Adipose Tissue Remodeling Beyond Weight Loss: New Insights Into Incretin-Based Therapies and Bariatric Surgery
Abstract Purpose of the Review This review summarizes obesity-induced adaptations in subcutaneous and visceral white adipose tissue (WAT) depots and discusses how incretin-based pharmacotherapies and bariatric surgery may influence WAT remodeling beyond weight loss, drawing on evidence from animal models and human studies. Recent Findings In obesity, adipose tissue undergoes pathological remodeling characterized by structural and cellular changes, extracellular matrix (ECM) remodeling, altered endocrine signaling, and impaired mitochondrial function that contribute to metabolic comorbidities. Weight-loss interventions, including incretin-based therapies and bariatric surgery, are associated with improvements in adiposity and metabolic outcomes, and multiple studies suggest accompanying changes in inflammatory, mitochondrial/thermogenic, and endocrine pathways within WAT; however, mechanistic evidence in humans remains heterogeneous and is often limited by tissue accessibility and study design. Summary This review highlights candidate cellular and molecular mechanisms through which incretin-based pharmacotherapies and bariatric surgery may modulate WAT plasticity, emphasizing convergent and distinct effects across depots and the need for more longitudinal, tissue-level human studies to define weight-dependent remodeling versus changes not fully explained by weight loss.
Authors
- Gabriela Ferreira Abud (ORCID: https://orcid.org/0000-0002-6301-3808)
- Ellen Cristini de Freitas (ORCID: https://orcid.org/0000-0002-7343-2002)
- Kristin I. Stanford (ORCID: https://orcid.org/0000-0002-0681-7746)
Institutions
- Universidade de Ribeirão Preto (BR)
- Universidade de São Paulo (BR)
- The Ohio State University Wexner Medical Center (US)
Publication Details
- Journal
- Current Obesity Reports
- Published
- 2026-09-10
- DOI
- https://doi.org/10.1007/s13679-026-00756-x
- Primary Topic
- Adipose Tissue and Metabolism
- Type
- article
- Field-Weighted Citation Impact
- 0.00