Novel Genetic Determinants of Dental Maturation in Children

全基因组关联研究 人口分层 颅面 人口 遗传学 混淆 等位基因 遗传关联 医学 生物 基因型 内科学 基因 单核苷酸多态性 环境卫生
作者
Olja Grgić,Vid Prijatelj,Amel Dudakovic,Strahinja Vučić,Brunilda Dhamo,Katerina Trajanoska,Claire Monnereau,Maša Zrimšek,Kaare M. Gautvik,Sjur Reppe,Emi Shimizu,Simon Haworth,Nicholas J. Timpson,Vincent W. V. Jaddoe,M. R. Jarvelin,David M. Evans,A G Uitterlinden,Edwin M. Ongkosuwito,André J. van Wijnen,Carolina Medina-Gómez,Fernando Rivadeneira,Eppo B. Wolvius
出处
期刊:Journal of Dental Research [SAGE]
卷期号:102 (3): 349-356 被引量:2
标识
DOI:10.1177/00220345221132268
摘要

Dental occlusion requires harmonious development of teeth, jaws, and other elements of the craniofacial complex, which are regulated by environmental and genetic factors. We performed the first genome-wide association study (GWAS) on dental development (DD) using the Demirjian radiographic method. Radiographic assessments from participants of the Generation R Study (primary study population, N 1 = 2,793; mean age of 9.8 y) were correlated with ~30 million genetic variants while adjusting for age, sex, and genomic principal components (proxy for population stratification). Variants associated with DD at genome-wide significant level ( P < 5 × 10 −8 ) mapped to 16q12.2 ( IRX5) (lead variant rs3922616, B = 0.16; P = 2.2 × 10 −8 ). We used Fisher’s combined probability tests weighted by sample size to perform a meta-analysis ( N = 14,805) combining radiographic DD at a mean age of 9.8 y from Generation R with data from a previous GWAS ( N 2 = 12,012) on number of teeth (NT) in infants used as proxy of DD at a mean age of 9.8 y (including the ALSPAC and NFBC1966). This GWAS meta-analysis revealed 3 novel loci mapping to 7p15.3 ( IGF2BP3: P = 3.2 × 10 −8 ), 14q13.3 ( PAX9: P = 1.9 × 10 −8 ), and 16q12.2 ( IRX5: P = 1.2 × 10 −9 ) and validated 8 previously reported NT loci. A polygenic allele score constructed from these 11 loci was associated with radiographic DD in an independent Generation R set of children ( N = 703; B = 0.05, P = 0.004). Furthermore, profiling of the identified genes across an atlas of murine and human stem cells observed expression in the cells involved in the formation of bone and/or dental tissues (>0.3 frequency per kilobase of transcript per million mapped reads), likely reflecting functional specialization. Our findings provide biological insight into the polygenic architecture of the pediatric dental maturation process.
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