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中国平衡复杂染色体重排携带者的遗传特征及生育风险分析

Analysis of genetic characteristics and reproductive risks of balanced complex chromosome rearrangement carriers in China.

作者信息

Liao Ya-ping, Wang Chun-jing, Liang Meng, Hu Xiao-mei, Wu Qi

机构信息

Department of Life Sciences, Bengbu Medical College, Bengbu 233030, China.

出版信息

Yi Chuan. 2017 May 20;39(5):396-412. doi: 10.16288/j.yczz.16-322.

Abstract

To examine the type, characteristics and meiotic behavior of balanced complex chromosome rearrangements (CCRs) and their relationship with reproductive abnormalities in Chinese people, karyotype analyses were performed in 1063 couples with reproductive abnormalities using G-banding technology. Additional data were retrieved from a Chinese database and analyzed statistically with the karyotype and clinic data of CCRs. Two CCR carriers were found among the 1063 couples, and in all a total of 124 CCR carriers with the complete information were identified in the karyotype analysis and the database search. Our results showed that simple 3-way or 4-way translocations were the most common types, present in 64/124 (51.6%) of CCRs. Double two-way translocations accounted for 26.6% and exceptional CCRs accounted for 21.6% of total cases. General risk of 77.6% for spontaneous abortions and 9.7% for an abnormal child were calculated based on 339 pregnancies of 124 carriers. Pregnancy consequences could be significantly associated with the type of CCRs. Abnormal pregnancy was frequently associated with CCRs on chromosome 8, while dyszoospermia was frequently associated with CCRs on chromosome 1 among the males. The most frequent mode of segregation was 3:3 adjacent-1 (8/12) in 12 abnormal karyotypes. Short chromosomes (groups D-G) were involved in 46.2% of CCRs showing 3:2, 4:2 and 5:3 segregation ratios. In conclusion, carriers of balanced CCRs have a high risk of an abortion and/or a chromosomally unbalanced child. The incidence of spermatogenic defect in male CCR carriers is high, and male infertility is associated with CCRs. Hence, identifying the types of CCRs, chromosomes involved, translocated segments of chromosomes, etc. will provide crucial information for prenatal diagnosis and genetic counseling for carriers of balanced CCRs.

摘要

为了研究中国人群中平衡复杂染色体重排(CCR)的类型、特征、减数分裂行为及其与生殖异常的关系,采用G显带技术对1063对有生殖异常的夫妇进行了核型分析。从中国数据库中检索了其他数据,并与CCR的核型和临床数据进行了统计学分析。在1063对夫妇中发现了2名CCR携带者,在核型分析和数据库搜索中总共鉴定出124名具有完整信息的CCR携带者。我们的结果表明,简单的三向或四向易位是最常见的类型,占CCR的64/124(51.6%)。双双向易位占26.6%,特殊CCR占总病例的21.6%。根据124名携带者的339次妊娠计算,自然流产的总体风险为77.6%,生出异常孩子的风险为9.7%。妊娠结局可能与CCR的类型显著相关。异常妊娠常与8号染色体上的CCR相关,而男性少精子症常与1号染色体上的CCR相关。在12个异常核型中,最常见的分离模式是3:3相邻-1(8/12)。短染色体(D-G组)参与了46.2%的显示3:2、4:2和5:3分离比例的CCR。总之,平衡CCR携带者有很高的流产和/或生出染色体不平衡孩子的风险。男性CCR携带者生精缺陷的发生率很高,男性不育与CCR有关。因此,确定CCR的类型、涉及的染色体、染色体的易位片段等,将为平衡CCR携带者的产前诊断和遗传咨询提供关键信息。

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