Evidence map›Paper›PMID 38771832›Full record

ArticlePloS one2024

Single Nucleotide Polymorphisms in RUNX2 and BMP2 contributes to different vertical facial profile.

Caio Luiz Bitencourt Reis, Mirian Aiko Nakane Matsumoto, Maria Bernadete Sasso Stuani, Fábio Lourenço Romano, Rafaela Scariot, Angela Graciela Deliga Schroder, Paulo Nelson-Filho, Christian Kirschneck, Svenja Beisel-Memmert, Erika Calvano Küchler

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Caio Luiz Bitencourt ReisDepartment of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Mirian Aiko Nakane MatsumotoDepartment of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Maria Bernadete Sasso StuaniDepartment of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Fábio Lourenço RomanoDepartment of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Rafaela ScariotDepartment of Stomatology, Federal University of Paraná, Curitiba, Brazil.ORCID 0000-0002-4911-6413
Angela Graciela Deliga SchroderSchool of Dentistry, Tuiuti University of Paraná, Curitiba, PR, Brazil.
Paulo Nelson-FilhoDepartment of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Christian KirschneckDepartment of Orthodontics, University Hospital Bonn, Medical Faculty, Bonn, Germany.
Svenja Beisel-MemmertDepartment of Orthodontics, University Hospital Bonn, Medical Faculty, Bonn, Germany.
Erika Calvano KüchlerDepartment of Orthodontics, University Hospital Bonn, Medical Faculty, Bonn, Germany.ORCID 0000-0001-5351-2526

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The vertical facial profile is a crucial factor for facial harmony with significant implications for both aesthetic satisfaction and orthodontic treatment planning. However, the role of single nucleotide polymorphisms (SNPs) in the development of vertical facial proportions is still poorly understood. This study aimed to investigate the potential impact of some SNPs in genes associated with craniofacial bone development on the establishment of different vertical facial profiles. Vertical facial profiles were assessed by two senior orthodontists through pre-treatment digital lateral cephalograms. The vertical facial profile type was determined by recommended measurement according to the American Board of Orthodontics. Healthy orthodontic patients were divided into the following groups: "Normodivergent" (control group), "Hyperdivergent" and "Hypodivergent". Patients with a history of orthodontic or facial surgical intervention were excluded. Genomic DNA extracted from saliva samples was used for the genotyping of 7 SNPs in RUNX2, BMP2, BMP4 and SMAD6 genes using real-time polymerase chain reactions (PCR). The genotype distribution between groups was evaluated by uni- and multivariate analysis adjusted by age (alpha = 5%). A total of 272 patients were included, 158 (58.1%) were "Normodivergent", 68 (25.0%) were "Hyperdivergent", and 46 (16.9%) were "Hypodivergent". The SNPs rs1200425 (RUNX2) and rs1005464 (BMP2) were associated with a hyperdivergent vertical profile in uni- and multivariate analysis (p-value < 0.05). Synergistic effect was observed when evaluating both SNPs rs1200425- rs1005464 simultaneously (Prevalence Ratio = 4.0; 95% Confidence Interval = 1.2-13.4; p-value = 0.022). In conclusion, this study supports a link between genetic factors and the establishment of vertical facial profiles. SNPs in RUNX2 and BMP2 genes were identified as potential contributors to hyperdivergent facial profiles.

Indexed as

Bone DevelopmentBone Morphogenetic Protein 2Core Binding Factor Alpha 1 SubunitFaceAdolescentChildFemaleHumansMaleOrthodonticsPolymorphism, Single NucleotideYoung AdultBMP2 protein, humanBone Morphogenetic Protein 2Core Binding Factor Alpha 1 SubunitRUNX2 protein, human

Identifiers

PMID38771832
PMCPMC11108145

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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.