dc.contributor.author
Warrington, Nicole M.
dc.contributor.author
Richmond, Rebecca C.
dc.contributor.author
Fenstra, Bjarke
dc.contributor.author
Myhre, Ronny
dc.contributor.author
Gaillard, Romy
dc.contributor.author
Paternoster, Lavinia
dc.contributor.author
Wang, Carol A.
dc.contributor.author
Beaumont, Robin N.
dc.contributor.author
Das, Shikta
dc.contributor.author
Murcia, Mario
dc.contributor.author
Barton, Sheila J.
dc.contributor.author
Espinosa Cardiel, Ana
dc.contributor.author
Thiering, Elisabeth
dc.contributor.author
Atalay, Mustafa
dc.contributor.author
Pitkanen, Niina
dc.contributor.author
Ntalla, Ioanna
dc.contributor.author
Jonsson, Anna E.
dc.contributor.author
Freathy, Rachel M.
dc.contributor.author
Karhunen, Ville
dc.contributor.author
Tiesler, Carla M. T.
dc.contributor.author
Allard, Catherine
dc.contributor.author
Crawford, Andrew
dc.contributor.author
Ring, Susan M.
dc.contributor.author
Melbye, Mads
dc.contributor.author
Magnus, Per
dc.contributor.author
Rivadeneira, Fernando
dc.contributor.author
Skotte, Line
dc.contributor.author
Hansen, Torben
dc.contributor.author
Marsh, Julie A.
dc.contributor.author
Guxens, Mònica
dc.contributor.author
Holloway, John W.
dc.contributor.author
Grallert, Harald
dc.contributor.author
Jaddoe, Vincent W.
dc.contributor.author
Lowe, William L.
dc.contributor.author
Roumeliotaki, Theano
dc.contributor.author
Hattersley, Andrew T.
dc.contributor.author
Lindi, Virpi
dc.contributor.author
Pahkala, Katja
dc.contributor.author
Panoutsopoulou, Kalliope
dc.contributor.author
Standl, Marie
dc.contributor.author
Flexeder, Claudia
dc.contributor.author
Bouchard, Luigi
dc.contributor.author
Nohr, Ellen Aagard
dc.contributor.author
Marina, Loreto Santa
dc.contributor.author
Kogevinas, Manolis
dc.contributor.author
Niinikoski, Harri
dc.contributor.author
Dedoussis, George
dc.contributor.author
Heinrich, Joachim
dc.contributor.author
Reynolds, Rebecca M.
dc.contributor.author
Lakka, Timo
dc.contributor.author
Zeggini, Eleftheria
dc.contributor.author
Raitakari, Olli T.
dc.contributor.author
Chatzi, Leda
dc.contributor.author
Inskip, Hazel M.
dc.contributor.author
Bustamante Pineda, Mariona
dc.contributor.author
Hivert, Marie-France
dc.contributor.author
Jarvelin, Marjo-Riitta
dc.contributor.author
Sorensen, Thorkild I. A.
dc.contributor.author
Pennell, Craig E.
dc.contributor.author
Felix, Janine F.
dc.contributor.author
Jacobsson, Bo
dc.contributor.author
Geller, Frank
dc.contributor.author
Evans, David M.
dc.contributor.author
Lawlor, Debbie A.
dc.date.issued
2017-11-07T14:15:52Z
dc.date.issued
2017-11-07T14:15:52Z
dc.date.issued
2017-10-09
dc.date.issued
2017-11-01T19:00:07Z
dc.identifier
https://hdl.handle.net/2445/117486
dc.description.abstract
BACKGROUND: Clinical recommendations to limit gestational weight
gain (GWG) imply high GWG is causally related to adverse
outcomes in mother or offspring, but GWG is the sum of several
inter-related complex phenotypes (maternal fat deposition and
vascular expansion, placenta, amniotic fluid and fetal growth).
Understanding the genetic contribution to GWG could help clarify
the potential effect of its different components on maternal and
offspring health. Here we explore the genetic contribution to
total, early and late GWG. PARTICIPANTS AND METHODS: A
genome-wide association study was used to identify maternal and
fetal variants contributing to GWG in up to 10 543 mothers and
16 317 offspring of European origin, with replication in 10 660
mothers and 7561 offspring. Additional analyses determined the
proportion of variability in GWG from maternal and fetal common
genetic variants and the overlap of established genome-wide
significant variants for phenotypes relevant to GWG (e.g.
maternal BMI and glucose, birthweight). RESULTS: Approximately
20% of the variability in GWG was tagged by common maternal
genetic variants, and the fetal genome made a surprisingly minor
contribution to explaining variation in GWG. Variants near the
Pregnancy Specific Beta-1-Glycoprotein 5 (PSG5) gene reached
genome-wide significance (P=1.71 x 10-8) for total GWG in the
offspring genome, but did not replicate. Some established
variants associated with increased BMI, fasting glucose and type
2 diabetes were associated with lower early, and higher later
GWG. Maternal variants related to higher systolic blood pressure
were related to lower late GWG. Established maternal and fetal
birthweight variants were largely unrelated to GWG. CONCLUSION:
We found a modest contribution of maternal common variants to
GWG and some overlap of maternal BMI, glucose and type 2
diabetes variants with GWG. These findings suggest that
associations between GWG and later offspring/maternal outcomes
may be due to the relationship of maternal BMI and diabetes with
GWG.International Journal of Obesity accepted article preview
online, 09 October 2017. doi:10.1038/ijo.2017.248.
dc.format
application/pdf
dc.publisher
Nature Publishing Group
dc.relation
Reproducció del document publicat a:
http://dx.doi.org/10.1038/ijo.2017.248
dc.relation
International Journal of Obesity, 2017, vol. , num. , p. Ahead
of print
dc.relation
http://dx.doi.org/10.1038/ijo.2017.248
dc.relation
info:eu-repo/grantAgreement/EC/H2020/733206/EU//LIFECYCLE
dc.relation
info:eu-repo/grantAgreement/EC/H2020/648916/EU//EMBRYOandLATERHEALTH
dc.relation
info:eu-repo/grantAgreement/EC/H2020/669545/EU//ObesityDevelop
dc.relation
info:eu-repo/grantAgreement/EC/H2020/633595/EU//DYNAHEALTH
dc.rights
cc-by-nc-sa (c) Warrington et al., 2017
dc.rights
http://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (ISGlobal)
dc.subject
Genètica mèdica
dc.subject
Medical genetics
dc.title
Maternal and fetal genetic contribution to gestational weight
gain
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion