Prepubertal Cushing's disease is more common in males, but there is no increase in severity at diagnosis

被引:50
作者
Storr, HL [1 ]
Isidori, AM [1 ]
Monson, JP [1 ]
Besser, GM [1 ]
Grossman, AB [1 ]
Savage, MO [1 ]
机构
[1] St Bartholomews & Royal London Sch Med & Dent, Dept Endocrinol, London EC1A 7BE, England
关键词
D O I
10.1210/jc.2003-031531
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sex distribution and severity of biochemical indices at the diagnosis of Cushing's disease (CD) were analyzed in 50 patients (21 males and 29 females; aged less than or equal to30 yr; range, 6.4-30.0 yr). Twenty-five (50%) presented aged 18 yr or younger ( 17 males and eight females) and 25 aged 18-30 yr ( four males and 21 females). CD diagnosed at less than 18 yr occurred predominantly in males, contrasting with 18 yr or older, which was more common in females. The difference between the two groups was significant (P = 0.0003). There was a significant difference (chi(2)) in sex distribution depending on pubertal status (P = 0.0002); in prepubertal patients (n = 11) males predominated (91%) compared with postpubertal patients (n = 27), where females predominated (81%). In patients in puberty (n = 12), there was an equal sex incidence (50% males). In adult patients with CD, males have been reported to have more severe disease. We found no difference in hypercortisolemia or ACTH at diagnosis in males compared with females in the patients less than 18 yr of age [serum 0000 h cortisol, 510.5 +/- 75.2 vs. 415.6 +/- 63.7 nmol/liter (P = 0.52); plasma ACTH, 48.5 +/- 7.9 vs. 42.9 +/- 10.9 ng/liter (P = 0.54); percent suppression of serum cortisol during low dose dexamethasone suppression test, 57.2 +/- 8.6% vs. 33.5 +/- 13.1% (P = 0.14); high dose dexamethasone suppression test, 85.9 +/- 3.1% vs. 85.7 +/- 4.9% (P = 0.55); percent increase in cortisol after iv CRH, 180.3 +/- 15.3% vs. 189.9 +/- 20.3% (P = 0.67)]. In conclusion, female preponderance of CD in adult patients was not present in childhood. In patients 18 yr of age or younger, there was no difference in the severity of hypercortisolemia or ACTH at diagnosis between males and females.
引用
收藏
页码:3818 / 3820
页数:3
相关论文
共 15 条
[1]  
BESSER GM, 2002, COMPREHENSIVE CLIN E, P193
[2]   Long-term outcome in children and adolescents after transsphenoidal surgery for Cushing's disease [J].
Devoe, DJ ;
Miller, WL ;
Conte, FA ;
Kaplan, SL ;
Grumbach, MM ;
Rosenthal, SM ;
Wilson, CB ;
Gitelman, SE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (10) :3196-3202
[3]   Gender-related differences in the presentation and course of Cushing's disease [J].
Giraldi, FP ;
Moro, M ;
Cavagnini, F .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (04) :1554-1558
[4]   A critical analysis of the value of simultaneous inferior petrosal sinus sampling in Cushing's disease and the occult ectopic adrenocorticotropin syndrome [J].
Kaltsas, GA ;
Giannulis, MG ;
Newell-Price, JDC ;
Dacie, JE ;
Thakkar, C ;
Afshar, F ;
Monson, JP ;
Grossman, AB ;
Besser, GM ;
Trainer, PJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (02) :487-492
[5]   Transnasal microsurgery in children and adolescents with Cushing's disease [J].
Knappe, UJ ;
Ludecke, DK .
NEUROSURGERY, 1996, 39 (03) :484-492
[6]   LONG-TERM FOLLOW-UP OF TRANSSPHENOIDAL SURGERY FOR THE TREATMENT OF CUSHINGS-DISEASE IN CHILDHOOD [J].
LEINUNG, MC ;
KANE, LA ;
SCHEITHAUER, BW ;
CARPENTER, PC ;
LAWS, ER ;
ZIMMERMAN, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (08) :2475-2479
[7]   CUSHINGS-SYNDROME IN CHILDREN AND ADOLESCENTS - PRESENTATION, DIAGNOSIS, AND THERAPY [J].
MAGIAKOU, MA ;
MASTORAKOS, G ;
OLDFIELD, EH ;
GOMEZ, MT ;
DOPPMAN, JL ;
CUTLER, GB ;
NIEMAN, LK ;
CHROUSOS, GP .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (10) :629-636
[8]   VARIATIONS IN PATTERN OF PUBERTAL CHANGES IN BOYS [J].
MARSHALL, WA ;
TANNER, JM .
ARCHIVES OF DISEASE IN CHILDHOOD, 1970, 45 (239) :13-+
[9]  
MARSHALL WA, 1969, ARCH DIS CHILD, V45, P291
[10]   Transsphenoidal surgery for pituitary tumours [J].
Massoud, AF ;
Powell, M ;
Williams, RA ;
Hindmarsh, PC ;
Brook, CGD .
ARCHIVES OF DISEASE IN CHILDHOOD, 1997, 76 (05) :398-404