The pathophysiology of abdominal adipose tissue depots in health and disease
Open accessAbstract
Obesity is currently the most important contributor to ill health and expenditure worldwide. More alarming is the fact that the pediatric population parallels adults, with obesity closely associated to type 2 diabetes mellitus (T2D), cardiovascular disease, hypertension, non-alcoholic fatty liver disease, vitamin D deficiency (VDD) and certain types of cancer. The observation in the early 1950s that android or truncal adipose tissue (AT) distribution compared to gynoid had a greater association with metabolic dysfunction, in particular T2D and cardiovascular disease risk, led to the hypothesis that obesity-associated complications are not associated with fat mass per se, but the pattern of fat distribution. This concept was further supported by groups of individuals with metabolic dysfunction despite a lean phenotype, and healthy obese people protected from metabolic dysfunction. It is now well recognized that an increase in visceral AT is an independent risk factor for the development of obesity-associated comorbidities with AT depot distribution, their anatomic, cellular and molecular features defining their role. The differences and the plasticity of subcutaneous, visceral and ectopic ATs to store and release fatty acids and to synthesize and secrete adipokines, defines the metabolic outcomes. The present review will examine the phenotypic and pathophysiological differences between the different AT depots, with a particular focus on the abdominal depots and their link to metabolic complications.
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Adipose depot location greatly influences metabolic health.
“The WAT secretome is composed of cytokines, adipokines, and other factors, which can be reviewed here (12), and adipose depot location greatly influences metabolic health (13, 14).”
From Metabolic impact of endogenously produced estrogens by adipose tissue in females and males across the lifespan (2025) · cites this paper as [14]
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“The WAT secretome is composed of cytokines, adipokines, and other factors, which can be reviewed here (12), and adipose depot location greatly in fl uences metabolic health (13, 14).”
- Authors
- Walker, G. E., Marzullo, P., Ricotti, R., Bona, G., & Prodam, F.
- Affiliations
- Università degli Studi del Piemonte Orientale “Amedeo Avogadro” (IT)
- IRCCS Istituto Auxologico Italiano (IT)
- Corresponding author
- Walker, Gillian E.
- Venue
- Hormone Molecular Biology and Clinical Investigation
- Publisher
- Walter de Gruyter GmbH
- Published
- 2014-07-01
- Volume
- 19
- Issue
- 1
- Pages
- 57-74
- ISSN
- 1868-1883 (ISSN-L)
- 1868-1891
- OpenAlex
- W2067204155
- Cited by
- 90
- References
- 164
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 8 · 2023: 6 · 2022: 8 · 2021: 10 · 2020: 4 · 2019: 8 · 2018: 7 · 2017: 8 · 2016: 14 · 2015: 12
- FWCI
- 1.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Hormone Molecular Biology and Clinical Investigation (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Keywords
- abdominal fat, visceral adipose tissue, subcutaneous adipose tissue, ectopic fat, obesity, type 2 diabetes, adipokines, metabolic dysfunction, cardiovascular disease, non-alcoholic fatty liver disease, vitamin D deficiency
- MeSH terms
- Cardiovascular Diseases, Diabetes Mellitus, Type 2, Humans, Insulin Resistance, Obesity, Risk Factors, Abdominal Fat
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