Skip to main content
Top
Published in: BMC Pregnancy and Childbirth 1/2024

Open Access 01-12-2024 | ICSI | Research

Diverse impacts of female chromosomal polymorphisms on assisted reproduction outcomes: a retrospective cohort study

Authors: Yongjie Lu, Tian Tian, Lixue Chen, Liying Yan, Liang Chang, Jie Qiao

Published in: BMC Pregnancy and Childbirth | Issue 1/2024

Login to get access

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.
Appendix
Available only for authorised users
Literature
1.
go back to reference Shaffer LG, McGowan-Jordan J, Schmid M. ISCN (2013): an international system for human cytogenetic nomenclature. Basel Switzerland: Karger; 2013. Shaffer LG, McGowan-Jordan J, Schmid M. ISCN (2013): an international system for human cytogenetic nomenclature. Basel Switzerland: Karger; 2013.
2.
go back to reference Cheng R, Ma Y, Nie Y, Qiao X, Yang Z, Zeng R, et al. Chromosomal polymorphisms are associated with female infertility and adverse reproductive outcomes after infertility treatment: a 7-year retrospective study. Reprod Biomed Online. 2017;35(1):72–80.CrossRefPubMed Cheng R, Ma Y, Nie Y, Qiao X, Yang Z, Zeng R, et al. Chromosomal polymorphisms are associated with female infertility and adverse reproductive outcomes after infertility treatment: a 7-year retrospective study. Reprod Biomed Online. 2017;35(1):72–80.CrossRefPubMed
3.
go back to reference Feng X, Liu J, Wang Y, Fu J, Qin Q, Cao Y, et al. Acrocentric chromosome polymorphic variants on Chinese female have possible association with unexplained recurrent pregnancy loss. Reproduct sci (Thousand Oaks Calif). 2021;28(2):575–84.CrossRef Feng X, Liu J, Wang Y, Fu J, Qin Q, Cao Y, et al. Acrocentric chromosome polymorphic variants on Chinese female have possible association with unexplained recurrent pregnancy loss. Reproduct sci (Thousand Oaks Calif). 2021;28(2):575–84.CrossRef
4.
go back to reference Madon PF, Athalye AS, Parikh FR. Polymorphic variants on chromosomes probably play a significant role in infertility. Reprod Biomed Online. 2005;11(6):726–32.CrossRefPubMed Madon PF, Athalye AS, Parikh FR. Polymorphic variants on chromosomes probably play a significant role in infertility. Reprod Biomed Online. 2005;11(6):726–32.CrossRefPubMed
5.
go back to reference Minocherhomji S, Athalye AS, Madon PF, Kulkarni D, Uttamchandani SA, Parikh FR. A case-control study identifying chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype. Fertil Steril. 2009;92(1):88–95.CrossRefPubMed Minocherhomji S, Athalye AS, Madon PF, Kulkarni D, Uttamchandani SA, Parikh FR. A case-control study identifying chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype. Fertil Steril. 2009;92(1):88–95.CrossRefPubMed
6.
go back to reference Morales R, Lledó B, Ortiz JA, Ten J, Llácer J, Bernabeu R. Chromosomal polymorphic variants increase aneuploidies in male gametes and embryos. Syst Biol Reprod Med. 2016;62(5):317–24.CrossRefPubMed Morales R, Lledó B, Ortiz JA, Ten J, Llácer J, Bernabeu R. Chromosomal polymorphic variants increase aneuploidies in male gametes and embryos. Syst Biol Reprod Med. 2016;62(5):317–24.CrossRefPubMed
7.
go back to reference Šípek A Jr, Mihalová R, Panczak A, Hrčková L, Janashia M, Kaspříková N, et al. Heterochromatin variants in human karyotypes: a possible association with reproductive failure. Reprod Biomed Online. 2014;29(2):245–50.CrossRefPubMed Šípek A Jr, Mihalová R, Panczak A, Hrčková L, Janashia M, Kaspříková N, et al. Heterochromatin variants in human karyotypes: a possible association with reproductive failure. Reprod Biomed Online. 2014;29(2):245–50.CrossRefPubMed
8.
go back to reference Wang Y, Li G, Zuo MZ, Fang JH, Li HR, Quan DD, et al. Y chromosome polymorphisms may contribute to an increased risk of male-induced unexplained recurrent miscarriage. Biosci Rep. 2017;37(2) Wang Y, Li G, Zuo MZ, Fang JH, Li HR, Quan DD, et al. Y chromosome polymorphisms may contribute to an increased risk of male-induced unexplained recurrent miscarriage. Biosci Rep. 2017;37(2)
