• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

分析中国东北地区 1738 名不育男性的 Y 染色体微缺失。

Analysis of Y chromosome microdeletion in 1738 infertile men from northeastern China.

机构信息

Centre for Reproductive Medicine, First Hospital of Jilin University, Changchun, China.

出版信息

Urology. 2013 Sep;82(3):584-8. doi: 10.1016/j.urology.2013.04.017. Epub 2013 Jun 13.

DOI:10.1016/j.urology.2013.04.017
PMID:23769119
Abstract

OBJECTIVE

To determine the frequencies and the characteristics of Y chromosome microdeletion in infertile men from northeastern China to perform appropriate therapeutic choices.

MATERIALS AND METHODS

The study included 1738 infertile men. Sperm concentration was measured according to standard methods and karyotype analysis was performed on peripheral blood lymphocytes with standard G-banding. Multiplex polymerase chain reaction amplification using 9 specific sequence-tagged sites were selected to detect Y chromosome microdeletions.

RESULTS

The data showed that the frequency of Y chromosome microdeletion was 8.57%. The most common microdeletion, among the azoospermia factor (AZF) regions, was detected in the AZFc region, followed by AZFb+c, AZFb, AZFa+b+c, AZFa, and AZFa+c. One-hundred seven patients with Y chromosome microdeletion developed azoospermia, 39 developed severe oligozoospermia (sperm concentration ≤5 × 10(6)/mL), and 3 developed moderate oligozoospermia (sperm concentration >5 × 10(6)/mL and ≤10 × 10(6)/mL). Karyotype analysis was available for 130 patients with Y chromosome microdeletion and abnormal karyotypes were found in 19 patients (14.6%). The most frequent abnormal karyotype was 46,X,Yqh-(n = 7).

CONCLUSION

In northeastern China, Y chromosome microdeletion diagnosis should be performed before the use of intracytoplasmic sperm injection in infertile men with sperm count ≤10 × 10(6)/mL, especially in men with azoospermia.

摘要

目的

确定东北地区不育男性中 Y 染色体微缺失的频率和特征,以便进行适当的治疗选择。

材料与方法

本研究纳入了 1738 例不育男性。精子浓度按照标准方法进行测量,外周血淋巴细胞的核型分析采用标准 G 带技术。选择 9 个特定的序列标签位点进行多重聚合酶链反应扩增,以检测 Y 染色体微缺失。

结果

数据显示,Y 染色体微缺失的频率为 8.57%。在无精子因子(AZF)区域中,最常见的微缺失发生在 AZFc 区域,其次是 AZFb+c、AZFb、AZFa+b+c、AZFa 和 AZFa+c。107 例 Y 染色体微缺失患者发生无精子症,39 例发生严重少精子症(精子浓度≤5×10^6/ml),3 例发生中度少精子症(精子浓度>5×10^6/ml 且≤10×10^6/ml)。对 130 例 Y 染色体微缺失患者进行了核型分析,发现 19 例(14.6%)存在异常核型。最常见的异常核型是 46,X,Yqh-(n=7)。

