Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/24268
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dc.contributor.authorWINCKELMANS, Ellen-
dc.contributor.authorVRIJENS, Karen-
dc.contributor.authorTSAMOU, Maria-
dc.contributor.authorJANSSEN, Bram-
dc.contributor.authorSAENEN, Nelly-
dc.contributor.authorROELS, Harry-
dc.contributor.authorKLEINJANS, J.-
dc.contributor.authorLefebvre, Wouter-
dc.contributor.authorVanpoucke, Charlotte-
dc.contributor.authorDE KOK, Theo-
dc.contributor.authorNAWROT, Tim-
dc.date.accessioned2017-08-18T12:00:23Z-
dc.date.available2017-08-18T12:00:23Z-
dc.date.issued2017-
dc.identifier.citationENVIRONMENTAL HEALTH, 16, p. 1-17 (Art N° 52)-
dc.identifier.issn1476-069X-
dc.identifier.urihttp://hdl.handle.net/1942/24268-
dc.description.abstractBackground: Air pollution exposure during pregnancy has been associated with adverse birth outcomes and health problems later in life. We investigated sex-specific transcriptomic responses to gestational long-and short-term exposure to particulate matter with a diameter < 2.5 mu m ( PM2.5) in order to elucidate potential underlying mechanisms of action. Methods: Whole genome gene expression was investigated in cord blood of 142 mother-newborn pairs that were enrolled in the ENVIRONAGE birth cohort. Daily PM2.5 exposure levels were calculated for each mother's home address using a spatial-temporal interpolation model in combination with a dispersion model to estimate both long- (annual average before delivery) and short- (last month of pregnancy) term exposure. We explored the association between gene expression levels and PM2.5 exposure, and identified modulated pathways by overrepresentation analysis and gene set enrichment analysis. Results: Some processes were altered in both sexes for long-(e.g. DNA damage) or short-term exposure (e.g. olfactory signaling). For long-term exposure in boys neurodevelopment and RhoA pathways were modulated, while in girls defensin expression was down-regulated. For short-term exposure we identified pathways related to synaptic transmission and mitochondrial function (boys) and immune response (girls). Conclusions: This is the first whole genome gene expression study in cord blood to identify sex-specific pathways altered by PM2.5. The identified transcriptome pathways could provide new molecular insights as to the interaction pattern of early life PM2.5 exposure with the biological development of the fetus.-
dc.description.sponsorshipThis research is funded by the European Research Council (ERC-2012-stG310898) and the Flemish Scientific Fund (FWO, G073315N). Ellen Winckelmans has a PhD. fellowship of Hasselt University (BOF program).-
dc.language.isoen-
dc.publisherBIOMED CENTRAL LTD-
dc.rights© The Author(s). 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.-
dc.subject.otherAmbient air pollution; Particulate matter; Microarray analysis; Fetal; Sex-
dc.subject.otherambient air pollution; particulate matter; microarray analysis; fetal; sex-
dc.titleNewborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort-
dc.typeJournal Contribution-
dc.identifier.epage17-
dc.identifier.spage1-
dc.identifier.volume16-
local.format.pages17-
local.bibliographicCitation.jcatA1-
dc.description.notes[Winckelmans, Ellen; Vrijens, Karen; Tsamou, Maria; Janssen, Bram G.; Saenen, Nelly D.; Roels, Harry A.; Nawrot, Tim S.] Hasselt Univ, Ctr Environm Sci, Agoralaan Gebouw D, B-3590 Diepenbeek, Belgium. [Roels, Harry A.] Catholic Univ Louvain, Louvain Ctr Toxicol & Appl Pharmacol LTAP, Brussels, Belgium. [Kleinjans, Jos; de Kok, Theo M.] Maastricht Univ, Dept Toxicogen, Maastricht, Netherlands. [Lefebvre, Wouter] Flemish Inst Tech Res VITO, Environm Risk & Hlth, Mol, Belgium. [Vanpoucke, Charlotte] Belgian Interreg Environm Agcy IRCEL, Brussels, Belgium. [Nawrot, Tim S.] Leuven Univ, Dept Publ Hlth & Primary Care, Kapucijnenvoer 35, B-3000 Leuven, Belgium.-
local.publisher.placeLONDON-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnr52-
local.classdsPublValOverrule/author_version_not_expected-
dc.identifier.doi10.1186/s12940-017-0264-y-
dc.identifier.isi000402648600001-
item.validationecoom 2018-
item.accessRightsOpen Access-
item.fullcitationWINCKELMANS, Ellen; VRIJENS, Karen; TSAMOU, Maria; JANSSEN, Bram; SAENEN, Nelly; ROELS, Harry; KLEINJANS, J.; Lefebvre, Wouter; Vanpoucke, Charlotte; DE KOK, Theo & NAWROT, Tim (2017) Newborn sex-specific transcriptome signatures and gestational exposure to fine particles: findings from the ENVIRONAGE birth cohort. In: ENVIRONMENTAL HEALTH, 16, p. 1-17 (Art N° 52).-
item.fulltextWith Fulltext-
item.contributorWINCKELMANS, Ellen-
item.contributorVRIJENS, Karen-
item.contributorTSAMOU, Maria-
item.contributorJANSSEN, Bram-
item.contributorSAENEN, Nelly-
item.contributorROELS, Harry-
item.contributorKLEINJANS, J.-
item.contributorLefebvre, Wouter-
item.contributorVanpoucke, Charlotte-
item.contributorDE KOK, Theo-
item.contributorNAWROT, Tim-
crisitem.journal.eissn1476-069X-
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