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GWAS Study

Novel Genetic Determinants of Dental Maturation in Children.

Grgic O, Prijatelj V, Dudakovic A et al.

36437532 PubMed ID
GWAS Study Type
14805 Participants
61 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GO
Grgic O
PV
Prijatelj V
DA
Dudakovic A
VS
Vucic S
DB
Dhamo B
TK
Trajanoska K
MC
Monnereau C
ZM
Zrimsek M
GK
Gautvik KM
RS
Reppe S
SE
Shimizu E
HS
Haworth S
TN
Timpson NJ
JV
Jaddoe VWV
JM
Jarvelin MR
ED
Evans D
UA
Uitterlinden AG
OE
Ongkosuwito EM
VW
van Wijnen AJ
MC
Medina-Gomez C
RF
Rivadeneira F
WE
Wolvius EB
Chapter II

Abstract

Summary of the research findings

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, N1 = 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 (N2 = 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.

14,805 European or unknown ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

14805
Total Participants
GWAS
Study Type
No
Replicated
European, NR
Ancestry
Netherlands, Finland, U.K.
Recruitment Country
Chapter IV

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