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1.
Biochem Pharmacol ; 223: 116137, 2024 May.
Article in English | MEDLINE | ID: mdl-38494065

ABSTRACT

Endogenous Cushing's syndrome (CS) is a rare condition due to prolonged exposure to elevated circulating cortisol levels that features its typical phenotype characterised by moon face, proximal myopathy, easy bruising, hirsutism in females and a centripetal distribution of body fat. Given the direct and indirect effects of hypercortisolism, CS is a severe disease burdened by increased cardio-metabolic morbidity and mortality in which visceral adiposity plays a leading role. Although not commonly found in clinical setting, endogenous CS is definitely underestimated leading to delayed diagnosis with consequent increased rate of complications and reduced likelihood of their reversal after disease control. Most of all, CS is a unique model for systemic impairment induced by exogenous glucocorticoid therapy that is commonly prescribed for a number of chronic conditions in a relevant proportion of the worldwide population. In this review we aim to summarise on one side, the mechanisms behind visceral adiposity and lipid metabolism impairment in CS during active disease and after remission and on the other explore the potential role of cortisol in promoting adipose tissue accumulation.


Subject(s)
Cushing Syndrome , Hydrocortisone , Female , Humans , Hydrocortisone/metabolism , Cushing Syndrome/complications , Cushing Syndrome/genetics , Cushing Syndrome/metabolism , Adipose Tissue/metabolism , Lipid Metabolism , Heart
2.
Front Endocrinol (Lausanne) ; 13: 934675, 2022.
Article in English | MEDLINE | ID: mdl-35979433

ABSTRACT

Since the introduction of glucocorticoid (GC) replacement therapy, congenital adrenal hyperplasia (CAH) is no longer a fatal disease. The development of neonatal screening programs and the amelioration of GC treatment strategies have improved significantly life expectancy in CAH patients. Thanks to these achievements, CAH patients are now in their adulthood, but an increased incidence of cardiovascular risk factors has been reported compared to general population in this stage of life. The aim of CAH treatment is to both prevent adrenal insufficiency and suppress androgen excess; in this delicate balance, under- as well as overtreatment might be equally harmful to long-term cardiovascular health. This work examines the prevalence of metabolic features and cardiovascular events, their correlation with hormone levels and GC replacement regimen in CAH patients and focuses on precocious markers to early detect patients at higher risk and new potential treatment approaches.


Subject(s)
Adrenal Hyperplasia, Congenital , Cardiovascular Diseases , Metabolic Syndrome , Adrenal Hyperplasia, Congenital/complications , Adrenal Hyperplasia, Congenital/diagnosis , Adrenal Hyperplasia, Congenital/epidemiology , Adult , Cardiovascular Diseases/complications , Cardiovascular Diseases/etiology , Glucocorticoids/therapeutic use , Hormone Replacement Therapy , Humans , Infant, Newborn , Metabolic Syndrome/complications , Metabolic Syndrome/epidemiology
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