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M Banti, E Van Zyl, D Kafetzis, P-109 Non-invasive Genetic Testing (niPGTA) and Laser Assisted Hatching (LAH) may improve pregnancy and ongoing pregnancy rates in patients of advanced maternal age, Human Reproduction, Volume 39, Issue Supplement_1, July 2024, deae108.483, https://doi.org/10.1093/humrep/deae108.483
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Abstract
Does niPGTA and LAH improve pregnancy and ongoing pregnancy rates in patients of advanced maternal age?
niPGTA increases pregnancy and clinical pregnancy rates in patients aged ≥38 years compared to those without tested embryos, while LAH may further improve pregnancy outcomes.
Embryos release cell-free DNA (cf-DNA) in the IVF culture media, which can be analyzed for chromosomal constitution. The benefit that niPGTA holds over PGT-A is that it is a non-invasive test and could potentially produce comparable results. Therefore, the time to pregnancy and the risk of miscarriage could be reduced in comparison to an IVF treatment with non-tested embryos. Previous studies have shown high concordance with trophectoderm biopsies in PGT-A patients and improved outcomes with LAH in frozen-thawed cycles. However, there is a lack of studies investigating clinical pregnancy rates with niPGTA.
Retrospective cohort study including 74 patients aged ≥38 years, who underwent Single Frozen Embryo Transfer (FET) from May 2021 to February 2023. Patients who had Endometrial Receptivity Assay (ERA) were excluded.
32 couples had niPGTA; Spent Blastocyst Media (SBM) for each blastocyst were collected on Day 6 and analyzed using the EMBRACE test. Embryos were vitrified. 42 couples had their blastocysts vitrified on Day 5/6 without testing. LAH was introduced to all patients in October 2021. Before that, no LAH was performed. Embryos were transferred to patients 2 hours post-warming after LAH. Pregnancy test was performed 10 days after FET and clinical pregnancy was established.
There was a statistical significant increase of pregnancy rate (p = 0.017, Pearson’s Chi-Squared test) and a trend towards higher clinical pregnancy rate for niPGTA patients versus those who had a transfer of not tested embryos. Regarding LAH, there was a trend towards higher pregnancy and clinical pregnancy rates in both niPGTA and not tested group. Results for pregnancies and clinical pregnancies are presented in Table 1.
. | Overall niPGTA . | Overall NOT TESTED . | niPGTA with LAH . | niPGTA without LAH . | Not Tested with LAH . | Not Tested without LAH . |
---|---|---|---|---|---|---|
Number of patients | 32 | 42 | 17 | 15 | 20 | 22 |
Pregnancy (%) | 22 (68.75) | 16 (38.10)* | 13 (76.47) | 9 (60.00) | 8 (40.00) | 8 (36.36) |
Clinical Pregnancy (%) | 15 (46.88) | 15 (35.71) | 9 (52.94) | 6 (40.00) | 8 (40.00) | 7 (31.82) |
. | Overall niPGTA . | Overall NOT TESTED . | niPGTA with LAH . | niPGTA without LAH . | Not Tested with LAH . | Not Tested without LAH . |
---|---|---|---|---|---|---|
Number of patients | 32 | 42 | 17 | 15 | 20 | 22 |
Pregnancy (%) | 22 (68.75) | 16 (38.10)* | 13 (76.47) | 9 (60.00) | 8 (40.00) | 8 (36.36) |
Clinical Pregnancy (%) | 15 (46.88) | 15 (35.71) | 9 (52.94) | 6 (40.00) | 8 (40.00) | 7 (31.82) |
p = 0.017
. | Overall niPGTA . | Overall NOT TESTED . | niPGTA with LAH . | niPGTA without LAH . | Not Tested with LAH . | Not Tested without LAH . |
---|---|---|---|---|---|---|
Number of patients | 32 | 42 | 17 | 15 | 20 | 22 |
Pregnancy (%) | 22 (68.75) | 16 (38.10)* | 13 (76.47) | 9 (60.00) | 8 (40.00) | 8 (36.36) |
Clinical Pregnancy (%) | 15 (46.88) | 15 (35.71) | 9 (52.94) | 6 (40.00) | 8 (40.00) | 7 (31.82) |
. | Overall niPGTA . | Overall NOT TESTED . | niPGTA with LAH . | niPGTA without LAH . | Not Tested with LAH . | Not Tested without LAH . |
---|---|---|---|---|---|---|
Number of patients | 32 | 42 | 17 | 15 | 20 | 22 |
Pregnancy (%) | 22 (68.75) | 16 (38.10)* | 13 (76.47) | 9 (60.00) | 8 (40.00) | 8 (36.36) |
Clinical Pregnancy (%) | 15 (46.88) | 15 (35.71) | 9 (52.94) | 6 (40.00) | 8 (40.00) | 7 (31.82) |
p = 0.017
More patients are required to confirm clinical significance of pregnancy and clinical pregnancy rates of niPGTA over not tested embryos and if LAH can improve the outcomes. A review of patients who had previous implantation failures and miscarriages in addition to ERA could yield clearer conclusions.
The results of this study are encouraging for niPGTA combined with LAH for patients aged ≥38 years. Further studies on niPGTA and modifications of the protocol for increased concordance rates and shorter time in embryo culture should be explored.
Not applicable
- pregnancy
- biopsy
- fertilization in vitro
- abortion, spontaneous
- embryo stage 3
- chromosomes
- culture media
- dna
- embryo
- embryo transfer
- lasers
- pregnancy outcome
- pregnancy rate
- pregnancy tests
- genetic screening
- intravenous fluid
- pregnancy with advanced maternal age
- transfer technique
- assisted embryo hatching
- cell-free dna
- clinical relevance