# The association between epicardial adipose tissue thickness and diabetes mellitus, hyperlipidemia, hepatosteatosis, pancreatic steatosis and pancreatitis

**Authors:** Ece Zengin, Aybuke Ucgun, Mehmet Emir Çevik, Sehnaz Evrimler, Ihsaniye Suer Dogan, Eyüp Serhat Çalık, Eyüp Serhat Çalık, Eyüp Serhat Çalık

PMC · DOI: 10.1371/journal.pone.0343831 · PLOS One · 2026-02-26

## TL;DR

This study finds that thicker epicardial fat is linked to diabetes, high cholesterol, and pancreatitis, suggesting it could be a useful marker for metabolic health.

## Contribution

The study provides new evidence that epicardial adipose tissue thickness is a potential imaging biomarker for broader cardiometabolic and inflammatory conditions.

## Key findings

- Epicardial adipose tissue thickness is significantly associated with diabetes mellitus and LDL cholesterol levels.
- Pancreatic steatosis and LAD-EAT are significantly linked to a history of pancreatitis.
- EAT thickness correlates with cardiometabolic risk factors and may reflect systemic metabolic burden.

## Abstract

Epicardial adipose tissue (EAT) is associated with cardiometabolic disorders such as diabetes mellitus (DM), hyperlipidemia, and nonalcoholic fatty liver disease. However, its potential relationship with pancreatic steatosis and pancreatitis remains unclear, and existing studies offer inconsistent findings. Therefore, a clearer understanding of whether EAT reflects broader systemic ectopic fat burden or inflammatory processes is needed.This study evaluated the relationships between EAT thickness and DM, hyperlipidemia, hepatosteatosis, pancreatic steatosis, and pancreatitis.

This retrospective, single-center study included 200 patients who underwent abdominal CT between 2022 and 2024. EAT thickness was measured at the mid-RCA and LAD levels, and subcutaneous fat was measured at the umbilical level. Liver and pancreatic steatosis were assessed with CT or MRI. Demographic and clinical data (age, gender, LDL cholesterol, diabetes, and history of pancreatitis) were collected. Mann-Whitney U, Spearman correlation, and logistic regression were used in analyses; p < 0.05 was considered significant.

Of the 200 patients, 31.4% had diabetes, 42% had hepatosteatosis, and 73.5% had a history of pancreatitis. EAT and subcutaneous fat were significantly higher in women at all levels (p < 0.05). Diabetes was associated with increased EAT in both the RCA (p = 0.002) and the LAD (p = 0.001). In multivariate analysis, RCA-EAT (OR=1.18, p = 0.002) and age (OR=1.03, p = 0.003) were significantly associated with diabetes. High LDL was associated with LAD-EAT (p = 0.030). For pancreatitis, multivariate analysis identified pancreatic steatosis (OR=5.78, p < 0.001) and LAD-EAT (OR=1.52, p = 0.002) as variables significantly associated with a history of pancreatitis.

EAT thickness is significantly associated with DM, LDL cholesterol, pancreatitis history, and age, supporting its role as a potential imaging biomarker of cardiometabolic risk. These findings suggest that EAT may serve as an imaging marker of broader metabolic and inflammatory burden, supporting its relevance for cardiometabolic risk assessment.

## Linked entities

- **Diseases:** diabetes mellitus (MONDO:0005015), hyperlipidemia (MONDO:0021187), pancreatitis (MONDO:0004982)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ADM (adrenomedullin) [NCBI Gene 133] {aka AM, PAMP}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, NGF (nerve growth factor) [NCBI Gene 4803] {aka Beta-NGF, HSAN5, NGFB}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, ITLN1 (intelectin 1) [NCBI Gene 55600] {aka HL-1, HL1, INTL, ITLN, LFR, hIntL}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, NAMPT (nicotinamide phosphoribosyltransferase) [NCBI Gene 10135] {aka 1110035O14Rik, PBEF, PBEF1, VF, VISFATIN}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, DLD (dihydrolipoamide dehydrogenase) [NCBI Gene 1738] {aka DLDD, DLDH, E3, GCSL, LAD, OGDC-E3}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, SERPINE1 (serpin family E member 1) [NCBI Gene 5054] {aka PAI, PAI-1, PAI1, PLANH1}
- **Diseases:** dyslipidemia (MESH:D050171), hyperlipidemia (MESH:D006949), cardiometabolic disorders (MESH:D024821), inflammation (MESH:D007249), ORCID iD (MESH:C535742), Pancreatitis (MESH:D010195), DM (MESH:D003920), malignancy (MESH:D009369), NAFLD (MESH:D065626), obesity (MESH:D009765), Hepatic Steatosis (MESH:D005234), ectopic fat (MESH:D004620), metabolic disease (MESH:D008659), atherogenesis (MESH:D050197), hypertension (MESH:D006973), LAD-EAT (MESH:C535887), insulin resistance (MESH:D007333), vascular injury (MESH:D057772), familial hypercholesterolemia (MESH:D006938), cardiovascular disease (MESH:D002318), EAT (MESH:D018205), Type 1 and Type 2 DM (MESH:D003924)
- **Chemicals:** free fatty acid (MESH:D005230), Calik (-), fatty acid (MESH:D005227), lipid (MESH:D008055), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944748/full.md

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Source: https://tomesphere.com/paper/PMC12944748