Aug 2026· Frontiers in Oncology· Vol 16· 0 citations· 52 references
Medicine
TL;DR
Current longitudinal evidence suggests that MetS is associated with a modest but significant increase in the risk of incident OC, and findings for individual MetS components are exploratory and hypothesis-generating.
Abstract
Background Metabolic syndrome (MetS) has been implicated in the development of several malignancies, but its association with oral cancer (OC) remains uncertain. This meta-analysis aimed to evaluate the association between MetS and the risk of incident OC. Methods PubMed, Embase, and Web of Science were systematically searched from inception to May 11, 2026. Longitudinal cohort studies comparing the incidence of OC between adults with and without MetS were included. Hazard ratios (HRs) and 95% confidence intervals (CIs) were pooled using random-effects models accounting for potential heterogeneity. Results Four cohort studies comprising 6,370,396 participants and 4,539 incident OC cases were included. One study reported sex-specific estimates, resulting in five datasets for the primary meta-analysis. Overall, MetS was associated with a significantly increased risk of OC (HR: 1.12, 95% CI: 1.04–1.20; p = 0.001), with low heterogeneity (I² = 8%). Leave-one-out sensitivity analyses yielded consistent results (pooled HRs: 1.08–1.16). Subgroup analysis showed no significant difference between men and women (HR: 1.14 vs. 1.02; p for subgroup difference = 0.35). Exploratory analyses indicated that hypertriglyceridemia (HR: 1.07, 95% CI: 1.00–1.14; p = 0.04) and hyperglycemia (HR: 1.22, 95% CI: 1.10–1.36; p < 0.001) were significantly associated with increased OC risk, whereas central obesity, low high-density lipoprotein cholesterol, and hypertension were not. Conclusions Current longitudinal evidence suggests that MetS is associated with a modest but significant increase in the risk of incident OC. Findings for individual MetS components are exploratory and hypothesis-generating. Systematic review registration https://www.crd.york.ac.uk/PROSPERO/, identifier CRD420261432959.
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BACKGROUND
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METHODS
We conducted a systematic review and meta-analysis following PRISMA guidelines. PubMed/MEDLINE, Embase, Scopus and CENTRAL were searched th...
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