ADULT HEIGHT IN WOMEN WITH EARLY-TREATED CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE TYPE) - RELATION TO BODY-MASS INDEX IN EARLIER CHILDHOOD

被引:35
作者
YU, ACM [1 ]
GRANT, DB [1 ]
机构
[1] GREAT ORMOND ST HOSP CHILDREN NHS TRUST,LONDON,ENGLAND
基金
英国惠康基金;
关键词
ADULT STATURE; BODY MASS INDEX; CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE TYPE); PREDICTED ADULT HEIGHT;
D O I
10.1111/j.1651-2227.1995.tb13789.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To investigate if obesity, as judged by increased body mass index (BMI), during childhood is associated with impaired adult stature in patients with 21-hydroxylase-type congenital adrenal hyperplasia (CAH), a retrospective analysis was carried out on outpatient records of 30 girls with CAH who had reached adult height. Height SD score for age (HtSDS(ca)), HtSDS for bone age (HtSDS(ba)), BMI and steroid dosage in early childhood (3.2-4.6 years) and later childhood (7.2-9.1 years), were compared with adult HtSDS (HtSDS(adlt)), adult HtSDS less mid-parental HtSDS (HtSDS(adlt)- HtSDS(mp)), predicted adult height SDS (HtSDS(pdct)), adult height SDS less predicted adult HtSDS (HtSDS(adlt) -HtSDS(pdct)) and age at menarche. Mean (SD) for HtSDS(adlt) was -1.13 (1.05), mean HtSDS(pdct) -0.12 (0.9) and mean age at menarche 13.5 (1.9) years. BMI in childhood was not correlated with HtSDS(adlt) but showed negative correlations with HtSDS(adlt) - HtSDS(mp) (r = -0.43; p < 0.02) and HtSDS(adlt) - HtSDS(pdct) (r -0.45; p < 0.02). BMI in later childhood showed negative correlations with HtSDS(adlt) - HtSDS(pdct) (r = -0.61;p < 0.001) and age at menarche (r = -0.63; p < 0.001). We conclude that in girls with early-treated CAH, a high BMI during early childhood is associated with loss of genetic height potential, and in later childhood with over-prediction of adult height and early menarche.
引用
收藏
页码:899 / 903
页数:5
相关论文
共 18 条
[1]   MONITORING TREATMENT IN CONGENITAL ADRENAL-HYPERPLASIA [J].
APPAN, S ;
HINDMARSH, PC ;
BROOK, CGD .
ARCHIVES OF DISEASE IN CHILDHOOD, 1989, 64 (09) :1235-1239
[2]   GROWTH AND SKELETAL MATURATION IN CONGENITAL ADRENAL-HYPERPLASIA - REVIEW OF 20 CASES [J].
BAILEY, CC ;
KOMROWER, GM .
ARCHIVES OF DISEASE IN CHILDHOOD, 1974, 49 (01) :4-7
[3]   THE MANAGEMENT OF CLASSICAL CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY [J].
BROOK, CGD .
CLINICAL ENDOCRINOLOGY, 1990, 33 (04) :559-567
[4]  
BROOK CGD, 1974, J PEDIATR-US, V85, P12, DOI 10.1016/S0022-3476(74)80277-5
[5]  
CLAYTON GW, 1986, ACTA ENDOCR-COP S, V279, P295
[6]  
GRANT D, 1983, Pediatric and Adolescent Gynecology, V1, P97
[7]   CONTINUING NEED FOR MINERALOCORTICOID THERAPY IN SALT-LOSING CONGENITAL ADRENAL-HYPERPLASIA [J].
HUGHES, IA ;
WILTON, A ;
LOLE, CA ;
GRAY, OP .
ARCHIVES OF DISEASE IN CHILDHOOD, 1979, 54 (05) :350-355
[8]   REINSTITUTION OF MINERALOCORTICOID THERAPY IN CONGENITAL ADRENAL-HYPERPLASIA - EFFECTS ON CONTROL AND GROWTH [J].
JANSEN, M ;
WIT, JM ;
VANDENBRANDE, JL .
ACTA PAEDIATRICA SCANDINAVICA, 1981, 70 (02) :229-233
[9]   GLUCOCORTICOID TREATMENT OF GIRLS WITH CONGENITAL ADRENAL-HYPERPLASIA - EFFECTS ON HEIGHT, SEXUAL-MATURATION, AND FERTILITY [J].
KLINGENSMITH, GJ ;
GARCIA, SC ;
JONES, HW ;
MIGEON, CJ ;
BLIZZARD, RM .
JOURNAL OF PEDIATRICS, 1977, 90 (06) :996-1004
[10]  
Knorr D, 1988, Acta Paediatr Jpn, V30 Suppl, P89