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Updated: Jan 10, 2026

Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Dynamics of postnatal upper airway bacteria colonization in preterm infants <1000g and bronchopulmonary dysplasia
Tina Frodermann1, Ulrich Rochwalsky2, Ariane Selting1
1Department of General Pediatrics and Neonatology, Justus-Liebig-University, Feulgenstrasse 12, D-35392, Giessen, Germany.
Insights
Delayed upper airway colonization with facultative pathogenic bacteria increases the risk of bronchopulmonary dysplasia (BPD) in premature infants. This risk factor is particularly relevant for infants weighing 800g or more at birth.
Area of Science:
- Neonatalogy
- Microbiology
- Pediatric Pulmonology
Background:
- Aberrant microbial colonization in premature infants is linked to severe acute morbidities.
- Bronchopulmonary dysplasia (BPD) is a significant complication in preterm infants.
Purpose of the Study:
- To evaluate the correlation between bacterial upper airway colonization in the first 6 weeks of life and the risk of moderate/severe BPD in preterm infants weighing less than 1000g.
- To identify specific bacterial colonization patterns associated with BPD development.
Main Methods:
- Retrospective two-center cohort study analyzing postnatal upper airway bacterial colonization.
- Categorization of bacteria into facultative and highly pathogenic.
- Classification tree analyses to determine risk factors for BPD.
Main Results:
- Birth weight <800g was a key discriminator for BPD risk.
- Factors associated with BPD included center, male sex, antibiotic therapy duration, and delayed facultative pathogenic bacteria detection after week 4.
- For infants <800g, antibiotic therapy was more critical; for infants ≥800g, delayed facultative bacterial colonization was more relevant than antibiotic exposure.
Conclusions:
- Delayed upper airway colonization with facultative pathogenic bacteria is identified as a risk factor for BPD.
- Microbial colonization variations must be considered in future BPD pathogenesis studies and treatment development.
Abstract:
Aberrant microbial colonization of premature infants is increasingly recognized as a risk factor for severe acute morbidities. The aim of this study was to evaluate the correlation of bacterial upper airway colonization within the first 6 weeks of life in preterm infants <1000g and risk of moderate/severe bronchopulmonary dysplasia (BPD). In this retrospective two-center cohort study postnatal upper airway bacterial colonization of premature infants with a birth weight <1000g was analyzed. Bacteria were categorized into facultative- and highly pathogenic. Within 242 infants, a birth weight cutoff of 800g prevailed as the most relevant discriminator for risk of BPD. Furthermore, center, male sex, duration of antibiotic therapy, and delayed detection of facultative pathogenic bacteria after week 4 was associated with the development of BPD. Using classification tree analyses for the binary outcome, antibiotic therapy was more importance in infants <800g, whereas in those with a birth weight ≥800g, delayed colonization with facultative pathogenic bacteria was more relevant than antibiotic exposure. We add delayed colonization of the upper airway with facultative pathogenic bacteria to the risks for BPD. The variations of microbial colonization should be considered in future studies on the pathogenesis of BPD and new treatment modalities.
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