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Published on: January 12, 2018
Pre-pregnancy endothelial dysfunction and birth outcomes: The Coronary Artery Risk Development in Young Adults
Abbi D Lane-Cordova1, Erica P Gunderson2, Mercedes R Carnethon3
1Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. lanecord@mailbox.sc.edu.
Insights
Biomarkers for endothelial dysfunction, measured before pregnancy, did not predict preterm birth or small-for-gestational-age deliveries. This suggests that the endothelial dysfunction linked to these pregnancy complications may not be detectable pre-conception.
Area of Science:
- Cardiovascular disease
- Reproductive health
- Biomarker research
Background:
- Endothelial dysfunction, a subclinical cardiovascular issue, is implicated in preterm birth and small-for-gestational-age (SGA) deliveries.
- Pre-pregnancy levels of endothelial dysfunction biomarkers are seldomly studied in relation to these adverse birth outcomes.
Purpose of the Study:
- To investigate if elevated pre-pregnancy levels of endothelial dysfunction biomarkers (cellular adhesion molecules, selectins) are associated with increased odds of preterm birth and/or SGA deliveries.
Main Methods:
- Utilized data from 235 nulliparous women in the Coronary Artery Risk Development in Young Adults (CARDIA) study.
- Measured biomarkers of endothelial dysfunction at Year 7 (approximately 3 years pre-pregnancy).
- Employed Poisson regression to assess associations between individual biomarkers, a composite endothelial dysfunction score, and birth outcomes, adjusting for confounders.
Main Results:
- No significant association was found between individual biomarkers or the total endothelial dysfunction score and the odds of preterm birth and/or SGA deliveries.
- The overall evidence of endothelial dysfunction was similar between women who did and did not experience these adverse birth outcomes.
- Adjusted incidence rate ratio for the total endothelial dysfunction score was 1.01 (95% CI: 0.74, 1.39; P=0.93).
Conclusions:
- Pre-pregnancy biomarkers of endothelial dysfunction do not appear to identify women at increased risk for preterm birth or SGA deliveries.
- The findings suggest that maternal endothelial dysfunction contributing to these pregnancy complications may not be detectable prior to conception.
Abstract:
Endothelial dysfunction is a form of subclinical cardiovascular disease that may be involved in preterm birth and small-for-gestational-age deliveries. However, concentrations of biomarkers of endothelial dysfunction before pregnancy have rarely been measured. We hypothesized that higher levels of biomarkers of endothelial dysfunction (cellular adhesion molecules and selectins) would be associated with odds of preterm birth and/or small-for-gestational-age deliveries. We included 235 women from the Coronary Artery Risk Development in Young Adults (CARDIA) study who were nulliparous at Y7, reported ≥1 live birth through Y25, and had ≥1 biomarker measured at Y7. We tested for associations between individual biomarkers and an averaged z-score representing total endothelial dysfunction with preterm birth and/or small-for-gestational-age deliveries using Poisson regression, adjusted for demographic and clinical characteristics at the exam immediately preceding index birth. At Y7, total evidence of endothelial dysfunction was similar in women who did (n = 59) and did not have (n = 176) preterm birth and/or small-for-gestational-age deliveries. There was no association between biomarkers of endothelial dysfunction (either individual biomarker or total score) with odds of preterm birth and/or small-for-gestational-age deliveries after adjustment: IRR = 1.01, 95% CI: 0.74, 1.39, p = 0.93 for total endothelial biomarker score. Associations were not modified by race. We conclude that biomarkers of endothelial dysfunction in nulliparous women, measured ~3 years before pregnancy, did not identify women at risk for preterm birth and/or small-for-gestational-age deliveries. This suggests that the maternal endothelial dysfunction that is believed to contribute to these birth outcomes may not be detectable before pregnancy.
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