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临床试验/NCT05346159
NCT05346159已完成不适用

Effects of Adrenal Androgens on Gender-typed Behavior in Girls With Turner Syndrome

Sohag University1 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2022年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
78
试验地点
1
主要终点
luteinizing hormone (LH)

研究概览

简要总结

Turner syndrome (TS) is a genetic disorder in which there is loss of all or part of the second X chromosome and occurs in 1/2500 live female births. TS is characterized by short stature and endocrine abnormalities, such as the loss of ovarian function (Gonadal dysgenesis) and estrogen deficiency.

The absence of pubertal development is one of the most common clinical features of patients with TS, who should have experienced a sex hormone surge if the hypothalamic-pituitary-gonadal axis was activated normally . Gonadarche and adrenarche are regarded as processes that are independent of each other. The function of adrenal gland is independent of true (central/complete/gonadotropin- dependent) puberty . Adrenal androgen in Turner syndrome shows a wide spectrum, ranging from normal to highly elevated.

X-linked genes affect the brain in at least two ways: by directly acting on the brain and by indirectly acting on the gonads to induce differences in specific gonadal secretions (i.e., hormones) that have specific effects on brain development. The changes in brain and behavioral/ cognitive phenotypes in TS individuals may be the result of a direct genetic factor, an indirect hormonal factor, or a combination of the two factors .

To evaluate direct effect of X chromosome, a lot of neuroimaging studies have revealed both neuroanatomical and neurofunctional changes in patients with TS. S. C. Mueller (2013) reported that oestrogen deficiency exhibits paradoxical healthy male-like patterns (i.e., a larger amygdala but reduced hippocampal volume). This finding confirms the indirect hormonal effect on the brain that are likely attributed to the effect of androgen on the brain or may be due to active role of estrogen in feminization of brain .

The cognitive phenotypes of TS include severe deficits in multiple cognitive domains: visual-spatial ability, mathematical processing, and social cognition. Regarding intelligence, numerous TS studies have a lower performance IQ in contrast to a within-normal verbal IQ in TS individuals .

The presence of hypogonadism with normal or may be elevated adrenal function in girls with turner syndrome provide a model to study the hormonal effect of adrenal androgen in absence of estrogen on gender-role behavior. Ehrhardt et al (1970) reported that Women with TS are described as clearly feminine in their behavior and interests .

To the best of our knowledge, there have been no previous studies on the correlation between level of adrenal androgen and gender-typed behavior in Girls with TS.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
— 至 18 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Girls with turner syndrome (TS) (karyotype 45, X) younger than 18 years of age and Tanner stage matched healthy control girls with normal karyotype attending outpatient clinic at Sohag University Hospital will be included in the study.

排除标准

  • failure to obtain informed consent

结局指标

主要结局

luteinizing hormone (LH)

时间窗: Baseline

to access ovarian function

estradiol (E2)

时间窗: Baseline

to access ovarian function

Gender-typed behavior The Children's Sex Role Inventory

时间窗: Baseline

we will measure children's gender-typed behavior using The Children's Sex Role Inventory

Parent-Report Gender Identity Questionnaire

时间窗: Baseline

we will measure children's gender-typed behavior using the Parent-Report Gender Identity Questionnaire

Serum dehydroepiandrosterone sulfate (DHEAS)

时间窗: Baseline

we use DHEAS level to access adrenal function

follicle stimulating hormone (FSH)

时间窗: Baseline

to access ovarian function

Gender-typed behavior

时间窗: Baseline

we will measure children's gender-typed behavior using the Pre school Activities Inventory

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Menatalla Moamen Ramadan Mohamed

resident doctor at pediatric department

Sohag University

研究点 (1)

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