• 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

复发性流产患者染色体异常分析,重点关注9号染色体倒位患者的预后。

The analysis of chromosomal abnormalities in patients with recurrent pregnancy loss, focusing on the prognosis of patients with inversion of chromosome (9).

作者信息

Nonaka Taro, Takahashi Makiko, Nonaka Chika, Enomoto Takayuki, Takakuwa Koichi

机构信息

Department of Obstetrics and Gynecology Niigata University Medical and Dental Hospital Niigata Japan.

Center for Perinatal, Maternal and Neonatal Medicine Niigata University Medical and Dental Hospital Niigata Japan.

出版信息

Reprod Med Biol. 2019 Jun 24;18(3):296-301. doi: 10.1002/rmb2.12281. eCollection 2019 Jul.

DOI:10.1002/rmb2.12281
PMID:31312110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6613022/
Abstract

PURPOSE

Inversion of chromosome 9 (inv[9]) is considered to be a normal variant, and the inv(9) in patients or husbands with recurrent pregnancy loss (RPL) is believed to be harmless. However, there are few reports concerning the outcomes of pregnancy in patients with RPL when the patient or their partner has inv(9). In this study, we analyzed the outcomes of pregnancy in this patient population.

METHODS

Chromosomal karyotyping was performed for 2006 couples with RPL (two or more consecutive early pregnancy losses including non-visualized cases) with their informed consent. The frequency of various chromosomal abnormalities in the patient population was then analyzed, and the outcomes of pregnancy in patients with inv(9) were investigated.

RESULTS

The frequency of inv(9) in the overall population was 2.6% (52/2006). Thus far, 32 patients have conceived repetitively, resulting in live births in 23 cases and early pregnancy losses in nine cases. Four of the nine cases obtained a good outcome in the subsequent pregnancy. Thus, a successful outcome was obtained in 27 of the 32 (84.4%) cases.

CONCLUSIONS

This study suggests that inv(9) has no adverse influence on subsequent pregnancy.

摘要

目的

9号染色体倒位(inv[9])被认为是一种正常变异,且认为复发性流产(RPL)患者或其丈夫的inv(9)无害。然而,关于RPL患者自身或其伴侣存在inv(9)时的妊娠结局的报道较少。在本研究中,我们分析了这一患者群体的妊娠结局。

方法

在2006对有复发性流产(两次或更多次连续早期妊娠丢失,包括未见到胎心搏动的情况)的夫妇知情同意的情况下,进行染色体核型分析。然后分析该患者群体中各种染色体异常的频率,并研究存在inv(9)的患者的妊娠结局。

结果

总体人群中inv(9)的频率为2.6%(52/2006)。到目前为止,32例患者再次怀孕,23例分娩活婴,9例早期妊娠丢失。9例中的4例在随后的妊娠中获得了良好结局。因此,32例中的27例(84.4%)获得了成功结局。

结论

本研究表明,inv(9)对随后的妊娠没有不良影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/938f/6613022/f9f9c2769edf/RMB2-18-296-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/938f/6613022/f9f9c2769edf/RMB2-18-296-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/938f/6613022/f9f9c2769edf/RMB2-18-296-g001.jpg

相似文献

1
The analysis of chromosomal abnormalities in patients with recurrent pregnancy loss, focusing on the prognosis of patients with inversion of chromosome (9).复发性流产患者染色体异常分析,重点关注9号染色体倒位患者的预后。
Reprod Med Biol. 2019 Jun 24;18(3):296-301. doi: 10.1002/rmb2.12281. eCollection 2019 Jul.
2
Recurrent pregnancy loss evaluation combined with 24-chromosome microarray of miscarriage tissue provides a probable or definite cause of pregnancy loss in over 90% of patients.复发性流产评估结合流产组织 24 染色体微阵列分析,为超过 90%的患者提供了流产的可能或明确病因。
Hum Reprod. 2018 Apr 1;33(4):579-587. doi: 10.1093/humrep/dey021.
3
Chromosomal Aberrations in 224 Couples with Recurrent Pregnancy Loss.224对复发性流产夫妇的染色体畸变
J Hum Reprod Sci. 2020 Oct-Dec;13(4):340-348. doi: 10.4103/jhrs.JHRS_11_20. Epub 2020 Dec 28.
4
Evaluation of chromosomal abnormalities from preimplantation genetic testing to the reproductive outcomes: a comparison between three different structural rearrangements based on next-generation sequencing.基于新一代测序的三种不同结构重排的比较:对胚胎植入前遗传学检测至生殖结局的染色体异常评估。
J Assist Reprod Genet. 2021 Mar;38(3):709-718. doi: 10.1007/s10815-020-02053-5. Epub 2021 Jan 6.
5
Evaluation of 1100 couples with recurrent pregnancy loss using conventional cytogenetic, PGD, and PGS: hype or hope.使用传统细胞遗传学、植入前基因诊断(PGD)和植入前基因筛查(PGS)对1100对复发性流产夫妇进行评估:炒作还是希望。
Gynecol Endocrinol. 2016 Jun;32(6):483-7. doi: 10.3109/09513590.2015.1134476. Epub 2016 Feb 8.
6
Prevalence, causes, and impact of non-visualized pregnancy losses in a recurrent pregnancy loss population.复发性妊娠丢失人群中非可见性妊娠丢失的发生率、原因和影响。
Hum Reprod. 2023 May 2;38(5):830-839. doi: 10.1093/humrep/dead040.
7
Acrocentric Chromosome Polymorphic Variants on Chinese Female Have Possible Association with Unexplained Recurrent Pregnancy Loss.中国女性的染色体臂间倒位多态性变异可能与不明原因复发性妊娠丢失有关。
Reprod Sci. 2021 Feb;28(2):575-584. doi: 10.1007/s43032-020-00332-1. Epub 2020 Oct 6.
8
Recurrent pregnancy loss: what is the impact of consecutive versus non-consecutive losses?复发性流产:连续流产与非连续流产的影响有何不同?
Hum Reprod. 2016 Nov;31(11):2428-2434. doi: 10.1093/humrep/dew169. Epub 2016 Sep 2.
9
Description of cytogenetic abnormalities and the pregnancy outcomes of couples with recurrent pregnancy loss in a tertiary-care center in Saudi Arabia.沙特阿拉伯一家三级医疗中心复发性流产夫妇的细胞遗传学异常描述及妊娠结局
Saudi Med J. 2018 Mar;39(3):239-242. doi: 10.15537/smj.2018.3.21592.
10
Recurrent pregnancy loss: diagnostic workup after two or three pregnancy losses? A systematic review of the literature and meta-analysis.复发性流产:两次或三次妊娠丢失后应进行哪些诊断检查?系统综述和荟萃分析。
Hum Reprod Update. 2020 Apr 15;26(3):356-367. doi: 10.1093/humupd/dmz048.

