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Published on: November 20, 2015
The impact of preterm adversity on cardiorespiratory function
Fiona B McDonald1,2, Eugene M Dempsey2,3, Ken D O'Halloran1,2
1Department of Physiology, School of Medicine, College of Medicine & Health, University College Cork, Cork, Ireland.
Insights
Preterm infants face cardiorespiratory challenges due to oxygen dysregulation and immune activation. Neonatal animal models reveal how early-life stress impacts neurodevelopment and cardiorespiratory homeostasis.
Area of Science:
- Neonatal physiology
- Cardiorespiratory system
- Developmental neuroscience
Background:
- Preterm birth is a major cause of neonatal mortality.
- Surviving infants experience short- and long-term morbidities due to early-life stress.
- Oxygen dysregulation (hypoxia, hyperoxia) is a primary concern for cardiorespiratory adaptation.
Purpose of the Study:
- To review the influence of prematurity on the cardiorespiratory system.
- To examine the consequences of altered oxygen tension and immune activation in preterm infants.
- To highlight advances in understanding stress effects on neurodevelopment and cardiorespiratory homeostasis.
Main Methods:
- Examination of clinical challenges in preterm birth.
- Review of neonatal animal models of intermittent hypoxia, hyperoxia, and infection.
- Focus on physiological pathways modulating the cardiorespiratory system.
Main Results:
- Oxygen dysregulation alters redox balance and immune signaling.
- Altered stress responses impact neurodevelopment and cardiorespiratory homeostasis.
- Neonatal animal models provide insights into early-life stress effects.
Conclusions:
- Preterm infants are vulnerable to cardiorespiratory complications.
- Understanding oxygen and immune system interactions is crucial.
- Animal models are valuable tools for studying preterm infant physiology and stress responses.
New Findings:
What is the topic of this review? We review the influence of prematurity on the cardiorespiratory system and examine the common sequel of alterations in oxygen tension, and immune activation in preterm infants. What advances does it highlight? The review highlights neonatal animal models of intermittent hypoxia, hyperoxia and infection that contribute to our understanding of the effect of stress on neurodevelopment and cardiorespiratory homeostasis. We also focus on some of the important physiological pathways that have a modulatory role on the cardiorespiratory system in early life.
Abstract:
Preterm birth is one of the leading causes of neonatal mortality. Babies that survive early-life stress associated with immaturity have significant prevailing short- and long-term morbidities. Oxygen dysregulation in the first few days and weeks after birth is a primary concern as the cardiorespiratory system slowly adjusts to extrauterine life. Infants exposed to rapid alterations in oxygen tension, including exposures to hypoxia and hyperoxia, have altered redox balance and active immune signalling, leading to altered stress responses that impinge on neurodevelopment and cardiorespiratory homeostasis. In this review, we explore the clinical challenges posed by preterm birth, followed by an examination of the literature on animal models of oxygen dysregulation and immune activation in the context of early-life stress.
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