4.6 Article

Maternal nonpregnant vascular function correlates with subsequent fetal growth

Journal

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
Volume 192, Issue 2, Pages 504-512

Publisher

MOSBY, INC
DOI: 10.1016/j.ajog.2004.08.035

Keywords

preeclampsia; pulsatility index; pregnancy; vascular compliance; distensibility; plasma volume; fetal growth

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Objective: Evidence is accumulating that fetal growth is influenced by preexisting maternal disorder(s) hampering endothelial function. We tested the hypothesis that in nonpregnant normotensive, formerly preeclamptic women, vascular function predicts the development of fetal growth restriction. Methods: In 60 formerly preeclamptic women, we measured central hemodynamic and vascular and clotting function mid follicular phase during the menstrual cycle. Inclusion for final analysis required besides normotension, a subsequent singleton pregnancy, established within I year after the prepregnant evaluation and ongoing beyond 16 weeks' gestation. In the ongoing pregnancy we determined birth weight and birth weight percentile. Results: Among 60 formerly preeclamptic women, 45 (75%) were normotensive. Thirty-one (69%) participants succeeded in establishing an ongoing pregnancy within I year and were included for final analysis. Of the 31 subsequent pregnancies, 8 (26%) were complicated by fetal growth restriction. Prepregnant left and right uterine artery pulsatility index (PI) correlated inversely with carotid artery compliance (r = 0.57, P = .005, r = 0.62, P = .002) and venous compliance (r = 0.49, P = .02 and r = 0.45, P = .04, respectively). The latter, in turn, correlates with plasma volume (r = 0.63, P = .001) and total peripheral vascular resistance index (r = -0.45, P = .02). Finally, prepregnant left and right uterine artery PI correlated inversely with subsequent achieved fetal growth (r = -0.68, P < .0001 and r = -0.58, P = .001, respectively). Conclusion: In nonpregnant normotensive, formerly preeclamptic women, an elevated uterine artery PI predisposes to subsequent restriction in fetal growth. (C) 2005 Elsevier Inc. All rights reserved.

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