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      Estados de pseudo-Cushing Translated title: Pseudo-Cushing states

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          Abstract

          Síndromes de pseudo-Cushing são um grupo heterogêneo de doenças, incluindo alcoolismo, anorexia nervosa, obesidade visceral e depressão, que compartilham muitas das características clínicas e bioquímicas da síndrome de Cushing. Os mecanismos responsáveis para a gênese da síndrome de pseudo-Cushing são fracamente compreendidos. Tem sido sugerido que o hipercortisolismo da síndrome de pseudo-Cushing pode ser resultante do aumento da secreção do hormônio liberador de corticotrofina (CRH) hipotalâmico no contexto de um eixo hipotálamo-hipofisário-adrenal que, de outra maneira, está normalmente constituído. A sobreposição substancial entre as características clínicas e laboratoriais entre muitos pacientes com síndrome de Cushing e aqueles com síndrome de pseudo-Cushing pode tornar o diagnóstico diferencial difícil. Distinguir entre síndrome de pseudo-Cushing e síndrome de Cushing verdadeira é crítico para se prevenir o tratamento desnecessário e potencialmente prejudicial de tais pacientes. Esta breve revisão sumariza os principais eventos patofisiológicos das síndromes de pseudo-Cushing e fornece uma estratégia útil para o seu diagnóstico diferencial.

          Translated abstract

          Pseudo-Cushing syndromes are a heterogeneous group of disorders, including alcoholism, anorexia nervosa, visceral obesity, and depression, which share many of the clinical and biochemical features of Cushing's syndrome. The mechanisms responsible for the genesis of pseudo-Cushing's syndrome are poorly understood. It has been suggested that hypercortisolism of pseudo-Cushing syndrome may be the result of increased hypothalamic corticotrophin-releasing hormone (CRH) secretion in the context of a hypothalamic-pituitary-adrenal axis that is otherwise normally constituted. The substantial overlap in clinical and biochemical features among several patients with Cushing syndrome and those with pseudo-Cushing syndromes can make the differential diagnosis difficult. Distinguishing between pseudo-Cushing's syndrome and true Cushing's syndrome is critical for preventing the unnecessary and potentially harmful treatment of such patients. This brief review summarizes the main pathophysiological events of pseudo-Cushing syndromes and provides a useful strategy for differential diagnosis.

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          Most cited references109

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          Steroids and depression.

          Patients with endogenous depression (major affective disorder) frequently have high cortisol levels, but the diurnal rhythm is usually maintained and they do not develop the physical signs of Cushing's syndrome. On the other hand, depression is a frequent feature of Cushing's syndrome regardless of etiology, and it is often relieved when the cortisol levels are reduced, by whatever means. The mechanisms of the hypercortisolemia and resistance to dexamethasone suppression commonly found in endogenous depression are poorly understood; contrary to expectations, ACTH levels are not clearly elevated. There is a striking difference in the psychiatric features seen in endogenous hypercorticism compared to those seen after exogenous administration of glucocorticoids or ACTH. This suggests that either there are other stimulating or modifying factors besides ACTH or that the steroids stimulated by ACTH or other peptides differ from those in control subjects, i.e. there may be an alteration in the metabolism of steroids in depression. Little is known about the metabolic changes or the many steroids besides glucocorticoids produced by the hyperactive steroid-producing tissue. Preliminary studies suggest that major depression may be improved by steroid suppression. It is hypothesized that steroids themselves may be important in causing and perpetuating depression.
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            Alterations in the hypothalamic-pituitary-adrenal axis in actively drinking alcoholics.

            A Dobs, G Wand (1991)
            The impact of chronic alcohol abuse on the hypothalamic-pituitary-adrenal (HPA) axis was investigated in actively drinking, nondepressed alcoholics with no evidence of liver disease. Fourteen male alcoholics and 13 matched nonalcoholics were studied. Although alcoholics and controls had similar decrements in cortisol levels after metyrapone blockade, plasma ACTH and 11-deoxycortisol levels in alcoholics were 60% (P less than 0.05) and 40% (P less than 0.05), respectively, of control values. To further clarify defects in the HPA axis of the alcoholic group, each subject underwent a CRH stimulation test. Compared to control subjects, alcoholics had a significantly blunted plasma ACTH response to CRH stimulation (P less than 0.05). Timing of the peak plasma ACTH response was altered in alcoholics. Whereas all control subjects had a peak plasma ACTH response 30 min after CRH administration, 50% of alcoholics demonstrated a peak plasma ACTH response 60 min after CRH administration, and 50% demonstrated a peak plasma ACTH response 30 min after CRH. To determine if adrenal function was also impaired, alcoholics and controls underwent a standard (250 micrograms) and a submaximal (0.250 micrograms) Cortrosyn stimulation test. Controls demonstrated a significant cortisol response to both standard and low dose Cortrosyn. Although alcoholics had a cortisol response similar to that of controls after the standard dose of Cortrosyn, they did not have a statistically significant rise in cortisol after the submaximal dose of Cortrosyn. Twenty-four-hour urinary free cortisol levels were 2-fold higher in alcoholics compared to controls. In summary, although a subset of alcoholics demonstrated enhanced basal production of cortisol, most alcoholics had a blunted response to acute intervening stress, including CRH, low dose ACTH-(1-24), and metyrapone blockade. These data suggest that alcoholics have ethanol-induced HPA axis injury, resulting in an inappropriately reduced response to nonethanol-induced stress.
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              Cushing's syndrome: a review of diagnostic tests.

              L M Crapo (1979)
              This review presents an analysis and interpretation of the published experimental data that form the basis for laboratory tests commonly used for screening, definitive diagnosis, and differential diagnosis in Cushing's syndrome. The single-dose overnight dexamethasone suppression test is excellent for screening outpatients since this test has a very low incidence of false-negative results (1.9% of 154 patients with Cushing's syndrome). The definitive diagnosis of Cushing's syndrome is best established by combining basal state measurements of the daily urine-free cortisol excretion and late evening plasma cortisol levels with the 2-mg low-dose dexamethasone suppression test. The etiology of Cushing's syndrome is best determined by combining measurements of basal state plasma adrenocorticotropin (ACTH) levels with the 8-mg high-dose dexamethasone suppression test. Under certain conditions, the basal state daily urine excretion of 17-hydroxycorticosteroids and 17-ketogenic steroids, the insulin tolerance test, and the metyrapone test may be useful in the definitive or differential diagnosis of Cushing's syndrome.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Journal
                abem
                Arquivos Brasileiros de Endocrinologia & Metabologia
                Arq Bras Endocrinol Metab
                Sociedade Brasileira de Endocrinologia e Metabologia (São Paulo )
                1677-9487
                November 2007
                : 51
                : 8
                : 1303-1313
                Affiliations
                [1 ] Universidade de São Paulo Brazil
                Article
                S0004-27302007000800016
                10.1590/S0004-27302007000800016
                5a95f1d1-4dce-436c-995e-ff7df7fe911e

                http://creativecommons.org/licenses/by/4.0/

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                SciELO Brazil

                Self URI (journal page): http://www.scielo.br/scielo.php?script=sci_serial&pid=0004-2730&lng=en
                Categories
                ENDOCRINOLOGY & METABOLISM

                Endocrinology & Diabetes
                Pseudo-Cushing,Hypercortisolism,ACTH,Cushing syndrome,Síndrome de Cushing,Hipercortisolismo

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