Department of Medicine DIMED, University of Padua, Padua, Italy; Endocrinology Unit, Department of Medicine DIMED, University-Hospital of Padua, Padua, Italy.
Department of Medicine DIMED, University of Padua, Padua, Italy; Endocrinology Unit, Department of Medicine DIMED, University-Hospital of Padua, Padua, Italy.
Biochem Pharmacol. 2024 May;223:116137. doi: 10.1016/j.bcp.2024.116137. Epub 2024 Mar 15.
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.
内源性库欣综合征(CS)是一种罕见的疾病,由于长时间暴露于升高的循环皮质醇水平,其特征为典型表型,表现为满月脸、近端肌无力、易瘀伤、女性多毛症和中心性体脂分布。由于皮质醇过多的直接和间接影响,CS 是一种严重的疾病,伴有增加的心血管代谢发病率和死亡率,内脏肥胖在其中起主要作用。尽管在内分泌科临床实践中并不常见,但内源性 CS 肯定被低估了,导致诊断延迟,随后并发症发生率增加,疾病控制后并发症逆转的可能性降低。最重要的是,CS 是一种由外源性糖皮质激素治疗引起的全身性损害的独特模型,在世界范围内相当一部分患有多种慢性疾病的人群中经常开这种药物。在这篇综述中,我们一方面旨在总结 CS 活动期和缓解后内脏肥胖和脂代谢受损的机制,另一方面探讨皮质醇在促进脂肪组织堆积中的潜在作用。