Elevated leukotriene B4 and 8-isoprostane in exhaled breath condensate from preterm-born infants

Abstract Background Inflammation and oxidative stress play a key role in the development of bronchopulmonary dysplasia (BPD), possibly contributing to persistent respiratory morbidity after preterm birth. We aimed to assess if inflammatory markers were elevated in exhaled breath condensate (EBC) of...

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Main Authors: Rhea Urs, Rubi Ni Chin, Naomi Hemy, Andrew C. Wilson, J. Jane Pillow, Graham L. Hall, Shannon J. Simpson
Format: Article
Language:English
Published: BMC 2023-08-01
Series:BMC Pediatrics
Subjects:
Online Access:https://doi.org/10.1186/s12887-023-04210-y
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author Rhea Urs
Rubi Ni Chin
Naomi Hemy
Andrew C. Wilson
J. Jane Pillow
Graham L. Hall
Shannon J. Simpson
author_facet Rhea Urs
Rubi Ni Chin
Naomi Hemy
Andrew C. Wilson
J. Jane Pillow
Graham L. Hall
Shannon J. Simpson
author_sort Rhea Urs
collection DOAJ
description Abstract Background Inflammation and oxidative stress play a key role in the development of bronchopulmonary dysplasia (BPD), possibly contributing to persistent respiratory morbidity after preterm birth. We aimed to assess if inflammatory markers were elevated in exhaled breath condensate (EBC) of infants born very prematurely (< 32 weeks gestation) at 12–16 corrected months of age, and if increased levels were associated with BPD diagnosis and respiratory morbidity. Methods EBC samples and respiratory questionnaires were collected from 15 term-born infants and 33 preterm-born infants, 12 with a neonatal BPD diagnosis. EBC samples were analysed for leukotriene B4 (inflammation) and 8-isoprostane (oxidative stress) concentrations using enzyme-linked immune-assays. Differences between groups were analysed by Kruskal-Wallis Test with post-hoc comparisons, independent samples t-test or Mann-Whitney U test depending on normality of the data. Results Leukotriene B4 and 8-isoprostane levels were elevated in exhaled breath condensate of preterm-born infants compared to those born at term (mean difference [95% CI]; 1.52 [0.45, 2.59], p = 0.02; 0.77 [0.52, 1.02], p < 0.001, respectively). Leukotriene B4 and 8-isoprostane levels were independent of BPD diagnosis and respiratory morbidity over the first year of life. Conclusions Infants born very prematurely exhibit elevated markers of airway neutrophilic inflammation and oxidative stress beyond the first year of life, regardless of a neonatal diagnosis of chronic lung disease or respiratory morbidity during infancy. These findings may have implications for future lung health. Trial Registration N/A.
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spelling doaj.art-173e652457454ac3b499a31fe588d2382023-11-26T14:15:04ZengBMCBMC Pediatrics1471-24312023-08-012311910.1186/s12887-023-04210-yElevated leukotriene B4 and 8-isoprostane in exhaled breath condensate from preterm-born infantsRhea Urs0Rubi Ni Chin1Naomi Hemy2Andrew C. Wilson3J. Jane Pillow4Graham L. Hall5Shannon J. Simpson6School of Allied Health, Curtin UniversityWal-yan Respiratory Centre, Telethon Kids InstituteWal-yan Respiratory Centre, Telethon Kids InstituteSchool of Allied Health, Curtin UniversityWal-yan Respiratory Centre, Telethon Kids InstituteSchool of Allied Health, Curtin UniversitySchool of Allied Health, Curtin UniversityAbstract Background Inflammation and oxidative stress play a key role in the development of bronchopulmonary dysplasia (BPD), possibly contributing to persistent respiratory morbidity after preterm birth. We aimed to assess if inflammatory markers were elevated in exhaled breath condensate (EBC) of infants born very prematurely (< 32 weeks gestation) at 12–16 corrected months of age, and if increased levels were associated with BPD diagnosis and respiratory morbidity. Methods EBC samples and respiratory questionnaires were collected from 15 term-born infants and 33 preterm-born infants, 12 with a neonatal BPD diagnosis. EBC samples were analysed for leukotriene B4 (inflammation) and 8-isoprostane (oxidative stress) concentrations using enzyme-linked immune-assays. Differences between groups were analysed by Kruskal-Wallis Test with post-hoc comparisons, independent samples t-test or Mann-Whitney U test depending on normality of the data. Results Leukotriene B4 and 8-isoprostane levels were elevated in exhaled breath condensate of preterm-born infants compared to those born at term (mean difference [95% CI]; 1.52 [0.45, 2.59], p = 0.02; 0.77 [0.52, 1.02], p < 0.001, respectively). Leukotriene B4 and 8-isoprostane levels were independent of BPD diagnosis and respiratory morbidity over the first year of life. Conclusions Infants born very prematurely exhibit elevated markers of airway neutrophilic inflammation and oxidative stress beyond the first year of life, regardless of a neonatal diagnosis of chronic lung disease or respiratory morbidity during infancy. These findings may have implications for future lung health. Trial Registration N/A.https://doi.org/10.1186/s12887-023-04210-yBronchopulmonary dysplasiaPretermInfantInflammation
spellingShingle Rhea Urs
Rubi Ni Chin
Naomi Hemy
Andrew C. Wilson
J. Jane Pillow
Graham L. Hall
Shannon J. Simpson
Elevated leukotriene B4 and 8-isoprostane in exhaled breath condensate from preterm-born infants
BMC Pediatrics
Bronchopulmonary dysplasia
Preterm
Infant
Inflammation
title Elevated leukotriene B4 and 8-isoprostane in exhaled breath condensate from preterm-born infants
title_full Elevated leukotriene B4 and 8-isoprostane in exhaled breath condensate from preterm-born infants
title_fullStr Elevated leukotriene B4 and 8-isoprostane in exhaled breath condensate from preterm-born infants
title_full_unstemmed Elevated leukotriene B4 and 8-isoprostane in exhaled breath condensate from preterm-born infants
title_short Elevated leukotriene B4 and 8-isoprostane in exhaled breath condensate from preterm-born infants
title_sort elevated leukotriene b4 and 8 isoprostane in exhaled breath condensate from preterm born infants
topic Bronchopulmonary dysplasia
Preterm
Infant
Inflammation
url https://doi.org/10.1186/s12887-023-04210-y
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