Literature DB >> 27560353

Chromosomal polymorphic variants increase aneuploidies in male gametes and embryos.

Ruth Morales1, Belén Lledó1, José A Ortiz1, Jorge Ten2, Joaquin Llácer2, Rafael Bernabeu2.   

Abstract

UNLABELLED: Chromosomal polymorphisms involve heterochromatic regions and occur in the general population. However, previous studies have reported a higher incidence of these variants in infertile patients. The aim of this study was to examine the relationship between polymorphic variants and infertility and their association with aneuploidies in male gametes and embryos. We retrospectively considered 1,551 cytogenetic studies involving infertile patients (study group; n=866) and oocyte/sperm donors as the control group (n=685). We had detected 168 polymorphisms in the study group and 92 in the control group. An increase in the frequency of polymorphic variants was observed among infertile patients (19.4% study group vs. 13.4% control group; P < 0.01). Sperm aneuploidies among 145 infertile men were evaluated by fluorescent in situ hybridization (FISH). The frequency of infertile men with increased rates of sperm aneuploidy was higher among polymorphism carriers. Twenty men showed an abnormal rate of sperm aneuploidy in the carrier group (n=53) vs. 15 in the non-carrier group (n=92) (37.7% vs. 16.3%, respectively; P < 0.01). Finally, aneuploidies in blastocysts (n=301) resulting from donated oocytes were also examined by array comparative genomic hybridization (array-CGH). Significant differences were reported in the embryo aneuploidy rate between female carriers and non-carriers in oocyte donation cycles (50.0% vs. 27.6%; P < 0.001). This study suggests that polymorphic variants have an impact on fertility. Moreover, our results show a relationship between polymorphisms and aneuploidy in spermatozoa and embryos. ABBREVIATIONS: FISH: fluorescent in situ hybridization; CGH: comparative genomic hybridization; ESHRE: European Society of Human Reproduction and Embryology; ASRM: American Society for Reproductive Medicine; RPL: recurrent pregnancy loss; WHO: World Health Organization; ISCN: International System for Human Cytogenetic Nomenclature guidelines; WGA: whole genome amplification; SPSS: Statistical Package for Social Sciences.

Entities:  

Keywords:  Aneuploidy rate; array-CGH; chromosomal polymorphic variants; embryo

Mesh:

Year:  2016        PMID: 27560353     DOI: 10.1080/19396368.2016.1212949

Source DB:  PubMed          Journal:  Syst Biol Reprod Med        ISSN: 1939-6368            Impact factor:   3.061


  9 in total

Review 1.  Genetic and epigenetic variations associated with idiopathic recurrent pregnancy loss.

Authors:  Luis Alejandro Arias-Sosa; Iván Darío Acosta; Elkin Lucena-Quevedo; Harold Moreno-Ortiz; Clara Esteban-Pérez; Maribel Forero-Castro
Journal:  J Assist Reprod Genet       Date:  2018-01-09       Impact factor: 3.412

2.  Chromosomal polymorphisms are independently associated with multinucleated embryo formation.

Authors:  Ling Sun; Zhi-Heng Chen; Li Yang; Cui-Xing Yi; Jun Liu; Chun-Quan Ou
Journal:  J Assist Reprod Genet       Date:  2017-09-12       Impact factor: 3.412

3.  Male chromosomal polymorphisms reduce cumulative live birth rate for IVF couples.

Authors:  Tianxiang Ni; Jing Li; Hong Chen; Yuan Gao; Xuan Gao; Junhao Yan; Zi-Jiang Chen
Journal:  J Assist Reprod Genet       Date:  2017-06-01       Impact factor: 3.412

4.  [Chromosomal polymorphisms are associated with blastomere multinucleation in IVF/ICSI cycles].

Authors:  Zhiheng Chen; Li Yang; Cuiqing Yi; Jun Liu; Ling Sun
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2020-01-30

5.  Chromosome heteromorphisms: do they entail a reproductive risk for male carriers?

Authors:  Ester Anton; Elena Garcia-Guixé; Mireia Ramos-Muntada; Anna Godo; Mireia Sandalinas; Joan Blanco
Journal:  Asian J Androl       Date:  2020 Sep-Oct       Impact factor: 3.285

6.  The Influence of Chromosomal Polymorphism on Embryo Development and Embryonic Molecular Karyotype in Preimplantation Genetic Testing for Chromosomal Translocation.

Authors:  Gang Li; Weiyi Shi; Wenbin Niu; Jiawei Xu; Yihong Guo; Yingchun Su; Yingpu Sun
Journal:  Front Physiol       Date:  2020-11-26       Impact factor: 4.566

7.  Analysis of Aneuploidy Rate and Pregnancy Outcomes in Unexplained Recurrent Pregnancy Loss Couples With Chromosome Polymorphism After PGT-A.

Authors:  Mingzhu Cao; Qian Zhang; Wei Zhou; Yueting Zhu; Hongchang Li; Junhao Yan
Journal:  Front Med (Lausanne)       Date:  2022-03-31

8.  Impact of parental chromosomal polymorphisms on the incidence of congenital anomalies and perinatal complications in a cohort of newborns conceived after ICSI + PGT-A.

Authors:  Freddy Rodriguez; Maria Cruz; Antonio Requena
Journal:  Reprod Biol Endocrinol       Date:  2022-09-27       Impact factor: 4.982

9.  Parental chromosomal heteromorphisms are not associated with an increased risk of embryo aneuploidy.

Authors:  Carlos Hernandez-Nieto; Sonia Gayete-Lafuente; Tamar Alkon-Meadows; Joseph Lee; Martha Luna-Rojas; Tanmoy Mukherjee; Alan B Copperman; Benjamin Sandler
Journal:  JBRA Assist Reprod       Date:  2021-10-04
  9 in total

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