# Distinct metabolic associations of subcutaneous and visceral adipocyte morphology in women with or without obesity

**Authors:** Pailin Maikaew, Trittamon Phattanakiatsakul, Chantacha Sitticharoon, Issarawan Keadkraichaiwat

PMC · DOI: 10.1038/s41598-025-25101-5 · Scientific Reports · 2025-11-21

## TL;DR

The study found that enlarged visceral fat cells are more strongly linked to metabolic issues in non-obese women than in obese women, suggesting a possible limit to fat cell expansion in obesity.

## Contribution

The study reveals distinct metabolic associations of adipocyte morphology in obese and non-obese women, emphasizing the adiponectin/leptin ratio as a sensitive biomarker.

## Key findings

- Enlarged visceral adipocytes correlate more strongly with metabolic dysregulation in non-obese individuals.
- The serum adiponectin/leptin ratio is an independent predictor of adipocyte geometry in both obese and non-obese participants.
- Obese individuals show weaker or no correlations between adipocyte size and metabolic parameters.

## Abstract

This study aimed to compare subcutaneous and visceral adipocyte geometries, clinical, metabolic, hormonal, and gene expression parameters, between participants with insulin resistance (IR; n = 6) and without IR (n = 28). Additionally, correlations between these factors and adipocyte geometries were analyzed in 27 participants, including 14 with obesity and 13 without obesity, due to limited tissue availability. In a cross-sectional study at a tertiary hospital, 34 female patients undergoing intra-abdominal surgery were recruited. Participants with IR had higher serum leptin and larger visceral adipocytes but lower serum omentin and adiponectin/leptin ratio, despite comparable gene expression. Visceral adipocyte geometries showed positive correlations with IR parameters (glucose and HOMA-IR) only in individuals without obesity, but exhibited negative correlations with QUICKI, serum adiponectin, adiponectin/leptin ratio, omentin, and/or visfatin in both groups, with generally stronger correlations observed in individuals without obesity. Importantly, enlarged adipocytes were associated with lower subcutaneous and visceral adiponectin, omentin, and visfatin mRNA expression in individuals with obesity, and with higher visceral LEP mRNA expression in individuals without obesity. Multiple regression analysis identified the serum adiponectin/leptin ratio as an independent predictor of adipocyte geometries in both participants with and without obesity, and body weight in individuals without obesity. In conclusion, enlarged visceral adipocytes were more strongly associated with metabolic dysregulation in individuals without obesity, while individuals with obesity exhibited mostly weaker or no correlations, possibly due to reduced capacity for further adipocyte expansion and pre-existing metabolic impairments. The serum adiponectin/leptin ratio is a sensitive biomarker reflecting adipocyte function and morphology.

The online version contains supplementary material available at 10.1038/s41598-025-25101-5.

## Linked entities

- **Genes:** LEP (leptin) [NCBI Gene 3952], ITLN1 (intelectin 1) [NCBI Gene 55600], NAMPT (nicotinamide phosphoribosyltransferase) [NCBI Gene 10135]
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** NAMPT (nicotinamide phosphoribosyltransferase) [NCBI Gene 10135] {aka 1110035O14Rik, PBEF, PBEF1, VF, VISFATIN}, 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}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}
- **Diseases:** metabolic (MESH:D008659), obesity (MESH:D009765), metabolic dysregulation (MESH:D021081), IR (MESH:D007333)
- **Chemicals:** glucose (MESH:D005947)
- **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/PMC12639111/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12639111/full.md

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Source: https://tomesphere.com/paper/PMC12639111