Oxidative stress biomarkers for fetal growth restriction in umbilical cord blood: A scoping review
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Updated: Jun 20, 2026

Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
Evelien L Blok1, Renée J Burger1, Jenny E Van Bergeijk2
1Amsterdam UMC Location University of Amsterdam, Department of Obstetrics and Gynaecology, Meibergdreef 9, Amsterdam, the Netherlands; Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands.
Insights
Cord blood oxidative stress biomarkers can help identify newborns with fetal growth restriction. Total oxidant/antioxidant status, catalase, glutathione, ischemia-modified albumin, and nucleated red blood cells show promise for a new diagnostic tool.
Area of Science:
- Perinatal Medicine
- Biomarker Discovery
- Oxidative Stress Research
Background:
- Fetal growth restriction (FGR) and placental insufficiency are linked to increased oxidative stress.
- Current diagnostic methods for FGR often miss affected newborns, focusing primarily on size.
- Early identification of FGR is crucial for timely monitoring and support due to associated health risks.
Purpose of the Study:
- To review and synthesize evidence on the utility of cord blood oxidative stress biomarkers for identifying growth-restricted newborns.
- To assess the potential of these biomarkers in developing a diagnostic tool for clinical application.
Main Methods:
- A scoping review of MEDLINE and EMBASE databases (inception to May 2024).
- Inclusion criteria: studies measuring oxidative stress biomarkers in cord blood of suspected FGR newborns.
- Biomarkers were categorized by origin/function, and associations with FGR were analyzed.
Main Results:
- 78 studies involving 39 biomarkers, 2707 FGR newborns, and 4568 controls were analyzed.
- Total oxidant/antioxidant status, catalase, glutathione, ischemia-modified albumin, and nucleated red blood cells were consistently associated with suspected FGR.
- Other biomarkers, including reactive oxygen species and antioxidant enzymes, showed inconsistent associations.
Conclusions:
- Cord blood oxidative stress biomarkers offer potential for identifying growth-restricted newborns.
- Total oxidant/antioxidant status, catalase, glutathione, ischemia-modified albumin, and nucleated red blood cells are promising candidates for a novel diagnostic tool.
- Further development could lead to improved clinical monitoring and support for affected infants.
Abstract:
Fetal growth restriction and underlying placental insufficiency are associated with increased oxidative stress. Current diagnostics fail to identify all growth restricted fetuses and newborns, due to focus on small size. This scoping review aims to summarize the available evidence on usefulness of cord blood oxidative stress biomarkers for identification of growth restricted newborns in need of monitoring and support because of associated health risks. MEDLINE and EMBASE were searched from inception to May 2024. Studies were included if oxidative stress biomarkers were measured in cord blood collected immediately after delivery in newborns suspected to be growth restricted. Biomarkers were categorized based on the origin and/or biological function and their interrelationships. Oxidative stress was determined for each individual biomarker and category. Literature search identified 78 studies on 39 different biomarkers, with a total of 2707 newborns with suspected growth restriction, and 4568 controls. Total oxidant/antioxidant status, catalase, glutathione, ischemia-modified albumin, and nucleated red blood cells were most consistently associated with suspected growth restriction. Reactive oxygen species/reactive nitrogen species, factors in their production, antioxidant enzymes, non-enzymatic antioxidants, and products of oxidative stress were not consistently associated. This review collates the evidence of associations between cord blood oxidative stress biomarkers and growth restriction. Total oxidant/antioxidant status, catalase, glutathione, ischemia-modified albumin, and nucleated red blood cells could potentially be candidates for developing a cord blood diagnostic tool for future clinical use.
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