ABSENCE OF MOLECULAR DEFECT IN THE TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) GENE IN PREMATURE PUBARCHE CHILDREN AND HIRSUTE FEMALE-PATIENTS WITH MODERATELY DECREASED ADRENAL 3-BETA-HSD ACTIVITY

被引:50
|
作者
CHANG, YT
ZHANG, L
ALKADDOUR, HS
MASON, JI
LIN, KM
YANG, XJ
GARIBALDI, LR
BOURDONY, CJ
DOLAN, LM
DONALDSON, DL
PANG, SY
机构
[1] UNIV ILLINOIS, COLL MED, DEPT PEDIAT MC856, DIV PEDIAT ENDOCRINOL, CHICAGO, IL 60612 USA
[2] UNIV TEXAS, SW MED CTR, GREEN CTR REPROD BIOL SCI, DALLAS, TX 75235 USA
[3] CARDINAL GLENNON MEM HOSP CHILDREN, ST LOUIS, MO 63104 USA
[4] SAN JUAN CITY HOSP, DEPT PEDIAT, SAN JUAN, PR USA
[5] CHILDRENS HOSP MED CTR, CINCINNATI, OH 45267 USA
[6] UNIV KANSAS, MED CTR, DEPT PEDIAT, KANSAS CITY, KS 66103 USA
关键词
D O I
10.1203/00006450-199506000-00024
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To date the molecular basis and hormonal criteria for inherited mild late-onset 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) deficiency congenital adrenal hyperplasia (CAH) have not been defined. We have thus investigated the presence or absence of mutation in the type II 3 beta-HSD gene encoding adrenal/gonadal 3 beta-HSD in each of five premature pubarche children and hirsute female patients manifesting moderately decreased adrenal 3 beta-HSD activity. ACTH-stimulated hormonal levels in all patients compared with mean levels in pubertal stage-matched normal subjects were between 2.5 and 6.5 SD for 17-hydroxypregnenolone levels, and between 2.5 and 7 SD for dehydroepiandrosterone levels in all except one patient. 17-Hydroxypregnenolone to cortisol ratios were between 2.5 and 4.3 SD, and dehydroepiandrosterone to androstenedione ratios were between 3 and 8.6 SD, The type II 3 beta-HSD gene regions of a putative promoter, exons I, II, III, and IV, and exon-intron boundaries in all subjects were amplified by polymerase chain reaction and then sequenced. All patients had normal sequences of the type II 3 beta-HSD gene in both alleles. Three female patients heterozygotic for severe 3 beta-HSD deficiency CAH with one allele mutation of the gene demonstrated normal ACTH-stimulated hormone profiles. These data indicate that moderately decreased adrenal 3 beta-HSD activity resulting in modestly increased Delta 5 precursor steroid levels and Delta 5 to Delta 4 steroid ratios in premature pubarche and hirsute patients is not caused by a mutation in the type II 3 beta-HSD gene. This suggests that the moderately decreased adrenal 3 beta-HSD activity in the patient is not due to mild late-onset variants of inherited 3 beta-HSD deficiency CAH, whereas the carriers for true 3 beta-HSD deficiency CAH do not express decreased adrenal 3 beta-HSD activity.
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收藏
页码:820 / 824
页数:5
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