.52), leukotriene B(4) (p = 0.11), transforming growth factor-β(1) (p = 0.68), nitrite (p = 0.15), and ASM (p = 0.94). Furthermore, most inflammatory mediators were strongly affected by the age of the infants and increased from postnatal day 2 to 21. BPD or death was observed in 14 out of 62 infants, who were distributed evenly between both groups. CONCLUSION: The results suggest that high PCO(2) target levels did not result in lower pulmonary inflammatory activity and thus reflect clinical results. This indicates that high PCO(2) target ranges are not effective in reducing ventilator-induced lung injury in preterm infants, as compared to control targets. TRIAL REGISTRATION: ISRCTN56143743.
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spelling pubmed-57024412017-12-05 Inflammatory Mediators in Tracheal Aspirates of Preterm Infants Participating in a Randomized Trial of Permissive Hypercapnia Gentner, Sarah Laube, Mandy Uhlig, Ulrike Yang, Yang Fuchs, Hans W. Dreyhaupt, Jens Hummler, Helmut D. Uhlig, Stefan Thome, Ulrich H. Front Pediatr Pediatrics BACKGROUND: Ventilator-induced lung injury is considered to be a main factor in the pathogenesis of bronchopulmonary dysplasia (BPD). Optimizing ventilator strategies may reduce respiratory morbidities in preterm infants. Permissive hypercapnia has been suggested to attenuate lung injury. We aimed to determine if a higher PCO(2) target range results in less lung injury compared to the control target range and possibly reduces pro-inflammatory cytokines and acid sphingomyelinase (ASM) in tracheal aspirates (TA), which has not been addressed before. METHODS: During a multicenter trial of permissive hypercapnia in extremely low birthweight infants (PHELBI), preterm infants (birthweight 400–1,000 g, gestational age 23 0/7–28 6/7 weeks) requiring mechanical ventilation within 24 h of birth were randomly assigned to a high PCO(2) target or a control group. The high target group aimed at PCO(2) values of 55–65, 60–70, and 65–75 mmHg and the control group at PCO(2) values of 40–50, 45–55 and 50–60 mmHg on postnatal days 1–3, 4–6, and 7–14, respectively. TA was analyzed for pro-inflammatory cytokines from postnatal day 2–21. BPD was determined at a postmenstrual age of 36 weeks ± 2 days. MAIN FINDINGS: Levels of inflammatory cytokines and ASM were similar in both groups: interleukin (IL)-6 (p = 0.14), IL-8 (p = 0.43), IL-10 (p = 0.24), IL-1β (p = 0.11), macrophage inflammatory protein 1α (p = 0.44), albumin (p = 0.41), neuropeptide Y (p = 0.52), leukotriene B(4) (p = 0.11), transforming growth factor-β(1) (p = 0.68), nitrite (p = 0.15), and ASM (p = 0.94). Furthermore, most inflammatory mediators were strongly affected by the age of the infants and increased from postnatal day 2 to 21. BPD or death was observed in 14 out of 62 infants, who were distributed evenly between both groups. CONCLUSION: The results suggest that high PCO(2) target levels did not result in lower pulmonary inflammatory activity and thus reflect clinical results. This indicates that high PCO(2) target ranges are not effective in reducing ventilator-induced lung injury in preterm infants, as compared to control targets. TRIAL REGISTRATION: ISRCTN56143743. Frontiers Media S.A. 2017-11-21 /pmc/articles/PMC5702441/ /pubmed/29209598 http://dx.doi.org/10.3389/fped.2017.00246 Text en Copyright © 2017 Gentner, Laube, Uhlig, Yang, Fuchs, Dreyhaupt, Hummler, Uhlig and Thome. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Gentner, Sarah
Laube, Mandy
Uhlig, Ulrike
Yang, Yang
Fuchs, Hans W.
Dreyhaupt, Jens
Hummler, Helmut D.
Uhlig, Stefan
Thome, Ulrich H.
Inflammatory Mediators in Tracheal Aspirates of Preterm Infants Participating in a Randomized Trial of Permissive Hypercapnia
title Inflammatory Mediators in Tracheal Aspirates of Preterm Infants Participating in a Randomized Trial of Permissive Hypercapnia
title_full Inflammatory Mediators in Tracheal Aspirates of Preterm Infants Participating in a Randomized Trial of Permissive Hypercapnia
title_fullStr Inflammatory Mediators in Tracheal Aspirates of Preterm Infants Participating in a Randomized Trial of Permissive Hypercapnia
title_full_unstemmed Inflammatory Mediators in Tracheal Aspirates of Preterm Infants Participating in a Randomized Trial of Permissive Hypercapnia
title_short Inflammatory Mediators in Tracheal Aspirates of Preterm Infants Participating in a Randomized Trial of Permissive Hypercapnia
title_sort inflammatory mediators in tracheal aspirates of preterm infants participating in a randomized trial of permissive hypercapnia
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702441/
https://www.ncbi.nlm.nih.gov/pubmed/29209598
http://dx.doi.org/10.3389/fped.2017.00246
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