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Published on: February 2, 2017
Cardiometabolic health in adults born with very low birth weight-a sibling study
Nina Kaseva1, Juho Kuula2,3, Samuel Sandboge2,4
1Finnish Institute for Health and Welfare, Helsinki, Finland. nina.kaseva@fimnet.fi.
Insights
Adults born at very low birth weight (VLBW) face higher risks for impaired glucose regulation and fatty acid metabolism compared to their siblings. Shared familial factors may explain some cardiometabolic differences.
Area of Science:
- Cardiology
- Metabolic Health
- Neonatology
Background:
- Individuals born preterm with very low birth weight (VLBW) exhibit an elevated risk for impaired cardiometabolic health in adulthood.
- This study investigates glucose regulation and cardiometabolic biomarkers in adult VLBW survivors, utilizing full siblings as controls to account for shared genetic and environmental factors.
Purpose of the Study:
- To assess and compare glucose metabolism and cardiometabolic biomarkers between adult very low birth weight survivors and their term-born siblings.
- To identify potential familial or environmental influences on cardiometabolic health disparities in VLBW individuals.
Main Methods:
- A cohort of 74 very low birth weight (VLBW) adults was matched with 70 term-born, same-sex siblings.
- Participants underwent a 2-hour, 75g oral glucose tolerance test and blood tests for cardiometabolic biomarker assessment at a mean age of 29.2 years.
Main Results:
- 31% of VLBW adults and 16% of siblings met criteria for impaired glucose regulation (OR 2.5).
- VLBW participants demonstrated significantly higher 2-hour glucose levels and free fatty acid concentrations compared to siblings, even after adjusting for confounders.
- No significant differences were observed in insulin resistance, lipid profiles, or liver function tests between the groups.
Conclusions:
- Adults born at very low birth weight exhibit poorer glucose regulation and fatty acid metabolism compared to their siblings.
- Observed differences in cardiometabolic biomarkers were less pronounced than in prior studies, suggesting shared familial, genetic, or environmental factors play a role.
- Impaired glucose regulation in VLBW adults appears independent of current body mass index, highlighting the lasting impact of prematurity.
Background:
Preterm survivors have increased risk for impaired cardiometabolic health. We assessed glucose regulation and cardiometabolic biomarkers in adult very low birth weight (VLBW, <1500 g) survivors, using siblings as controls.
Methods:
VLBW-participants were matched with term-born, same-sex siblings. At mean age 29.2 years (SD 3.9), 74 VLBW-adults and 70 siblings underwent a 2-h 75 g oral glucose tolerance test and blood tests for assessment of cardiometabolic biomarkers.
Results:
Of participants, 23 (31%) VLBW and 11 (16%) sibling-controls met World Health Organization criteria for impaired glucose regulation (OR adjusted for age and sex 2.5, 95% CI: 1.1 to 5.8). Adjusting for age and sex, VLBW-participants showed 9.2% higher 2-h glucose (95% CI: 0.4% to 18.8%) than their siblings. Also, fasting (13.4%, -0.3% to 29.0%) and 2-h free fatty acids (15.6%, -2.4% to 36.9%) were higher in VLBW-participants. These differences were statistically significant only after further adjusting for confounders. No statistically significant differences were found regarding other measured biomarkers, including insulin resistance, atherogenic lipid profiles or liver tests.
Conclusions:
VLBW-adults showed more impaired fatty acid metabolism and glucose regulation. Differences in cardiometabolic biomarkers were smaller than in previous non-sibling studies. This may partly be explained by shared familial, genetic, or environmental factors.
Impact:
At young adult age, odds for impaired glucose regulation were 3.4-fold in those born at very low birth weight, compared to same-sex term-born siblings. Taking into consideration possible unmeasured, shared familial confounders, we compared cardiometabolic markers in adults born preterm at very low birth weight with term-born siblings. Prematurity increased risk for impaired glucose regulation, unrelated to current participant characteristics, including body mass index. In contrast to previous studies, differences in insulin resistance were not apparent, suggesting that insulin resistance may partially be explained by factors shared between siblings. Also, common cardiometabolic biomarkers were similar within sibling pairs.
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