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Published on: November 20, 2015
Family social risks on neurodevelopmental outcomes in preterm infants without severe brain injury
Li-Wen Chen1, Min-Lan Tsai2,3, Yung-Chieh Lin1
1Department of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Insights
Family social risks and male sex are linked to neurodevelopmental impairment (NDI) in preterm infants without severe brain injury (SBI). Oxygen exposure further increases NDI risk, highlighting the need for targeted support for vulnerable infants.
Area of Science:
- Neonatal Medicine
- Developmental Pediatrics
- Public Health
Background:
- Preterm infants without severe brain injury (SBI) are still at risk for neurodevelopmental impairment (NDI).
- Family and social factors are increasingly recognized as significant contributors to infant development.
- Understanding these risks is crucial for early intervention and improved outcomes.
Purpose of the Study:
- To investigate the association between family-social risks and neurodevelopmental impairment (NDI) in preterm infants without SBI.
- To identify specific family-social factors that impact NDI outcomes.
- To analyze the combined effects of clinical factors like oxygen exposure on NDI.
Main Methods:
- Assessed infants born <29 weeks gestation without high-grade brain injury using Bayley Scales of Infant Development.
- Defined NDI as cognitive/motor delay, cerebral palsy, or bilateral blindness/deafness.
- Utilized logistic and linear regression to analyze family-social (maternal age, education, ethnicity, SES, single-parent status) and clinical risks for NDI severity at 24 months.
Main Results:
- 82% of infants had no/mild NDI, 14% moderate, and 4% severe NDI.
- Each additional family-social risk factor increased severe NDI odds by 1.6 times.
- Family-social risks and male sex were associated with lower cognitive, language, and motor scores; each extra day of oxygen therapy worsened scores by 0.1 points.
Conclusions:
- Family social risks, male sex, and oxygen exposure are significant predictors of NDI in preterm infants without SBI.
- These factors are associated with increased NDI severity and lower developmental scores.
- High-risk preterm infants require enhanced surveillance and early intervention services to improve neurodevelopmental outcomes.
Background:
To assess family-social risks on neurodevelopmental impairment (NDI) outcomes in preterm infants without severe brain injury (SBI).
Method:
Infants born <29 weeks' gestation without high-grade intraventricular hemorrhage, periventricular leukomalacia, or cerebellar hemorrhage in the population were assessed using the Bayley Scales of Infant Development. NDI included cognitive/motor delay, cerebral palsy, and bilateral blindness/deafness. Family-social risks included young maternal age, low maternal educational level, minority ethnicity, low family socioeconomic status, and single-parent family. Ordered logistic and linear regression models analyzed family-social and clinical risks for NDI severity outcomes at 24 months.
Results:
Among 459 infants, 82% had no/mild NDI, 14% moderate NDI, and 4% severe NDI. Each additional family-social risk increased severe NDI odds by 1.6 times (95% CI: 1.2-2.0), with each extra day of oxygen therapy raising NDI risk by 3% (2-4%). Family-social risks lowered cognitive (-3.3), language (-3.2), and motor (-2.2) scores at 24 months. Males had lower cognitive (-2.7), language (-4.0), and motor (-1.8) scores than females. Each oxygen therapy day reduced all developmental domain scores by 0.1.
Conclusions:
Family social risks, male sex, and oxygen exposure are associated with NDI outcomes in preterm infants without SBI. Additional support for high-risk infants may improve outcomes.
Impact:
Nearly one-fifth of preterm infants without severe neonatal brain injury (SBI) have moderate/severe neurodevelopmental impairment (NDI), showing developmental deviations from those with no/mild NDI since age 12 months. Family social risks increase the odds of more severe NDI, complicated by additional days of oxygen therapy. Family social risks and male sex are associated with lower developmental scores at 24 months in cognition, language, and motor abilities. Prolonged oxygen therapy contributes to poorer neurodevelopmental performance in all domains. Preterm infants without SBI but with identifiable demographic and clinical risk factors may benefit from surveillance and early intervention services.
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