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卵巢早衰的细胞遗传学:对269名患病女性的调查

Cytogenetics of premature ovarian failure: an investigation on 269 affected women.

作者信息

Baronchelli Simona, Conconi Donatella, Panzeri Elena, Bentivegna Angela, Redaelli Serena, Lissoni Sara, Saccheri Fabiana, Villa Nicoletta, Crosti Francesca, Sala Elena, Martinoli Emanuela, Volontè Marinella, Marozzi Anna, Dalprà Leda

机构信息

Dipartimento di Neuroscienze e Tecnologie Biomediche, Università degli Studi di Milano-Bicocca, Via Cadore 48, 20900 Monza, Italy.

出版信息

J Biomed Biotechnol. 2011;2011:370195. doi: 10.1155/2011/370195. Epub 2011 Jan 17.

Abstract

The importance of X chromosome in the aetiology of premature ovarian failure (POF) is well-known but in many cases POF still remains idiopathic. Chromosome aneuploidy increase is a physiological phenomenon related to aging, but the role of low-level sex chromosome mosaicism in ovarian function is still undiscovered. Standard cytogenetic analysis was carried out in a total of 269 patients affected by POF: 27 chromosomal abnormalities were identified, including X chromosome and autosomal structural and numerical abnormalities. In 47 patients with 46,XX karyotype we performed interphase FISH using X alpha-satellite probe in order to identify X chromosome mosaicism rate. Aneuploidy rate in the patient group was significantly higher than the general population group. These findings underline the importance of X chromosome in the aetiology of POF and highlight the potential role of low-level sex chromosome mosaicism in ovarian aging that may lead to a premature onset of menopause.

摘要

X染色体在卵巢早衰(POF)病因学中的重要性已广为人知,但在许多情况下,POF仍为特发性。染色体非整倍体增加是一种与衰老相关的生理现象,但低水平性染色体嵌合体在卵巢功能中的作用仍未被发现。对总共269例POF患者进行了标准细胞遗传学分析:共鉴定出27种染色体异常,包括X染色体以及常染色体的结构和数目异常。在47例核型为46,XX的患者中,我们使用Xα卫星探针进行了间期荧光原位杂交(FISH),以确定X染色体嵌合体率。患者组的非整倍体率显著高于一般人群组。这些发现强调了X染色体在POF病因学中的重要性,并突出了低水平性染色体嵌合体在卵巢衰老中可能导致绝经提前发生的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c12a/3026995/2a396481be7f/JBB2011-370195.001.jpg

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