Autologous endometrial cell co-culture improves human embryo development to high-quality blastocysts: a randomized controlled trial.
Adult
Blastocyst
/ cytology
Coculture Techniques
Double-Blind Method
Embryo Culture Techniques
/ methods
Embryo Transfer
/ methods
Embryonic Development
/ physiology
Endometrium
/ cytology
Female
Fertilization in Vitro
/ methods
Humans
Live Birth
Oocytes
/ cytology
Pregnancy
Pregnancy Outcome
Pregnancy Rate
Treatment Outcome
Autologous endometrial co-culture
Good-quality blastocysts
ICSI
IVF
Journal
Reproductive biomedicine online
ISSN: 1472-6491
Titre abrégé: Reprod Biomed Online
Pays: Netherlands
ID NLM: 101122473
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
received:
18
05
2018
revised:
18
12
2018
accepted:
20
12
2018
pubmed:
21
1
2019
medline:
31
3
2020
entrez:
21
1
2019
Statut:
ppublish
Résumé
Does autologous endometrial cell co-culture (AECC) improve the number of good-quality blastocysts obtained by IVF/intracytoplasmic sperm injection (ICSI), compared with conventional embryo culture medium in a broad group of patients referred to assisted reproductive technology (ART)? This interventional, randomized, double-blind study took place at Clinique Ovo from March 2013 to October 2015 and included 207 healthy patients undergoing an IVF or ICSI protocol, of which 71 were excluded before randomization. On the previous cycle, all participants underwent an endometrial biopsy at D5 to D7 post-ovulation, following which the endometrial cells were prepared for AECC. The data demonstrated that AECC significantly increased the incidence of good-quality blastocysts compared with culture in conventional media (42.6% vs 28.4%, P < 0.001). No significant differences were found in pregnancy and live birth rates. This study demonstrated the benefits of AECC on blastocyst quality compared with conventional embryo culture medium, in a broader category of patients referred to ART as opposed to other studies that concentrated on specific causes of infertility only. However, limitations of the study design should be taken into consideration; the analysis was performed using embryos rather than patients and a follow-up of children born following the treatments could not be conducted.
Identifiants
pubmed: 30660602
pii: S1472-6483(19)30001-X
doi: 10.1016/j.rbmo.2018.12.039
pii:
doi:
Types de publication
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
321-329Informations de copyright
Copyright © 2019 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.