# A positive linear association between uric acid and the risk of gestational diabetes mellitus: a single-center retrospective study

**Authors:** Mengfan Zhang, Chunbo Li, Xiaoli Zhao, Mengchun Li, Zhaohua Tian

PMC · DOI: 10.3389/fendo.2026.1685036 · Frontiers in Endocrinology · 2026-02-10

## TL;DR

Higher uric acid levels in pregnant women before 24 weeks are linked to a greater risk of gestational diabetes mellitus later in pregnancy.

## Contribution

This study identifies a positive linear association between maternal uric acid levels and gestational diabetes mellitus risk in a Chinese cohort.

## Key findings

- Each 1 µmol/L increase in uric acid was associated with a 0.5% higher risk of GDM.
- Women in the highest UA tertile had over double the risk of GDM compared to the lowest tertile.
- Uric acid showed limited but significant predictive value for GDM (AUC = 0.623).

## Abstract

This study aimed to examine the association between maternal uric acid (UA) concentrations measured prior to 24 weeks of pregnancy and the risk of gestational diabetes mellitus (GDM) between 24 and 28 weeks.

In this retrospective cohort conducted at a single institution, 847 expectant mothers receiving prenatal services at Zhengzhou People’s Hospital from August to December 2024 were enrolled. All participants had their UA levels measured prior to 24 gestational weeks, followed by a 75 g oral glucose tolerance assessment conducted between weeks 24 and 28. Multivariable logistic regression analysis was performed to evaluate the association between UA levels and the risk of GDM, supplemented by subgroup analysis, sensitivity analysis, and analytical procedures including receiver operating characteristic (ROC) curve evaluation and modeling with restricted cubic spline (RCS).

Among 847 enrolled pregnancies, the proportion with GDM was 21.1% (n = 179). Multivariate logistic regression showed that each 1 µmol/L or each one-standard-deviation elevation in serum UA corresponded to a markedly greater risk of GDM (OR: 1.005, 95% CI: 1.001–1.009; OR: 1.274, 95% CI: 1.062–1.528, respectively). In comparison to the lowest UA tertile (T1), T2 and T3 exhibited elevated risk for GDM, with ORs of 1.976 (95% CI: 1.203–3.247) and 2.468 (95% CI: 1.520–4.007), respectively. Subgroup analyses revealed that in women aged > 30, with gravidity < 2, parity < 2, or body mass index before conception below 24 kg/m2, both continuous and categorical UA demonstrated a clear and statistically meaningful association with GDM. Sensitivity analyses supported consistent results, with both median- and quartile-based groupings showing a significant association between higher UA levels and greater GDM risk (P < 0.05). ROC curve analysis suggested that serum UA provided limited yet statistically significant discriminative information for GDM (AUC = 0.623). RCS modeling revealed a notable positive linear association between UA concentrations and the risk of GDM (P for nonlinearity = 0.140).

Higher maternal serum UA measurements taken prior to 24 gestational weeks were strongly linked to GDM risk during weeks 24–28.

## Linked entities

- **Chemicals:** uric acid (PubChem CID 1175)
- **Diseases:** gestational diabetes mellitus (MONDO:0005406)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, SLC2A9 (solute carrier family 2 member 9) [NCBI Gene 56606] {aka GLUT9, GLUTX, UAQTL2, URATv1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** hyperuricemia (MESH:D033461), glucose intolerance (MESH:D018149), type 2 diabetes (MESH:D003924), adipose tissue (MESH:D018205), UA (MESH:D011015), heart diseases (MESH:D006331), preterm birth (MESH:D047928), neonatal hypoglycemia (MESH:D007003), endocrine or metabolic disorders (MESH:D004700), insulin resistance (MESH:D007333), hypertensive disorders (MESH:D006973), CL (MESH:D002971), metabolic (MESH:D008659), respiratory distress syndrome (MESH:D012128), systemic lupus erythematosus (MESH:D008180), GDM (MESH:D016640), Diabetes (MESH:D003920), endothelial dysfunction (MESH:D014652), macrosomia (MESH:D005320), preeclampsia (MESH:D011225), chronic kidney disease (MESH:D051436), abnormal glucose metabolism (MESH:D044882), inflammation (MESH:D007249), metabolic syndrome (MESH:D024821), gout (MESH:D006073)
- **Chemicals:** glucose (MESH:D005947), creatinine (MESH:D003404), lipid (MESH:D008055), purine (MESH:C030985), FPG (-), sodium (MESH:D012964), C-peptide (MESH:D002096), cholesterol (MESH:D002784), bilirubin (MESH:D001663), UA (MESH:D014527), triglycerides (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929156/full.md

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Source: https://tomesphere.com/paper/PMC12929156