Amed Soliz, Jorge Soliz
Florida International University and Memorial Regional Hospital. Institute Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ) and Université Laval. Altitude Baby Association.
United States and Canada
Respiratory Physiology and Neurobiology
Respir Physiol Neurobiol 2026;
DOI: 10.1016/j.resp.2026.104609
Abstract
High altitude exposes the human fetus and newborn to chronic hypobaric hypoxia, markedly reducing oxygen availability during critical windows of development. While adults tolerate moderate hypoxia through well-described acclimatization mechanisms, neonates (particularly those born preterm) exhibit substantially greater vulnerability. Despite more than one million infants being born annually at high or very high altitude, neonatal care practices are still largely derived from sea-level evidence, often neglecting altitude-specific physiology. This review synthesizes current evidence on the effects of high-altitude hypobaric hypoxia on neonatal development, morbidity, and survival. We examine how reduced oxygen availability influences birth weight, prematurity, neonatal mortality, congenital heart disease, pulmonary hypertension, respiratory morbidity, retinopathy of prematurity, hematologic adaptations, infection susceptibility, and neurodevelopment. Across diverse populations and study designs, high altitude is consistently associated with lower birth weight, increased prematurity, higher neonatal mortality, and a greater burden of cardiopulmonary and ocular disease. Notably, many of these risks emerge at altitudes considered physiologically innocuous for adults. Mechanistically, hypobaric hypoxia disrupts oxygen homeostasis at systemic and cellular levels, affecting placental function, pulmonary vascular transition at birth, cerebral blood flow regulation, mitochondrial energy metabolism, and redox balance. Compensatory responses in the fetus and newborn, including increased hemoglobin concentration and erythropoietin production, may partially improve oxygen transport but can also contribute to secondary complications such as hyperbilirubinemia and altered vascular signaling. Importantly, high-altitude ancestry confers partial protection against fetal growth restriction, underscoring the potential influence of evolutionary and developmental context. Collectively, the evidence indicates that neonatal responses to hypobaric hypoxia are developmentally distinct from adult physiological adaptations. Altitude-adapted clinical thresholds, monitoring strategies, and therapeutic approaches grounded in neonatal physiology are urgently needed to improve outcomes for infants born and treated at high altitude worldwide.
Category
Environmental Factors Associated with Pulmonary Vascular Disease
Class III. Pulmonary Hypertension Associated with Alveolar Hypoxia
Review Articles Concerning Pulmonary Vascular Disease
Age Focus: Pediatric Pulmonary Vascular Disease
Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication
Article Access
Free PDF File or Full Text Article Available Through PubMed or DOI: Yes