Cushing's syndrome is a serious endocrine disease caused by chronic, autonomous, and excessive secretion of cortisol. The syndrome is associated with increased mortality and impaired quality of life because of the occurrence of comorbidities. These clinical complications include metabolic syndrome, consisting of systemic arterial hypertension, visceral obesity, impairment of glucose metabolism, and dyslipidaemia; musculoskeletal disorders, such as myopathy, osteoporosis, and skeletal fractures; neuropsychiatric disorders, such as impairment of cognitive function, depression, or mania; impairment of reproductive and sexual function; and dermatological manifestations, mainly represented by acne, hirsutism, and alopecia. Hypertension in patients with Cushing's syndrome has a multifactorial pathogenesis and contributes to the increased risk for myocardial infarction, cardiac failure, or stroke, which are the most common causes of death; risks of these outcomes are exacerbated by a prothrombotic diathesis and hypokalaemia. Neuropsychiatric disorders can be responsible for suicide. Immune disorders are common; immunosuppression during active disease causes susceptibility to infections, possibly complicated by sepsis, an important cause of death, whereas immune rebound after disease remission can exacerbate underlying autoimmune diseases. Prompt treatment of cortisol excess and specific treatments of comorbidities are crucial to prevent serious clinical complications and reduce the mortality associated with Cushing's syndrome.

Complications of Cushing's syndrome: state of the art / Pivonello, Rosario; Isidori, Andrea; De Martino, Maria Cristina; Newell Price, John; Biller, Beverly M. K; Colao, Annamaria. - In: THE LANCET DIABETES & ENDOCRINOLOGY. - ISSN 2213-8587. - STAMPA. - 4:7(2016), pp. 611-629. [10.1016/S2213-8587(16)00086-3]

Complications of Cushing's syndrome: state of the art

ISIDORI, Andrea;
2016

Abstract

Cushing's syndrome is a serious endocrine disease caused by chronic, autonomous, and excessive secretion of cortisol. The syndrome is associated with increased mortality and impaired quality of life because of the occurrence of comorbidities. These clinical complications include metabolic syndrome, consisting of systemic arterial hypertension, visceral obesity, impairment of glucose metabolism, and dyslipidaemia; musculoskeletal disorders, such as myopathy, osteoporosis, and skeletal fractures; neuropsychiatric disorders, such as impairment of cognitive function, depression, or mania; impairment of reproductive and sexual function; and dermatological manifestations, mainly represented by acne, hirsutism, and alopecia. Hypertension in patients with Cushing's syndrome has a multifactorial pathogenesis and contributes to the increased risk for myocardial infarction, cardiac failure, or stroke, which are the most common causes of death; risks of these outcomes are exacerbated by a prothrombotic diathesis and hypokalaemia. Neuropsychiatric disorders can be responsible for suicide. Immune disorders are common; immunosuppression during active disease causes susceptibility to infections, possibly complicated by sepsis, an important cause of death, whereas immune rebound after disease remission can exacerbate underlying autoimmune diseases. Prompt treatment of cortisol excess and specific treatments of comorbidities are crucial to prevent serious clinical complications and reduce the mortality associated with Cushing's syndrome.
2016
Cushing's syndrome, clinical complications, Hypertension, Immune disorders, metabolic syndrome, diabetes, reproductive disorders, neuropsychiatric disorders
01 Pubblicazione su rivista::01a Articolo in rivista
Complications of Cushing's syndrome: state of the art / Pivonello, Rosario; Isidori, Andrea; De Martino, Maria Cristina; Newell Price, John; Biller, Beverly M. K; Colao, Annamaria. - In: THE LANCET DIABETES & ENDOCRINOLOGY. - ISSN 2213-8587. - STAMPA. - 4:7(2016), pp. 611-629. [10.1016/S2213-8587(16)00086-3]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/869810
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