Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/117486
Title: Maternal and fetal genetic contribution to gestational weight gain
Author: Warrington, Nicole M.
Richmond, Rebecca C.
Fenstra, Bjarke
Myhre, Ronny
Gaillard, Romy
Paternoster, Lavinia
Wang, Carol A.
Beaumont, Robin N.
Das, Shikta
Murcia, Mario
Barton, Sheila J.
Espinosa Cardiel, Ana
Thiering, Elisabeth
Atalay, Mustafa
Pitkanen, Niina
Ntalla, Ioanna
Jonsson, Anna E.
Freathy, Rachel M.
Karhunen, Ville
Tiesler, Carla M. T.
Allard, Catherine
Crawford, Andrew
Ring, Susan M.
Melbye, Mads
Magnus, Per
Rivadeneira, Fernando
Skotte, Line
Hansen, Torben
Marsh, Julie A.
Guxens, Mònica
Holloway, John W.
Grallert, Harald
Jaddoe, Vincent W.
Lowe, William L.
Roumeliotaki, Theano
Hattersley, Andrew T.
Lindi, Virpi
Pahkala, Katja
Panoutsopoulou, Kalliope
Standl, Marie
Flexeder, Claudia
Bouchard, Luigi
Nohr, Ellen Aagard
Marina, Loreto Santa
Kogevinas, Manolis
Niinikoski, Harri
Dedoussis, George
Heinrich, Joachim
Reynolds, Rebecca M.
Lakka, Timo
Zeggini, Eleftheria
Raitakari, Olli T.
Chatzi, Leda
Inskip, Hazel M.
Bustamante Pineda, Mariona
Hivert, Marie-France
Jarvelin, Marjo-Riitta
Sorensen, Thorkild I. A.
Pennell, Craig E.
Felix, Janine F.
Jacobsson, Bo
Geller, Frank
Evans, David M.
Lawlor, Debbie A.
Keywords: Genètica mèdica
Pes corporal
Embaràs
Medical genetics
Body weight
Pregnancy
Issue Date: 9-Oct-2017
Publisher: Nature Publishing Group
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.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1038/ijo.2017.248
It is part of: International Journal of Obesity, 2017, vol. , num. , p. Ahead of print
URI: http://hdl.handle.net/2445/117486
Related resource: http://dx.doi.org/10.1038/ijo.2017.248
ISSN: 0307-0565
Appears in Collections:Articles publicats en revistes (ISGlobal)

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