The application of PGT-A for carriers of balanced structural chromosomal rearrangements.


Journal

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology
ISSN: 1473-0766
Titre abrégé: Gynecol Endocrinol
Pays: England
ID NLM: 8807913

Informations de publication

Date de publication:
2019
Historique:
entrez: 19 9 2019
pubmed: 19 9 2019
medline: 5 3 2020
Statut: ppublish

Résumé

The aim of this study was to analyze differences in chromosomal aberrations and euploidy in embryos of each translocation type and gender of carrier in the case series of 10 couples with balanced translocations who underwent IVF with embryos trophectoderm (TE) biopsy and PGT-A to detect chromosomal aberrations. This is a Case Series (Retrospective study). In each case, controlled ovarian hyperstimulation, oocyte insemination with intracytoplasmic sperm injection (ICSI) and cultivation gave multiple blastocysts, that underwent trophectoderm (TE) biopsy with PGT-A analysis using aCGH and NGS. Number of total unbalanced translocations compared to the number of sporadic aneuploid embryos was 39.6% to 39.6% (50% to 50% of all 37 aneuploid embryos). The highest euploidy rate was in male carrier group - 26.7% and the lowest in the Robertsonian translocation carrier group - 18.2%. Sporadic aneuploidy - 68.2% was highest in Robertsonian translocation carrier group and lowest in female group - 11.1%. Chromosomal aberrations related to translocation were highest in female carrier group - 77.8% and lowest in Robertsonian translocation carrier group - 13.6%. Our study showed that expectancy of total embryo aneuploidy rates will be higher in carriers, than in people with normal karyotype. The prevalence of chromosomal aberrations related to translocation was 4.5 times higher in Reciprocal carrier group than in Robertsonian translocation carrier group. Among maternal and paternal carrier groups, the embryos from female carriers had the lowest euploidy rate, unbalanced translocation rate 4.7 times higher than in the male carrier group and higher total aneuploidy rates.

Identifiants

pubmed: 31532310
doi: 10.1080/09513590.2019.1632091
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

18-23

Auteurs

Violeta Fodina (V)

Department of Gynecology and Reproduction, Clinic "IVF-Riga" , Riga , Latvia.

Alesja Dudorova (A)

Genetic laboratory, Clinic "IVF-Riga" , Riga , Latvia.

Baiba Alksere (B)

Genetic laboratory, Clinic "IVF-Riga" , Riga , Latvia.

Aigars Dzalbs (A)

Genetic laboratory, Clinic "IVF-Riga" , Riga , Latvia.
Center of Medical Genetics and Prenatal Diagnostics, Children's Clinical University Hospital , Riga , Latvia.

Natalija Vedmedovska (N)

Department of Gynecology and Reproduction, Clinic "IVF-Riga" , Riga , Latvia.

Santa Andersone (S)

Genetic laboratory, Clinic "IVF-Riga" , Riga , Latvia.

Conka Una (C)

Genetic laboratory, Clinic "IVF-Riga" , Riga , Latvia.

Erenpreiss Juris (E)

Department of Andrology, Clinic "IVF-Riga" , Riga , Latvia.
Riga Stradins University , Latvia.

Berzina Dace (B)

Genetic laboratory, Clinic "IVF-Riga" , Riga , Latvia.

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Classifications MeSH