Evidence map›Paper›PMID 32030567›Full record

ArticleClinical and translational medicine2020

Embryos derived from donor or patient oocytes are not different for in vitro fertilization outcomes when PGT allows euploid embryo selection: a retrospective study.

Elizabeth Schaeffer, Leonardo M Porchia, Adina Neumann, Almena Luna, Tania Rojas, Esther López-Bayghen

Abstract read
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Article in Clinical and translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Elizabeth SchaefferLaboratorio de Investigación y Diagnóstico Molecular, Instituto de Infertilidad y Genética, Ingenes, México City, Mexico.
Leonardo M PorchiaDepartamento de Toxicología, Centro de Investigación de Estudios Avanzados del Instituto Politécnico Nacional, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, CP 07360, México City, Distrito Federal, Mexico.
Adina NeumannLaboratorio de Investigación y Diagnóstico Molecular, Instituto de Infertilidad y Genética, Ingenes, México City, Mexico.
Almena LunaLaboratorio de Investigación y Diagnóstico Molecular, Instituto de Infertilidad y Genética, Ingenes, México City, Mexico.
Tania RojasLaboratorio de Investigación y Diagnóstico Molecular, Instituto de Infertilidad y Genética, Ingenes, México City, Mexico.
Esther López-BayghenDepartamento de Toxicología, Centro de Investigación de Estudios Avanzados del Instituto Politécnico Nacional, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, CP 07360, México City, Distrito Federal, Mexico. ebayghen@cinvestav.mx.ORCID http://orcid.org/0000-0002-2849-7587

Funding

Consejo Nacional de Ciencia y Tecnología 212650Consejo Nacional de Ciencia y Tecnología 231793
6 · The paper itself

Abstract

backgroundAt our facilities, patients that received embryos using donor oocyte during in vitro fertilization (IVF), usually have had at least one failed attempt to produce at least one euploid embryo with their own oocytes; however, the current debate between using donor over patient oocytes remains inconclusive. We examined the aneuploidy rate and IVF clinical outcomes from embryos derived from either donor or patient oocytes.

methodsRetrospectively, 973 cycles were examined of patients who underwent a standard IVF protocol. Chromosomal content was determined using Pre-implantation Genetic Testing (PGT) by either microarray-comparative genomic hybridization or Next-generation sequencing from either Day 3 (blastocysts) or Day 5 (trophectoderm) embryo biopsies, respectively. Embryo implantation was confirmed by serum β-hCG (> 10 m IU/mL/Day 14), whereas clinical pregnancy by a fetal heartbeat (Week 6.5-8).

resultsEmbryos derived from donor oocytes presented with more monosomies than embryos derived from patient oocytes (41.2% vs. 25.4%, p < 0.05, respectively); however, only Trisomy 7 (0.4% vs. 2.3%, p < 0.05) and Trisomy in X (0.7% vs. 2.3%, p < 0.05) were significantly less present when compared to patient oocyte derived embryos. Interestingly, rates for embryo implantation (46.7% vs. 50.8%, p = 0.35), clinical pregnancy (38.5% vs. 43.1%, p = 0.30), and live birth (30.5% vs. 30.5%, p = 0.99) were similar for embryos derived from donor and patient oocytes. These results did not change when adjusted for the number of embryos implanted.

conclusionHere, we show no significant differences in achieving pregnancy when using donor oocytes. Taking into consideration that aneuploidy rates are > 30% in embryos, independent of the oocyte origin, PGT should be recommended with donor oocytes as well.

Indexed as

AneuploidyImplantationPreimplantation genetic diagnosis

Identifiers

PMID32030567
PMCPMC7005195

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