Archives of Disease in Childhood - Fetal and Neonatal Edition 2006;91:F36-F39
ORIGINAL ARTICLE
NF-
B in tracheal lavage fluid from intubated premature infants: association with inflammation, oxygen, and outcome
Virginia Commonwealth University, Richmond, VA 23298-0276, USA
Correspondence to:
Correspondence to:
Dr Rozycki
Division of Neonatal-Perinatal Medicine, Department of Pediatrics, Virginia Commonwealth University School of Medicine, Richmond, VA 23298-0276, USA; hrozycki{at}hsc.vcu.edu
Objectives: To determine if tracheal lavage concentrations of the transcription factor NF-
B, which is activated by risk factors associated with bronchopulmonary dysplasia (BPD) and induces expression of cytokines associated with BPD, is related to BPD in premature infants.
Design: Serial tracheal lavage samples from intubated premature infants were analysed for cell count and concentrations of interleukin (IL)8 and NF-
B, corrected for dilution by secretory component concentrations.
Setting: Level III university hospital neonatal intensive care unit.
Patients: Thirty three intubated infants (mean (SD) birth weight 903 (258) g, median gestation 27 weeks (range 2431)) in the first 14 days of life.
Main outcome measures: Tracheal effluent NF-
B, IL8, and cell counts, corrected for dilution by secretory component measurement.
Results: Square root transformed NF-
B concentrations were significantly related to signs of inflammation (cell count, p = 0.002; IL8, p = 0.019) and to simultaneous fraction of inspired oxygen in samples from the first 3 days of life (r = 0.512, p<0.003). Of the 32 subjects with samples in the first 3 days of life, the half who either died or had BPD had higher NF-
B concentrations than those without BPD (square root concentration 0.097 (0.043) v 0.062 (0.036) µg/µg protein/µg secretory component, p = 0.018).
Conclusions: Tracheobronchial lavage NF-
B concentrations are related to lung inflammation, oxygen exposure, and pulmonary outcome in intubated preterm infants. NF-
B activation may be an early critical step leading to BPD.
Abbreviations: BPD, bronchopulmonary dysplasia; FIO2, fraction of inspired oxygen; IL, interleukin; NF-
B, nuclear factor-kappa B; SC, secretory component
Keywords: bronchopulmonary dysplasia; lung injury; respiratory distress syndrome; cytokines
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
-
Chauhan, M, Bombell, S, McGuire, W
(2009). Tumour necrosis factor (-308A) polymorphism in very preterm infants with bronchopulmonary dysplasia: a meta-analysis. Arch. Dis. Child. Fetal Neonatal Ed.
94: F257-F259
[Abstract] [Full Text] -
Bhandari, A., Bhandari, V.
(2009). Pitfalls, Problems, and Progress in Bronchopulmonary Dysplasia. Pediatrics
123: 1562-1573
[Abstract] [Full Text] -
Wright, C. J., Zhuang, T., La, P., Yang, G., Dennery, P. A.
(2009). Hyperoxia-induced NF-{kappa}B activation occurs via a maturationally sensitive atypical pathway. Am. J. Physiol. Lung Cell. Mol. Physiol.
296: L296-L306
[Abstract] [Full Text] -
Yoder, B. A., Albertine, K. H.
(2008). Inflammation and Lung Disease in the Neonatal Period. NeoReviews
9: e447-e457
[Abstract] [Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.



