Assisted Reproduction · Safety and Risks

Obstetric, neonatal, and child health outcomes following embryo biopsy for preimplantation genetic testing

Alteri A, Cermisoni GC, Pozzoni M, Gaeta G, Cavoretto PI, Viganò P

Published May 2, 2023 Human reproduction update
DOI 10.1093/humupd/dmad001 PMID 36655536 PMC PMC10152168

RRM Academy Synopsis

Embryo biopsy for PGT shows possible links to pregnancy hypertension

Embryo biopsy for preimplantation genetic testing (PGT) showed possible links to high blood pressure in pregnancy, a 2023 scoping review of 31 studies found. The studies compared pregnancies from biopsied and unbiopsied embryos. Limited, controversial data also pointed to preterm birth, birth defects and low birthweight, depending on biopsy stage.

Key Findings

  • One retrospective cohort of singletons after blastomere biopsy for monogenic disorders (345 biopsied, 422 not) found more hypertensive disorders (aOR 5.9, 95% CI 1.9–18.2) and small-for-gestational-age births (aOR 2.5, 95% CI 1.2–5.0).
  • In a registry-based cohort of singletons, frozen biopsied embryos (n = 6244) had a slightly higher likelihood of preterm delivery than non-biopsied blastocysts (n = 10002): aOR 1.20, 95% CI 1.09–1.33.
  • Of five trophectoderm biopsy studies, two found higher hypertensive risk (pre-eclampsia aOR 3.02, 95% CI 1.10–8.29; hypertensive disorders aOR 1.94, 95% CI 1.07–3.52) and three frozen-transfer studies found no significant difference.
  • All long-term studies (follow-up 18 months to 9 years) involved blastomere biopsy. In one series, neurological optimality scores were lower at 2 years and similar at 9 years (43 biopsied, 56 controls).
  • For polar body biopsy, one retrospective study (106 women with biopsy, 220 without) found similar median birthweight, and no other obstetric or neonatal outcome data were available.

Interpretation

A scoping review maps the studies on a topic and summarizes them in words. Most obstetric and neonatal studies were retrospective cohorts. Adjustment for maternal age, body mass index, cause of infertility and embryo freezing was limited. Most studies were too small to detect subtle differences. The authors note that low birthweight and adverse neurological outcomes are also associated with multiple pregnancy. They call the evidence controversial, scarce and weak. Polar body biopsy has almost no outcome data, and trophectoderm biopsy has no long-term data.

RRM Context

Preimplantation genetic testing happens only inside IVF. IVF bypasses infertility and does not establish why conception fails. The review concludes that the short- and long-term risks of embryo biopsy for pregnancy and later health remain uncertain. The authors also state that infertility itself is related to adverse pregnancy and birth outcomes. Restorative reproductive medicine looks for the cause of infertility in both partners.

Abstract

Preimplantation genetic testing (PGT) of embryos developed in vitro requires a biopsy for obtaining cellular samples for the analysis. Signs of cell injury have been described in association with this procedure. Thus, the consequences of the biopsy on obstetric and neonatal outcomes have been the subject of some quantitative analyses, although the reliability of data pooling may be limited by important issues in the various reports. The present review identifies evidence for whether pregnancies conceived after embryo biopsy are associated with a higher risk of adverse obstetric, neonatal, and long-term outcomes. Available evidence has been summarized considering manipulation at various stages of embryo development. We used the scoping review methodology. Searches of article databases were performed with keywords pertaining to the embryo biopsy technique and obstetric, neonatal, and postnatal outcomes. Studies in which embryos were biopsied at different stages (i.e. both at the cleavage and blastocyst stages) were excluded. We included data on fresh and frozen embryo transfers. The final sample of 31 documents was subjected to qualitative thematic analysis. Sound evidence is lacking to fully address the issues on the potential obstetric, neonatal or long-term consequences of embryo biopsy. For polar body biopsy, the literature is too scant to draw any conclusion. Some data, although limited and controversial, suggest a possible association of embryo biopsy at the cleavage stage with an increased risk of low birthweight and small for gestational age neonates compared to babies derived from non-biopsied embryos. An increase in preterm deliveries and birth defects in cases of trophectoderm biopsy was suggested. For both biopsy methods (at the cleavage and blastocyst stages), an increased risk for hypertensive disorders of pregnancy was found. However, these findings may be explained by confounders such as other embryo manipulation procedures or by intrinsic patient or population characteristics. Since there is inadequate evidence to assess obstetric, neonatal, and long-term health outcomes following embryo biopsy, an invasive PGT strategy should be developed with a cautious approach. A non-invasive approach, based on the analysis of embryo cell-free DNA, needs to be pursued to overcome the potential limitations of embryo biopsy.

Topics

By this author

Related research

Assisted Reproduction › Safety and Risks › Procedure-Attributable Risk · Pregnancy › Neonatal Outcomes › Neonatal Morbidity · Birth and Delivery › Birth Outcomes › Maternal Morbidity
Alessandra Alteri, Greta Chiara Cermisoni, Mirko Pozzoni, Gerarda Gaeta, Paolo Ivo Cavoretto, Paola Viganò
A Alteri, G Cermisoni, M Pozzoni, G Gaeta, P Cavoretto, P Viganò
PMID 36655536 36655536 DOI 10.1093/humupd/dmad001 10.1093/humupd/dmad001 Alteri et al. 2023, Alteri 2023