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Wnt Signaling-Related Biomarkers in Gestational Diabetes Mellitus: Diagnostic Performance and Integrated Statistical
Yeliz Çeçen Dönmez1, Esra Keles2, İsmail Bağlar1
1Department of Obstetrics and Gynecology, University of Health Sciences, Kartal Dr. Lütfi Kırdar City Hospital, Istanbul 34865, Turkey.
Diagnostics (Basel, Switzerland)
|June 26, 2026
Summary
Wnt signaling biomarkers, Wnt-inhibitory factor 1 (WIF-1), secreted frizzled-related protein-4 (SFRP-4), and beta-catenin-1 (CTNNB1), are elevated in gestational diabetes mellitus (GDM). A combined biomarker approach shows promising diagnostic value for GDM risk stratification.
Area of Science:
- Endocrinology and Metabolism
- Molecular Biology
- Biomarker Discovery
Background:
- Gestational diabetes mellitus (GDM) is a prevalent metabolic disorder linked to insulin resistance and inflammation.
- The Wnt/β-catenin signaling pathway is implicated in metabolic dysregulation, but its role in GDM is not fully understood.
- Wnt signaling-related molecules like Wnt-inhibitory factor 1 (WIF-1), secreted frizzled-related protein-4 (SFRP-4), and beta-catenin-1 (CTNNB1) are potential biomarkers.
Purpose of the Study:
- To investigate the diagnostic value of WIF-1, SFRP-4, and CTNNB1 in gestational diabetes mellitus (GDM).
- To assess the combined diagnostic performance of these Wnt signaling biomarkers for GDM.
- To explore the relationship between these biomarkers and GDM status.
Main Methods:
- A case-control study involving 60 GDM patients and 60 healthy pregnant controls.
- Serum levels of WIF-1, SFRP-4, and CTNNB1 were quantified.
- Diagnostic performance was evaluated using Receiver Operating Characteristic (ROC) analysis and multivariable logistic regression; biomarker relationships were assessed via correlation and principal component analysis (PCA).
Main Results:
- Serum concentrations of WIF-1, SFRP-4, and CTNNB1 were significantly elevated in the GDM group (p < 0.001).
- Individual biomarkers showed moderate diagnostic ability, with CTNNB1 being the most discriminative.
- The combined biomarker panel significantly enhanced diagnostic accuracy (AUC, sensitivity, specificity) and all biomarkers remained independent predictors of GDM.
Conclusions:
- Wnt signaling biomarkers (WIF-1, SFRP-4, CTNNB1) are significantly upregulated in GDM, indicating their diagnostic potential.
- A combined biomarker strategy offers superior diagnostic performance over individual markers for GDM.
- These findings suggest a role for Wnt signaling in GDM pathogenesis and highlight potential for improved risk stratification and personalized management.
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