9.
go back to reference Rodriguez F, Cruz M, Requena A. Impact of parental chromosomal polymorphisms on the incidence of congenital anomalies and perinatal complications in a cohort of newborns conceived after ICSI + PGT-A. Reproduct biol endocrinol: RB&E. 2022;20(1):145.CrossRef Rodriguez F, Cruz M, Requena A. Impact of parental chromosomal polymorphisms on the incidence of congenital anomalies and perinatal complications in a cohort of newborns conceived after ICSI + PGT-A. Reproduct biol endocrinol: RB&E. 2022;20(1):145.CrossRef
10.
go back to reference Xu X, Zhang R, Wang W, Liu H, Liu L, Mao B, et al. The effect of chromosomal polymorphisms on the outcomes of fresh IVF/ICSI-ET cycles in a Chinese population. J Assist Reprod Genet. 2016;33(11):1481–6.CrossRefPubMedPubMedCentral Xu X, Zhang R, Wang W, Liu H, Liu L, Mao B, et al. The effect of chromosomal polymorphisms on the outcomes of fresh IVF/ICSI-ET cycles in a Chinese population. J Assist Reprod Genet. 2016;33(11):1481–6.CrossRefPubMedPubMedCentral
11.
go back to reference Liang J, Zhang Y, Yu Y, Sun W, Jing J, Liu R. Effect of chromosomal polymorphisms of different genders on fertilization rate of fresh IVF-ICSI embryo transfer cycles. Reprod Biomed Online. 2014;29(4):436–44.CrossRefPubMed Liang J, Zhang Y, Yu Y, Sun W, Jing J, Liu R. Effect of chromosomal polymorphisms of different genders on fertilization rate of fresh IVF-ICSI embryo transfer cycles. Reprod Biomed Online. 2014;29(4):436–44.CrossRefPubMed
12.
go back to reference Li SJ, Cheng YX, Ye S, Zhou DN, Zhang Y, Yin TL, et al. Chromosomal polymorphisms associated with reproductive outcomes after IVF-ET. J Assist Reprod Genet. 2020;37(7):1703–10.CrossRefPubMedPubMedCentral Li SJ, Cheng YX, Ye S, Zhou DN, Zhang Y, Yin TL, et al. Chromosomal polymorphisms associated with reproductive outcomes after IVF-ET. J Assist Reprod Genet. 2020;37(7):1703–10.CrossRefPubMedPubMedCentral
13.
go back to reference Ni T, Li J, Chen H, Gao Y, Gao X, Yan J, et al. Male chromosomal polymorphisms reduce cumulative live birth rate for IVF couples. J Assist Reprod Genet. 2017;34(8):1017–25.CrossRefPubMedPubMedCentral Ni T, Li J, Chen H, Gao Y, Gao X, Yan J, et al. Male chromosomal polymorphisms reduce cumulative live birth rate for IVF couples. J Assist Reprod Genet. 2017;34(8):1017–25.CrossRefPubMedPubMedCentral
14.
go back to reference Hong Y, Zhou YW, Tao J, Wang SX, Zhao XM. Do polymorphic variants of chromosomes affect the outcome of in vitro fertilization and embryo transfer treatment? Hum Reprod. 2011;26(4):933–40.CrossRefPubMedPubMedCentral Hong Y, Zhou YW, Tao J, Wang SX, Zhao XM. Do polymorphic variants of chromosomes affect the outcome of in vitro fertilization and embryo transfer treatment? Hum Reprod. 2011;26(4):933–40.CrossRefPubMedPubMedCentral
15.
go back to reference Ralapanawe MSB, Gajaweera SL, Karunaratne N, Price MJ, Melo P, Coomarasamy A, et al. Chromosomal polymorphisms in assisted reproduction: an analysis of 942 cycles. Reproduct fertil. 2022;3(3):133–9.CrossRef Ralapanawe MSB, Gajaweera SL, Karunaratne N, Price MJ, Melo P, Coomarasamy A, et al. Chromosomal polymorphisms in assisted reproduction: an analysis of 942 cycles. Reproduct fertil. 2022;3(3):133–9.CrossRef
16.
go back to reference Zhao J, Huang B, Hao J, Xu B, Li Y. Chromosomal polymorphisms have no negative effect on reproductive outcomes after IVF/ICSI-ET/FET. Sci Rep. 2022;12(1):19052.CrossRefPubMedPubMedCentral Zhao J, Huang B, Hao J, Xu B, Li Y. Chromosomal polymorphisms have no negative effect on reproductive outcomes after IVF/ICSI-ET/FET. Sci Rep. 2022;12(1):19052.CrossRefPubMedPubMedCentral
17.
