# Fats and Facts: A Meta-Analysis of Lipid Biomarkers in Endometrial Cancer

**Authors:** Ioana Adelina Clim, Ionut Flaviu Faur, Catalin Prodan-Barbulescu, Andreea-Adriana Neamtu, Paul Pasca, Cosmin Burta, Sergiu Florin Bara, Dan Brebu, Vlad Braicu, Ciprian Duta, Bogdan Totolici, Carmen Neamtu, Amadeus Dobrescu

PMC · DOI: 10.3390/life16020330 · 2026-02-14

## TL;DR

This study finds that abnormal lipid levels, like high triglycerides and low HDL, are linked to a higher risk of endometrial cancer, suggesting lipid profiling could help assess cancer risk.

## Contribution

The study provides a meta-analysis confirming a significant association between dyslipidemia and endometrial cancer risk.

## Key findings

- Elevated triglyceride levels are significantly associated with endometrial cancer.
- Reduced HDL-C levels are linked to increased endometrial cancer risk.
- Higher LDL-C levels are observed in endometrial cancer patients compared to controls.

## Abstract

Background: Endometrial cancer (EC) represents one of the most prevalent gynecological malignancies worldwide, with increasing incidence rates attributed to rising obesity, metabolic syndrome, and demographic aging. Recent evidence suggests that dyslipidemia, including elevated triglycerides (TG), low-density lipoprotein cholesterol (LDL-C), and reduced high-density lipoprotein cholesterol (HDL-C), may have a significant role in the pathogenesis of EC through inflammatory, oxidative stress, and hormonal mechanisms. Objective: This meta-analysis aims to systematically evaluate the association between serum lipid biomarkers and endometrial cancer risk by synthesizing quantitative data from observational studies. Methods: We conducted a comprehensive search of five electronic databases (PubMed, Web of Science, Scopus, EMBASE, and Cochrane) to identify studies examining lipid biomarkers in patients with EC compared to healthy controls. After screening 639 articles and applying rigorous inclusion/exclusion criteria, six studies were selected for final analysis. The standardized mean differences (SMD) were calculated with 95% confidence intervals using random-effects and fixed-effects models, considering heterogeneity assessed by the I2 statistic. Publication bias was evaluated using funnel plots and Egger’s regression test. Results: The meta-analysis revealed significantly elevated TG levels in EC patients compared to controls (SMD +0.87, 95% CI [+0.65, +1.10]), markedly reduced HDL-C levels (SMD −0.92, 95% CI [−1.15, −0.69]), and increased LDL-C levels (SMD +0.74, 95% CI [+0.50, +0.98]). The heterogeneity was moderate to substantial, with an I2 ranging from 49% to 62%. Subgroup analyses demonstrated stronger associations in Type I EC and obese patients (BMI > 30 kg/m2). Conclusions: This meta-analysis establishes a significant association between dyslipidemia and endometrial cancer risk, with elevated triglycerides and LDL-C conferring increased risk while HDL-C appears protective. These findings support the integration of lipid profiling into EC risk assessment protocols and suggest the potential preventive value of lipid-modulating interventions. Further studies are needed to establish causality and evaluate therapeutic applications.

## Linked entities

- **Diseases:** endometrial cancer (MONDO:0002447), metabolic syndrome (MONDO:0000816)

## Full-text entities

- **Genes:** CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** lipid abnormalities (MESH:D011017), lymph node metastasis (MESH:D008207), insulin resistance (MESH:D007333), gynecological malignancies (MESH:D005833), hypertension (MESH:D006973), carcinogenic (MESH:D011230), EC (MESH:D016889), lipid metabolism abnormalities (MESH:D052439), I (MESH:D006969), endometrial carcinogenesis (MESH:D063646), obese (MESH:D009765), diabetes mellitus (MESH:D003920), tumor (MESH:D009369), Dyslipidemia (MESH:D050171), metabolic syndrome (MESH:D024821), injury to (MESH:D014947), inflammation (MESH:D007249)
- **Chemicals:** Lipid (MESH:D008055), cholesterol (MESH:D002784), TG (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942389/full.md

---
Source: https://tomesphere.com/paper/PMC12942389