首页> 美国卫生研究院文献>Clinical Pediatric Endocrinology >Mutational Analysis of Androgen Receptor (AR) Gene in 46XY Patients withAmbiguous Genitalia and Normal Testosterone Secretion: Endocrinological Characteristics ofThree Patients with AR Gene Mutations
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Mutational Analysis of Androgen Receptor (AR) Gene in 46XY Patients withAmbiguous Genitalia and Normal Testosterone Secretion: Endocrinological Characteristics ofThree Patients with AR Gene Mutations

机译:46XY患者的雄激素受体(AR)基因突变分析生殖器歧义和睾丸激素正常分泌:内分泌特征三例AR基因突变患者

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摘要

The prevalence of abnormalities in androgen receptor gene (AR) among patients with ambiguous genitalia is unknown. Moreover, endocrinological data from prepubertal patients with AR mutation are very limited. Thus, the aim of this study was to examine the prevalence of abnormalities in AR among patients with both ambiguous genitalia, which was defined as a combination of two or more genital abnormalities (i.e. hypospadias, microphallus (penile length < 25 mm), hypoplastic scrotum, bifid scrotum, undescended testis) in this study, and normal to elevated T levels. We also compared the endocrinological data of prepubertal patients with AR mutation and ambiguous genitalia with that of those without the AR mutation. We screened 26 Japanese prepubertal 46,XY patients (five from three families were included) with both ambiguous genitalia and normal to elevated T levels. Mutations in AR were found in three (two of the three were related). Among the 23 patients without mutation in AR, the steroid 5-alpha-reductase 2 gene (SRD5A2) was also examined in eight patients with elevated T/dehydrotestosterone ratio after the hCG (>10) or with undervirilized family members. No mutation in SRD5A2 was found. Characteristics of the three patients with mutation in AR were compared with the 23 patients without mutation. In two patients, basal T levels (0.3, 0.2 ng/ml) and peak T levels after the hCG tests (8.3, 8.5 ng/ml) tended to be higher, and the peak LH/ peak FSHratios after the GnRH tests (4.6, 4.0) were higher than in patients without mutation, atthe ages of 1 yr and 9 mo and 3 yr and 8 mo, respectively. In conclusion, an abnormalityin either AR or SRD5A2 was not common among patients with ambiguous genitalia and normaltestosterone secretion. Elevated peak LH/peak FSH ratio (≥4) after the GnRH test inaddition to detectable basal T levels and elevated peak T levels after the hCG test mayinfer AR abnormality in prepubertal patients with ambiguous genitalia at the age of oneand over, although further study is needed, because our data were limited.
机译:生殖器歧义患者中雄激素受体基因(AR)异常的患病率尚不清楚。而且,来自AR突变的青春期前患者的内分泌数据非常有限。因此,本研究的目的是检查两个生殖器模棱两可的患者中AR的患病率,这被定义为两个或多个生殖器异常(即尿道下裂,微孔(阴茎长度<25 mm),阴囊发育不良)的组合,双阴囊,睾丸未降,并且T水平正常至升高。我们还比较了具有AR突变和不明确生殖器的青春期前患者与未患有AR突变的患者的内分泌数据。我们筛选了26名日本女性青春期前的46,XY患者(包括三个家庭的五名患者),他们的生殖器模棱两可且T水平正常至升高。在三个人中发现了AR突变(三个人中有两个相关)。在23例AR中无突变的患者中,还对8例hCG后T /脱氢睾丸激素比率升高(> 10)或未充分免疫的家庭成员的患者进行了类固醇5-α-还原酶2基因(SRD5A2)的检查。在SRD5A2中未发现突变。比较了3例AR突变患者和23例无突变患者的特征。两名患者的基础T水平(0.3,0.2 ng / ml)和hCG试验后的最高T水平(8.3,8.5 ng / ml)倾向于更高,并且LH / FSH峰值GnRH试验后的比率(4.6,4.0)高于无突变的患者分别为1岁和9个月,3岁和8个月。总之,异常生殖器歧义和正常的患者中,AR或SRD5A2的发生并不常见睾丸激素分泌。在GnRH测试后,峰值LH /峰值FSH比(≥4)升高hCG测试后除了可检测的基础T水平和峰值T水平升高外一岁时生殖器歧义的青春期前患者推断AR异常而且,由于我们的数据有限,因此需要进一步研究。

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