21-羟化酶缺乏症基因型和临床表型分析  

Correlation between CYP21A2 genotype and phenotype in patients with 21-hydroxylase deficiency

作　　者：孙云[1] 马定远[1] 蒋涛[1] 陈玉林[1] 孙亦骏[1] 杨冰[1] 张瑾[1] 黄美莲[1] 许争锋[1] 

机构地区：[1]南京医科大学附属南京妇幼保健院产前诊断中心,江苏南京210004

出　　处：《临床儿科杂志》2013年第7期622-625,共4页Journal of Clinical Pediatrics

基　　金：江苏省医学创新团队与领军人才课题(No.LJ201109);南京市科技发展计划项目(No.201201064);南京医科大学科技发展基金重点项目(No.2010NJMUZ17)

摘　　要：目的了解21-羟化酶缺乏症(21-OHD)患儿CYP21A2基因突变热点,并分析其基因型和表型的关系。方法对在新生儿17α羟孕酮(17-αOHP)筛查中发现并诊断的18例21-OHD患儿及其父母,采用等位基因特异性PCR-直接测序联合多重连接依赖探针扩增技术测定其基因型。结果共检出6种CYP21A2基因突变类型,最常见的为I2G(44.4%)和de(l33.3%),这两种也是失盐型常见的突变;单纯男性化型患儿I172N突变检出率达75%。根据对21-羟化酶活性影响程度将患儿分为重度、中度和轻度组,三组间反映病情严重性的指标17-αOHP、促肾上腺皮质激素、睾酮的差异均有统计学意义(P<0.05)。结论 21-OHD基因诊断技术的建立揭示了基因型和临床表型的一致性。Abstract： Objectives To study the mutation spectrum in CYP21A2 ene in patients with 21-hydroxylase deficiency （21-OHD）, and to analyze the relationship between genotype and phenotype. Methods Eighteen patients with 21-OHD were identified by neonatal screening of 17or-OH progesterone （17tt-OHP）. The allele specific PCR-DNA sequencing com- bining with multiplex ligation-dependent probe amplification was applied to determine the genotype in the patients and their parents. Results Six mutations of CYP21A2 gene were identified. I2G （44.4%） and del （33.3%） were the most frequent mutations and also were the most common mutations in salt-wasting form. The detection rate of I172N mutation in simple virilizing form was 75%. Patients were classified into three groups according to the degree of 21-hydroylase enzymatic compromise caused by the mutation. The serum 17ct-OHP, ACTH and T levels which reflected the severity of disease were significantly different among three groups （P〈0.05）. Conclusions The genetic diagnosis of 21-OHD reveals the consistencybetween genotype and phenotype.

关 键 词：21羟化酶缺乏症 突变 基因型 筛查 

分 类 号：R725.8[医药卫生—儿科]