Evidence map›Paper›PMID 39294450›Full record

SynthesisCalcified tissue international2024

Dental Abnormalities in Osteogenesis Imperfecta: A Systematic Review.

Laura Ventura, Sara J E Verdonk, Lidiia Zhytnik, Angela Ridwan-Pramana, Marjolijn Gilijamse, Willem H Schreuder, Kirsten A van Gelderen-Ziesemer, Ton Schoenmaker, Dimitra Micha, Elisabeth M W Eekhoff

Abstract readSystematic Review
In one paragraph

Synthesis in Calcified tissue international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  10. Review
  11. Article
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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.

Laura Ventura *Department of Human Genetics, Amsterdam UMC Location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0009-0005-1732-6618
Sara J E Verdonk *Amsterdam Movement Sciences, Amsterdam, The Netherlands.ORCID 0000-0001-5992-6789
Lidiia ZhytnikDepartment of Human Genetics, Amsterdam UMC Location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-4682-0402
Angela Ridwan-PramanaDepartment of Oral and Maxillofacial Surgery, Amsterdam UMC Location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Marjolijn GilijamseAmsterdam Movement Sciences, Amsterdam, The Netherlands.ORCID 0000-0003-0609-9227
Willem H SchreuderAmsterdam Bone Center, Amsterdam, The Netherlands.
Kirsten A van Gelderen-ZiesemerMedical Library, Vrije Universiteit, Amsterdam, The Netherlands.
Ton Schoenmaker *Amsterdam Movement Sciences, Amsterdam, The Netherlands.ORCID 0000-0001-6649-374X
Dimitra Micha *Department of Human Genetics, Amsterdam UMC Location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0001-7890-4411
Elisabeth M W Eekhoff *Amsterdam Reproduction and Development, Amsterdam, The Netherlands. emw.eekhoff@amsterdamumc.nl.ORCID 0000-0001-5399-676X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by fragile bones and skeletal deformities. Individuals with OI may have dental abnormalities such as dentinogenesis imperfecta (DI) type I, malocclusions, and unerupted or missing teeth. This review comprehensively examines these dental abnormalities to assess their prevalence among the OI population and explore potential differences across different clinical types of OI and pathogenic variants. In accordance with the PRISMA guidelines, a systematic literature search in PubMed, Embase, and Web of Science was conducted that included articles up to June 2024. Out of 672 articles screened, 34 were included. The included studies confirmed that dental abnormalities are prevalent in OI, with DI prevalence ranging from approximately 20 to 48%. Those with a more severe skeletal phenotype (OI type III/IV) exhibited more dental abnormalities than those with a milder skeletal phenotype (OI type I). Notably, OI type V individuals generally do not have DI, although a few isolated cases have been reported. The prevalence of occlusion types varied: Class I occlusion ranged from 14.8 to 50% and Class II malocclusion ranged from 0 to 37.5%, while Class III malocclusion from 4.1 to 84%. This differs from the general population, where Class III malocclusion is typically the least common. Open bites, cross-bites, and unerupted and missing teeth are also commonly reported, particularly in OI types III and IV. This review emphasizes the need for comprehensive dental examinations in OI due to the high prevalence of dental abnormalities. Additionally, the review draws attention to the lack of clear guidelines for diagnosing DI.

Indexed as

Osteogenesis ImperfectaDentinogenesis ImperfectaHumansMalocclusionPrevalenceTooth AbnormalitiesCollagen type IDental abnormalitiesDentinogenesis imperfectaOsteogenesis imperfecta

Identifiers

PMID39294450
PMCPMC11531448

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.