Angiogenic proteins, placental weight and perinatal outcomes among pregnant women in Tanzania

PLoS One. 2016 Dec 9;11(12):e0167716. doi: 10.1371/journal.pone.0167716. eCollection 2016.

Abstract

Introduction: Placental vascular development, and ultimately placental weight, is essential to healthy fetal development. Here, we examined placental weight in a cohort of Tanzanian women in association with angiogenic proteins known to regulate placental vascular development and perinatal outcomes.

Methods: A total of n = 6579 women with recorded placental weight were included in this study. The relative risk of adverse perinatal outcomes (Apgar score, death, asphyxia, respiratory distress, seizures, pneumonia and sepsis) was compared between placental weight in the bottom and top 10th percentiles. We quantified angiogenic mediators (Ang-1, Ang-2, VEGF, PGF and sFlt-1) in plasma samples (n = 901) collected between 12 to 27 weeks of pregnancy using ELISA and assessed the relative risk of placental weight in the bottom and top 10th percentiles by protein levels in quartiles.

Results: Women with Ang-2 levels in the highest quartile had an increased relative risk of placental weight in the bottom 10th percentile (RR = 1.45 (1.10, 1.91), p = 0.01). Women with VEGF-A (RR = 0.73 (0.56, 0.96), p = 0.05) and PGF (RR = 0.58 (0.44, 0.72), p = 0.002) in the highest quartile had a reduced relative risk of placental weight in the bottom 10th percentile. Low placental weight (in bottom 10th percentile) was associated with an increased relative risk of Apgar score of <7 at 1 minute (RR = 2.31 (1.70, 3.13), p = 0.001), at 5 minutes (RR = 3.53 (2.34, 5.33), p = 0.001), neonatal death (RR = 5.02 (3.61, 7.00), p = 0.001), respiratory distress (RR = 4.80(1.71, 13.45), p = 0.001), and seizures (RR = 4.18 (1.16, 15.02), p = 0.03).

Discussion: The association between low placental weight and risk of adverse perinatal outcomes in this cohort suggests that placental weight could serve as a useful indicator, providing additional insight into high-risk pregnancies and identifying neonates that may require additional monitoring and follow-up.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Angiogenic Proteins / analysis*
  • Apgar Score
  • Female
  • Humans
  • Organ Size
  • Placenta / anatomy & histology
  • Placenta / blood supply
  • Placenta / physiology*
  • Pregnancy
  • Pregnancy Complications / epidemiology*
  • Pregnancy Outcome / epidemiology*
  • Tanzania / epidemiology
  • Young Adult

Substances

  • Angiogenic Proteins

Grants and funding

This work was supported by the National Institute of Child Health and Human Development (NICHD R01 37701 [WF]), the Global Alliance to Prevent Prematurity and Stillbirth and Grand Challenges in Global Health: Preventing Preterm Birth Initiative Grant No. 12003 [KK]; the Canadian Institutes of Health Research MOP-115160 and 13721 [KK], Canadian Institutes of Health Research Fellowship [CM] and Canada Research Chair [KK].