Evidence map›Paper›PMID 34610834›Full record

ArticleBMC oral health2021

Polymorphic variants in genes related to stress coping are associated with the awake bruxism.

Zofia Maciejewska-Szaniec, Marta Kaczmarek-Ryś, Szymon Hryhorowicz, Agnieszka Przystańska, Tomasz Gredes, Barbara Maciejewska, Justyna Hoppe-Gołębiewska, Ryszard Słomski, Andrzej Pławski, Agata Czajka-Jakubowska

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. 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 at 3 institutions in 2 countries.

Zofia Maciejewska-Szaniec *Department of Temporomandibular Disorders, Poznan University of Medical Sciences, Poznan, Poland.
Marta Kaczmarek-Ryś *Institute of Human Genetics, Polish Academy of Sciences, Poznan, Poland. m.kaczmarekrys@gmail.com.
Szymon HryhorowiczInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Agnieszka PrzystańskaDepartment of Temporomandibular Disorders, Poznan University of Medical Sciences, Poznan, Poland.
Tomasz GredesDepartment of Temporomandibular Disorders, Poznan University of Medical Sciences, Poznan, Poland.
Barbara MaciejewskaDepartment and Clinic of Phoniatrics and Audiology, Poznan University of Medical Sciences, Poznan, Poland.
Justyna Hoppe-GołębiewskaInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Ryszard SłomskiInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Andrzej PławskiInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Agata Czajka-JakubowskaDepartment of Temporomandibular Disorders, Poznan University of Medical Sciences, Poznan, Poland. agatacj@gmail.com.
Polish Academy of Sciences · PLPoznan University of Medical Sciences · PLUniversity Hospital Carl Gustav Carus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic stress is one of the leading predisposing factors in bruxism aetiology, but the influence of genetic factors is also suggested. We aimed to study whether sequence variants in genes involved in stress regulation pathways: NTRK2 and BDNF, may be associated with awake bruxism susceptibility, clinical presentation, and patients' perceived stress level.

methodsThe study group included 104 patients with probable awake bruxism and 191 population controls. Patients underwent dental examination concerning the symptoms of bruxism and psychological testing. Genotyping was performed using HRMA and sequencing. Statistical analyses were conducted, and P values below 0.05 were considered statistically significant.

resultsWe observed a positive correlation of measured stress level and pathological teeth attrition in the anterior segment (r = 0.45, P < 0.001), enamel attritions (r = 0.44, P < 0.001), tongue impressions (r = 0.50, P < 0.001) and posterior teeth attrition (r = 0.27, P = 0.005). Moreover, the c.196A variant (p.66Met) of the BDNF gene and c.1397-31392G allele of the NTRK2 gene were present with elevated frequency, comparing to controls.

conclusionsThis study hence the thesis that perceived stress level is a substantial contributing factor to awake bruxism occurrence and its clinical manifestations. Moreover, sequence variants in genes related to stress coping may be correlated with awake bruxism's susceptibility via elevated perceived stress level.

Indexed as

Adaptation, PsychologicalBruxismTooth AttritionAllelesBrain-Derived Neurotrophic FactorHumansMembrane GlycoproteinsReceptor, trkBWakefulnessBDNF protein, humanBrain-Derived Neurotrophic FactorMembrane GlycoproteinsReceptor, trkBtropomyosin-related kinase-B, humanAssociation analysisAwake bruxismBDNF geneNTRK2 geneStress copingSusceptibility

Identifiers

PMID34610834
PMCPMC8491599
OpenAlexW3202887575

What OpenQuestion 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 OpenQuestion graph.