Key result
Adiposopathy linked to multisystem endocrine and metabolic derangements that augment cardiovascular risk.
Why the study?
Adiposopathy is linked to immune, metabolic, and endocrine disturbances that promote inflammation and cardiovascular disease, with unclear pathways involving thyroid disease and cardiovascular risk.
Adiposopathy may warrant endocrine assessment in CV risk stratification; leaves open causal pathways and therapeutic targets for validation.
Adiposopathy, defined as functionally disturbed adipose tissue mainly composed of large adipocytes and induced by chronic excess of food intake, has been associated with immune, metabolic and endocrine derangements promoting inflammation and, eventually, cardiovascular disease. Adiposopathy may positively influence thyrotropin-stimulating hormone, by raising leptin levels, and triggering autoimmunity. In this regard, it is hypothesized that the increased thyrotropin-stimulating hormone is independent of the negative regulation of the thyroid hormone, thereby constituting a secondary phenomenon and not a causal effect. Replacement therapy with thyroid hormones should therefore be applied following strict individualized consideration. Leptin is involved in the immune response and neuroendocrine appetite regulation, while leptin resistance may further promote autoimmune disease. The lipid derangement in adiposopathy may be aggravated in the presence of hypothyroidism and thus considerably augment cardiovascular risk. Lifestyle-modification counselling, including low-fat dietary intake and regular physical exercise, is today the cornerstone of adiposopathy treatment. Meanwhile, new drug formulations, such as leptin and leptin analogs, 5-HT2C-receptor agonist, and potent thyromimetics, currently comprise a promising armamentarium against adiposity and adiposopathy.
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Duntas et al. (2012) conducted a review in Adiposopathy and thyroid disease. Adiposopathy was evaluated. Adiposopathy is associated with immune, metabolic, and endocrine derangements, including altered thyroid function, which may considerably augment cardiovascular risk.
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