Literature DB >> 18418713

Secondary hypoadrenalism.

Giuseppe Reimondo1, Silvia Bovio, Barbara Allasino, Massimo Terzolo, Alberto Angeli.   

Abstract

Secondary adrenal insufficiency (SAI) is a clinical disorder that results from hypothalamic or hypophyseal damage or from prolonged administration of supraphysiological doses of glucocorticoids. Since glucocorticoids are widely used for a variety of diseases, the prevalence of SAI is by far exceeding that of primary adrenal insufficiency. Although the presentation of adrenal insufficiency may be insidious and difficult to recognize, an appropriate adrenocortical hormone replacement could lead to a normal quality of life and longevity can be achieved. The spectrum of adrenal insufficiency ranges from overt adrenal crises to subtle dysfunctions in asymptomatic patients who may be at risk of developing acute adrenal insufficiency since their hypothalamic-pituitary-adrenal (HPA) axis cannot appropriately react to stress. Thus, identification of patients with subtle abnormalities of the HPA is mandatory for avoiding this life-threatening event in stressful conditions. The optimal tests and the optimal testing sequence for adrenal insufficiency are still matter of debate. Insulin tolerance test (ITT) could be the gold standard, as it tests the whole HPA axis, but there are some patients who pass the ITT failing the ACTH test. Various alternatives to the ITT, including the standard cosyntropin stimulation test (SST) and low-dose SST, have been proposed since the adrenal gland in SAI loses the capacity for a prompt response to ACTH stimulation. The standard ACTH dose, but not the 1 microg dose, increases adrenal blood flow and this may contribute to produce an early cortisol response of greater magnitude. Moreover, the loss of the early cortisol response to ACTH stimulation could be a specific property of adrenal insufficiency, thus being a sensitive and early marker of failing adrenal function. While the results of the SSTs are often positive in patients with long-standing and severe disease, in patients with mild or recent-onset SAI these tests, using either 250 microg or 1 microg ACTH, tend to give normal results; thus, a negative cosyntropin test result does not rule out the possibility of SAI. Further studies with a systematic comparison of the different tests in large series of patients submitted to a prolonged follow-up are needed to solve the controversy of the optimal diagnostic strategy of SAI.

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Year:  2008        PMID: 18418713     DOI: 10.1007/s11102-008-0108-4

Source DB:  PubMed          Journal:  Pituitary        ISSN: 1386-341X            Impact factor:   4.107


  70 in total

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3.  Physiological dosing of exogenous ACTH.

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4.  Threshold adrenocortical sensitivity in man and its possible application to corticotrophin bioassay.

Authors:  J Landon; V H James; M J Wharton; M Friedman
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5.  Reproducibility of the cortisol response to stimulation with a low dose of ACTH(1-24): the effect of basal cortisol levels and comparison of low-dose with high-dose secretory dynamics.

Authors:  S Crowley; P C Hindmarsh; J W Honour; C G Brook
Journal:  J Endocrinol       Date:  1993-01       Impact factor: 4.286

6.  Optimizing the diagnostic criteria for standard (250-microg) and low dose (1-microg) adrenocorticotropin tests in the assessment of adrenal function.

Authors:  M Zarković; J Cirić; M Stojanović; Z Penezić; B Trbojević; M Drezgić; M Nesovic
Journal:  J Clin Endocrinol Metab       Date:  1999-09       Impact factor: 5.958

7.  The low-dose ACTH test does not provide a useful assessment of the hypothalamic-pituitary-adrenal axis in secondary adrenal insufficiency.

Authors:  Abdulwahab M Suliman; Thomas P Smith; Mourad Labib; Tarek M Fiad; T Joseph McKenna
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8.  Adrenocorticotropin stimulation tests in patients with hypothalamic-pituitary disease: low dose, standard high dose and 8-h infusion tests.

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9.  Late-night salivary cortisol as a screening test for Cushing's syndrome.

Authors:  H Raff; J L Raff; J W Findling
Journal:  J Clin Endocrinol Metab       Date:  1998-08       Impact factor: 5.958

10.  Low-dose adrenocorticotropin test reveals impaired adrenal function in patients taking inhaled corticosteroids.

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1.  Performance of low-dose cosyntropin stimulation test handled via plastic tube.

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Review 2.  Adrenal insufficiency in pregnancy: challenging issues in diagnosis and management.

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5.  Revised GH and cortisol cut-points for the glucagon stimulation test in the evaluation of GH and hypothalamic-pituitary-adrenal axes in adults: results from a prospective randomized multicenter study.

Authors:  Amir H Hamrahian; Kevin C J Yuen; Murray B Gordon; Karen J Pulaski-Liebert; James Bena; Beverly M K Biller
Journal:  Pituitary       Date:  2016-06       Impact factor: 4.107

6.  Evaluation of antioxidant systems in pituitary-adrenal axis diseases.

Authors:  A Mancini; E Leone; A Silvestrini; R Festa; V Di Donna; L De Marinis; A Pontecorvi; G P Littarru; E Meucci
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7.  Acute adrenal crisis in an asthmatic child treated with inhaled fluticasone proprionate.

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8.  Low-dose and high-dose synacthen tests and the hemodynamic response to hydrocortisone in acute traumatic brain injury.

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Review 9.  Isolated acquired ACTH deficiency and primary hypothyroidism: a short series and review.

Authors:  M J Hannon; D J O'Halloran
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10.  Technical details influence the diagnostic accuracy of the 1 microg ACTH stimulation test.

Authors:  Matthew Wade; Smita Baid; Karim Calis; Hershel Raff; Ninet Sinaii; Lynnette Nieman
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