Does underlying infertility in natural conception modify the epigenetic control of imprinted genes and transposable elements in newborns?


Journal

Reproductive biomedicine online
ISSN: 1472-6491
Titre abrégé: Reprod Biomed Online
Pays: Netherlands
ID NLM: 101122473

Informations de publication

Date de publication:
04 2022
Historique:
received: 30 08 2021
revised: 30 11 2021
accepted: 10 01 2022
pubmed: 28 2 2022
medline: 6 5 2022
entrez: 27 2 2022
Statut: ppublish

Résumé

Does the epigenetic control of imprinted genes and transposable elements at birth differ according to time to conception in natural conception and after intrauterine insemination (IUI)? A total of 144 singletons were included in four groups: 50 natural pregnancies obtained within 6 months after stopping contraception (group 1); 34 natural pregnancies with infertility period between 6 and 12 months (group 2); 36 pregnancies with an infertility period of more than 12 months (group 3) and 24 pregnancies obtained after IUI (group 4). The placental DNA methylation levels of H19/IGF2 and KCNQ1OT1 were lower in groups 2, 3 and 4 than in group 1 (P = 0.025 in the overall comparison). The DNA methylation rate for LINE-1 was higher in placentas from group 2 than in group 1 (P = 0.022). In cord blood, DNA methylation levels were not significantly different between groups except for H19/IGF2 for which the DNA methylation levels were higher in group 2 than in group 1 (H19/IGF2-seq1 and seq2: P = 0.023 and P = 0.002, respectively). In placenta tissue, compared with group 1, relative expression for SNRPN and for LINE-1 was significantly higher in group 2 (P = 0.002 and P < 0.001, respectively). The relative expression of KCNQ1 in placenta was lower in group 4 than in group 1 (P = 0.013). In cord blood, compared with group 1, the relative expression for H19 was significantly higher in group 3 (P = 0.026), and the relative expression of LINE-1 was higher in groups 2 and 3 and in group 4 (P < 0.001). Infertility itself, and not only ART techniques, could contribute to potential epigenetic risks for children.

Identifiants

pubmed: 35219588
pii: S1472-6483(22)00032-3
doi: 10.1016/j.rbmo.2022.01.004
pii:
doi:

Substances chimiques

DNA Transposable Elements 0
RNA, Long Noncoding 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

706-715

Informations de copyright

Copyright © 2022 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.

Auteurs

Julie Barberet (J)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Laboratoire de Biologie de la Reproduction - CECOS, 14 rue Gaffarel, Dijon F-21000, France.

Christine Binquet (C)

CHU Dijon Bourgogne, Centre d'Investigation Clinique, module Epidémiologie Clinique/essais cliniques (CIC-EC), 7 boulevard Jeanne d'Arc, Dijon F-21000, France; INSERM, CIC1432, module épidémiologie clinique, 7 boulevard Jeanne d'Arc, Dijon F-21000, France.

Magali Guilleman (M)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Laboratoire de Biologie de la Reproduction - CECOS, 14 rue Gaffarel, Dijon F-21000, France.

Gaelle Romain (G)

CHU Dijon Bourgogne, Centre d'Investigation Clinique, module Epidémiologie Clinique/essais cliniques (CIC-EC), 7 boulevard Jeanne d'Arc, Dijon F-21000, France; INSERM, CIC1432, module épidémiologie clinique, 7 boulevard Jeanne d'Arc, Dijon F-21000, France.

Céline Bruno (C)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Laboratoire de Biologie de la Reproduction - CECOS, 14 rue Gaffarel, Dijon F-21000, France.

Aurélie Martinaud (A)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Laboratoire de Biologie de la Reproduction - CECOS, 14 rue Gaffarel, Dijon F-21000, France.

Perrine Ginod (P)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Service de Gynécologie-Obstétrique, 14 rue Gaffarel, Dijon F-21000, France.

Mathilde Cavalieri (M)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Service de Gynécologie-Obstétrique, 14 rue Gaffarel, Dijon F-21000, France.

Céline Amblot (C)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Service de Gynécologie-Obstétrique, 14 rue Gaffarel, Dijon F-21000, France.

Cécile Choux (C)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Service de Gynécologie-Obstétrique, 14 rue Gaffarel, Dijon F-21000, France.

Patricia Fauque (P)

Université Bourgogne Franche-Comté - Equipe Génétique des Anomalies du Développement (GAD) INSERM UMR1231, 2 Rue Angélique Ducoudray, Dijon F-21000, France; CHU Dijon Bourgogne, Laboratoire de Biologie de la Reproduction - CECOS, 14 rue Gaffarel, Dijon F-21000, France. Electronic address: patricia.fauque@chu-dijon.fr.

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