Adrenomedullary dysplasia and hypofunction in patients with classic 21-hydroxylase deficiency.

被引:174
作者
Merke, DP
Chrousos, GP
Eisenhofer, G
Weise, M
Keil, MF
Rogol, AD
Van Wyk, JJ
Bornstein, SR
机构
[1] NIH, Warren Grant Magnuson Clin Ctr, Bethesda, MD 20892 USA
[2] NICHHD, Pediat & Reprod Endocrinol Branch, Bethesda, MD 20892 USA
[3] NINDS, Clin Neurocardiol Sect, Bethesda, MD 20892 USA
[4] Univ Virginia Hlth Syst, Charlottesville, VA USA
[5] Univ N Carolina, Sch Med, Dept Pediat, Chapel Hill, NC USA
关键词
D O I
10.1056/NEJM200011093431903
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Glucocorticoids are essential for the normal development and functioning of the adrenal medulla. Whether adrenomedullary structure and function are normal in patients with congenital adrenal hyperplasia is not known. Methods: We measured plasma and urinary catecholamines and plasma metanephrines in 38 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (25 children with the salt-wasting form and 13 with the simple virilizing form), 39 age-matched normal subjects, and 20 patients who had undergone bilateral adrenalectomy. Adrenal specimens obtained from three other patients with 21-hydroxylase deficiency who had undergone bilateral adrenalectomy and specimens obtained at autopsy from eight other patients were examined histologically. Results: Plasma epinephrine and metanephrine concentrations and urinary epinephrine excretion were 40 to 80 percent lower in the patients with congenital adrenal hyperplasia than in the normal subjects (P<0.05), and the values were lowest in the patients with the most severe deficits in cortisol production. Urinary epinephrine excretion and plasma epinephrine concentrations were at or below the limit of detection of the assay in 8 (21 percent) of the patients with congenital adrenal hyperplasia and in 19 (95 percent) of the patients who had undergone adrenalectomy. In the group of patients with congenital adrenal hyperplasia, plasma epinephrine and metanephrine concentrations and urinary epinephrine excretion were approximately 50 percent lower in those who had been hospitalized for adrenal crises than in those who had not. In three patients with congenital adrenal hyperplasia who had undergone bilateral adrenalectomy, the formation of the adrenal medulla was incomplete, and electron-microscopical studies revealed a depletion of secretory vesicles in chromaffin cells. Conclusions: Congenital adrenal hyperplasia compromises both the development and the functioning of the adrenomedullary system. (N Engl J Med 2000;343:1362-8.) (C) 2000, Massachusetts Medical Society.
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页码:1362 / 1368
页数:7
相关论文
共 26 条
[1]   STRESS HORMONES - THEIR INTERACTION AND REGULATION [J].
AXELROD, J ;
REISINE, TD .
SCIENCE, 1984, 224 (4648) :452-459
[2]   Adrenomedullary function is severely impaired in 21-hydroxylase-deficient mice [J].
Bornstein, SR ;
Tajima, T ;
Eisenhofer, G ;
Haidan, A ;
Aguilera, G .
FASEB JOURNAL, 1999, 13 (10) :1185-1194
[3]   PLASMA-CATECHOLAMINES IN PATIENTS WITH ADDISONS-DISEASE [J].
BORNSTEIN, SR ;
BREIDERT, M ;
EHRHARTBORNSTEIN, M ;
KLOOS, B ;
SCHERBAUM, WA .
CLINICAL ENDOCRINOLOGY, 1995, 42 (02) :215-218
[4]  
Bornstein SR, 1999, J CLIN ENDOCR METAB, V84, P1729
[5]  
BORNSTEIN SR, 1994, J CLIN ENDOCR METAB, V78, P225, DOI 10.1210/jc.78.1.225
[6]  
Ehrhart-Bornstein M, 1998, ENDOCR REV, V19, P301
[7]   17 alpha-hydroxylase and chromogranin A in 6th week human fetal adrenals [J].
EhrhartBornstein, M ;
Breidert, M ;
Guadanucci, P ;
Wozniak, W ;
BocianSobkowska, J ;
Malendowicz, LK ;
Bornstein, SR .
HORMONE AND METABOLIC RESEARCH, 1997, 29 (01) :30-32
[8]   SYMPATHOADRENAL REGULATION OF ADRENOCORTICAL STEROIDOGENESIS [J].
EHRHARTBORNSTEIN, M ;
BORNSTEIN, SR ;
GONZALEZHERNANDEZ, J ;
HOLST, JJ ;
WATERMAN, MR ;
SCHERBAUM, WA .
ENDOCRINE RESEARCH, 1995, 21 (1-2) :13-24
[9]   PLASMA METADRENALINES - DO THEY PROVIDE USEFUL INFORMATION ABOUT SYMPATHOADRENAL FUNCTION AND CATECHOLAMINE METABOLISM [J].
EISENHOFER, G ;
FRIBERG, P ;
PACAK, K ;
GOLDSTEIN, DS ;
MURPHY, DL ;
TSIGOS, C ;
QUYYUMI, AA ;
BRUNNER, HG ;
LENDERS, JWM .
CLINICAL SCIENCE, 1995, 88 (05) :533-542
[10]   REGIONAL RELEASE AND REMOVAL OF CATECHOLAMINES AND EXTRANEURONAL METABOLISM TO METANEPHRINES [J].
EISENHOFER, G ;
RUNDQUIST, B ;
ANEMAN, A ;
FRIBERG, P ;
DAKAK, N ;
KOPIN, IJ ;
JACOBS, MC ;
LENDERS, JWM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (10) :3009-3017