Prematurity and cardiovascular risk at early adulthood
Mary C Sullivan1, Suzy Barcelos Winchester1, Michael E Msall2
1College of Nursing, University of Rhode Island, Providence, Rhode Island.
Child: Care, Health and Development
|September 22, 2018
Summary
Former preterm infants show early cardiovascular risks, like higher blood pressure, by adulthood. Metabolic risks were not significantly different between preterm and term-born groups at age 23.
Area of Science:
- Neonatology
- Pediatric Cardiology
- Endocrinology
Background:
- Theories of early stress and allostatic load link early life stressors to adult health.
- Prematurity and neonatal illness can impact endocrine and metabolic systems, influencing long-term health.
- This study investigates cardiovascular and metabolic risks in adults who were preterm infants.
Purpose of the Study:
- To compare cardiovascular and metabolic risks at age 23 between healthy preterm (HPT), sick preterm (SPT), and term-born (FT) individuals.
- To identify early indicators of adult health risks associated with prematurity and neonatal illness.
- To assess the utility of clinical and subclinical ranges in identifying early cardiovascular risk.
Main Methods:
- A cohort of 215 infants (45 FT, 24 HPT, 111 SPT) was followed to age 23 (84% participation).
- Cardiovascular outcomes measured included blood pressure (BP), weight, waist-hip ratio (WHR), and body mass index (BMI).
- Metabolic outcomes included fasting glucose and lipid profiles, compared across neonatal groups and by gender.
Main Results:
- HPT and SPT groups exhibited higher systolic BP than the FT group at age 23.
- The SPT group had lower weight compared to FT and HPT groups.
- Preterm males showed increased systolic hypertension and lower high-density lipids; both preterm males and females had high WHR and BMI.
Conclusions:
- Young adults with a history of prematurity (HPT and SPT) display early signs of cardiovascular risk.
- No significant metabolic risks were identified in young adults based on prematurity status.
- Utilizing clinical and subclinical ranges effectively identifies early cardiovascular risk in young adulthood.
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