Evidence map›Paper›PMID 34016088›Full record

ArticleBMC oral health2021

Replication of GWAS significant loci in a sub-Saharan African Cohort with early childhood caries: a pilot study.

Olubukola O Olatosi, Mary Li, Azeez A Alade, Afolabi Oyapero, Tamara Busch, John Pape, Joy Olotu, Waheed Awotoye, Mohaned Hassan, Chinyere Adeleke and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC oral health, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

Olubukola O OlatosiDepartment of Child Dental Health, Faculty of Dental Sciences, College of Medicine, University of Lagos, Lagos, Nigeria. bukkyolatosi@gmail.com.
Mary LiDepartment of Oral Pathology, Radiology and Medicine, College of Dentistry, University of Iowa, Iowa City , USA.
Azeez A AladeDepartment of Oral Pathology, Radiology and Medicine, College of Dentistry, University of Iowa, Iowa City , USA.
Afolabi OyaperoDepartment of Preventive Dentistry, Faculty of Dentistry, Lagos State University College of Medicine, Lagos, Nigeria.
Tamara BuschIowa Institute of Oral Health Research, University of Iowa, Iowa City, IA, USA.
John PapeIowa Institute of Oral Health Research, University of Iowa, Iowa City, IA, USA.
Joy OlotuDepartment of Anatomy, University of Port Harcourt, Port Harcourt, Nigeria.
Waheed AwotoyeDepartment of Oral Pathology, Radiology and Medicine, College of Dentistry, University of Iowa, Iowa City , USA.
Mohaned HassanIowa Institute of Oral Health Research, University of Iowa, Iowa City, IA, USA.
Chinyere AdelekeIowa Institute of Oral Health Research, University of Iowa, Iowa City, IA, USA.
Wasiu L AdeyemoDepartment of Oral and Maxillofacial Surgery, University of Lagos, Lagos, Nigeria.
Elizabeth O SoteDepartment of Child Dental Health, Faculty of Dental Sciences, College of Medicine, University of Lagos, Lagos, Nigeria.
John R ShafferDepartment of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Mary MarazitaDepartment of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Azeez ButaliDepartment of Oral Pathology, Radiology and Medicine, College of Dentistry, University of Iowa, Iowa City , USA.
University of Iowa · USUniversity of Lagos · NGUniversity of Pittsburgh · USLagos State University · NGUniversity of Port Harcourt · NG

Funding

Whole Genome Sequencing for Orofacial Clefts, Incidental Findings and Role of Community GatekeepersR01DE028300 · NIDCR · UNIVERSITY OF IOWA · PI BUTALI, AZEEZ · 2020 to 2024
$3.9M
Building Research And Innovation in Nigeria's Science - (BRAINS)D43TW010134 · FIC · COLLEGE OF MEDICINE, UNIVERSITY OF LAGOS · PI OGUNSOLA, FOLASADE TOLULOPE · 2015 to 2020
$3.2M
University of Iowa Institutional Training Program in Oral Health ResearchR90DE024296 · NIDCR · UNIVERSITY OF IOWA · PI STEVEN M. LEVY · 2013 to 2026
$1.8M
Genetic studies of nonsyndromic clefts in populations of African Descent.R00DE022378 · NIDCR · UNIVERSITY OF IOWA · PI BUTALI, AZEEZ · 2014 to 2016
$747k
FIC NIH HHS D43 TW010134NIDCR NIH HHS R00 DE022378NIDCR NIH HHS R01 DE028300NIDCR NIH HHS R90 DE024296
6 · The paper itself

Abstract

backgroundEarly childhood caries (ECC) is a rapidly progressing form of dental infection and a significant public health problem, especially among socially and economically disadvantaged populations. This study aimed to assess the risk factors for ECC among a cohort of Sub-Saharan African children and to determine the role of genetics in the etiology of ECC.

methodsA sample of 691 children (338 with ECC, 353 without ECC, age < 6 years) was recruited from schools in Lagos, Nigeria. Socio-demographic, dental services utilization and infant dietary data were obtained with interviewer-administered questionnaire. Oral examination was conducted using the WHO oral health diagnostic criteria. Saliva samples were collected from the children for genetic analysis. Single nucleotide polymorphisms were selected from previous study for genotyping. Genetic association analyses to investigate the role of genetics in the etiology of ECC was done. Bivariate comparisons and Multivariate logistic regression analyses were conducted to assess associations between ECC and predictor variables, p < 0.05.

resultsOf the 338 children with ECC, 64 (18.9%) had Severe-Early Childhood Caries (S-ECC). Children aged 48-59 months comprised the highest proportion of subjects with ECC (165; 48.8%) and S-ECC (24; 37.5%) while female subjects had higher dt (3.13 ± 2.56) and dmft values 3.27 ± 2.64. ECC was significantly more prevalent among children who were breastfed at night ≥ 12 months (OR 3.30; CI 0.39, 4.75), those with no previous dental visit (OR 1.71; CI 0.24, 2.77), those who used sweetened pacifiers (OR 1.85; CI 0.91, 3.79) and those who daily consumed sugar-sweetened drinks/snacks (OR 1.35; CI 0.09, 18.51). A suggestive increased risk for ECC (OR 1.26, p = 0. 0.0397) was observed for the genetic variant rs11239282 on chromosome 10. We also observed a suggestive reduced risk for ECC (OR 0.80, p = 0.03) for the rs131777 on chromosome 22. None of the genetic variants were significant after correction for multiple testing (Bonferroni p value p = 0.004).

conclusionsProlonged night-time breastfeeding, poor utilization of dental services and daily consumption of sugar were risk factors for ECC. Larger sample size is needed to confirm the results of the genetic analysis and to conduct genome wide studies in order to discover new risk loci for ECC.

Indexed as

Dental CariesDental Caries SusceptibilityAfrica South of the SaharaChildChild, PreschoolCross-Sectional StudiesFemaleGenome-Wide Association StudyHumansInfantNigeriaPilot ProjectsPrevalenceRisk FactorsEarly childhood caries (ECC)GeneticsPrevalenceRisk factorsSevere early childhood caries

Identifiers

PMID34016088
PMCPMC8139096
OpenAlexW3160576804

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.