1E-4 Cardiovascular risk factors at age 30 following preterm birth

2007 ◽  
Vol 83 ◽  
pp. S51-S52 ◽  
Author(s):  
S.R. Dalziel ◽  
V. Parag ◽  
A. Rodgers ◽  
J.E. Harding
2009 ◽  
Vol 85 (4) ◽  
pp. 239-245 ◽  
Author(s):  
Kari Anne Indredavik Evensen ◽  
Sigurd Steinshamn ◽  
Arnt Erik Tjønna ◽  
Tomas Stølen ◽  
Morten Andre Høydal ◽  
...  

2011 ◽  
Vol 31 (12) ◽  
pp. 2975-2981 ◽  
Author(s):  
Michael R. Skilton ◽  
Jorma S.A. Viikari ◽  
Markus Juonala ◽  
Tomi Laitinen ◽  
Terho Lehtimäki ◽  
...  

2017 ◽  
Vol 106-107 ◽  
pp. 53-58 ◽  
Author(s):  
Robinson Ramírez-Vélez ◽  
Jorge Enrique Correa-Bautista ◽  
Emilio Villa-González ◽  
Javier Martínez-Torres ◽  
Anthony C. Hackney ◽  
...  

Hypertension ◽  
2020 ◽  
Vol 75 (3) ◽  
pp. 796-805 ◽  
Author(s):  
Adrien Flahault ◽  
Katryn Paquette ◽  
Rafael Oliveira Fernandes ◽  
Jacques Delfrate ◽  
Anik Cloutier ◽  
...  

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.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Eirin B. Haug ◽  
Amanda R. Markovitz ◽  
Abigail Fraser ◽  
Håvard Dalen ◽  
Pål R. Romundstad ◽  
...  

AbstractA history of preterm or small (SGA) or large (LGA) for gestational age offspring is associated with smoking and unfavorable levels of BMI, blood pressure, glucose and lipids. Whether and to what extent the excess cardiovascular risk observed in women with these pregnancy complications is explained by conventional cardiovascular risk factors (CVRFs) is not known. We examined the association between a history of SGA, LGA or preterm birth and cardiovascular disease among 23,284 parous women and quantified the contribution of individual CVRFs to the excess cardiovascular risk using an inverse odds weighting approach. The hazard ratios (HR) between SGA and LGA offspring and CVD were 1.30 (95% confidence interval (CI) 1.15, 1.48) and 0.89 (95% CI 0.76, 1.03), respectively. Smoking explained 49% and blood pressure may have explained ≈12% of the excess cardiovascular risk in women with SGA offspring. Women with preterm birth had a 24% increased risk of CVD (HR 1.24, 95% CI 1.06, 1.45), but we found no evidence for CVRFs explaining any of this excess cardiovascular risk. While smoking explains a substantial proportion of excess cardiovascular risk in women with SGA offspring and blood pressure may explain a small proportion in these women, we found no evidence that conventional CVRFs explain any of the excess cardiovascular risk in women with preterm birth.


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