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Tobi, E.W.* ; Juvinao-Quintero, D.L.* ; Ronkainen, J.* ; Ott, R. ; Alfano, R.* ; Canouil, M.* ; Geurtsen, M.L.* ; Khamis, A.* ; Küpers, L.K.* ; Lim, I.Y.* ; Perron, P.* ; Pesce, G.* ; Tuhkanen, J.* ; Starling, A.P.* ; Andrew, T.* ; Binder, E.* ; Caiazzo, R.* ; Chan, J.K.Y.* ; Gaillard, R.* ; Gluckman, P.D.* ; Keikkala, E.* ; Karnani, N.* ; Mustaniemi, S.* ; Nawrot, T.S.* ; Pattou, F.* ; Plusquin, M.* ; Raverdy, V.* ; Tan, K.H.* ; Tzala, E.* ; Räikkönen, K.* ; Winkler, C. ; Ziegler, A.-G. ; Annesi-Maesano, I.* ; Bouchard, L.* ; Chong, Y.S.* ; Dabelea, D.* ; Felix, J.F.* ; Heude, B.* ; Jaddoe, V.W.V.* ; Lahti, J.* ; Reimann, B.* ; Vääräsmäki, M.* ; Bonnefond, A.* ; Froguel, P.* ; Hummel, S. ; Kajantie, E.* ; Jarvelin, M.R.* ; Steegers-Theunissen, R.P.M.* ; Howe, C.G.* ; Hivert, M.F.* ; Sebert, S.*

Maternal glycemic dysregulation during pregnancy and neonatal blood DNA methylation: Meta-analyses of epigenome-wide association studies.

Diabetes Care 45, 614-623 (2022)
Verlagsversion Forschungsdaten DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
OBJECTIVE: Maternal glycemic dysregulation during pregnancy increases the risk of adverse health outcomes in her offspring, a risk thought to be linearly related to maternal hyperglycemia. It is hypothesized that changes in offspring DNA methylation (DNAm) underline these associations. RESEARCH DESIGN AND METHODS: To address this hypothesis, we conducted fixed-effects meta-analyses of epigenome-wide association study (EWAS) results from eight birth cohorts investigating relationships between cord blood DNAm and fetal exposure to maternal glucose (Nmaximum = 3,503), insulin (Nmaximum = 2,062), and area under the curve of glucose (AUCgluc) following oral glucose tolerance tests (Nmaximum = 1,505). We performed lookup analyses for identified cytosine-guanine dinucleotides (CpGs) in independent observational cohorts to examine associations between DNAm and cardiometabolic traits as well as tissue-specific gene expression. RESULTS: Greater maternal AUCgluc was associated with lower cord blood DNAm at neighboring CpGs cg26974062 (β [SE] = 0.013 [2.1 × 10-3], P value corrected for false discovery rate [PFDR] = 5.1 × 10-3) and cg02988288 (β [SE]-0.013 [2.3 × 10-3], PFDR = 0.031) in TXNIP. These associations were attenuated in women with GDM. Lower blood DNAm at these two CpGs near TXNIP was associated with multiple metabolic traits later in life, including type 2 diabetes. TXNIP DNAm in liver biopsies was associated with hepatic expression of TXNIP. We observed little evidence of associations between either maternal glucose or insulin and cord blood DNAm. CONCLUSIONS: Maternal hyperglycemia, as reflected by AUCgluc, was associated with lower cord blood DNAm at TXNIP. Associations between DNAm at these CpGs and metabolic traits in subsequent lookup analyses suggest that these may be candidate loci to investigate in future causal and mediation analyses.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 0149-5992
e-ISSN 1935-5548
Zeitschrift Diabetes Care
Quellenangaben Band: 45, Heft: 3, Seiten: 614-623 Artikelnummer: , Supplement: ,
Verlag American Diabetes Association
Verlagsort Alexandria, Va.
Begutachtungsstatus Peer reviewed