Increased Incidence but Lack of Association Between Cardiovascular Risk Factors in Adults Born Preterm

医学 优势比 内科学 人口 糖化血红素 背景(考古学) 生理学 内分泌学 糖尿病 2型糖尿病 生物 环境卫生 古生物学
作者
Adrien Flahault,Katryn Paquette,Rafael Oliveira Fernandes,Jacques Delfrate,Anik Cloutier,Mélanie Henderson,Jean-Claude Lavoie,Benoı̂t Mâsse,Anne Monique Nuyt,Thuy Mai Luu,Nathalie Alos,Mariane Bertagnolli,Jean‐Luc Bigras,Daniel Curnier,Daniela Ravizzoni Dartora,Thiérry Ducruet,Ramy El-Jalbout,Camille Girard‐Bock,Geneviève Gyger,Patrick Hamel
出处
期刊:Hypertension [Ovid Technologies (Wolters Kluwer)]
卷期号:75 (3): 796-805 被引量:47
标识
DOI:10.1161/hypertensionaha.119.14335
摘要

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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