Evidence map›Paper›PMID 40653461›Full record

ArticleBMC oral health2025

Oxidative genomic damage in pediatric patients exposed to mercury released by dental amalgam.

Guadalupe Nalleli Macías-Lamas, Yveth Marlene Ortiz-García, Blanca Patricia Lazalde-Ramos, Guillermo Moisés Zúñiga-González, Belinda Claudia Gómez-Meda, Cristina Hermila Martínez-Bugarín, Susana Vanessa Sánchez-De-La-Rosa, Saulo Oswaldo Sánchez-Rivera, Gabriela Morales-Velazquez, Celia Guerrero-Velázquez and 1 more

Abstract read
In one paragraph

Article in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Guadalupe Nalleli Macías-LamasInstituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, José Maria Echauri y Juan Díaz Covarrubias s/n, Col. Independencia, Guadalajara, 44340, Jalisco, México.
Yveth Marlene Ortiz-GarcíaInstituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, José Maria Echauri y Juan Díaz Covarrubias s/n, Col. Independencia, Guadalajara, 44340, Jalisco, México.
Blanca Patricia Lazalde-RamosMaestría en Ciencias y Tecnología Química, Unidad Académica de Ciencias Químicas, Universidad Autónoma de Zacatecas, Zacatecas, 98000, México.
Guillermo Moisés Zúñiga-GonzálezLaboratorio de Mutagenesis, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, 44340, México.
Belinda Claudia Gómez-MedaInstituto de Genética Humana "Enrique Corona Rivera" Departamento de Biología Molecular y Genómica, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, 44340, México.
Cristina Hermila Martínez-BugarínInstituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, José Maria Echauri y Juan Díaz Covarrubias s/n, Col. Independencia, Guadalajara, 44340, Jalisco, México.
Susana Vanessa Sánchez-De-La-RosaInstituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, José Maria Echauri y Juan Díaz Covarrubias s/n, Col. Independencia, Guadalajara, 44340, Jalisco, México.
Saulo Oswaldo Sánchez-RiveraInstituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, José Maria Echauri y Juan Díaz Covarrubias s/n, Col. Independencia, Guadalajara, 44340, Jalisco, México.
Gabriela Morales-VelazquezInstituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, José Maria Echauri y Juan Díaz Covarrubias s/n, Col. Independencia, Guadalajara, 44340, Jalisco, México.
Celia Guerrero-VelázquezInstituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, José Maria Echauri y Juan Díaz Covarrubias s/n, Col. Independencia, Guadalajara, 44340, Jalisco, México.
Ana Lourdes Zamora-PerezInstituto de Investigación en Odontología, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, José Maria Echauri y Juan Díaz Covarrubias s/n, Col. Independencia, Guadalajara, 44340, Jalisco, México. anazamora@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMercury (Hg) is the major component of dental amalgam which has been utilized for decades because it is durable, inexpensive and easy to manipulate and position, as well as having a relatively low cost. Hg from dental amalgam fillings has been shown to be released into the buccal cavity due to processes such as abrasion and corrosion, and which could represent a continuous source of oxidative damage to mouth tissues. Therefore, this study assessed the impact of Hg-containing dental amalgams exposure on the oxidative genomic damage using a means of the buccal micronucleus cytome assay by counting the nuclear abnormalities (NAs) in buccal mucosa cells and by analyzing in whole saliva the molecules 8-hydroxy-2′-deoxyguanosine (8-OHdG) and malondialdehyde (MDA) in whole saliva.

methodsThis study was conducted on 120 healthy children divided into two groups-group 1 (or the control group) (n = 60), including participants without dental caries, no history of dental amalgam (Hg-containing) restorations, and no other dental treatments, and group 2 (the intervention group) (n = 60), including participants with dental caries involving enamel or dentin, who received dental amalgam restorations in two posterior teeth. Oral epithelial cell and whole saliva samples were taken at baseline and 30 days later for group 1, while for group 2, samples were obtained at different pre-treatment (baseline) and post-amalgam placement time points at 15 and 30 days.

resultsAn increased frequency of NAs (p < 0.05) and higher levels of 8-OHdG (p < 0.05) and MDA (p < 0.05) were observed after Hg-dental amalgams exposure. In addition, a positive correlation existed between NAs and oxidative stress induced by Hg from dental amalgam.

conclusionsThe presents study shows that individuals exposed to Hg-containing dental amalgam exhibit increased NAs in oral epithelial cells, as well as increased levels of 8-OHdG and MDA in saliva, which are directly related to genotoxicity, oxidative DNA damage and lipid peroxidation, respectively. Exposure to Hg- containing dental amalgams may contribute to oxidative stress and genetic damage, potentially leading to long-term implications for both oral and systemic health.

Indexed as

Dental AmalgamDNA DamageMercuryOxidative Stress8-Hydroxy-2'-DeoxyguanosineChildDental CariesDeoxyguanosineFemaleHumansMaleMalondialdehydeMicronucleus TestsMouth MucosaSaliva8-Hydroxy-2'-DeoxyguanosineDental AmalgamDeoxyguanosineMalondialdehydeMercuryBuccal mucosa cellsDental amalgamDNA damageMercuryNuclear abnormalitiesOxidative stressSaliva

Identifiers

PMID40653461
PMCPMC12257660

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LicenceCC BY-NC-ND
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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.