Evidence map›Paper›PMID 16538639›Full record

ArticleJournal of clinical laboratory analysis2006

Association of the OGG1 Ser326Cys polymorphism with tooth loss.

Yoshinori Hasui, Yuichiro Hamanaka, Naoko Okayama, Yutaka Suehiro, Fumihiko Shinozaki, Yoshiya Ueyama, Yuji Hinoda

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Yoshinori HasuiDepartment of Oral and Maxillofacial Surgery, Yamaguchi University School of Medicine, Yamaguchi, Japan.
Yuichiro Hamanaka
Naoko Okayama
Yutaka Suehiro
Fumihiko Shinozaki
Yoshiya Ueyama
Yuji Hinoda

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although tooth loss is a serious health problem for elderly people, little is known about the genetic basis for susceptibility to it. In the present study we aimed to find a single nucleotide polymorphism (SNP) associated with tooth loss. DNA samples from 119 outpatients (mean age=78.8 years) were genotyped on seven polymorphisms (tumor necrosis factor-alpha -1031T/C, interleukin-1beta -511C/T, interleukin-6 -634C/G, macrophage migration inhibitory factor -173G/C, interleukin-1 receptor antagonist variable number of tandem repeat in intron 2, matrix metalloproteinase-1 -16071G/2G, and oxoguanine glycosylase 1 (OGG1) Ser326Cys (1245C/G)), and the results were statistically evaluated. Of the seven polymorphisms tested, only OGG1 Ser326Cys was revealed to associate with tooth loss at a statistically significant level (P=0.0086). In addition, a multivariate logistic regression analysis in which age, gender, body mass index (BMI), and ischemic heart disease were included as independent variables indicated that Ser326Cys could be an independent factor affecting tooth loss (OR, 3.191; 95%CI, 1.174-8.672). The data suggest that the OGG1 Ser326Cys polymorphism may be associated with tooth loss.

Indexed as

AgedAged, 80 and overCysteineDNA GlycosylasesFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedPolymorphism, Single NucleotideRegression AnalysisSerineTooth LossCysteineDNA Glycosylasesoxoguanine glycosylase 1, humanSerine

Identifiers

PMID16538639
PMCPMC6807533

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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.