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@ARTICLE{Parmar:142509,
author = {P. Parmar and E. Lowry and G. Cugliari and M. Suderman and
R. Wilson and V. Karhunen and T. Andrew and P. Wiklund and
M. Wielscher and S. Guarrera and A. Teumer and B. Lehne and
L. Milani and N. de Klein and P. P. Mishra and P. E. Melton
and P. R. Mandaviya and S. Kasela and J. Nano and W. Zhang
and Y. Zhang and A. G. Uitterlinden and A. Peters and B.
Schöttker$^*$ and C. Gieger and D. Anderson and D. I.
Boomsma and H. J. Grabe and S. Panico and J. H. Veldink and
J. B. J. van Meurs and L. van den Berg and L. J. Beilin and
L. Franke and M. Loh and M. M. J. van Greevenbroek and M.
Nauck and M. Kähönen and M. A. Hurme and O. T. Raitakari
and O. H. Franco and P. E. Slagboom and P. van der Harst and
S. Kunze and S. B. Felix and T. Zhang and W. Chen and T. A.
Mori and A. Bonnefond and B. T. Heijmans and T. Muka and J.
S. Kooner and K. Fischer and M. Waldenberger and P. Froguel
and R.-C. Huang and T. Lehtimäki and W. Rathmann and C. L.
Relton and G. Matullo and H. Brenner$^*$ and N. Verweij and
S. Li and J. C. Chambers and M.-R. Järvelin and S. Sebert},
collaboration = {B. Consortium and G. M. Q. Consortium},
title = {{A}ssociation of maternal prenatal smoking {GFI}1-locus and
cardio-metabolic phenotypes in 18,212 adults.},
journal = {EBioMedicine},
volume = {38},
issn = {2352-3964},
address = {Amsterdam [u.a.]},
publisher = {Elsevier},
reportid = {DKFZ-2019-00227},
pages = {206 - 216},
year = {2018},
abstract = {DNA methylation at the GFI1-locus has been repeatedly
associated with exposure to smoking from the foetal period
onwards. We explored whether DNA methylation may be a
mechanism that links exposure to maternal prenatal smoking
with offspring's adult cardio-metabolic health.We
meta-analysed the association between DNA methylation at
GFI1-locus with maternal prenatal smoking, adult own
smoking, and cardio-metabolic phenotypes in 22
population-based studies from Europe, Australia, and USA
(n = 18,212). DNA methylation at the GFI1-locus was
measured in whole-blood. Multivariable regression models
were fitted to examine its association with exposure to
prenatal and own adult smoking. DNA methylation levels were
analysed in relation to body mass index (BMI), waist
circumference (WC), fasting glucose (FG), high-density
lipoprotein cholesterol (HDL-C), triglycerides (TG),
diastolic, and systolic blood pressure (BP).Lower DNA
methylation at three out of eight GFI1-CpGs was associated
with exposure to maternal prenatal smoking, whereas, all
eight CpGs were associated with adult own smoking. Lower DNA
methylation at cg14179389, the strongest maternal prenatal
smoking locus, was associated with increased WC and BP when
adjusted for sex, age, and adult smoking with
Bonferroni-corrected P < 0·012. In contrast, lower DNA
methylation at cg09935388, the strongest adult own smoking
locus, was associated with decreased BMI, WC, and BP
(adjusted 1 × 10-7 < P < 0.01). Similarly,
lower DNA methylation at cg12876356, cg18316974, cg09662411,
and cg18146737 was associated with decreased BMI and WC
(5 × 10-8 < P < 0.001). Lower DNA methylation
at all the CpGs was consistently associated with higher TG
levels.Epigenetic changes at the GFI1 were linked to smoking
exposure in-utero/in-adulthood and robustly associated with
cardio-metabolic risk factors. FUND: European Union's
Horizon 2020 research and innovation programme under grant
agreement no. 633595 DynaHEALTH.},
cin = {C070 / G110},
ddc = {610},
cid = {I:(DE-He78)C070-20160331 / I:(DE-He78)G110-20160331},
pnm = {323 - Metabolic Dysfunction as Risk Factor (POF3-323)},
pid = {G:(DE-HGF)POF3-323},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30442561},
pmc = {pmc:PMC6306313},
doi = {10.1016/j.ebiom.2018.10.066},
url = {https://inrepo02.dkfz.de/record/142509},
}