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Modeling Neonatal Intraventricular Hemorrhage Through Intraventricular Injection of Hemoglobin
Published on: August 25, 2022
Male sex and intraventricular hemorrhage
Jennifer A Tioseco1, Hany Aly, Jonah Essers
1Department of Neonatology, The Children's National Medical Center, Washington, DC, USA.
Insights
Male infants with low birth weight show higher rates of intraventricular hemorrhage (IVH), death, and bilirubin levels. These sex-biased outcomes highlight potential biological factors influencing neonatal health in vulnerable populations.
Area of Science:
- Neonatology
- Perinatal Medicine
- Pediatric Research
Background:
- Neonatal mortality and morbidity exhibit sex-based disparities in low birth weight infants.
- The "Y chromosome effect" is a proposed factor contributing to sex-specific maturational differences.
Purpose of the Study:
- To investigate the association between infant sex and neonatal outcomes.
- To identify sex-specific risks in low birth weight infants.
Main Methods:
- Retrospective observational study of low birth weight infants surviving >48 hours.
- Comparison of neonatal outcomes between male and female infants.
- Regression analysis to assess the influence of sex, controlling for confounders, with subgroup analysis by birth weight (<1000g, 1000-1499g, 1500-2499g).
Main Results:
- Male infants demonstrated higher rates of intraventricular hemorrhage (IVH) and severe IVH (grades 3-4).
- Elevated bilirubin levels were observed in male infants.
- Male sex was a significant predictor for IVH, severe IVH, death, and bilirubin levels in regression models.
- In the lowest birth weight group (<1000g), male infants had a significantly increased prevalence of death, independent of IVH.
Conclusions:
- Male sex is associated with significantly higher rates of bilirubin, IVH, and death in low birth weight infants.
- These sex-based differences were particularly significant in the extremely low birth weight subgroup (<1000g).
- Further research is needed to elucidate whether a single biological factor or a multifactorial process underlies these observed sex disparities.
Background:
Neonatal mortality and morbidity are sex biased in low birth weight infants. The "Y chromosome effect" has been suggested to be responsible for these maturational differences.
Objective:
To examine the association of sex and neonatal outcomes.
Design And Methods:
A retrospective observational study. Data on all low birth weight infants who survived for >48 hrs were analyzed. Neonatal outcomes were compared between male and female infants. A regression model was used to detect the influence of sex on outcomes after controlling for confounders. Analysis was repeated after stratification of infants into three groups: group A (<1000 g), group B (1000-1499 g), and group C (1500-2499 g).
Results:
A total of 833 infants were included in this study; 419 female infants and 414 male infants. Male infants had an increased rate of overall intraventricular hemorrhage (IVH) (12.2% vs. 7.2%, p = .02) and IVH grades 3-4 (4.8% vs. 2.3%, p = .04). In addition, male infants had higher bilirubin levels (10.19 +/- 3.1 mg/dL vs. 9.32 +/- 2.94 mg/dL, p = .001). In a regression model, male sex continued to have significant influence on IVH, IVH grades 3-4, death, and bilirubin. In group A, male infants had a significantly increased prevalence of death (regression coefficient, 1.82 +/- 0.65; p = .005) that could not be explained by the increased prevalence of IVH (p = .18) in regression analysis. In group B, male sex was significantly associated with a higher bilirubin level (regression coefficient, 0.94 + 0.3; p = .002). In bivariate analyses, IVH and IVH grades 3-4 were significantly higher in male compared with female infants (19.8% vs. 3.9%, p < .0001) and (8.5% vs. 0.97%, p = .02), respectively, but these differences lost significance in multiple-regression analysis. In group C, male sex positively influenced the prevalence of IVH (regression coefficient, 1.7 +/- 0.57; p = .003). Bilirubin measured higher in male infants (11.38 +/- 2.87 mg/dL vs. 10.19 +/- 3.22 mg/dL, p = .0004), but the difference lost significance in regression analysis (regression coefficient, 0.21 +/- 0.31; p = .5).
Conclusions:
Bilirubin, IVH, and death were significantly higher in male infants. In subgroup analysis, significance was retained in group A (<1000 g). Whether a single biological factor is responsible for these differences or perhaps a multi-causal process involving a complex interaction of physiologic, environmental, and pathologic responses needs to be further addressed in future research.
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