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Gut and Lung Microbiota in Preterm Infants: Immunological Modulation and Implication in Neonatal Outcomes
Chiara Tirone1,2, Lucilla Pezza1,2, Angela Paladini1,2
1Fondazione Policlinico Universitario A. Gemelli IRCCS, U.O.C. di Neonatologia, Dipartimento di Scienze della Salute della Donna, del Bambino e di Sanità Pubblica, Rome, Italy.
Insights
Gut dysbiosis in preterm infants increases risks for sepsis, necrotizing enterocolitis (NEC), and growth issues. Understanding the gut-lung axis and microbiota
Area of Science:
- Neonatal Medicine
- Microbiology
- Gastroenterology
Background:
- Aberrant gastrointestinal colonization is linked to adverse outcomes in preterm infants, including sepsis, necrotizing enterocolitis (NEC), and growth impairment.
- Intestinal dysbiosis in this vulnerable population is a growing area of research.
- Emerging evidence highlights the gut-lung axis and gut-brain crosstalk, influencing neonatal immunity and outcomes.
Purpose of the Study:
- To review studies on gut and lung microbiota in preterm infants.
- To analyze data on microbial patterns and their association with growth impairment, NEC, bronchopulmonary dysplasia (BPD), and sepsis.
- To explore the role of microbiota in neonatal health and disease prevention.
Main Methods:
- Systematic literature review of studies examining gut and lung microbiota in preterm infants.
- Qualitative analysis of data correlating microbial patterns with specific neonatal morbidities.
- Synthesis of existing research on the gut-lung axis and its implications.
Main Results:
- Microbiota play a critical role in establishing gut barrier integrity and immune modulation.
- The gut-lung axis development is interconnected, potentially leading to inflammatory responses implicated in BPD pathogenesis.
- Gut dysbiosis and a predominance of facultative anaerobes are associated with the development of these neonatal diseases.
Conclusions:
- Gut microbiota composition significantly impacts neonatal outcomes, particularly in preterm infants.
- Dysbiosis and specific microbial patterns are key factors in the pathogenesis of NEC, BPD, and sepsis.
- Targeting the gut microbiome may offer strategies for preventing these serious neonatal conditions.
Abstract:
In recent years, an aberrant gastrointestinal colonization has been found to be associated with an higher risk for postnatal sepsis, necrotizing enterocolitis (NEC) and growth impairment in preterm infants. As a consequence, the reasons of intestinal dysbiosis in this population of newborns have increasingly become an object of interest. The presence of a link between the gut and lung microbiome's development (gut-lung axis) is emerging, and more data show as a gut-brain cross talking mediated by an inflammatory milieu, may affect the immunity system and influence neonatal outcomes. A revision of the studies which examined gut and lung microbiota in preterm infants and a qualitative analysis of data about characteristic patterns and related outcomes in terms of risk of growing impairment, Necrotizing Enterocolitis (NEC), Bronchopulmonary Dysplasia (BPD), and sepsis have been performed. Microbiota take part in the establishment of the gut barrier and many data suggest its immune-modulator role. Furthermore, the development of the gut and lung microbiome (gut-lung axis) appear to be connected and able to lead to abnormal inflammatory responses which have a key role in the pathogenesis of BPD. Dysbiosis and the gut predominance of facultative anaerobes appear to be crucial to the pathogenesis and subsequently to the prevention of such diseases.
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