Obesity

Sex-specific Association Between Adipose Tissue Inflammation and Vascular and Metabolic Complications of Obesity

J Clin Endocrinol MetabPublished Cross-sectional study

Authors' conclusion

Inflammation in abdominal subcutaneous adipose tissue is more related to the metabolic than the atherosclerotic complications of obesity, and there are profound sex-specific differences in the association between BMI, adipocyte size, AT inflammation, and systemic inflammation, which are much stronger in men than women.

Study context

Population
Adults with body mass index (BMI) ≥ 27 kg/m², university hospital in the Netherlands
Participants
302 adults
Exposure
Associations of adipose tissue (AT) inflammation parameters with metabolic and atherosclerotic complications, men vs women
Outcome
Associations of AT inflammation parameters (adipocyte size, macrophage content, crown-like structures, gene expression) with systemic inflammation biomarkers, leukocyte number and function, metabolic syndrome, insulin resistance and carotid atherosclerotic plaques (US)
Methodological detailssingle-centre, sex-specific analysis
  • Single-centre
  • Sex-specific analysis

Main finding

As reported in the abstract

AT inflammation and obesity complications
  • Adipocyte size associated with metabolic syndrome
  • AT macrophage content associated with insulin resistance
  • No AT parameter associated with carotid atherosclerosis
  • AT IL-37 mRNA expression associated with lower intima-media thickness
  • Associations between BMI and adipocyte size, and between adipocyte size and metabolic syndrome, in men only
  • In men only: association between adipocyte size, AT leptin and MCP-1 expression and AT macrophage numbers, and between crown-like structure number and circulating inflammatory proteins incl. high specificity C-reactive protein and IL-6

Observational data: associations, not effects.

Original publication

Sex-specific Association Between Adipose Tissue Inflammation and Vascular and Metabolic Complications of Obesity. J Clin Endocrinol Metab. Published 4 April 2023. doi:10.1210/clinem/dgad193

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