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This version published online on May 29, 2007
Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2007-0493
A more recent version of this article appeared on August 1, 2007
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Submitted on March 5, 2007
Accepted on May 22, 2007

Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glycemic Control During Prolonged Moderate-Intensity Exercise

Liza Green-Golan, Catherine Yates, Bart Drinkard, Carol VanRyzin, Graeme Eisenhofer, Martina Weise, and Deborah P. Merke*

National Institutes of Health Clinical Center, Pediatric Endocrinology, Walter Reed Army Medical Center, Washington, DC, Rehabilitation Medicine Department, National Institutes of Health, Clinical Neurocardiology Section, National Institute of Neurological Disorders and Stroke, Reproductive Biology and Medicine Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD

* To whom correspondence should be addressed. E-mail: dmerke{at}mail.nih.gov.

Context: Patients with classic congenital adrenal hyperplasia (CAH) have adrenomedullary dysplasia and hypofunction and their lack of adrenomedullary reserve has been associated with defective glucose response to brief high-intensity exercise.

Objective: To assess hormonal, metabolic and cardiovascular response to prolonged moderate-intensity exercise comparable to brisk walking in adolescents with classic CAH.

Subjects and Methods: We compared six adolescents with classic CAH (16 to 20 yr) with seven age, sex, and BMI group-matched controls (16 to 23 yr) using a 90-minute standardized ergometer test. Metabolic, hormonal and cardiovascular parameters were studied during exercise and recovery.

Results: Glucose did not change throughout exercise and recovery for controls, whereas CAH patients showed a steady decline in glucose during exercise with an increase in glucose in the post-exercise period. Glucose levels were significantly lower in CAH patients at 60 (P=0.04), 75 (P=0.01) and 90 (P=0.03) minutes of exercise and 15 (P=0.02) minutes post-exercise; while glucose levels were comparable between the two groups early in exercise and at 30 (P=0.19) minutes post-exercise. As compared to controls, CAH patients had significantly lower epinephrine (P=0.002) and cortisol (P≤0.001) levels throughout the study and similar norepinephrine, glucagon and growth hormone levels. Patients with CAH and controls had comparable cardiovascular parameters and perceived level of exertion. Despite having lower glucose levels, insulin levels were slightly higher in CAH patients during the testing period (P=0.17), suggesting insulin insensitivity.

Conclusion: CAH patients have defective glycemic control and altered metabolic and hormonal responses during prolonged moderate-intensity exercise comparable to brisk walking.


Key words: exercise • epinephrine • glucose • congenital adrenal hyperplasia • adrenal




This article has been cited by other articles:


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J. Clin. Endocrinol. Metab.Home page
D. P. Merke
Approach to the Adult with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
J. Clin. Endocrinol. Metab., March 1, 2008; 93(3): 653 - 660.
[Abstract] [Full Text] [PDF]




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