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Genetic Factors Contribute to Risk for Neonatal Respiratory Distress Syndrome among Moderately Preterm, Late Preterm,
Carol L Shen1, Qunyuan Zhang2, Julia Meyer Hudson1
1Division of Newborn Medicine, Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, St. Louis, MO.
Genetic factors contribute significantly to respiratory distress syndrome (RDS) risk in preterm and term infants. Understanding these genetic influences is key for predicting and managing RDS.
Area of Science:
- Perinatology
- Genetics
- Neonatal Research
Background:
- Respiratory distress syndrome (RDS) is a significant concern in preterm and term infants.
- Understanding the etiology of RDS is crucial for effective prevention and management strategies.
Purpose of the Study:
- To quantify the genetic contribution to the risk of developing respiratory distress syndrome (RDS).
- To investigate genetic influences on RDS in infants with estimated gestational age of 32 weeks or greater, across different ancestries.
Main Methods:
- Twin study design analyzing 524 twin pairs (monozygotic and dizygotic) with at least one twin diagnosed with RDS.
- Utilized mixed-effects logistic regression to identify risk factors and employed genetic modeling to estimate variance components.
Main Results:
- Higher concordance for RDS was observed in monozygotic twins compared to dizygotic twins.
- Independent risk factors for RDS included lower gestational age, European descent, male sex, cesarean delivery, and lower 5-minute Apgar scores.
- Genetic factors accounted for 58% of the variance in RDS risk after adjusting for identified covariates.
Conclusions:
- Genetic predisposition plays a substantial role in RDS risk, alongside environmental factors.
- Identifying specific risk alleles for RDS could enhance prediction and inform clinical management approaches.
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