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中国香港地区生育力低下男性的染色体异常及Y染色体微缺失

Chromosomal anomalies and Y-microdeletions among Chinese subfertile men in Hong Kong.

作者信息

Ng Paulina P Y, Tang Mary H Y, Lau Elizabeth T, Ng Lucy K L, Ng Ernest H Y, Tam P C, Yeung William S B, Ho P C

机构信息

Department of Obstetrics and Gynaecology, The University of Hong Kong, Tsan Yuk Hospital, Hong Kong.

出版信息

Hong Kong Med J. 2009 Feb;15(1):31-8.

Abstract

OBJECTIVE

To report the type and frequency of chromosomal anomalies and Y-microdeletions among Hong Kong Chinese subfertile men with sperm concentrations lower than 5 million/mL. DESIGN. Retrospective study.

SETTING

A reproductive centre in Hong Kong.

PARTICIPANTS

A total of 295 Chinese subfertile men who underwent both karyotyping and Y-microdeletion studies from 2000 to 2007 were categorised as having non-obstructive azoospermia (n=71), very severe oligospermia (sperm concentration>0 and <or=2 million/mL, n=158), and severe oligospermia (sperm concentration>2 and <5 million/mL, n=66).

MAIN OUTCOME MEASURES

Karyotyping and Y-microdeletion studies.

RESULTS

The prevalence of chromosomal anomalies and Y-microdeletions in the study population were 8.5% (25/295; 95% confidence interval, 5.6-12.3%) and 6.4% (19/295; 3.9-9.9%), respectively. The total prevalence of chromosomal anomalies and Y-microdeletions was 13.2% (39/295; 95% confidence interval, 9.6-17.6%) as five cases of non-obstructive azoospermia showed both Y structural alterations and AZFbc deletion. The corresponding figures for chromosomal anomalies in the groups with non-obstructive azoospermia, very severe oligospermia, and severe oligospermia were 21.1% (15/71; 95% confidence interval, 12.3-32.4%), 5.7% (9/158; 2.6-10.5%), and 1.5% (1/66; 0.0-8.2%). While for Y-microdeletions they were 8.5% (6/71; 3.2-17.5%), 8.2% (13/158; 4.5-13.7%) and 0% (0/66; 0.0-4.4%), respectively. The respective overall prevalence rates for chromosomal anomalies and Y-microdeletions in these groups were: 22.5% (16/71; 13.5-34.0%), 13.9% (22/158; 8.9-20.3%), and 1.5% (1/66; 0.0-8.2%).

CONCLUSIONS

Our findings strongly support the recommendation for both karyotyping and Y-microdeletion analyses in subfertile men with sperm concentrations of 2 million/mL or lower before they undergo assisted reproduction treatment.

摘要

目的

报告香港华裔精子浓度低于500万/mL的不育男性的染色体异常和Y染色体微缺失的类型及发生率。设计:回顾性研究。

地点

香港的一个生殖中心。

研究对象

2000年至2007年间共295名接受了染色体核型分析和Y染色体微缺失检测的华裔不育男性,被分为非梗阻性无精子症组(n = 71)、极重度少精子症组(精子浓度>0且≤200万/mL,n = 158)和重度少精子症组(精子浓度>200万且<500万/mL,n = 66)。

主要观察指标

染色体核型分析和Y染色体微缺失检测。

结果

研究人群中染色体异常和Y染色体微缺失的发生率分别为8.5%(25/295;95%置信区间,5.6 - 12.3%)和6.4%(19/295;3.9 - 9.9%)。染色体异常和Y染色体微缺失的总发生率为13.2%(39/295;95%置信区间,9.6 - 17.6%),因为有5例非梗阻性无精子症患者同时存在Y染色体结构改变和AZFbc缺失。非梗阻性无精子症组、极重度少精子症组和重度少精子症组中染色体异常的相应数字分别为21.1%(15/71;95%置信区间,12.3 - 32.4%)、5.7%(9/158;2.6 - 10.5%)和1.5%(1/66;0.0 - 8.

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