Abstract
Although obesity is an important determinant of metabolic disease, specific accumulation of visceral fat is strongly and independently associated with important metabolic alterations such as insulin resistance, hypertension, and dyslipidemia. A marked sex dimorphism and large interindividual variations are observed in fat distribution, and excess accumulation of visceral fat is a strong predictor of cardiometabolic risk in both sexes. However, adipose tissue cellularity and function are distinctly related to obesity in women and men. Women are more likely to store lipids in lower body fat compartments through adipocyte hyperplasia, while visceral adipose tissue depots of men are more prone to manage incoming lipids through adipocyte hypertrophy. Proneness to adipocyte hypertrophy appears as a critical determinant of sex-related and depot-related differences in lipid metabolism and may contribute to the chronic, low-grade inflammation observed in abdominally obese individuals. Regarding the hormonal etiology of abdominal obesity, adipose tissue exposure to active androgens is known to inhibit adipogenesis and lipogenesis. Estrogens have important central effects on energy balance, but may also directly modulate central fat accumulation through direct effects on adipose tissue metabolism. Moreover, a relatively high adipose tissue glucocorticoid reactivation by 11β-hydroxysteroid dehydrogenase type 1 appears to promote specific accumulation of visceral fat and to alter adipocyte function in humans. Interventions targeting visceral fat accumulation such as moderate weight loss are known to exert beneficial effects on cardiometabolic disease risk.
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Veilleux, A., Tchernof, A. (2012). Sex Differences in Body Fat Distribution. In: Symonds, M. (eds) Adipose Tissue Biology. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0965-6_5
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