4.4 Article

The effect of trophectoderm biopsy technique and sample handling on artefactual mosaicism

期刊

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
卷 39, 期 6, 页码 1333-1340

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10815-022-02453-9

关键词

PGT-A; Blastocyst; Biopsy; Tubing; Mosaicism; Artefactual

资金

  1. Catedra d'Investigacio en Obstetricia i Ginecologia of the Department of Obstetrics and Gynecology, Hospital Universitari Dexeus, Universitat Autnoma de Barcelona

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The prevalence of embryo mosaicism in preimplantation genetic testing for aneuploidy (PGT-A) cycles is not significantly associated with the trophectoderm biopsy technique or the time to tubing. As long as standardized high quality procedures are followed, the specific approach to trophectoderm biopsy does not increase the generation of artefactual mosaicism. The study suggests that minimizing blastocyst manipulation should be the goal during biopsy procedures.
Purpose To determine whether embryo mosaicism prevalence in preimplantation genetic testing for aneuploidy (PGT-A) cycles is associated with the trophectoderm biopsy technique used (a. number of laser pulses or b. the use of flicking or pulling) or the time to tubing. Methods Prospective observational study performed in a single IVF-PGT-A setting from May 2019 to May 2021. Trophectoderm biopsies were analysed by next-generation sequencing. Mosaicism was analysed in relation to the biopsy methodology (number of laser pulses and pulling vs flicking), time elapsed from biopsy to tubing (min), and time of sample cryostorage from tubing to amplification (days). As a secondary objective, the number of laser pulses and biopsy methodology were studied in relation to clinical outcomes of transferred euploid blastocysts. Results None of the analysed variables were associated to mosaicism prevalence. Multivariable regression analysis demonstrated that mosaicism prevalence was comparable either when > 3 laser pulses were used as compared to <= 3 (13.9% vs 13.8%, aOR = 0.8726 [0.60-1.28]) and pulling compared to flicking (13.1% vs 14.0%, aOR = 0.86 [0.60-1.23]). Moreover, neither the number of laser pulses during biopsy (> 3 vs <= 3) nor the technique used (pulling vs flicking) were associated with clinical pregnancy after the transfer of frozen-thawed euploid blastocysts (54.9% vs 55.2%, aOR = 1.05 [0.53-2.09]; 61.1% vs 52.9%, aOR = 1.11 [0.55-2.25], respectively). Conclusion Our results suggest that, as long as the biopsy and tubing procedures are performed following standardized high quality procedures, no specific approach would increase the generation of artefactual mosaicism as a result of trophectoderm biopsy. Trophectoderm biopsies should be performed regardless of the methodology but always aiming on minimising blastocyst manipulation.

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