go back to reference Lu YJ, Li Q, Chen LX, Tian T, Kang J, Hao YX, et al. Association between maternal MTHFR C677T/A1298C combination polymorphisms and IVF/ICSI outcomes: a retrospective cohort study. Hum Reprod Open. 2023;2023(1):hoac055.CrossRefPubMed Lu YJ, Li Q, Chen LX, Tian T, Kang J, Hao YX, et al. Association between maternal MTHFR C677T/A1298C combination polymorphisms and IVF/ICSI outcomes: a retrospective cohort study. Hum Reprod Open. 2023;2023(1):hoac055.CrossRefPubMed
18.
go back to reference Obstetrics-Subgroup, Chinese-Society-of-Obstetrics-and-Gynecology, Chinese-Medical-Association, Chinese-Expert-Consensus-Group-on-Diagnosis-and-Management-of-Recurrent-Spontaneous-Abortion.: Chinese expert consensus on diagnosis and management of recurrent spontaneous abortion (2022). Zhonghua fu chan ke za zhi., 57(9):653–667. Obstetrics-Subgroup, Chinese-Society-of-Obstetrics-and-Gynecology, Chinese-Medical-Association, Chinese-Expert-Consensus-Group-on-Diagnosis-and-Management-of-Recurrent-Spontaneous-Abortion.: Chinese expert consensus on diagnosis and management of recurrent spontaneous abortion (2022). Zhonghua fu chan ke za zhi., 57(9):653–667.
19.
go back to reference Zong X, Guo Y, Li H, Li R, Qiao J. Obstetric and perinatal outcomes following frozen and fresh embryo transfer in patients with endometrial hyperplasia and carcinoma: a retrospective study in a high-volume reproductive center. BMC pregnancy childbirth. 2023;23(1):92.CrossRefPubMedPubMedCentral Zong X, Guo Y, Li H, Li R, Qiao J. Obstetric and perinatal outcomes following frozen and fresh embryo transfer in patients with endometrial hyperplasia and carcinoma: a retrospective study in a high-volume reproductive center. BMC pregnancy childbirth. 2023;23(1):92.CrossRefPubMedPubMedCentral
20.
go back to reference van de Werken C, van der Heijden GW, Eleveld C, Teeuwssen M, Albert M, Baarends WM, et al. Paternal heterochromatin formation in human embryos is H3K9/HP1 directed and primed by sperm-derived histone modifications. Nat Commun. 2014;5:5868.CrossRefPubMed van de Werken C, van der Heijden GW, Eleveld C, Teeuwssen M, Albert M, Baarends WM, et al. Paternal heterochromatin formation in human embryos is H3K9/HP1 directed and primed by sperm-derived histone modifications. Nat Commun. 2014;5:5868.CrossRefPubMed
22.
23.
go back to reference Sullivan LL, Chew K, Sullivan BA. Alpha satellite DNA variation and function of the human centromere. Nucleus (Austin Tex). 2017;8(4):331–9.PubMedPubMedCentral Sullivan LL, Chew K, Sullivan BA. Alpha satellite DNA variation and function of the human centromere. Nucleus (Austin Tex). 2017;8(4):331–9.PubMedPubMedCentral
24.
go back to reference Janssen A, Colmenares SU, Karpen GH. Heterochromatin: Guardian of the genome. Annu Rev Cell Dev Biol. 2018;34:265–88.CrossRefPubMed Janssen A, Colmenares SU, Karpen GH. Heterochromatin: Guardian of the genome. Annu Rev Cell Dev Biol. 2018;34:265–88.CrossRefPubMed
25.
go back to reference Sun L, Chen ZH, Yang L, Yi CX, Liu J, Ou CQ. Chromosomal polymorphisms are independently associated with multinucleated embryo formation. J Assist Reprod Genet. 2018;35(1):149–56.CrossRefPubMed Sun L, Chen ZH, Yang L, Yi CX, Liu J, Ou CQ. Chromosomal polymorphisms are independently associated with multinucleated embryo formation. J Assist Reprod Genet. 2018;35(1):149–56.CrossRefPubMed
26.
Metadata
Title
Diverse impacts of female chromosomal polymorphisms on assisted reproduction outcomes: a retrospective cohort study
Authors
Yongjie Lu
Tian Tian
Lixue Chen
Liying Yan
Liang Chang
Jie Qiao
Publication date
01-12-2024
Publisher
BioMed Central
Published in
BMC Pregnancy and Childbirth / Issue 1/2024
Electronic ISSN: 1471-2393
DOI
https://doi.org/10.1186/s12884-024-06532-w

Other articles of this Issue 1/2024

BMC Pregnancy and Childbirth 1/2024 Go to the issue