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Oxidative Stress and Bronchopulmonary Dysplasia: Evidences From Microbiomics, Metabolomics, and Proteomics
Letizia Capasso1, Giovanni Vento2, Cristina Loddo3
1Neonatology, Section of Pediatrics, Department of Translational Sciences, University of Naples Federico II, Naples, Italy.
Insights
Bronchopulmonary dysplasia (BPD) in premature infants is linked to oxidative stress. New "omics" research, including microbiomics, metabolomics, and proteomics, offers insights into BPD
Area of Science:
- Neonatal Medicine
- Pediatric Respiratory Medicine
- Biochemistry
Background:
- Bronchopulmonary dysplasia (BPD) significantly impacts premature infant survival and health.
- Premature infants are highly vulnerable to oxidative stress, a key factor in BPD development.
- Oxidative stress patterns are evident in early-stage BPD, highlighting its pathogenic role.
Purpose of the Study:
- To review emerging evidence from "omics" research in BPD.
- To explore the relationship between microbiomics, metabolomics, proteomics, oxidative stress, and BPD pathogenesis.
- To identify potential avenues for improved BPD prevention and treatment strategies.
Main Methods:
- Literature review focusing on recent "omics" studies in BPD research.
- Analysis of data linking oxidative stress markers with BPD.
- Synthesis of findings from microbiomics, metabolomics, and proteomics.
Main Results:
- "Omics" technologies are providing novel insights into BPD.
- Specific oxidation patterns in infants suggest a critical role for oxidative stress in BPD pathogenesis.
- Emerging data highlight the interconnectedness of microbial, metabolic, and protein profiles with oxidative stress in BPD.
Conclusions:
- Oxidative stress is a crucial component in the pathogenesis of bronchopulmonary dysplasia.
- Microbiomics, metabolomics, and proteomics offer promising new perspectives on BPD.
- Further research integrating "omics" data is essential for developing effective BPD management strategies.
Abstract:
Bronchopulmonary dysplasia is a major issue affecting morbidity and mortality of surviving premature babies. Preterm newborns are particularly susceptible to oxidative stress and infants with bronchopulmonary dysplasia have a typical oxidation pattern in the early stages of this disease, suggesting the important role of oxidative stress in its pathogenesis. Bronchopulmonary dysplasia is a complex disease where knowledge advances as new investigative tools become available. The explosion of the "omics" disciplines has recently affected BPD research. This review focuses on the new evidence coming from microbiomics, metabolomics and proteomics in relation to oxidative stress and pathogenesis of bronchopulmonary dysplasia. Since the pathogenesis is not yet completely understood, information gained in this regard would be important for planning an efficacious prevention and treatment strategy for the future.
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