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Diverse impacts of female chromosomal polymorphisms on assisted reproduction outcomes: a retrospective cohort study.
Lu, Yongjie; Tian, Tian; Chen, Lixue; Yan, Liying; Chang, Liang; Qiao, Jie.
Afiliação
  • Lu Y; State Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, 100191, China.
  • Tian T; National Clinical Research Center for Obstetrics and Gynecology, Peking University Third Hospital, Beijing, 100191, China.
  • Chen L; Key Laboratory of Assisted Reproduction (Peking University), Ministry of Education, Beijing, 100191, China.
  • Yan L; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing, 100191, China.
  • Chang L; National Clinical Key Specialty Construction Program, P. R. China 2023, Beijing, 100191, China.
  • Qiao J; State Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, 100191, China.
BMC Pregnancy Childbirth ; 24(1): 331, 2024 Apr 27.
Article em En | MEDLINE | ID: mdl-38678230
ABSTRACT

BACKGROUND:

The effects of female chromosomal polymorphisms (FCPs) on various aspects of reproductive health have been investigated, yet the findings are frequently inconsistent. This study aims to clarify the role of FCPs on the outcomes of in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI).

METHODS:

This retrospective cohort study comprised 951 couples with FCPs and 10,788 couples with normal karyotypes who underwent IVF/ICSI treatment at Peking University Third Hospital between 2015 and 2021. The exposure was FCPs. The embryological outcomes and clinical outcomes were compared.

RESULTS:

The FCPs, as a whole, compromised the oocyte maturation rate (76.0% vs. 78.8%, P = 0.008), while they did not adversely affect other IVF/ICSI outcomes. Further detailed analyses showed that every type of FCPs contributed to the lower oocyte maturation rate, particularly the rare FCPs (69.0% vs. 78.8%, P = 0.008). The female qh + was associated with a higher normal fertilization rate (63.0% vs. 59.2%, adjusted P = 0.022), a higher clinical pregnancy rate (37.0% vs. 30.7%, adjusted P = 0.048), and a higher live birth rate (27.0% vs.19.0%, adjusted P = 0.003) in couples undergoing IVF. Conversely, in couples undergoing ICSI, female qh + was found to be related to a lower normal fertilization rate (58.8% vs. 63.8%, P = 0.032), a comparable clinical pregnancy rate (25.7% vs. 30.9%, P = 0.289), and a comparable live birth rate (19.8% vs. 19.2%, P = 0.880) compared to the control group. Additionally, an increased risk of preterm birth was observed in women undergoing IVF with multiple polymorphisms (62.5% vs. 16.9%, adjusted P <  0.001) and in women undergoing ICSI with pstk+ (36.4% vs. 15.4%, P = 0.036).

CONCLUSIONS:

Our research unravels the diverse impacts of various FCPs on IVF/ICSI outcomes, highlighting the detrimental effects of FCPs on oocyte maturation and the risk of preterm birth.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Fertilização in vitro / Taxa de Gravidez / Injeções de Esperma Intracitoplásmicas Limite: Adult / Female / Humans / Male / Pregnancy Idioma: En Revista: BMC Pregnancy Childbirth Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Fertilização in vitro / Taxa de Gravidez / Injeções de Esperma Intracitoplásmicas Limite: Adult / Female / Humans / Male / Pregnancy Idioma: En Revista: BMC Pregnancy Childbirth Ano de publicação: 2024 Tipo de documento: Article