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原发性闭经的染色体畸变:一项回顾性研究。

Chromosomal Aberrations in Primary Amenorrhea: A Retrospective Study.

作者信息

Korgaonkar Seema, Dhangar Somprakash, Kulkarni Vinayak, Kerketta Lily, Vundinti Babu Rao

机构信息

Department of Cytogenetics, National Institute of Immunohematology, Mumbai, Maharashtra, India.

出版信息

J Hum Reprod Sci. 2019 Apr-Jun;12(2):92-97. doi: 10.4103/jhrs.JHRS_107_16.

Abstract

OBJECTIVES

The aim of this study was to estimate the frequency of chromosomal abnormalities and establish the association with clinical of factors such as secondary sexual characters and gonad development in primary amenorrhea (PA).

STUDY DESIGN

The study was carried out in a large cohort of PA. The chromosomal aberrations were correlated with secondary sexual characters and anatomical abnormalities.

MATERIALS AND METHODS

The data of 490 cases of PA were collected retrospectively. The chromosomal preparations were done from the peripheral blood and subjected to giemsa-trypsin-giemsa banding and karyotyped according to the International System of Human Cytogenetic Nomenclature 2013. The fluorescence hybridization was carried out using centromeric and whole painting probes for X and Y chromosome.

STATISTICAL ANALYSIS

Statistical analysis of the data was performed using online version of social science statistics software.

RESULTS

A high frequency of abnormal uterus (81.9%) and ovaries (86.7%) were detected in our study. A total of 121 (24.7%) cases were identified with abnormal karyotype. The numerical chromosomal abnormalities were identified in 53 (43.8%) cases while structural abnormalities were identified in 32 (26.4%) cases. The XY karyotype was detected in 29.8% females with PA. The PA individuals with anatomical abnormalities (84.3%) had a high frequency (24.6%) of chromosomal aberrations.

CONCLUSIONS

The present study concluded that cytogenetics plays an important role in precise diagnosis which helps in the management of PA. The cytogenetic analysis should be carried out to know the genetic basis of PA.

摘要

目的

本研究旨在评估原发性闭经(PA)患者染色体异常的发生率,并确定其与第二性征和性腺发育等临床因素之间的关联。

研究设计

该研究在一大群PA患者中进行。将染色体畸变与第二性征和解剖学异常进行关联分析。

材料与方法

回顾性收集490例PA患者的数据。染色体标本取自外周血,采用吉姆萨 - 胰蛋白酶 - 吉姆萨显带技术,并根据2013年国际人类细胞遗传学命名系统进行核型分析。使用X和Y染色体的着丝粒探针和全染色体涂染探针进行荧光杂交。

统计分析

使用社会科学统计软件的在线版本对数据进行统计分析。

结果

在我们的研究中检测到高比例的子宫异常(81.9%)和卵巢异常(86.7%)。共有121例(24.7%)患者被鉴定为核型异常。其中,53例(43.8%)为染色体数目异常,32例(26.4%)为结构异常。在PA女性中,XY核型的检出率为29.8%。有解剖学异常的PA个体(84.3%)染色体畸变的发生率较高(24.6%)。

结论

本研究得出结论,细胞遗传学在PA的精确诊断中起着重要作用,有助于PA的管理。应进行细胞遗传学分析以了解PA的遗传基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a57d/6594125/5ccfb836a019/JHRS-12-92-g001.jpg

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