Metabolomics Insights in Early Childhood Caries
Created by W.Langdon from
gp-bibliography.bib Revision:1.8010
- @Article{Heimisdottir:2021:JDR,
-
author = "L. H. Heimisdottir and B. M. Lin and H. Cho and
A. Orlenko and A. A. Ribeiro and A. Simon-Soro and
J. Roach and D. Shungin and J. Ginnis and
M. A. Simancas-Pallares and H. D. Spangler and
A. G. {Ferreira Zandona} and J. T. Wright and
P. Ramamoorthy and J. H. Moore and H. Koo and D. Wu and K. Divaris",
-
title = "Metabolomics Insights in Early Childhood Caries",
-
journal = "Journal of Dental Research",
-
year = "2021",
-
month = "9 " # jan,
-
note = "Epub ahead of print",
-
keywords = "genetic algorithms, genetic programming, TPOT,
children, biofilm, dental caries, microbiome, machine
learning, risk assessment",
-
ISSN = "0022-0345",
-
DOI = "doi:10.1177/0022034520982963",
-
abstract = "Dental caries is characterized by a dysbiotic shift at
the biofilm-tooth surface interface, yet comprehensive
biochemical characterisations of the biofilm are scant.
We used metabolomics to identify biochemical features
of the supragingival biofilm associated with early
childhood caries (ECC) prevalence and severity. The
study analytical sample comprised 289 children ages 3
to 5 (51percent with ECC) who attended public
preschools in North Carolina and were enrolled in a
community-based cross-sectional study of early
childhood oral health. Clinical examinations were
conducted by calibrated examiners in community
locations using International Caries Detection and
Classification System (ICDAS) criteria. Supragingival
plaque collected from the facial/buccal surfaces of all
primary teeth in the upper-left quadrant was analysed
using ultra-performance liquid chromatography-tandem
mass spectrometry. Associations between individual
metabolites and 18 clinical traits (based on different
ECC definitions and sets of tooth surfaces) were
quantified using Brownian distance correlations (dCor)
and linear regression modeling of log2-transformed
values, applying a false discovery rate multiple
testing correction. A tree-based pipeline optimization
tool (TPOT), machine learning process was used to
identify the best-fitting ECC classification metabolite
model. There were 503 named metabolites identified,
including microbial, host, and exogenous biochemicals.
Most significant ECC-metabolite associations were
positive (i.e., upregulations/enrichments). The
localized ECC case definition (ICDAS ge 1 caries
experience within the surfaces from which plaque was
collected) had the strongest correlation with the
metabolome (dCor P = 8 10-3). Sixteen metabolites were
significantly associated with ECC after multiple
testing correction, including fucose (P = 3.0 10-6) and
N-acetylneuraminate (p = 6.8 10-6) with higher ECC
prevalence, as well as catechin (P = 4.7 10-6) and
epicatechin (P = 2.9 10-6) with lower. Catechin,
epicatechin, imidazole propionate, fucose, 9,10-DiHOME,
and N-acetylneuraminate were among the top 15
metabolites in terms of ECC classification importance
in the automated TPOT model. These supragingival
biofilm metabolite findings provide novel insights in
ECC biology and can serve as the basis for the
development of measures of disease activity or risk
assessment.",
-
notes = "Division of Pediatric and Public Health, Adams School
of Dentistry, University of North Carolina, Chapel
Hill, NC, USA
PMID: 33423574",
- }
Genetic Programming entries for
L H Heimisdottir
B M Lin
H Cho
Alena Orlenko
A A Ribeiro
A Simon-Soro
J Roach
D Shungin
J Ginnis
M A Simancas-Pallares
H D Spangler
A G Ferreira Zandona
J T Wright
P Ramamoorthy
Jason H Moore
H Koo
D Wu
K Divaris
Citations