Abstract

Background: After very preterm birth, male infants show higher mortality than females, with higher incidence of lung immaturity, neurological deficits, infections, and growth failure. In modern pig production, piglets dying in the perinatal period (up to 20%) often show signs of immature organs, but sex-specific effects are not clear. Using preterm pigs as model for immature infants and piglets, we hypothesized that neonatal survival and initial growth and immune development depend on sex.Methods: Using data from a series of previous intervention trials with similar delivery and rearing procedures, we established three cohorts of preterm pigs (90% gestation), reared for 5, 9, or 19 days before sample collection (total n = 1,938 piglets from 109 litters). Partly overlapping endpoints among experiments allowed for multiple comparisons between males and females for data on mortality, body and organ growth, gut, immunity, and brain function.Results: Within the first 2 days, males showed higher mortality than females (18 vs. 8%, P < 0.001), but less severe immune response to gram-positive infection. No effect of sex was observed for thermoregulation or plasma cortisol. Later, infection resistance did not differ between sexes, but growth rate was reduced for body (up to −40%) and kidneys (−6%) in males, with higher leucocyte counts (+15%) and lower CD4 T cell fraction (−5%) on day 9 and lower monocyte counts (−18%, day 19, all P < 0.05). Gut structure, function and necrotizing enterocolitis (NEC) incidence were similar between groups, but intestinal weight (−3%) and brush-border enzyme activities were reduced at day 5 (lactase, DPP IV, −8%) in males. Remaining values for blood biochemistry, hematology, bone density, regional brain weights, and visual memory (tested in a T maze) were similar.Conclusion: Following preterm birth, male pigs show higher mortality and slower growth than females, despite limited differences in organ growth, gut, immune, and brain functions. Neonatal intensive care procedures may be particularly important for compromised newborns of the male sex. Preterm pigs can serve as good models to study the interactions of sex- and maturation-specific survival and physiological adaptation in mammals.

Highlights

  • Across the lifespan, overall morbidity and mortality is higher in males than in females, caused by a multifaceted interaction among biological factors, societal conditions, and environmental determinants [1]

  • Deficient respiratory and immune functions may increase mortality [4, 5], potentially linked to later reduced body growth [6, 7] and more frequent neurological sequelae [4]. While such complications may be specific for preterm birth, indications of increased mortality of term male infants, across the entire lifespan, imply that differences in survival capacity may exist between sexes, even after term birth [1, 8]

  • Mortality within the first 48 h was recorded for 833 live-born preterm pigs (48% male) from 18 experiments and 44 of these litters

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Summary

Introduction

Overall morbidity and mortality is higher in males than in females, caused by a multifaceted interaction among biological factors, societal conditions, and environmental determinants [1]. Deficient respiratory and immune functions may increase mortality [4, 5], potentially linked to later reduced body growth [6, 7] and more frequent neurological sequelae [4]. While such complications may be specific for preterm birth, indications of increased mortality of term male infants, across the entire lifespan, imply that differences in survival capacity may exist between sexes, even after term birth [1, 8]. Using preterm pigs as model for immature infants and piglets, we hypothesized that neonatal survival and initial growth and immune development depend on sex

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