Expression and diagnostic value of plasma protein Z and protein Z-dependent protease inhibitor in fetal growth

Ci Pan1, Yulian Huang2, Xiaopei Guo2

  • 1Prenatal Diagnosis Center, 3rd Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Ginekologia Polska
|January 24, 2022
PubMed

Insights

Plasma protein Z (PZ) and protein Z-dependent protease inhibitor (ZPI) levels are significantly lower in pregnancies affected by fetal growth restriction (FGR). These markers show diagnostic potential for FGR screening in pregnant women.

Area of Science:

  • Biochemistry
  • Reproductive Medicine
  • Clinical Diagnostics

Background:

  • Fetal growth restriction (FGR) is a significant obstetric complication with serious implications for fetal well-being.
  • Protein Z (PZ) and its inhibitor ZPI play roles in coagulation and may be implicated in pregnancy complications.
  • Understanding the role of PZ and ZPI in FGR is crucial for developing diagnostic tools.

Purpose of the Study:

  • To investigate the expression levels of plasma PZ and ZPI in pregnancies complicated by FGR.
  • To evaluate the diagnostic value of plasma PZ and ZPI levels for identifying FGR.

Main Methods:

  • Plasma PZ and ZPI levels were measured using ELISA in three groups: FGR (n=79), healthy controls (HC, n=79), and non-pregnant controls (BC, n=60).
  • Spearman analysis was used to assess correlations between PZ, ZPI, and FGR.
  • Receiver operating characteristic (ROC) curves were employed to evaluate diagnostic performance.

Main Results:

  • Plasma PZ and ZPI levels were significantly decreased in both HC and FGR groups compared to the BC group (P < 0.001).
  • Levels of PZ and ZPI were notably lower in the FGR group than in the HC group (P < 0.01).
  • A combination of PZ and ZPI demonstrated high diagnostic accuracy (AUC = 0.92, sensitivity = 0.82, specificity = 0.88).

Conclusions:

  • Plasma PZ and ZPI levels are significantly reduced in pregnant women with FGR.
  • These decreased levels suggest that PZ and ZPI can serve as valuable biomarkers for FGR screening in pregnant populations.
Abstract

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