结论

在中国东北地区,对于精子计数≤10×10^6/ml 的不育男性,尤其是无精子症患者,在使用胞浆内精子注射之前,应进行 Y 染色体微缺失诊断。

相似文献

1
Analysis of Y chromosome microdeletion in 1738 infertile men from northeastern China.分析中国东北地区 1738 名不育男性的 Y 染色体微缺失。
Urology. 2013 Sep;82(3):584-8. doi: 10.1016/j.urology.2013.04.017. Epub 2013 Jun 13.
2
Molecular microdeletion analysis of infertile men with karyotypic Y chromosome abnormalities.对核型Y染色体异常的不育男性进行分子微缺失分析。
J Int Med Res. 2018 Jan;46(1):307-315. doi: 10.1177/0300060517719394. Epub 2017 Aug 23.
3
Chromosomal abnormalities and Y chromosome microdeletions in infertile men with azoospermia and oligozoospermia in Eastern China.中国东部无精子症和少精子症不育男性的染色体异常及Y染色体微缺失
J Int Med Res. 2020 Apr;48(4):300060519896712. doi: 10.1177/0300060519896712. Epub 2019 Dec 29.
4
Detection of AZF microdeletions and analysis of reproductive hormonal profiles in Hainan men undergoing assisted reproductive technology.海南接受辅助生殖技术男性中AZF微缺失的检测及生殖激素谱分析
BMC Urol. 2024 Jun 12;24(1):123. doi: 10.1186/s12894-024-01503-x.
5
[Screening for the microdeletions of azoospermia factor on the Y chromosome in male infertile patients from Guangzhou].[广州地区男性不育患者Y染色体无精子症因子微缺失的筛查]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):564-6.
6
[Analysis of Y chromosome microdeletion in non-obstructive male infertile patients with azoospermia and severe oligozoospermia].[无梗阻性无精子症和严重少精子症男性不育患者Y染色体微缺失分析]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2013 Mar;44(2):188-92.
7
Chromosomal abnormality and Y chromosome microdeletion in Chinese patients with azoospermia or severe oligozoospermia.中国无精子症或严重少精子症患者的染色体异常与Y染色体微缺失
Yi Chuan Xue Bao. 2006 Feb;33(2):111-6. doi: 10.1016/s0379-4172(06)60029-2.
8
Genetic screening for chromosomal abnormalities and Y chromosome microdeletions in Chinese infertile men.中文不育男性的染色体异常和 Y 染色体微缺失的遗传筛查。
J Assist Reprod Genet. 2012 Jun;29(6):521-7. doi: 10.1007/s10815-012-9741-y. Epub 2012 Mar 14.
9
Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast Turkey.土耳其东南部少精子症和无精子症不育男性的细胞遗传学和Y染色体微缺失筛查研究
J Assist Reprod Genet. 2008 Nov-Dec;25(11-12):559-65. doi: 10.1007/s10815-008-9272-8. Epub 2008 Oct 25.
10
Detection of AZF microdeletions and reproductive hormonal profile analysis of infertile sudanese men pursuing assisted reproductive approaches.苏丹男性不育患者采用辅助生殖技术,检测 AZF 微缺失与生殖激素谱分析。
BMC Urol. 2021 Apr 23;21(1):69. doi: 10.1186/s12894-021-00834-3.

引用本文的文献

1
Karyotypic analysis of 62,587 Han Chinese infertile couples undergoing assisted reproductive technology treatments: insights into chromosomal variations.对62587对接受辅助生殖技术治疗的汉族不育夫妇进行核型分析:对染色体变异的见解。
BMC Genomics. 2025 Jul 7;26(1):640. doi: 10.1186/s12864-025-11851-z.
2
Endosulfan induces reproductive & genotoxic effect in male and female Swiss albino mice.硫丹对雄性和雌性瑞士白化小鼠具有生殖毒性和遗传毒性作用。
Lab Anim Res. 2024 May 22;40(1):22. doi: 10.1186/s42826-024-00208-4.
3
Cytogenetics investigation in 151 Brazilian infertile male patients and genomic analysis in selected cases: experience of 14 years in a public genetic service.
151 例巴西不育男性患者的细胞遗传学研究及部分病例的基因组分析:14 年公共遗传服务的经验。
BMC Res Notes. 2024 Mar 5;17(1):67. doi: 10.1186/s13104-024-06710-1.
4
Prevalence of Y chromosome microdeletions among infertile Mongolian men.蒙古族不育男性Y染色体微缺失的患病率
Clin Exp Reprod Med. 2022 Jun;49(2):101-109. doi: 10.5653/cerm.2021.05099. Epub 2022 Apr 8.
5
Genetic counseling prior to assisted reproductive technology.辅助生殖技术前的遗传咨询。
Reprod Med Biol. 2020 Dec 31;20(2):133-143. doi: 10.1002/rmb2.12361. eCollection 2021 Apr.
6
-negative 45,X/46,XY adult male with complete masculinization and infertility: A case report and review of literature.45,X/46,XY成年男性,表现为完全男性化及不育:病例报告并文献复习
World J Clin Cases. 2020 Dec 26;8(24):6380-6388. doi: 10.12998/wjcc.v8.i24.6380.
7
Cytogenetic and molecular detection of a rare unbalanced Y;3 translocation in an infertile male: A case report.一名不育男性罕见的不平衡Y;3易位的细胞遗传学和分子检测:病例报告
Medicine (Baltimore). 2020 Jun 26;99(26):e20863. doi: 10.1097/MD.0000000000020863.
8
The association between the two more common genetic causes of spermatogenic failure: a 7-year retrospective study.两种更常见的生精失败遗传病因之间的关联:一项 7 年回顾性研究。
Asian J Androl. 2020 Nov-Dec;22(6):642-648. doi: 10.4103/aja.aja_13_20.
9
Molecular cytogenetic analysis and genetic counseling: a case report of eight 46,XX males and a literature review.分子细胞遗传学分析与遗传咨询:8例46,XX男性病例报告及文献复习
Mol Cytogenet. 2019 Nov 4;12:44. doi: 10.1186/s13039-019-0456-y. eCollection 2019.
10
Genotyping of the Gene in Iranian Patients with Non-Obstructive Azoospermia.伊朗非梗阻性无精子症患者中该基因的基因分型
Curr Urol. 2019 Sep;13(1):46-50. doi: 10.1159/000499295. Epub 2019 Sep 10.