# The serum gamma-glutamyl transpeptidase-to-platelet ratio predicts HELLP syndrome

**Authors:** Jiaying Chen, Hao Gu, Hongqin Wu, Minhui Jiang, Ying Gu, Yaling Feng

PMC · DOI: 10.1186/s12884-025-07431-4 · 2025-03-15

## TL;DR

The study finds that a blood test measuring gamma-glutamyl transpeptidase to platelet ratio (GPR) can predict HELLP syndrome, a serious pregnancy complication.

## Contribution

The study introduces GPR as a novel non-invasive predictor for HELLP syndrome and its adverse outcomes during pregnancy.

## Key findings

- GPR levels were significantly higher in late pregnancy and before delivery in HELLP syndrome patients compared to controls.
- GPR showed higher predictive accuracy than other markers like AST, ALT, and PLT in detecting HELLP syndrome.
- Abnormal GPR elevation was correlated with preterm birth and identified as an independent risk factor for HELLP syndrome.

## Abstract

HELLP (Hemolysis, elevated liver enzymes, and low platelets) syndrome is a dangerous obstetric condition that is in great need of simple and inexpensive non-invasive early predictors, but it has been poorly studied. This study was conducted to investigate the predictive role of serum gamma-glutamyl transpeptidase to platelet ratio (GPR) during pregnancy in HELLP syndrome and its adverse pregnancy outcomes.

This was a retrospective study in a tertiary hospital. One hundred parturients were allocated into two groups: HELLP group (n = 50) and control group (n = 50).

① In the HELLP group, the maternal GPR levels showed a continuous upward trend from middle pregnancy to before-delivery, with significantly higher values observed in late pregnancy and before-delivery compared to the control group (P < 0.05). ② A comparison was made between the counts of platelets (PLT), plasma fibrinogen (FIB), alanine transaminase (ALT), aspartate transaminase (AST), uric acid (UA), γ-glutamyl transferase (GGT), and GPR in two groups of the pregnant women during their late pregnancy and before-delivery to the hospital, all of which showed statistically significant differences (P < 0.05). ③Multivariate logistic regression analysis showed that higher GPR, ALT, and UA were independent risk factors for the development of HELLP syndrome (OR = 23.382, 1.169,1.016, P < 0.05), while higher FIB was a protective factor (OR = 0.057, P < 0.05). ④ Spearman correlation analysis indicated that the abnormal elevation of GPR in late pregnancy and before-delivery was correlated with preterm birth (r = 0.510, 0.450, P < 0.05). ⑤ROC curve analysis revealed that the predictive efficacy of GPR in late pregnancy (AUC = 0.8441) was higher than AST (AUC = 0.7960), ALT (AUC = 0.7952), and PLT (AUC = 0.7691) in late pregnancy, with an AUC of 0.8656 for GPR before delivery When GPR values were 0.22 and 0.27 in late pregnancy and before-delivery, the sensitivity for predicting HELLP syndrome was 77.6% and 78%, and the specificity was 85% and 90%.

The abnormal increase of GPR during pregnancy has a certain predictive effect on HELLP syndrome and its adverse pregnancy outcomes.

## Linked entities

- **Diseases:** HELLP syndrome (MONDO:0008585)

## Full-text entities

- **Genes:** LOC102724197 (inactive glutathione hydrolase 2) [NCBI Gene 102724197] {aka GGT2}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** low platelets (MESH:D009800), HELLP (MESH:D017359), preterm birth (MESH:D047928), Hemolysis (MESH:D006461), liver enzymes (MESH:D017093)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11910866/full.md

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Source: https://tomesphere.com/paper/PMC11910866