Literature DB >> 15292287

Stress dose of hydrocortisone is not beneficial in patients with classic congenital adrenal hyperplasia undergoing short-term, high-intensity exercise.

Martina Weise1, Bart Drinkard, Sarah L Mehlinger, Stuart M Holzer, Graeme Eisenhofer, Evangelia Charmandari, George P Chrousos, Deborah P Merke.   

Abstract

Classic congenital adrenal hyperplasia (CAH) is associated with impaired function of the adrenal cortex and medulla leading to decreased production of cortisol and epinephrine. As a result, the normal exercise-induced rise in blood glucose is markedly blunted in such individuals. We examined whether an extra dose of hydrocortisone, similar to that given during other forms of physical stress such as intercurrent illness, would normalize blood glucose levels during exercise in patients with CAH. We studied hormonal, metabolic, and cardiorespiratory parameters in response to a standardized high-intensity exercise protocol in nine adolescent patients with classic CAH. Patients were assigned to receive either an additional morning dose of hydrocortisone or placebo, in addition to their usual glucocorticoid and mineralocorticoid replacement in a randomized, double-blind, crossover design 1 h before exercising. Although plasma cortisol levels approximately doubled after administration of the additional hydrocortisone dose compared with the usual single dose, fasting and exercise-induced blood glucose levels did not differ. In addition, no differences were observed in the serum concentrations of the glucose-modulating hormones epinephrine, insulin, glucagon, and GH and of the metabolic parameters lactate and free fatty acids. Although maximal heart rate was slightly higher after stress dosing (193 +/- 3 vs. 191 +/- 3 beats/min, mean +/- sem, P < 0.05), this did not affect exercise performance or perceived exertion. We conclude that patients with classic CAH do not benefit from additional hydrocortisone during short-term, high-intensity exercise. Although this has not been tested with long-term exercise, a high degree of caution should be used when considering the frequent use of additional hydrocortisone administration with exercise, given the adverse side effects of glucocorticoid excess.

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Year:  2004        PMID: 15292287     DOI: 10.1210/jc.2003-032051

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  18 in total

1.  Adrenomedullary function in patients with nonclassic congenital adrenal hyperplasia.

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2.  Hypoglycemia during acute illness in children with classic congenital adrenal hyperplasia.

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Journal:  J Pediatr Nurs       Date:  2008-11-04       Impact factor: 2.145

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4.  Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline.

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Journal:  J Clin Endocrinol Metab       Date:  2010-09       Impact factor: 5.958

Review 5.  [Addison's disease].

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Review 6.  Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

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Authors:  Mimi S Kim; Anna Ryabets-Lienhard; Bhavna Bali; Christianne J Lane; Ashley H Park; Sandra Hall; Mitchell E Geffner
Journal:  J Clin Endocrinol Metab       Date:  2014-05-30       Impact factor: 5.958

8.  Investigation of cortisol dynamics in human sweat using a graphene-based wireless mHealth system.

Authors:  Rebeca M Torrente-Rodríguez; Jiaobing Tu; Yiran Yang; Jihong Min; Minqiang Wang; Yu Song; You Yu; Changhao Xu; Cui Ye; Waguih William IsHak; Wei Gao
Journal:  Matter       Date:  2020-02-26

9.  Corticosteroid physiology and principles of therapy.

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Journal:  Indian J Pediatr       Date:  2008-11-21       Impact factor: 1.967

10.  Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline.

Authors:  Phyllis W Speiser; Wiebke Arlt; Richard J Auchus; Laurence S Baskin; Gerard S Conway; Deborah P Merke; Heino F L Meyer-Bahlburg; Walter L Miller; M Hassan Murad; Sharon E Oberfield; Perrin C White
Journal:  J Clin Endocrinol Metab       Date:  2018-11-01       Impact factor: 5.958

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