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芳香化酶过度综合征患者芳香化酶抑制剂治疗的长期效果。

Long term effects of aromatase inhibitor treatment in patients with aromatase excess syndrome.

作者信息

Giannopoulou Eleni Z, Brandt Stephanie, Zorn Stefanie, Denzer Christian, von Schnurbein Julia, Fukami Maki, Kaiser Alexander, Schmidt Martin, Wabitsch Martin

机构信息

Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.

Center for Rare Endocrine Disease at the University of Ulm, Ulm, Germany.

出版信息

Front Endocrinol (Lausanne). 2024 Nov 20;15:1487884. doi: 10.3389/fendo.2024.1487884. eCollection 2024.

Abstract

INTRODUCTION

Aromatase excess syndrome (AEXS) is a rare, autosomal dominant disorder, characterized by enhanced aromatization of androgens and estrogen excess. In males it is characterized by pre-/peripubertal gynecomastia, hypogonadotropic hypogonadism, advanced bone age and short adult height. Only a few female patients have been described so far.

METHODS

We report on a family with four members with AEXS and present the long-term effects of aromatase inhibitor use in three of them. Genetic analysis showed a monoallelic 0.3-Mb deletion in 15q21, involving parts of , and in all four patients with AEXS.

RESULTS

The index patient (male, 8 years old) presented with gynecomastia and accelerated growth and bone age. With start of puberty, estradiol levels increased, while testosterone levels remained low. Gynecomastia progressed and a mastectomy was performed twice. Presuming AEXS, a therapy with letrozole was initiated at the age of 19 years. Low-dose letrozole treatment was associated with an increase in testicular volume, increase in virilization and improvement in physical strength and libido. His brother (age 3 years) presented with accelerated growth and bone age. Treatment with letrozole, which was started at the age of 7 years, resulted in achieving an adult height of 179 cm and prevented the appearance of gynecomastia. His sister (age 6 years), who presented with premature thelarche and accelerated growth and bone age, was treated with an estrogen receptor modulator and a GnRH analog followed by letrozole treatment. Menarche occurred at age 13.5 years and adult height was 158 cm. Their father had an early, accelerated growth with an adult height of 171 cm, a delayed puberty and no gynecomastia. studies provided evidence for involvement of aromatase induction in atypical cells and an increased range of potential mechanisms regulating aromatase activity due to the presence of the mutated allele.

DISCUSSION

In conclusion, we observed a phenotypic variability within family members with AEXS carrying the same microdeletion. When started early, treatment with letrozole was found to prevent the development of gynecomastia and increase adult height in one patient. In adult life, low-dose letrozole treatment resulted in improved physical strength and libido in the index patient.

摘要

引言

芳香化酶过剩综合征(AEXS)是一种罕见的常染色体显性疾病,其特征为雄激素芳香化增强和雌激素过剩。在男性中,其特征为青春期前/青春期乳腺增生、低促性腺激素性性腺功能减退、骨龄提前和成人身高矮小。迄今为止,仅报道了少数女性患者。

方法

我们报告了一个有四名成员患AEXS的家族,并介绍了其中三名患者使用芳香化酶抑制剂的长期效果。基因分析显示,所有四名患AEXS的患者在15q21均存在一个单等位基因0.3-Mb的缺失,涉及 、 和 的部分区域。

结果

索引患者(男性,8岁)出现乳腺增生以及生长加速和骨龄提前。随着青春期开始,雌二醇水平升高,而睾酮水平仍较低。乳腺增生进展,进行了两次乳房切除术。推测为AEXS后,19岁时开始使用来曲唑治疗。低剂量来曲唑治疗与睾丸体积增加、男性化增强以及体力和性欲改善有关。他的弟弟(3岁)出现生长加速和骨龄提前。7岁开始使用来曲唑治疗,最终成人身高达到179厘米,并预防了乳腺增生的出现。他的妹妹(6岁)出现乳房过早发育以及生长加速和骨龄提前,先接受雌激素受体调节剂和促性腺激素释放激素类似物治疗,随后使用来曲唑治疗。月经初潮发生在13.5岁,成人身高为158厘米。他们的父亲生长提前且加速,成人身高为171厘米,青春期延迟,无乳腺增生。 研究为非典型细胞中芳香化酶诱导的参与以及由于突变等位基因的存在而增加的调节芳香化酶活性的潜在机制范围提供了证据。

讨论

总之,我们观察到携带相同微缺失的AEXS家族成员存在表型变异。早期开始使用来曲唑治疗可预防一名患者乳腺增生的发展并增加成人身高。在成年期,低剂量来曲唑治疗使索引患者的体力和性欲得到改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a0d/11614628/20237ef31f3c/fendo-15-1487884-g001.jpg

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