AI Article Synopsis

  • The study aimed to compare tissue factor (TF) and tissue factor pathway inhibitor (TFPI) levels in pregnant women with preeclampsia (PE) or small for gestational age (SGA) infants to those in normal pregnancies.
  • Results showed that women with PE had significantly higher plasma TF activity compared to those with normal pregnancies and SGA infants, while TFPI levels did not differ significantly.
  • The findings suggest that elevated TF activity in women with PE may contribute to increased thrombin generation, but there is no direct link between TF/TFPI activity and having an SGA infant.

Article Abstract

Objective: The aim of this study was to determine whether the activity of tissue factor (TF) and tissue factor pathway inhibitor (TFPI) in the plasma of women with preeclampsia (PE) and small for gestational age (SGA) neonate differ from that of normal pregnant women and whether they are related to specific placental lesions.

Methods: This cross-sectional study included the following groups: (1) normal pregnancy (n = 68); (2) PE (n= 128); and (3) SGA (n = 56). Maternal plasma TF and TFPI activity was determined with chromogenic assays.

Results: (1) The median maternal plasma TF activity, but not TFPI activity, differed among the study groups (p < .0001 and p = .4, respectively); (2) patients with PE had a higher median maternal plasma TF activity than women with normal pregnancies (p < .0001) and mothers with SGA fetuses (p = .002); (3) among patients with PE, those with distal villous hypoplasia had a higher median maternal TF activity than those without these placental lesions (p = .018); and (4) following adjustment for confounding variables, maternal plasma TF and TFPI activity were not associated with an SGA neonate.

Conclusions: Plasma TF activity is higher in women with PE than in those with SGA or normal pregnancies. We propose that these changes may be responsible, at least in part, for the increased in-vivo thrombin generation observed in this obstetrical syndrome.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694704PMC
http://dx.doi.org/10.1080/14767058.2017.1320543DOI Listing

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