Evaluating the association between placenta DNA methylation and cognitive functions in the offspring

The placenta plays a crucial role in protecting the fetus from environmental harm and supports the development of its brain. In fact, compromised placental function could predispose an individual to neurodevelopmental disorders. Placental epigenetic modifications, including DNA methylation, could be...

Descripción completa

Detalles Bibliográficos
Autores: Diez-Ahijado, Laia, Cilleros-Portet, Ariadna, Fernández-Jiménez, Nora, Fernández, Mariana F., Guxens Junyent, Mònica, Júlvez Calvo, Jordi, Llop, Sabrina, Lopez-Espinosa, Maria-José, Subiza-Pérez, Mikel, Lozano, Manuel, Ibarluzea, Jesús, Sunyer Deu, Jordi, Bustamante Pineda, Mariona, Cosín Tomàs, Marta
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Universitat Pompeu Fabra
Repositorio:Repositorio Digital de la UPF
OAI Identifier:oai:repositori.upf.edu:10230/68816
Acceso en línea:http://hdl.handle.net/10230/68816
http://dx.doi.org/10.1038/s41398-024-03094-5
Access Level:acceso abierto
Palabra clave:Epigenetics and behaviour
Personalized medicine
id ES_65c99f97be700dabf3da30ca8bb96d67
oai_identifier_str oai:repositori.upf.edu:10230/68816
network_acronym_str ES
network_name_str España
repository_id_str
dc.title.none.fl_str_mv Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
title Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
spellingShingle Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
Diez-Ahijado, Laia
Epigenetics and behaviour
Personalized medicine
title_short Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
title_full Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
title_fullStr Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
title_full_unstemmed Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
title_sort Evaluating the association between placenta DNA methylation and cognitive functions in the offspring
dc.creator.none.fl_str_mv Diez-Ahijado, Laia
Cilleros-Portet, Ariadna
Fernández-Jiménez, Nora
Fernández, Mariana F.
Guxens Junyent, Mònica
Júlvez Calvo, Jordi
Llop, Sabrina
Lopez-Espinosa, Maria-José
Subiza-Pérez, Mikel
Lozano, Manuel
Ibarluzea, Jesús
Sunyer Deu, Jordi
Bustamante Pineda, Mariona
Cosín Tomàs, Marta
author Diez-Ahijado, Laia
author_facet Diez-Ahijado, Laia
Cilleros-Portet, Ariadna
Fernández-Jiménez, Nora
Fernández, Mariana F.
Guxens Junyent, Mònica
Júlvez Calvo, Jordi
Llop, Sabrina
Lopez-Espinosa, Maria-José
Subiza-Pérez, Mikel
Lozano, Manuel
Ibarluzea, Jesús
Sunyer Deu, Jordi
Bustamante Pineda, Mariona
Cosín Tomàs, Marta
author_role author
author2 Cilleros-Portet, Ariadna
Fernández-Jiménez, Nora
Fernández, Mariana F.
Guxens Junyent, Mònica
Júlvez Calvo, Jordi
Llop, Sabrina
Lopez-Espinosa, Maria-José
Subiza-Pérez, Mikel
Lozano, Manuel
Ibarluzea, Jesús
Sunyer Deu, Jordi
Bustamante Pineda, Mariona
Cosín Tomàs, Marta
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Epigenetics and behaviour
Personalized medicine
topic Epigenetics and behaviour
Personalized medicine
description The placenta plays a crucial role in protecting the fetus from environmental harm and supports the development of its brain. In fact, compromised placental function could predispose an individual to neurodevelopmental disorders. Placental epigenetic modifications, including DNA methylation, could be considered a proxy of placental function and thus plausible mediators of the association between intrauterine environmental exposures and genetics, and childhood and adult mental health. Although neurodevelopmental disorders such as autism spectrum disorder have been investigated in relation to placenta DNA methylation, no studies have addressed the association between placenta DNA methylation and child's cognitive functions. Thus, our goal here was to investigate whether the placental DNA methylation profile measured using the Illumina EPIC array is associated with three different cognitive domains (namely verbal score, perceptive performance score, and general cognitive score) assessed by the McCarthy Scales of Children's functions in childhood at age 4. To this end, we conducted epigenome-wide association analyses, including data from 255 mother-child pairs within the INMA project, and performed a follow-up functional analysis to help the interpretation of the findings. After multiple-testing correction, we found that methylation at 4 CpGs (cg1548200, cg02986379, cg00866476, and cg14113931) was significantly associated with the general cognitive score, and 2 distinct differentially methylated regions (DMRs) (including 27 CpGs) were significantly associated with each cognitive dimension. Interestingly, the genes annotated to these CpGs, such as DAB2, CEP76, PSMG2, or MECOM, are involved in placenta, fetal, and brain development. Moreover, functional enrichment analyses of suggestive CpGs (p < 1 × 10-4) revealed gene sets involved in placenta development, fetus formation, and brain growth. These findings suggest that placental DNA methylation could be a mechanism contributing to the alteration of important pathways in the placenta that have a consequence on the offspring's brain development and cognitive function.
publishDate 2024
dc.date.none.fl_str_mv 2024
2024
2024
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/10230/68816
http://dx.doi.org/10.1038/s41398-024-03094-5
url http://hdl.handle.net/10230/68816
http://dx.doi.org/10.1038/s41398-024-03094-5
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Transl Psychiatry. 2024 Sep 20;14(1):383
info:eu-repo/grantAgreement/EC/H2020/874583
