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Folate and vitamin B12 status: associations with maternal glucose and neonatal DNA methylation sites related to dysglycaemia, in pregnant women with obesity

Abstract:
AbstractRecent studies implicate maternal gestational diabetes mellitus (GDM) in differential methylation of infant DNA. Folate and vitamin B12 play a role in DNA methylation, and these vitamins may also influence GDM risk. The aims of this study were to determine folate and vitamin B12 status in obese pregnant women and investigate associations between folate and vitamin B12 status, maternal dysglycaemia and neonatal DNA methylation at cytosine-phosphate-guanine sites previously observed to be associated with dysglycaemia. Obese pregnant women who participated in the UK Pregnancies Better Eating and Activity Trial were included. Serum folate and vitamin B12 were measured at the oral glucose tolerance test (OGTT) visit. Cord blood DNA methylation was assessed using the Infinium MethylationEPIC BeadChip. Regression models with adjustment for confounders were used to examine associations. Of the 951 women included, 356 (37.4%) were vitamin B12 deficient, and 44 (4.6%) were folate deficient. Two-hundred and seventy-one women (28%) developed GDM. Folate and vitamin B12 concentrations were not associated with neonatal DNA methylation. Higher folate was positively associated with 1-h plasma glucose after OGTT (β = 0.031, 95% CI 0.001–0.061, p = 0.045). There was no relationship between vitamin B12 and glucose concentrations post OGTT or between folate or vitamin B12 and GDM. In summary, we found no evidence to link folate and vitamin B12 status with the differential methylation of neonatal DNA previously observed in association with dysglycaemia. We add to the evidence that folate status may be related to maternal glucose homoeostasis although replication in other maternal cohorts is required for validation.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1017/s2040174421000246

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Role:
Author
ORCID:
0000-0002-9660-4006
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Role:
Author
ORCID:
0000-0001-7904-7933
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-9477-1564
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Role:
Author
ORCID:
0000-0002-4643-0618
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Role:
Author
ORCID:
0000-0001-7518-9096


Publisher:
Cambridge University Press
Journal:
Journal of Developmental Origins of Health and Disease More from this journal
Volume:
13
Issue:
2
Pages:
168-176
Publication date:
2021-05-11
DOI:
EISSN:
2040-1752
ISSN:
2040-1744


Language:
English
Keywords:
Pubs id:
1307409
Local pid:
pubs:1307409
Source identifiers:
W3162156137
Deposit date:
2026-04-30
ARK identifier:
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