Spontaneous natural conception and live birth in three patients with likely pathogenic variants in TUBB8, ZP2, and ZP3 associated with female subfertility.

IF 5.3 3区 医学 Q1 REPRODUCTIVE BIOLOGY
Juepu Zhou, Hui He, Ruolin Mao, Meng Wang, Rui Long, Xiangfei Wang, Hong Chen, Lei Jin, Lixia Zhu
{"title":"Spontaneous natural conception and live birth in three patients with likely pathogenic variants in TUBB8, ZP2, and ZP3 associated with female subfertility.","authors":"Juepu Zhou, Hui He, Ruolin Mao, Meng Wang, Rui Long, Xiangfei Wang, Hong Chen, Lei Jin, Lixia Zhu","doi":"10.1186/s13048-026-02200-z","DOIUrl":null,"url":null,"abstract":"<p><strong>Case: </strong>Three patients with genetically confirmed female subfertility due to heterozygous likely pathogenic variants in TUBB8 (c.613G > A), ZP2 (c.1421T > C), or ZP3 (c.518 C > G), respectively, had histories of recurrent adverse assisted reproductive technology (ART) outcomes, including zona pellucida (ZP) abnormalities or oocyte degeneration, reduced fertilization, poor embryo development or limited viable embryo availability, and implantation failure.</p><p><strong>Outcome: </strong>Notably, all three patients eventually achieved successful live births. Patient 1, after two failed ART cycles, delivered a male infant following a third ICSI attempt, and later conceived naturally, delivering a female infant. Patient 2, after five unsuccessful IVF/ICSI cycles and no implantation, conceived naturally years later and delivered a male infant. Patient 3, following two failed IVF/ICSI attempts, conceived via donor oocytes and later delivered a male infant through natural conception.</p><p><strong>Conclusion: </strong>These cases expand the reported reproductive outcome spectrum of women carrying likely pathogenic variants in oocyte- and ZP-related genes. The findings suggest that reproductive outcomes in selected heterozygous carriers may be more variable than previously appreciated and that residual reproductive potential may occasionally be retained. These observations may help refine reproductive genetic counseling for women with genetically associated subfertility, while further case accumulation and functional studies are required.</p>","PeriodicalId":16610,"journal":{"name":"Journal of Ovarian Research","volume":" ","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2026-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13651015/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Ovarian Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13048-026-02200-z","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"REPRODUCTIVE BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Case: Three patients with genetically confirmed female subfertility due to heterozygous likely pathogenic variants in TUBB8 (c.613G > A), ZP2 (c.1421T > C), or ZP3 (c.518 C > G), respectively, had histories of recurrent adverse assisted reproductive technology (ART) outcomes, including zona pellucida (ZP) abnormalities or oocyte degeneration, reduced fertilization, poor embryo development or limited viable embryo availability, and implantation failure.

Outcome: Notably, all three patients eventually achieved successful live births. Patient 1, after two failed ART cycles, delivered a male infant following a third ICSI attempt, and later conceived naturally, delivering a female infant. Patient 2, after five unsuccessful IVF/ICSI cycles and no implantation, conceived naturally years later and delivered a male infant. Patient 3, following two failed IVF/ICSI attempts, conceived via donor oocytes and later delivered a male infant through natural conception.

Conclusion: These cases expand the reported reproductive outcome spectrum of women carrying likely pathogenic variants in oocyte- and ZP-related genes. The findings suggest that reproductive outcomes in selected heterozygous carriers may be more variable than previously appreciated and that residual reproductive potential may occasionally be retained. These observations may help refine reproductive genetic counseling for women with genetically associated subfertility, while further case accumulation and functional studies are required.

TUBB8、ZP2和ZP3可能致病变异与女性低生育能力相关的3例患者的自然受孕和活产
病例:3例遗传上证实女性低生育能力的患者,原因是TUBB8 (C . 613g b> A)、ZP2 (C . 1421t > C)或ZP3 (C .518)可能的杂合致病变异C > G)分别有复发性不良辅助生殖技术(ART)结果的历史,包括透明带(ZP)异常或卵母细胞变性,受精减少,胚胎发育不良或活胚可用性有限,以及着床失败。结果:值得注意的是,所有3例患者最终都成功活产。患者1在两次ART周期失败后,在第三次ICSI尝试后产下一名男婴,后来自然受孕,产下一名女婴。患者2在经历了5次不成功的IVF/ICSI周期和未着床后,数年后自然受孕并产下一名男婴。患者3在两次IVF/ICSI尝试失败后,通过供体卵母细胞受孕,后来通过自然受孕产下一名男婴。结论:这些病例扩大了报道的携带卵母细胞和zp相关基因可能致病变异的妇女的生殖结局谱。研究结果表明,选择的杂合子携带者的生殖结果可能比以前认为的更加可变,并且偶尔可能保留剩余的生殖潜力。这些观察结果可能有助于改进与遗传相关的低生育能力妇女的生殖遗传咨询,同时需要进一步的病例积累和功能研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Ovarian Research
Journal of Ovarian Research REPRODUCTIVE BIOLOGY-
CiteScore
6.20
自引率
2.50%
发文量
125
审稿时长
>12 weeks
期刊介绍: Journal of Ovarian Research is an open access, peer reviewed, online journal that aims to provide a forum for high-quality basic and clinical research on ovarian function, abnormalities, and cancer. The journal focuses on research that provides new insights into ovarian functions as well as prevention and treatment of diseases afflicting the organ. Topical areas include, but are not restricted to: Ovary development, hormone secretion and regulation Follicle growth and ovulation Infertility and Polycystic ovarian syndrome Regulation of pituitary and other biological functions by ovarian hormones Ovarian cancer, its prevention, diagnosis and treatment Drug development and screening Role of stem cells in ovary development and function.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书