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Published on: November 20, 2015
Increased Incidence but Lack of Association Between Cardiovascular Risk Factors in Adults Born Preterm
Adrien Flahault1, Katryn Paquette1, Rafael Oliveira Fernandes1
1From the Department of Pediatrics (A.F., K.P., R.O.F., J.D., A.C., M.H., A.M.N., T.M.L.), Sainte-Justine University Hospital and Research Center, Université de Montréal, Quebec, Canada.
Insights
Young adults born preterm face higher risks of hypertension, glucose intolerance, and lung issues. Cardiovascular risks in this group may stem from different pathways than in full-term individuals.
Area of Science:
- Cardiology
- Neonatology
- Public Health
Background:
- Preterm birth (gestation ≤29 weeks) is linked to later cardiovascular events.
- Cardiovascular risk factors often cluster with inflammation and oxidative stress in the general population.
- The clustering of cardiovascular risk factors in young adults born preterm is not well understood.
Purpose of the Study:
- To investigate cardiovascular risk factors in healthy young adults born preterm compared to those born full-term.
- To explore the roles of inflammation and oxidative stress in these risk factors.
- To identify potential differences in pathophysiological pathways.
Main Methods:
- A cohort study comparing 101 young adults born preterm (≤29 weeks) with 105 full-term controls.
- Comprehensive clinical evaluation: blood pressure, spirometry, glucose metabolism (OGTT).
- Biomarker analysis for inflammation and oxidative stress.
Main Results:
- Individuals born preterm showed significantly higher risks of hypertension (aOR 2.91), glucose intolerance (aOR 2.22), and airflow limitation (aOR 3.47).
- In preterm individuals, cardiovascular risk factors were not interrelated, unlike in full-term controls where hypertension associated with adiposity and glucose intolerance.
- No significant group differences in inflammation or oxidative stress biomarkers were found; these were linked to adiposity in preterm individuals.
Conclusions:
- Young adults born preterm exhibit distinct cardiovascular risk profiles, with risk factors not clustering as expected.
- Different pathophysiological mechanisms may underlie cardiovascular risk development after preterm birth.
- Clinical screening for hypertension, glucose intolerance, and airflow limitation is recommended for preterm-born individuals, independent of other risk factors.
Abstract:
Preterm birth incurs an increased risk of early cardiovascular events and death. In the general population, cardiovascular risk factors cluster in the context of inflammation and oxidative stress. Whether this also occurs in young adults born preterm is unknown. We analyzed 101 healthy young adults (ages 18-29) born preterm (≤29 weeks of gestation) and 105 full-term controls, predominantly (90%) white. They underwent a comprehensive clinical and biological evaluation, including measurement of blood pressure, lung function (spirometry), glucose metabolism (fasting glucose, glycated hemoglobin, and oral glucose tolerance test), as well as biomarkers of inflammation and oxidative stress. Individuals born preterm were at higher risk than those born full-term of stage ≥1 hypertension (adjusted odds ratio, 2.91 [95% CI, 1.51-5.75]), glucose intolerance (adjusted odds ratio, 2.22 [95% CI, 1.13-4.48]), and airflow limitation (adjusted odds ratio, 3.47 [95% CI, 1.76-7.12]). Hypertension was strongly associated with adiposity and with glucose intolerance in participants born full-term but not in those born preterm. We did not find any group difference in levels of biomarkers of inflammation and oxidative stress. In individuals born preterm, inflammation, and oxidative stress were not related to hypertension or glucose intolerance but were associated with adiposity. In those born preterm, cardiovascular risk factors were not related to each other suggesting different pathophysiological pathways leading to the development of cardiovascular risk following preterm birth. Clinicians should consider screening for these abnormalities irrespectively of other risk factors in this at-risk population. Clinical Trial Registration URL: http://www.clinicaltrials.gov. Unique identifier: NCT03261609.
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