Suppr超能文献

21-羟化酶缺乏所致经典型先天性肾上腺皮质增生症患者的肾上腺初现延迟。

Blunted adrenarche in patients with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

作者信息

Sellers E P, MacGillivray M H

机构信息

Children's Hospital of Buffalo, Department of Pediatrics, School of Medicine, State University of New York at Buffalo 14222, USA.

出版信息

Endocr Res. 1995 Aug;21(3):537-44. doi: 10.1080/07435809509030471.

Abstract

Dehydroepiandrosterone sulfate (DHEAS) concentration levels were measured by a specific RIA in 23 female and 7 male patients with classical congenital adrenal hyperplasia (CAH) salt-losing type due to steroid 21-hydroxylase (21-OH) deficiency. The patients were divided into four groups by age and the DHEAS concentrations (mean +/- SD; micrograms/dl) for each age group were: 5 to 8 years (10.2 +/- 6.5; range 5-23 micrograms/dl); 8 to 10 years (18.3 +/- 14.9; range 5-44 micrograms/dl); 10 to 18 years (41.9 +/- 40; range 5-160 micrograms/dl); and above 18 years (49.7 +/- 65.9; range 9 to 242 micrograms/dl). These DHEAS levels were compared to age-matched normal values and it was found that DHEAS concentrations in 29 of the 30 patients were less than or in the lower part of the normal range for all age groupings. The DHEAS levels did not correlate with 17 alpha-hydroxyprogesterone (17-OHP), androstenedione, and testosterone values. The data indicate that blunted adrenarche occurs in classical CAH patients with 21-OH deficiency.

摘要

采用特异性放射免疫分析法(RIA)测定了23例女性和7例男性因类固醇21-羟化酶(21-OH)缺乏导致的典型失盐型先天性肾上腺皮质增生症(CAH)患者的硫酸脱氢表雄酮(DHEAS)浓度水平。根据年龄将患者分为四组,各年龄组的DHEAS浓度(均值±标准差;微克/分升)分别为:5至8岁(10.2±6.5;范围5 - 23微克/分升);8至10岁(18.3±14.9;范围5 - 44微克/分升);10至18岁(41.9±40;范围5 - 160微克/分升);18岁以上(49.7±65.9;范围9至242微克/分升)。将这些DHEAS水平与年龄匹配的正常值进行比较,发现30例患者中有29例的DHEAS浓度在所有年龄组中均低于或处于正常范围的下限。DHEAS水平与17α-羟孕酮(17-OHP)、雄烯二酮及睾酮值无关。数据表明,21-OH缺乏的典型CAH患者出现肾上腺初现延迟。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验