First-Trimester Leukoglycemic Index and the Risk of Gestational Diabetes Mellitus: Diagnostic Performance and Predictive Value (Analytical-Retrospective Cohort Study)
Journal of Clinical Obstetrics and Gynecology, cilt.36, sa.2, ss.43-50, 2026 (ESCI, Scopus, TRDizin)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 36 Sayı: 2
- Basım Tarihi: 2026
- Doi Numarası: 10.5336/jcog.2026-117624
- Dergi Adı: Journal of Clinical Obstetrics and Gynecology
- Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, Central & Eastern European Academic Source (CEEAS), EMBASE, TR DİZİN (ULAKBİM), Academic Search Ultimate (EBSCO)
- Sayfa Sayıları: ss.43-50
- Anahtar Kelimeler: Gestational diabetes mellitus, Leukoglycemic Index, early pregnancy, oral glucose tolerance test
- Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
- Sağlık Bilimleri Üniversitesi Adresli: Evet
Özet
Objective: To assess whether the first-trimester Leukoglycemic Index (LGI) predicts the later development of gestational diabetes mellitus (GDM) and what its diagnostic performance is, as well as the incremental predictive value beyond conventional clinical risk factors. Material and Methods: This single-center retrospective cohort study included 986 pregnant women who had first-trimester leukocyte count and fasting plasma glucose values available, with documented 75-g oral glucose tolerance test results at 24-28 weeks. LGI was calculated by multiplying leukocyte count by fasting plasma glucose. Diagnostic performance was assessed by receiver operating characteristic analysis and area under the curve (AUC) for independent predictors identified through multivariable logistic regression. Model improvement will be assessed using net reclassification improvement (NRI) and integrated discrimination improvement (IDI), while clinical usefulness can be determined through decision curve analysis. Results: GDM was developed in 24.9% of participants. LGI was significantly higher in women who developed GDM (p<0.001) and remained an independent predictor together with age and body mass index. LGI has a good discriminatory ability (AUC=0.74), outperforming fasting glucose and leukocyte count. Adding LGI to the clinical model increased the AUC from 0.73 to 0.81 with meaningful reclassification gains (NRI=0.17; IDI=0.04). Conclusion: First-trimester LGI is a simple index reflecting both inflammatory burden and glycemic load that significantly improves early GDM prediction when added to routine clinical models; hence, supporting it as a promising adjunct biomarker but requiring prospective multicenter validation for wide implementation.