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青春期克莱恩费尔特综合征患者生育力保存的可行性。

The feasibility of fertility preservation in adolescents with Klinefelter syndrome.

机构信息

Laboratoire de Biologie de la Reproduction-CECOS, Rouen University Hospital, Rouen, France.

出版信息

Hum Reprod. 2013 Jun;28(6):1468-79. doi: 10.1093/humrep/det084. Epub 2013 Mar 28.

Abstract

STUDY QUESTION

Is fertility preservation feasible after the onset of puberty in adolescents with Klinefelter syndrome (KS)?

SUMMARY ANSWER

Fertility preservation counseling should be an integral part of the care of XXY adolescents. Frozen ejaculated or testicular spermatozoa and even frozen immature germ cells can give them the potential to conceive their genetic progeny. However, no biological or clinical parameters were predictive of mature or immature germ cell retrieval.

WHAT IS KNOWN ALREADY

KS is the commonest sex chromosome disorder observed in azoospermic infertile males. Testicular sperm extraction success decreases with age and after testosterone therapy. Arguably, spermatozoa should be retrieved from KS males at the onset of puberty and before testosterone therapy to increase the chance of success.

STUDY DESIGN, SIZE, DURATION: A retrospective study was performed in eight KS adolescents, aged between 15 and 17 years, who were referred for counseling about their future fertility to the center CECOS (Centre d'Etude et de Conservation des Oeufs et du Sperme humain) at Rouen University Hospital between October 2008 and December 2011.

PARTICIPANTS/MATERIALS, SETTING, METHODS: The patients were first seen with their parents and then separately. It was proposed to them that they should provide a semen sample, if this was azoospermic, two other semen samples spaced by 3 months were collected. If azoospermia was confirmed, a bilateral testicular biopsy was proposed for sperm retrieval and testicular tissue preservation. Each adolescent met the psychologist before undergoing testicular biopsy. Paraffin-embedded testicular tissue was evaluated after staining with hematoxylin-eosin and saffron and immunostaining using vimentin, anti-Müllerian hormone, androgen receptor and MAGE-A4 antibodies. Sertoli cell maturity, germ cell identification and lamina propria alteration were assessed on seminiferous tubules.

MAIN RESULTS AND THE ROLE OF CHANCE

KS adolescents were not deeply concerned about their future fertility and only became involved in the process of fertility preservation after at least three medical consultations. The parents agreed immediately that fertility preservation should be attempted. Seven non-mosaic XXY adolescents presented with azoospermia and one XXY/XY adolescent had oligozoospermia. Increased plasma levels of FSH and LH as well as bilateral testicular hypotrophy were observed in all patients. The XXY/XY adolescent banked four semen samples before testosterone replacement therapy. Two patients refused testicular biopsy. Five patients accepted a bilateral testicular biopsy. Spermatozoa were retrieved in one patient, elongated spermatids and spermatocytes I in a second patient.

LIMITATIONS, REASONS FOR CAUTION: The number of patients enrolled in our study was low because the diagnosis of KS is only rarely made before or at the onset of puberty. Most XXY males are diagnosed in adulthood within the context of male infertility.

WIDER IMPLICATIONS OF THE FINDINGS

Spermatozoa can be retrieved in semen sample and in testicular tissue of adolescent Klinefelter patients. Furthermore, the testis may also harbor spermatogonia and incompletely differentiated germ cells. However, the physician should discuss with the patient and his parents over a period of several months before collecting a semen sample and performing bilateral testicular biopsy. Fertility preservation might best be proposed to adolescent Klinefelter patients just after the onset of puberty when it is possible to collect a semen sample and when the patient is able to consider alternative options to achieve fatherhood and also to accept the failure of spermatozoa or immature germ cell retrieval.

摘要

研究问题

青春期后克氏综合征(KS)患者的生育力保存是否可行?

总结答案

应将生育力保存咨询作为 XXY 青少年护理的一个组成部分。冷冻射出或睾丸精子,甚至冷冻未成熟的生殖细胞,都可以使他们有可能孕育自己的遗传后代。然而,没有生物学或临床参数可以预测成熟或未成熟生殖细胞的获取。

已知情况

KS 是在无精子症不育男性中观察到的最常见的性染色体疾病。睾丸精子提取的成功率随着年龄的增长和睾酮治疗而降低。可以说,应该在青春期开始和睾酮治疗之前从 KS 男性中获取精子,以增加成功的机会。

研究设计、大小和持续时间:这是一项回顾性研究,在 2008 年 10 月至 2011 年 12 月期间,在鲁昂大学医院的 CECOS(人类卵子和精子保存与研究中心)中心,对 8 名年龄在 15 至 17 岁之间的 KS 青少年进行了咨询,以了解他们未来的生育能力。

参与者/材料、设置、方法:首先让患者及其父母一起就诊,然后分别与他们交谈。如果精液样本呈无精子症,建议他们提供精液样本,如果确认无精子症,将在 3 个月的时间间隔内收集另外两份精液样本。如果确认无精子症,则建议进行双侧睾丸活检以获取精子和保存睾丸组织。每位青少年在接受睾丸活检前都要见一次心理学家。用苏木精-伊红和藏红花染色以及用波形蛋白、抗苗勒管激素、雄激素受体和 MAGE-A4 抗体进行免疫染色后,评估石蜡包埋的睾丸组织。评估生精小管的 Sertoli 细胞成熟度、生殖细胞识别和固有层改变。

主要结果和机会的作用

KS 青少年对未来的生育能力并不十分关注,只有在至少三次医疗咨询后,他们才开始参与生育力保存的过程。家长们立即同意尝试生育力保存。7 名非嵌合性 XXY 青少年出现无精子症,1 名 XXY/XY 青少年出现少精子症。所有患者均出现血浆 FSH 和 LH 水平升高以及双侧睾丸萎缩。在接受睾酮替代治疗之前,XXY/XY 青少年储存了四份精液样本。两名患者拒绝进行睾丸活检。五名患者接受了双侧睾丸活检。一名患者中获取了精子,另一名患者中获取了延长的精子和精母细胞 I。

局限性、谨慎的原因:由于 KS 的诊断很少在青春期前或青春期时做出,因此我们研究中纳入的患者数量较低。大多数 XXY 男性在成年后因男性不育而被诊断为 KS。

研究结果的更广泛意义

可以从青春期 KS 患者的精液样本和睾丸组织中获取精子。此外,睾丸中也可能存在精原细胞和未分化的生殖细胞。然而,医生应该在收集精液样本和进行双侧睾丸活检前与患者及其父母讨论数月。青春期后,当可以收集精液样本且患者能够考虑实现父亲身份的替代方案,并接受精子或未成熟生殖细胞获取失败的可能性时,最好向青春期 KS 患者提出生育力保存建议。

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