scholarly journals sIgA and Lisozim as Biomarker of Early Childhood Caries Risk

Author(s):  
Essie Octiara ◽  
Heriandi Sutadi ◽  
Yahwardiah Siregar ◽  
Ameta Primasari
2009 ◽  
Vol 19 (2) ◽  
pp. 174-180 ◽  
Author(s):  
Sukaeni Ibrahim ◽  
Michiko Nishimura ◽  
Seishi Matsumura ◽  
Omar M.M. Rodis ◽  
Ayami Nishida ◽  
...  

2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Morenike O Folayan ◽  
Kikelomo A Kolawole ◽  
Elizabeth O Oziegbe ◽  
Titus Oyedele ◽  
Olusegun V Oshomoji ◽  
...  

2020 ◽  
Vol 30 (6) ◽  
pp. 798-804
Author(s):  
Morenike Oluwatoyin Folayan ◽  
Ayodeji Babatunde Oginni ◽  
Maha El Tantawi ◽  
Micheal Alade ◽  
Abiola A. Adeniyi ◽  
...  

2020 ◽  
Vol 99 (5) ◽  
pp. 537-543
Author(s):  
B. Heaton ◽  
S.T. Cherng ◽  
W. Sohn ◽  
R.I. Garcia ◽  
S. Galea

Early childhood caries (ECC) is a largely preventable condition that occurs when children develop caries in their primary teeth before the age of six. National trends of ECC indicate that prevalence is decreasing, but disparities between various sociodemographic groups may be increasing, despite intervention efforts. Dynamic mechanisms in caries development are hypothesized to be responsible for the observed population distributions of disease. Agent-based models (ABMs) have been utilized to explore similar hypotheses in many areas of health research. Therefore, we developed an ABM of ECC development mechanisms and examined population outcomes of hypothetical preventive intervention scenarios. We found that risk-based targeting had minimal impact on population averages or disparities and was largely due to the strength of the dynamic mechanisms among those considered to be at high caries risk. Universally increasing intervention access reduced population caries prevalence, but increased disparities between different groups of caries risk profiles. We show that population distributions of ECC can emerge as a result of dynamic mechanisms that have been shown to drive disease development. Understanding the effectiveness of a proposed intervention in relation to the hypothesized mechanism(s) that contributes to the outcome of interest is critical to future efforts to address population disparities in ECC.


2020 ◽  
pp. 002203452097992
Author(s):  
A. Grier ◽  
J.A. Myers ◽  
T.G. O’Connor ◽  
R.G. Quivey ◽  
S.R. Gill ◽  
...  

As the most common chronic disease in preschool children in the United States, early childhood caries (ECC) has a profound impact on a child’s quality of life, represents a tremendous human and economic burden to society, and disproportionately affects those living in poverty. Caries risk assessment (CRA) is a critical component of ECC management, yet the accuracy, consistency, reproducibility, and longitudinal validation of the available risk assessment techniques are lacking. Molecular and microbial biomarkers represent a potential source for accurate and reliable dental caries risk and onset. Next-generation nucleotide-sequencing technology has made it feasible to profile the composition of the oral microbiota. In the present study, 16S ribosomal RNA (rRNA) gene sequencing was applied to saliva samples that were collected at 6-mo intervals for 24 mo from a subset of 56 initially caries-free children from an ongoing cohort of 189 children, aged 1 to 3 y, over the 2-y study period; 36 children developed ECC and 20 remained caries free. Analyses from machine learning models of microbiota composition, across the study period, distinguished between affected and nonaffected groups at the time of their initial study visits with an area under the receiver operating characteristic curve (AUC) of 0.71 and discriminated ECC-converted from healthy controls at the visit immediately preceding ECC diagnosis with an AUC of 0.89, as assessed by nested cross-validation. Rothia mucilaginosa, Streptococcus sp., and Veillonella parvula were selected as important discriminatory features in all models and represent biomarkers of risk for ECC onset. These findings indicate that oral microbiota as profiled by high-throughput 16S rRNA gene sequencing is predictive of ECC onset.


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