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Review of human oocyte cryopreservation in ART programs: Current challenges and opportunities

Journal

CRYOBIOLOGY
Volume 113, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cryobiol.2023.104590

Keywords

Infertility; Slow -freezing; Vitrification; Human oocyte; Oocyte donation; Egg bank; Fertility preservation; Clinical pregnancy outcomes

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The use of oocyte cryopreservation has significantly increased in recent years, with advancements in vitrification techniques and cryoprotectants improving clinical infertility treatment. Biosafety concerns arise due to potential contamination from liquid nitrogen, and research suggests the need to further understand the impact of vitrification-induced stress on epigenetic modifications. It is important to explore the benefits, efficiency, and potential long-term consequences of human oocyte vitrification for offspring health.
Oocyte cryopreservation has notably increased in recent times, to become an essential part of clinical infertility treatment. Since the 1980s, many improvements in oocyte cryopreservation (OC) have been adopted, including the great advance with the application of vitrification. The commonly used vitrification protocol applies different cryoprotectants (Ethylene glycol and/or DMSO and/or PROH and sucrose and/or Trehalose) and two different steps: firstly, exposure in equilibration solution for 5-15 min, followed by a vitrification solution for 60-90 s at room temperature. The warming method includes a first step for 1 min at 37 degrees C and 3 subsequent steps at room temperature to remove the cryoprotectant for a total of 9-12 min. In addition, biosafety is a critical aspect to mention, and it is related to devices used during the vitrification, mainly in terms of whether the biological vitrified material comes in direct contact with liquid nitrogen (open vitrification) or not (closed vitrification), where LN2 may contain potentially contaminating viruses or pathogens. Furthermore, during early development major waves of epigenetic reprogramming take place. Recent literature suggests that epigenetic and tran-scriptomic profiles are sensitive to the stress induced by vitrification, including osmotic shock, temperature, rapid changes of pH and toxicity of cryoprotectants. It is, therefore, important to better understand the potential perturbations of epigenetic modifications that may be associated with the globally used vitrification methods. Therefore, we here discuss the benefits and efficiency of human oocyte vitrification; we also review the evidence surrounding oocyte cryopreservation-related epigenetic modifications and potential epigenetic dysregulations, together with long-term consequences for offspring health.

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