The one-carbon metabolism as an underlying pathway for placental DNA methylation – a systematic review

ABSTRACTEpigenetic modifications, including DNA methylation, are proposed mechanisms explaining the impact of parental exposures to foetal development and lifelong health. Micronutrients including folate, choline, and vitamin B12 provide methyl groups for the one-carbon metabolism and subsequent DNA...

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Main Authors: Marjolein M van Vliet, Sam Schoenmakers, Joost Gribnau, Régine P.M. Steegers-Theunissen
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Epigenetics
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/15592294.2024.2318516
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author Marjolein M van Vliet
Sam Schoenmakers
Joost Gribnau
Régine P.M. Steegers-Theunissen
author_facet Marjolein M van Vliet
Sam Schoenmakers
Joost Gribnau
Régine P.M. Steegers-Theunissen
author_sort Marjolein M van Vliet
collection DOAJ
description ABSTRACTEpigenetic modifications, including DNA methylation, are proposed mechanisms explaining the impact of parental exposures to foetal development and lifelong health. Micronutrients including folate, choline, and vitamin B12 provide methyl groups for the one-carbon metabolism and subsequent DNA methylation processes. Placental DNA methylation changes in response to one-carbon moieties hold potential targets to improve obstetrical care. We conducted a systematic review on the associations between one-carbon metabolism and human placental DNA methylation. We included 22 studies. Findings from clinical studies with minimal ErasmusAGE quality score 5/10 (n = 15) and in vitro studies (n = 3) are summarized for different one-carbon moieties. Next, results are discussed per study approach: (1) global DNA methylation (n = 9), (2) genome-wide analyses (n = 4), and (3) gene specific (n = 14). Generally, one-carbon moieties were not associated with global methylation, although conflicting outcomes were reported specifically for choline. Using genome-wide approaches, few differentially methylated sites associated with S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), or dietary patterns. Most studies taking a gene-specific approach indicated site-specific relationships depending on studied moiety and genomic region, specifically in genes involved in growth and development including LEP, NR3C1, CRH, and PlGF; however, overlap between studies was low. Therefore, we recommend to further investigate the impact of an optimized one-carbon metabolism on DNA methylation and lifelong health.
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spelling doaj.art-5acf3656bf254eac90b294618b4d0c532024-03-14T20:39:46ZengTaylor & Francis GroupEpigenetics1559-22941559-23082024-12-0119110.1080/15592294.2024.2318516The one-carbon metabolism as an underlying pathway for placental DNA methylation – a systematic reviewMarjolein M van Vliet0Sam Schoenmakers1Joost Gribnau2Régine P.M. Steegers-Theunissen3Department of Obstetrics and Gynaecology, Erasmus MC, Rotterdam, the NetherlandsDepartment of Obstetrics and Gynaecology, Erasmus MC, Rotterdam, the NetherlandsDepartment of Developmental Biology, Erasmus MC, Rotterdam, the NetherlandsDepartment of Obstetrics and Gynaecology, Erasmus MC, Rotterdam, the NetherlandsABSTRACTEpigenetic modifications, including DNA methylation, are proposed mechanisms explaining the impact of parental exposures to foetal development and lifelong health. Micronutrients including folate, choline, and vitamin B12 provide methyl groups for the one-carbon metabolism and subsequent DNA methylation processes. Placental DNA methylation changes in response to one-carbon moieties hold potential targets to improve obstetrical care. We conducted a systematic review on the associations between one-carbon metabolism and human placental DNA methylation. We included 22 studies. Findings from clinical studies with minimal ErasmusAGE quality score 5/10 (n = 15) and in vitro studies (n = 3) are summarized for different one-carbon moieties. Next, results are discussed per study approach: (1) global DNA methylation (n = 9), (2) genome-wide analyses (n = 4), and (3) gene specific (n = 14). Generally, one-carbon moieties were not associated with global methylation, although conflicting outcomes were reported specifically for choline. Using genome-wide approaches, few differentially methylated sites associated with S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), or dietary patterns. Most studies taking a gene-specific approach indicated site-specific relationships depending on studied moiety and genomic region, specifically in genes involved in growth and development including LEP, NR3C1, CRH, and PlGF; however, overlap between studies was low. Therefore, we recommend to further investigate the impact of an optimized one-carbon metabolism on DNA methylation and lifelong health.https://www.tandfonline.com/doi/10.1080/15592294.2024.2318516DoHADepigeneticsnutritionhuman
spellingShingle Marjolein M van Vliet
Sam Schoenmakers
Joost Gribnau
Régine P.M. Steegers-Theunissen
The one-carbon metabolism as an underlying pathway for placental DNA methylation – a systematic review
Epigenetics
DoHAD
epigenetics
nutrition
human
title The one-carbon metabolism as an underlying pathway for placental DNA methylation – a systematic review
title_full The one-carbon metabolism as an underlying pathway for placental DNA methylation – a systematic review
title_fullStr The one-carbon metabolism as an underlying pathway for placental DNA methylation – a systematic review
title_full_unstemmed The one-carbon metabolism as an underlying pathway for placental DNA methylation – a systematic review
title_short The one-carbon metabolism as an underlying pathway for placental DNA methylation – a systematic review
title_sort one carbon metabolism as an underlying pathway for placental dna methylation a systematic review
topic DoHAD
epigenetics
nutrition
human
url https://www.tandfonline.com/doi/10.1080/15592294.2024.2318516
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