Evidence map›Paper›PMID 34744270›Full record

ArticleActa clinica Croatica2021

ASSESSMENT OF CYTOGENETIC DAMAGE TO EXFOLIATED GINGIVAL CELLS IN PATIENTS WITH CHRONIC GENERALIZED PERIODONTITIS.

Antonija Tadin, Lidia Gavić, Marija Roguljić, Mario Babić, Ivan Galić, Davor Želježić

Open access · diamondAbstract read
In one paragraph

Article in Acta clinica Croatica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Antonija Tadin1Department of Restorative Dental Medicine and Endodontics, Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 2Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 3Division for Mutagenesis, Institute for Medical Research and Occupational Health, Zagreb, Croatia.
Lidia Gavić1Department of Restorative Dental Medicine and Endodontics, Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 2Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 3Division for Mutagenesis, Institute for Medical Research and Occupational Health, Zagreb, Croatia.
Marija Roguljić1Department of Restorative Dental Medicine and Endodontics, Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 2Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 3Division for Mutagenesis, Institute for Medical Research and Occupational Health, Zagreb, Croatia.
Mario Babić1Department of Restorative Dental Medicine and Endodontics, Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 2Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 3Division for Mutagenesis, Institute for Medical Research and Occupational Health, Zagreb, Croatia.
Ivan Galić1Department of Restorative Dental Medicine and Endodontics, Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 2Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 3Division for Mutagenesis, Institute for Medical Research and Occupational Health, Zagreb, Croatia.
Davor Želježić1Department of Restorative Dental Medicine and Endodontics, Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 2Study of Dental Medicine, School of Medicine, University of Split, Split, Croatia; 3Division for Mutagenesis, Institute for Medical Research and Occupational Health, Zagreb, Croatia.
University of Split · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this cross-sectional study was to investigate the occurrence of chromosomal abnormalities through the frequency of micronuclei and other genomic damage markers in patients with chronic generalized periodontitis and without periodontal disease. Micronucleus assay was performed in exfoliated gingival epithelial cells of 35 patients with generalized chronic periodontitis and 30 control subjects with healthy periodontium. Full mouth clinical examination was performed to define periodontal condition. The mean number of cells with micronuclei observed in chronic periodontitis and control groups was 1.8 (±1.49) and 2.0 (±1.34), respectively. Differences between the groups were not significant (p=0.574). Compared to control subjects, patients with chronic periodontitis showed a significant increase in the number of binucleated cells (p≤0.001) and number of cells with nucleoplasmic bridges (p=0.042). Study results indicated that chronic periodontitis was not associated with higher occurrence of chromosomal damage in gingival cells compared to individuals with healthy periodontium.

Indexed as

Chronic PeriodontitisCross-Sectional StudiesCytogenetic AnalysisHumansPeriodontiumCytotoxicityGenotoxicityGingival cellMicronucleus assayPeriodontitis

Identifiers

PMID34744270
PMCPMC8564832
OpenAlexW3206406894

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.