# Influence of diabetes on survival of patients with glioma: a meta-analysis

**Authors:** Jing Yi, Jiangli Wen, Nianhua Wang, Min Yuan, Haibin Leng, Hua Chen

PMC · DOI: 10.3389/fendo.2026.1667242 · Frontiers in Endocrinology · 2026-02-12

## TL;DR

This study finds that having diabetes before being diagnosed with glioma is linked to worse survival outcomes.

## Contribution

A meta-analysis clarifying that preexisting diabetes is associated with poorer survival in glioma patients.

## Key findings

- Preexisting diabetes is associated with a 22% higher risk of death in glioma patients.
- The association between diabetes and poorer progression-free survival is statistically significant.
- The results are consistent across subgroups like tumor grade and age.

## Abstract

The prognostic impact of preexisting diabetes on glioma survival remains unclear, with conflicting evidence across studies. This meta-analysis aimed to assess the association between diabetes and survival outcomes in patients with glioma.

We systematically searched PubMed, Embase, and Web of Science up to April 30, 2025, for cohort studies reporting hazard ratios (HRs) for overall survival (OS) or progression-free survival (PFS) in glioma patients with and without preexisting diabetes. A random-effects model was used to pool multivariate-adjusted HRs accounting for the possible influence of heterogeneity.

Twelve retrospective cohort studies comprising 8,948 patients were included. Eleven studies reported on OS, and four on PFS. Pooled analysis showed that preexisting diabetes was associated with poorer OS (HR: 1.22, 95% CI: 1.10–1.36, p < 0.001; I² = 33%). Sensitivity analysis confirmed result robustness (HR range: 1.18–1.26). Subgroup analyses revealed consistent associations regardless of tumor grade (Grade III–IV: HR: 1.42; GBM: HR: 1.19; p for subgroup difference = 0.47), age (< 60 vs. ≥ 60 years, p = 0.15), sex distribution (< 60% vs. ≥ 60% men, p = 0.91), diabetes type (type 2 vs. overall diabetes, p = 0.33), or follow-up duration (≤ 12 vs. >12 months, p = 0.69). Preexisting diabetes was also associated with poorer PFS (HR: 1.36, 95% CI: 1.01–1.83, p = 0.04; I² = 0%).

Preexisting diabetes is associated with reduced survival in glioma patients. These findings highlight the importance of integrating metabolic comorbidities into glioma prognostic assessment.

https://www.crd.york.ac.uk/PROSPERO/view/CRD420251086248, identifier CRD420251086248.

## Linked entities

- **Diseases:** diabetes (MONDO:0005015), glioma (MONDO:0021042)

## Full-text entities

- **Genes:** MGMT (O-6-methylguanine-DNA methyltransferase) [NCBI Gene 4255], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** oligodendroglioma (MESH:D009837), ependymoma (MESH:D004806), HL (MESH:C538324), inflammation (MESH:D007249), GBM (MESH:D005910), metabolic disturbances (MESH:D024821), hyperglycemia (MESH:D006943), Diabetes (MESH:D003920), Tumors (MESH:D009369), prediabetes (MESH:D011236), DM (MESH:D009223), type 1 or type 2 (MESH:D003924), III to IV (MESH:D006011), pancreatic, breast, and colorectal cancers (MESH:D001943), GBM (MESH:D005909), astrocytoma (MESH:D001254), chronic (MESH:D002908), brain cancer (MESH:D001932), metastasis (MESH:D009362), III (MESH:C537189), death (MESH:D003643), Hyperinsulinemia (MESH:D006946), infections (MESH:D007239), insulin resistance (MESH:D007333)
- **Chemicals:** metformin (MESH:D008687), steroid (MESH:D013256), glucose (MESH:D005947), reactive oxygen species (MESH:D017382), dexamethasone (MESH:D003907), TMZ (MESH:D000077204)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12935661/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935661/full.md

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Source: https://tomesphere.com/paper/PMC12935661