info:eu-repo/grantAgreement/EC/FP7/282957
dc.rights.none.fl_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Nature Research
publisher.none.fl_str_mv Nature Research
dc.source.none.fl_str_mv reponame:Repositorio Digital de la UPF
instname:Universitat Pompeu Fabra
instname_str Universitat Pompeu Fabra
reponame_str Repositorio Digital de la UPF
collection Repositorio Digital de la UPF
repository.name.fl_str_mv
repository.mail.fl_str_mv
_version_ 1869409768440856576
spelling Evaluating the association between placenta DNA methylation and cognitive functions in the offspringDiez-Ahijado, LaiaCilleros-Portet, AriadnaFernández-Jiménez, NoraFernández, Mariana F.Guxens Junyent, MònicaJúlvez Calvo, JordiLlop, SabrinaLopez-Espinosa, Maria-JoséSubiza-Pérez, MikelLozano, ManuelIbarluzea, JesúsSunyer Deu, JordiBustamante Pineda, MarionaCosín Tomàs, MartaEpigenetics and behaviourPersonalized medicineThe placenta plays a crucial role in protecting the fetus from environmental harm and supports the development of its brain. In fact, compromised placental function could predispose an individual to neurodevelopmental disorders. Placental epigenetic modifications, including DNA methylation, could be considered a proxy of placental function and thus plausible mediators of the association between intrauterine environmental exposures and genetics, and childhood and adult mental health. Although neurodevelopmental disorders such as autism spectrum disorder have been investigated in relation to placenta DNA methylation, no studies have addressed the association between placenta DNA methylation and child's cognitive functions. Thus, our goal here was to investigate whether the placental DNA methylation profile measured using the Illumina EPIC array is associated with three different cognitive domains (namely verbal score, perceptive performance score, and general cognitive score) assessed by the McCarthy Scales of Children's functions in childhood at age 4. To this end, we conducted epigenome-wide association analyses, including data from 255 mother-child pairs within the INMA project, and performed a follow-up functional analysis to help the interpretation of the findings. After multiple-testing correction, we found that methylation at 4 CpGs (cg1548200, cg02986379, cg00866476, and cg14113931) was significantly associated with the general cognitive score, and 2 distinct differentially methylated regions (DMRs) (including 27 CpGs) were significantly associated with each cognitive dimension. Interestingly, the genes annotated to these CpGs, such as DAB2, CEP76, PSMG2, or MECOM, are involved in placenta, fetal, and brain development. Moreover, functional enrichment analyses of suggestive CpGs (p < 1 × 10-4) revealed gene sets involved in placenta development, fetus formation, and brain growth. These findings suggest that placental DNA methylation could be a mechanism contributing to the alteration of important pathways in the placenta that have a consequence on the offspring's brain development and cognitive function.We acknowledge support from the grant CEX2018-000806-S funded by MCIN/AEI/10.13039/501100011033, from the Generalitat de Catalunya through the CERCA Programme; and from the European Union’s Horizon 2020 research and innovation programme-EU.3.1.2. (874583–ATHLETE project); grants from UE (FP7-ENV-2011 cod 282957 and HEALTH.2010.2.4.5-1), Spain: ISCIII (Red INMA G03/176, CB06/02/0041; FIS-FEDER: PI03/1615, PI04/1509, PI04/1112, PI04/1931, PI05/1079, PI05/1052, PI06/1213, PI07/0314, PI09/02647, PI11/01007, PI11/02591, PI11/02038, PI12/00610, PI13/1944, PI13/2032, PI14/00891, PI14/01687, PI16/1288, PI17/00663, PI16/1288 and PI1338;; Miguel Servet-FEDER CP11/00178, CP15/00025, MS20/0005, and CPII16/00051, G03/176; Generalitat Valenciana (CIAICO/2021/132): FISABIO (UGP-15-230, UGP-15-244, and UGP-15-249), Ministry of Universities (CAS21/00008 and NextGeneration EU), and Alicia Koplowitz Foundation 2017; grants from Instituto de Salud Carlos III (Red INMA G03/176; CB06/02/0041; PI041436; PI081151 incl. FEDER funds), Generalitat de Catalunya-CIRIT 1999SGR 00241, Fundació La marató de TV3 (090430); grants from Instituto de Salud Carlos III (PI06/0867, PI11/00610, FIS-PI09/00090, FIS-PI13/02187, FIS-PI13/02406, and FIS-PI18/01142 incl. FEDER funds), CIBERESP, Department of Health of the Basque Government (2005111093, 2009111069, 2013111089 and 2015111065), Provincial Government of Gipuzkoa (DFG06/002), and annual agreements with the municipalities of the study area (Zumarraga, Urretxu, Legazpi, Azkoitia y Azpeitia y Beasain). MG was funded by a Miguel Servet-II fellowship (CPII18/00018) awarded by the Spanish Institute of Health Carlos III. MCT is funded by a Beatriu de Pinós Postdoctoral Contract awarded by Generalitat de Catalunya-AGAUR and European Commission-Horizon 2020 (2019 BP 00107). JJ was funded by a Miguel Servet-II fellowship (CPII19/00015) awarded by the Instituto de Salud Carlos III (Co-funded by the European Union Social Fund “Investing in your future”). We acknowledge all volunteers participating in the study, and interviewers and psychologists.Nature Research202420242024info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/68816http://dx.doi.org/10.1038/s41398-024-03094-5reponame:Repositorio Digital de la UPFinstname:Universitat Pompeu FabraInglésTransl Psychiatry. 2024 Sep 20;14(1):383info:eu-repo/grantAgreement/EC/H2020/874583info:eu-repo/grantAgreement/EC/FP7/282957© The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:repositori.upf.edu:10230/688162026-06-12T07:21:37Z
score 15,812429