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46,XX型先天性类脂性肾上腺增生患者的自然青春期。尽管类固醇生成急性调节蛋白(StAR)基因存在失活突变,但卵巢类固醇生成在一定程度上得以保留。

Spontaneous puberty in 46,XX subjects with congenital lipoid adrenal hyperplasia. Ovarian steroidogenesis is spared to some extent despite inactivating mutations in the steroidogenic acute regulatory protein (StAR) gene.

作者信息

Fujieda K, Tajima T, Nakae J, Sageshima S, Tachibana K, Suwa S, Sugawara T, Strauss J F

机构信息

Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

J Clin Invest. 1997 Mar 15;99(6):1265-71. doi: 10.1172/JCI119284.

Abstract

Congenital lipoid adrenal hyperplasia (lipoid CAH) is the most severe form of CAH in which the synthesis of all gonadal and adrenal cortical steroids is markedly impaired. We report here the clinical, endocrinological, and molecular analyses of two unrelated Japanese kindreds of 46,XX subjects affected with lipoid CAH who manifested spontaneous puberty. Phenotypic female infants with 46,XX karyotypes were diagnosed with lipoid CAH as newborns based on a clinical history of failure to thrive, hyperpigmentation, hyponatremia, hyperkalemia, and low basal values of serum cortisol and urinary 17-hydroxycorticosteroid and 17-ketosteroid. These patients responded to treatment with glucocorticoid and 9alpha-fludrocortisone. Spontaneous thelarche occurred in association with increased serum estradiol levels at the age of 10 and 11 yr, respectively. Pubic hair developed at the age of 12 yr 11 mo in one subject and menarche was at the age of 12 yr in both cases. Both subjects reported periodic menstrual bleeding and subsequently developed polycystic ovaries. To investigate the molecular basis of the steroidogenic lesion in these patients, the StAR gene was characterized by PCR and direct DNA sequence analyses. DNA sequence analysis revealed that one patient is homozygous for the Gln 258 Stop mutation in exon 7 and that the other patient is a compound heterozygote with the Gln 258 Stop mutation and a single A deletion at codon 238 in the other allele causing a frame-shift, which renders the StAR protein nonfunctional. These findings demonstrate that ovarian steroidogenesis can be spared to some extent through puberty when the StAR gene product is inactive. This is in marked contrast to the early onset of severe defects in testicular and adrenocortical steroidogenesis which are characteristics of this disease.

摘要

先天性类脂质性肾上腺增生症(类脂质性先天性肾上腺皮质增生症,lipoid CAH)是先天性肾上腺皮质增生症(CAH)最严重的一种形式,其中所有性腺和肾上腺皮质类固醇的合成均受到显著损害。我们在此报告了两例无亲缘关系的46,XX型日本患者的临床、内分泌学及分子分析情况,这两名患者均患有类脂质性先天性肾上腺皮质增生症且出现了自然青春期发育。具有46,XX核型的表型为女性的婴儿在新生儿期时,基于生长发育不良、色素沉着、低钠血症、高钾血症以及血清皮质醇、尿17 - 羟皮质类固醇和17 - 酮类固醇基础值低的临床病史,被诊断为类脂质性先天性肾上腺皮质增生症。这些患者对糖皮质激素和9α - 氟氢可的松治疗有反应。分别在10岁和11岁时,随着血清雌二醇水平升高出现了自发乳房发育。一名患者在12岁11个月时出现阴毛生长,两名患者均在12岁时出现月经初潮。两名患者均报告有周期性月经出血,随后都出现了多囊卵巢。为了研究这些患者类固醇生成病变的分子基础,通过聚合酶链反应(PCR)和直接DNA序列分析对类固醇急性调节蛋白(StAR)基因进行了特征分析。DNA序列分析显示,一名患者在第7外显子的谷氨酰胺258位点发生了终止突变,为纯合子;另一名患者是复合杂合子,一个等位基因发生了谷氨酰胺258位点终止突变,另一个等位基因在第238密码子处发生了单个A缺失,导致移码,使StAR蛋白失去功能。这些发现表明,当StAR基因产物无活性时,卵巢类固醇生成在青春期可在一定程度上得以幸免。这与该疾病特征性的睾丸和肾上腺皮质类固醇生成严重缺陷的早期出现形成了显著对比。

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