Clinical Presentation of Children With Premature Adrenarche

被引:14
作者
von Oettingen, Julia [1 ,2 ]
Sola Pou, Joaquim [3 ]
Levitsky, Lynne L. [1 ,2 ]
Misra, Madhusmita [1 ,2 ]
机构
[1] Massachusetts Gen Hosp Children, Div Pediat Endocrinol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Hosp Univ Girona, Girona, Spain
关键词
congenital adrenal hyperplasia; 17-hydroxyprogesterone; dehydroepiandrosterone sulfate; small for gestational age; low birth weight; bone age; advanced; precocious puberty; PRECOCIOUS PUBARCHE; EXAGGERATED ADRENARCHE; METABOLIC SYNDROME; NATURAL-HISTORY; WEIGHT-GAIN; PUBIC HAIR; GIRLS; ONSET; HYPERINSULINISM; HYPERPLASIA;
D O I
10.1177/0009922812456238
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives. To describe the phenotype of premature adrenarche (PA) patients, elucidate historical and physical correlates, and distinguish PA from late-onset congenital adrenal hyperplasia (LOCAH). Study design. Retrospective chart review of 122 patients (91 female and 31 male) with PA and 11 with LOCAH. Results. In PA patients, birth weight was < 2 standard deviation scores (SDSs) in 6%, and 14% were premature. Body mass index SDSs were high (2.00 +/- 1.84). Bone age (BA) SDS was > 2 in 31% and was greater in boys than in girls; PA subjects were taller, and the predicted height was at or above genetic potential. Dehydroepiandrosterone sulfate (DHEAS) was higher in boys. LOCAH patients had earlier pubic hair, more advanced BA, lower height SDSs, lower adult height prediction, and higher adrenal androgen levels. Conclusion. Patients with PA tend to be overweight with BA acceleration but normal height prediction. LOCAH is distinguished by earlier presentation and higher 17-hydrocyprogesterone and adrenal androgens.
引用
收藏
页码:1140 / 1149
页数:10
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