引用本文的文献

1
Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9 in a patient with a good prognosis.患者存在预后良好的嵌合体 22 三体和 9 号染色体着丝粒周围倒位。
BMC Med Genomics. 2023 Nov 13;16(1):286. doi: 10.1186/s12920-023-01709-2.
2
Chromosomal Instability in Genome Evolution: From Cancer to Macroevolution.基因组进化中的染色体不稳定性:从癌症到宏观进化
Biology (Basel). 2023 Apr 28;12(5):671. doi: 10.3390/biology12050671.
3
Pericentric inversion (Inv) 9 variant-reproductive risk factor or benign finding?着丝粒倒位(Inv)9 变异——生殖风险因素还是良性发现?

本文引用的文献

1
Complex chromosomal rearrangements in couples affected by recurrent spontaneous abortion.受复发性自然流产影响的夫妇中的复杂染色体重排。
Int J Gynaecol Obstet. 2015 Jan;128(1):36-9. doi: 10.1016/j.ijgo.2014.07.018. Epub 2014 Aug 16.
2
Two cases of recurrent abortion in which isodicentric chromosome 15 was observed in the husbands.两例复发性流产病例,其丈夫的染色体检查发现有等臂染色体15。
J Obstet Gynaecol Res. 2014 Jun;40(6):1795-8. doi: 10.1111/jog.12401.
3
Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective study.
J Assist Reprod Genet. 2019 Dec;36(12):2557-2561. doi: 10.1007/s10815-019-01601-y. Epub 2019 Nov 16.
反复流产夫妇的染色体异常:一项印度回顾性研究。
Indian J Hum Genet. 2013 Oct;19(4):415-22. doi: 10.4103/0971-6866.124369.
4
Association of pericentric inversion of chromosome 9 and infertility in romanian population.罗马尼亚人群中9号染色体臂间倒位与不孕的关联。
Maedica (Bucur). 2012 Jan;7(1):25-9.
5
Frequency of recurrent spontaneous abortion and its influence on further marital relationship and illness: the Okazaki Cohort Study in Japan.复发性自然流产的发生率及其对后续婚姻关系和疾病的影响:日本冈崎队列研究
J Obstet Gynaecol Res. 2013 Jan;39(1):126-31. doi: 10.1111/j.1447-0756.2012.01973.x. Epub 2012 Aug 13.
6
Clinical practice. Recurrent miscarriage.临床实践。复发性流产。
N Engl J Med. 2010 Oct 28;363(18):1740-7. doi: 10.1056/NEJMcp1005330.
7
Cytogenetic abnormalities in 1162 couples with recurrent miscarriages in southern region of India: report and review.印度南部地区 1162 对复发性流产夫妇的细胞遗传学异常:报告与综述。
J Assist Reprod Genet. 2011 Feb;28(2):145-9. doi: 10.1007/s10815-010-9492-6. Epub 2010 Oct 8.
8
Chromosomal abnormalities in couples with reproductive disorders.患有生殖障碍的夫妇的染色体异常。
Gynecol Obstet Invest. 2008;66(4):237-40. doi: 10.1159/000147170. Epub 2008 Jul 22.
9
Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling.9号染色体臂间倒位与临床表型的相关性及遗传咨询
Saudi Med J. 2008 Jul;29(7):946-51.
10
Prevalence of chromosomal abnormalities in couples with recurrent miscarriage.复发性流产夫妇中染色体异常的患病率。
Fertil Steril. 2007 Sep;88(3):721-3. doi: 10.1016/j.fertnstert.2006.11.160. Epub 2007 Feb 23.