Analysis of the clinical value of serum MMP-9 and VEGF expression levels in the prenatal diagnosis of patients with aggressive placenta previa.

Authors

Pei Zhang

Published in

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. Volume 38. Issue 1. Pages 2470414. Epub Mar 16, 2025.

Abstract

To investigate the diagnostic efficacy and detection value of matrix metalloproteinase-9 (MMP-9) and VEGF in menacing pernicious placenta previa (PPP).
Among all the cases of PPP, a critical condition within the Placenta Accreta Spectrum (PAS) caused by aberrant implantation of the placenta in the uterine wall, which were analyzed between April 2021 and March 2023, there were sixty-three cases. The control group consisted of those sixty-three women who had a normal placenta. Serum levels of MMP-9 and VEGF were measured and compared in both groups. The expression levels of MMP-9 and VEGF were analyzed along with ultrasound scores related to different degrees of placental implantation. Comparisons between groups were performed using t-tests and one-way ANOVA. The diagnostic efficacy of each of the indicators was determined using receiver operating characteristic (ROC) curves by calculating the area under the curve (AUC) and Youden's index.
MMP-9, VEGF expression, and ultrasound scores of pregnant women in the PPP group were significantly higher than those in the control group (p < 0.05). Logistic regression analysis demonstrated that MMP-9, VEGF, and ultrasound scores were significantly associated with PPP (p < 0.05). ROC curves indicated that serum MMP-9, VEGF, and ultrasound scores predicted the AUC of 0.802, 0.817, and 0.983 for PPP, respectively. The Youden's index values were 0.492, 0.540, and 0.826, respectively.
MMP-9, VEGF, and ultrasound scores help predict placental implantation in PPP, which, in turn, provides significant support for clinical understanding.

PMID:
40090739
Bibliographic data and abstract were imported from PubMed on 17 Mar 2025.

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