Impact of trophectoderm biopsy on obstetric and perinatal outcomes following frozen-thawed embryo transfer cycles.

ART frozen–thawed embryo transfer obstetric complications perinatal complications preimplantation genetic testing trophectoderm biopsy

Journal

Human reproduction (Oxford, England)
ISSN: 1460-2350
Titre abrégé: Hum Reprod
Pays: England
ID NLM: 8701199

Informations de publication

Date de publication:
25 01 2021
Historique:
received: 09 05 2020
revised: 19 10 2020
pubmed: 15 12 2020
medline: 26 5 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

Does trophectoderm biopsy for preimplantation genetic testing (PGT) increase the risk of obstetric or perinatal complications in frozen-thawed embryo transfer (FET) cycles? Trophectoderm biopsy may increase the risk of hypertensive disorders of pregnancy (HDP) in pregnancies following FET cycles. Trophectoderm biopsy has replaced blastomere biopsy as the standard of care to procure cells for PGT analysis. Recently, there has been concern that trophectoderm biopsy may adversely impact obstetric and perinatal outcomes. Previous studies examining this question are limited by use of inappropriate control groups, small sample size or reporting on data that no longer reflects current IVF practice. This was a retrospective cohort study conducted at a single university-affiliated fertility center. A total of 756 patients who underwent FET with transfer of previously vitrified blastocysts that had either trophectoderm biopsy or were unbiopsied and resulted in a singleton live birth between 2013 and 2019 were included. Obstetric and perinatal outcomes for patients aged 20-44 years who underwent FET with transfer of previously vitrified blastocysts that were either biopsied (n = 241) or unbiopsied (n = 515) were analyzed. Primary outcome was odds of placentation disorders including HDP and rate of fetal growth restriction (FGR). Binary logistic regression was performed to control for potential covariates. The biopsy group was significantly older, had fewer anovulatory patients, was more often nulliparous and had fewer embryos transferred compared to the unbiopsied group. After controlling for potential covariates, the probability of developing HDP was significantly higher in the biopsy group compared with unbiopsied group (adjusted odds ratio (aOR) 1.943, 95% CI 1.072-3.521; P = 0.029).There was no significant difference between groups in the probability of placenta previa or placenta accreta. There was also no significant difference in the rate of FGR (aOR 1.397; 95% CI, 0.815-2.395; P = 0.224) or the proportion of low (aOR 0.603; 95% CI, 0.336-1.084; P = 0.091) or very low (aOR 2.948; 95% CI, 0.613-14.177; P = 0.177) birthweight infants comparing biopsied to unbiopsied groups. This was a retrospective study performed at a single fertility center, which may limit the generalizability of our findings. Trophectoderm biopsy may increase the risk of HDP in FET cycles, however, a prospective multicenter randomized trial should be performed to confirm these findings. No specific funding was obtained for this study. The authors declare no conflict of interest. NA.

Identifiants

pubmed: 33313768
pii: 6032760
doi: 10.1093/humrep/deaa316
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

340-348

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Reeva Makhijani (R)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

Chantal Barbara Bartels (CB)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

Prachi Godiwala (P)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

Alison Bartolucci (A)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

Andrea DiLuigi (A)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

John Nulsen (J)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

Daniel Grow (D)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

Claudio Benadiva (C)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

Lawrence Engmann (L)

Division of Reproductive Endocrinology and Infertility, Center for Advanced Reproductive Services, University of Connecticut School of Medicine, Farmington, CT, USA.

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