Consortium-based genome-wide meta-analysis for childhood dental caries traits. (20th June 2018)
- Record Type:
- Journal Article
- Title:
- Consortium-based genome-wide meta-analysis for childhood dental caries traits. (20th June 2018)
- Main Title:
- Consortium-based genome-wide meta-analysis for childhood dental caries traits
- Authors:
- Haworth, Simon
Shungin, Dmitry
van der Tas, Justin T
Vucic, Strahinja
Medina-Gomez, Carolina
Yakimov, Victor
Feenstra, Bjarke
Shaffer, John R
Lee, Myoung Keun
Standl, Marie
Thiering, Elisabeth
Wang, Carol
Bønnelykke, Klaus
Waage, Johannes
Jessen, Leon Eyrich
Nørrisgaard, Pia Elisabeth
Joro, Raimo
Seppälä, Ilkka
Raitakari, Olli
Dudding, Tom
Grgic, Olja
Ongkosuwito, Edwin
Vierola, Anu
Eloranta, Aino-Maija
West, Nicola X
Thomas, Steven J
McNeil, Daniel W
Levy, Steven M
Slayton, Rebecca
Nohr, Ellen A
Lehtimäki, Terho
Lakka, Timo
Bisgaard, Hans
Pennell, Craig
Kühnisch, Jan
Marazita, Mary L
Melbye, Mads
Geller, Frank
Rivadeneira, Fernando
Wolvius, Eppo B
Franks, Paul W
Johansson, Ingegerd
Timpson, Nicholas J
… (more) - Abstract:
- Abstract: Prior studies suggest dental caries traits in children and adolescents are partially heritable, but there has been no large-scale consortium genome-wide association study (GWAS) to date. We therefore performed GWAS for caries in participants aged 2.5–18.0 years from nine contributing centres. Phenotype definitions were created for the presence or absence of treated or untreated caries, stratified by primary and permanent dentition. All studies tested for association between caries and genotype dosage and the results were combined using fixed-effects meta-analysis. Analysis included up to 19 003 individuals (7530 affected) for primary teeth and 13 353 individuals (5875 affected) for permanent teeth. Evidence for association with caries status was observed at rs1594318-C for primary teeth [intronic within ALLC, odds ratio (OR) 0.85, effect allele frequency (EAF) 0.60, P 4.13e-8] and rs7738851-A (intronic within NEDD9, OR 1.28, EAF 0.85, P 1.63e-8) for permanent teeth. Consortium-wide estimated heritability of caries was low [ h 2 of 1% (95% CI: 0%: 7%) and 6% (95% CI 0%: 13%) for primary and permanent dentitions, respectively] compared with corresponding within-study estimates [ h 2 of 28% (95% CI: 9%: 48%) and 17% (95% CI: 2%: 31%)] or previously published estimates. This study was designed to identify common genetic variants with modest effects which are consistent across different populations. We found few single variants associated with caries status under theseAbstract: Prior studies suggest dental caries traits in children and adolescents are partially heritable, but there has been no large-scale consortium genome-wide association study (GWAS) to date. We therefore performed GWAS for caries in participants aged 2.5–18.0 years from nine contributing centres. Phenotype definitions were created for the presence or absence of treated or untreated caries, stratified by primary and permanent dentition. All studies tested for association between caries and genotype dosage and the results were combined using fixed-effects meta-analysis. Analysis included up to 19 003 individuals (7530 affected) for primary teeth and 13 353 individuals (5875 affected) for permanent teeth. Evidence for association with caries status was observed at rs1594318-C for primary teeth [intronic within ALLC, odds ratio (OR) 0.85, effect allele frequency (EAF) 0.60, P 4.13e-8] and rs7738851-A (intronic within NEDD9, OR 1.28, EAF 0.85, P 1.63e-8) for permanent teeth. Consortium-wide estimated heritability of caries was low [ h 2 of 1% (95% CI: 0%: 7%) and 6% (95% CI 0%: 13%) for primary and permanent dentitions, respectively] compared with corresponding within-study estimates [ h 2 of 28% (95% CI: 9%: 48%) and 17% (95% CI: 2%: 31%)] or previously published estimates. This study was designed to identify common genetic variants with modest effects which are consistent across different populations. We found few single variants associated with caries status under these assumptions. Phenotypic heterogeneity between cohorts and limited statistical power will have contributed; these findings could also reflect complexity not captured by our study design, such as genetic effects which are conditional on environmental exposure. … (more)
- Is Part Of:
- Human molecular genetics. Volume 27:Number 17(2018:Sep. 01)
- Journal:
- Human molecular genetics
- Issue:
- Volume 27:Number 17(2018:Sep. 01)
- Issue Display:
- Volume 27, Issue 17 (2018)
- Year:
- 2018
- Volume:
- 27
- Issue:
- 17
- Issue Sort Value:
- 2018-0027-0017-0000
- Page Start:
- 3113
- Page End:
- 3127
- Publication Date:
- 2018-06-20
- Subjects:
- Human molecular genetics -- Periodicals
Human chromosome abnormalities -- Periodicals
572.8 - Journal URLs:
- http://hmg.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/hmg/ddy237 ↗
- Languages:
- English
- ISSNs:
- 0964-6906
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.198000
British Library DSC - BLDSS-3PM
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- 25164.xml