# Association of Lifestyle‐Induced Weight Loss With Gene Expression in Subcutaneous Adipose Tissue in Metabolic Syndrome

**Authors:** Silke Zimmermann, Kirsten Roomp, Hans‐Jonas Meyer, Akash Mathew, Manuel Florian Struck, Matthias Blüher, Hugo N. G. Martin, Maria Keller, Kathrin Landgraf, Antje Körner, Anne Hoffmann, Yvonne Böttcher, Kathleen Biemann, Adhideb Ghosh, Christian Wolfrum, Falko Noé, Berend Isermann, Jochen G. Schneider, Ronald Biemann

PMC · DOI: 10.1111/1753-0407.70083 · Journal of Diabetes · 2025-04-14

## TL;DR

This study shows that lifestyle-induced weight loss changes gene activity in fat tissue, which could help predict long-term weight loss success in people with metabolic syndrome.

## Contribution

The study identifies a gene signature in subcutaneous adipose tissue associated with sustained weight loss after lifestyle interventions.

## Key findings

- 642 differentially expressed genes were identified in subcutaneous adipose tissue after 6 months of lifestyle-induced weight loss.
- Three genes (SUMO3, PRKG2, ADAP2) were strongly associated with sustained weight loss of more than 10% of initial body weight.
- Differentially expressed genes were linked to cholesterol metabolism and correlated with lipid parameters like HDL, LDL, and triglycerides.

## Abstract

Lifestyle‐induced weight loss (LIWL) is considered an effective therapy for the treatment of metabolic syndrome (MetS). The role of differentially expressed genes (DEGs) in adipose tissue function and in the success of LIWL in MetS is still unclear. We investigated the effect of 6 months of LIWL on transcriptional regulation in subcutaneous adipose tissue (SAT). Aiming to identify a LIWL‐associated “gene signature” in SAT, DEGs were fitted into a linear regression model.

The study is embedded in a prospective, two‐arm, controlled, monocentric, randomized, 6‐month interventional trial in individuals with MetS following LIWL. The trial included 43 nonsmoking, nondiabetic men aged 45–55 years with MetS.

In total, we identified 642 DEGs in SAT after 6 months of LIWL. The identified DEGs were validated in two cross‐sectional cohorts analyzing SAT from individuals with and without obesity. Gene enrichment analysis of the DEGs revealed the strongest association with cholesterol metabolic processes. Accordingly, DEGs were correlated with the lipid parameters HDL cholesterol, LDL cholesterol, and triglycerides in corresponding serum samples. We identified 3 genes with an AUC of 0.963 (95% CI: 0.906–1.0) associated with a loss of more than 10% of initial body weight that was maintained for at least 12 months after LIWL, namely SUMO3 (Small ubiquitin‐related modifier 3), PRKG2 (Protein Kinase CGMP‐Dependent 2), and ADAP2 (ArfGAP with Dual PH Domains 2).

In summary, we have identified DEGs in SAT after LIWL, which may play an important role in metabolic functions. In particular, altered gene expression in SAT may predict sustained weight loss.

## Linked entities

- **Genes:** SUMO3 (small ubiquitin like modifier 3) [NCBI Gene 6612], PRKG2 (protein kinase cGMP-dependent 2) [NCBI Gene 5593], ADAP2 (ArfGAP with dual PH domains 2) [NCBI Gene 55803]
- **Diseases:** metabolic syndrome (MONDO:0000816)

## Full-text entities

- **Genes:** PRKG2 (protein kinase cGMP-dependent 2) [NCBI Gene 5593] {aka AMD4, PKG2, PRKGR2, SMDP, cGK2, cGKII}, SUMO3 (small ubiquitin like modifier 3) [NCBI Gene 6612] {aka SMT3A, SMT3H1, SUMO-3}, ADAP2 (ArfGAP with dual PH domains 2) [NCBI Gene 55803] {aka CENTA2, HSA272195, cent-b}
- **Diseases:** LIWL (MESH:D015431), MetS (MESH:D024821), obesity (MESH:D009765)
- **Chemicals:** cholesterol (MESH:D002784), triglycerides (MESH:D014280), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC11996622/full.md

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Source: https://tomesphere.com/paper/PMC11996622