# Effects of vitamin D supplementation on glucose metabolism and pregnancy outcomes in GDM: a systematic review and meta-analysis

**Authors:** Rong Luo, Huijing Wang, Yangli Cao

PMC · DOI: 10.3389/fmed.2026.1743776 · Frontiers in Medicine · 2026-02-09

## TL;DR

This study finds that vitamin D supplementation may improve glucose metabolism and reduce adverse outcomes in pregnancies with gestational diabetes.

## Contribution

A systematic review and meta-analysis showing vitamin D's potential benefits in gestational diabetes management.

## Key findings

- Vitamin D reduced fasting and postprandial glucose levels in GDM patients.
- Supplementation was linked to lower risks of cesarean delivery, preterm birth, and neonatal complications.
- No significant effects were observed for amniotic fluid excess or pre-eclampsia.

## Abstract

This systematic review and meta-analysis aimed to evaluate the efficacy and safety of vitamin D supplementation on glucose metabolism and pregnancy outcomes in gestational diabetes mellitus (GDM).

To achieve this, we searched Chinese and English databases (PubMed, EMBASE, Cochrane Library, China National Knowledge Infrastructure, Wanfang Med Online, and VipInfo Chinese Journal Service Platform) up to September 2024. Data were analyzed using Review Manager 5.3 and Stata 15.1, presenting continuous variables as standardized mean difference (SMD) and dichotomous variables as relative risk (RR), both with 95% confidence intervals (CI). The Cochrane tool assessed the risk of bias.

Twenty studies involving 1,737 patients were included. Meta-analysis showed that compared to placebo, vitamin D supplementation significantly reduced fasting glucose (SMD: −1.01, p = 0.0002), 2-h postprandial glucose (SMD: −0.89, p = 0.0002), insulin levels (SMD: −0.64, p < 0.0001), and insulin resistance (SMD: −0.91, p = 0.001). Furthermore, it was associated with lower incidences of cesarean delivery (RR: 0.68, p < 0.0001), forceps-assisted delivery (RR: 0.44, p = 0.02), preterm birth (RR: 0.28, p < 0.0001), postpartum hemorrhage (RR: 0.27, p = 0.01), fetal distress (RR: 0.17, p = 0.004), neonatal asphyxia (RR: 0.22, p = 0.006), macrosomia (RR: 0.34, p = 0.001), and neonatal hyperbilirubinemia (RR: 0.49, p = 0.001). No significant differences were found for amniotic fluid excess (RR: 0.46, p = 0.10) or pre-eclampsia (RR: 0.60, p = 0.38).

Vitamin D supplementation may improve glucose metabolism and reduce adverse pregnancy outcomes in GDM patients. However, the findings should be interpreted with caution due to substantial heterogeneity among studies and the methodological limitations of the included trials. These exploratory results highlight the need for further rigorous research to confirm the effects.

## Linked entities

- **Diseases:** gestational diabetes mellitus (MONDO:0005406), pre-eclampsia (MONDO:0005081), neonatal hyperbilirubinemia (MONDO:0006584)

## Full-text entities

- **Genes:** CSH2 (chorionic somatomammotropin hormone 2) [NCBI Gene 1443] {aka CS-2, CSB, GHB1, PL, hCS-B}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}
- **Diseases:** shoulder dystocia (MESH:D000080883), death (MESH:D003643), hypocalcemia (MESH:D006996), Polyhydramnios (MESH:D006831), toxicity (MESH:D064420), hypercalcemia (MESH:D006934), Insulin resistance (MESH:D007333), asphyxia (MESH:D001237), infection (MESH:D007239), hypoglycemia (MESH:D007003), CVD (MESH:D002318), preterm birth (MESH:D047928), premature delivery (MESH:C536271), postpartum hemorrhage (MESH:D006473), T2DM (MESH:D003924), Fetal distress (MESH:D005316), preterm labor (MESH:D007752), hyperbilirubinemia (MESH:D006932), fractures (MESH:D050723), inflammation (MESH:D007249), metabolic syndrome (MESH:D024821), Pre-eclampsia (MESH:D011225), abnormal glucose metabolism (MESH:D044882), Macrosomia (MESH:D005320), Diabetes (MESH:D003920), ischemic (MESH:D002545), jaundice (MESH:D007565), vitamin D deficiency (MESH:D014808), overweight (MESH:D050177), hypoxic encephalopathy (MESH:D002534), obese (MESH:D009765), hemorrhage (MESH:D006470), Neonatal hyperbilirubinemia (MESH:D051556), GDM (MESH:D016640), respiratory distress syndrome (MESH:D012128)
- **Chemicals:** glucose (MESH:D005947), calcium (MESH:D002118), phosphate (MESH:D010710), Vitamin D (MESH:D014807), blood glucose (MESH:D001786), progesterone (MESH:D011374), vitamin C (MESH:D001205)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926356/full.md

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Source: https://tomesphere.com/paper/PMC12926356