Evidence mapPaperPMID 41345979Full record

ArticleMicrobiome2025

Diabetes alters the supragingival microbiome through plasma-to-saliva migration of glucose and fructose.

Akito Sakanaka, Masahiro Furuno, Asuka Ishikawa, Naoto Katakami, Moe Inoue, Shota Mayumi, Daiki Kurita, Hitoshi Nishizawa, Kazuo Omori, Naohiro Taya and 7 more

Abstract read
In one paragraph

Article in Microbiome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

17 authors.

Akito SakanakaDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan. sakanaka.akito.dent@osaka-u.ac.jp.
Masahiro FurunoDepartment of Biotechnology, Graduate School of Engineering, The University of Osaka, Osaka, Japan.
Asuka IshikawaDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan.
Naoto KatakamiDepartment of Metabolic Medicine, Graduate School of Medicine, The University of Osaka, Osaka, Japan.
Moe InoueDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan.
Shota MayumiDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan.
Daiki KuritaDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan.
Hitoshi NishizawaDepartment of Metabolic Medicine, Graduate School of Medicine, The University of Osaka, Osaka, Japan.
Kazuo OmoriDepartment of Metabolic Medicine, Graduate School of Medicine, The University of Osaka, Osaka, Japan.
Naohiro TayaDepartment of Metabolic Medicine, Graduate School of Medicine, The University of Osaka, Osaka, Japan.
Emiko Tanaka IsomuraDepartment of Oral and Maxillofacial Surgery, Graduate School of Dentistry, The University of Osaka, Osaka, Japan.
Mashu KudohDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan.
Hiroki TakeuchiDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan.
Atsuo AmanoDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan.
Iichiro ShimomuraDepartment of Metabolic Medicine, Graduate School of Medicine, The University of Osaka, Osaka, Japan.
Eiichiro FukusakiDepartment of Biotechnology, Graduate School of Engineering, The University of Osaka, Osaka, Japan.
Masae KuboniwaDepartment of Preventive Dentistry, Graduate School of Dentistry, The University of Osaka, Osaka, Japan. kuboniwa.masae.dent@osaka-u.ac.jp.

Funding

Japan Agency for Medical Research and Development JP16gm0710005Japan Society for the Promotion of Science 22H03300, 22H00487, 22K10311, 21K18281
6 · The paper itself

Abstract

backgroundDental caries, a dysbiotic biofilm disease driven by polymicrobial acidogenesis, often coexists with type 2 diabetes (T2D). Previous studies suggest covarying relationships between circulating and salivary metabolites in patients with T2D. However, the role of hyperglycemia-induced saccharide migration from plasma to saliva in caries pathogenesis remains unclear. Here, we developed a novel method for untargeted metabolomics profiling of trace saliva from sublingual and submandibular glands, comparing this profile with those of plasma and whole saliva in participants with T2D (n = 31) and those with normoglycemia (n = 30). This comparison aimed to determine how circulating saccharide migration into the oral cavity and its subsequent microbial consumption are linked to dental caries. Additionally, shotgun metagenomic sequencing was combined with this analysis to investigate the cariogenic impact of circulating saccharide migration on the composition and function of supragingival biofilm using MetaPhlAn4 and HUMAnN3 pipelines.

resultsThe metabolomics profiles of glandular saliva showed intermediate dissimilarity between plasma and whole saliva, reflecting cardiometabolic traits more sensitively than whole saliva. Glucose and fructose showed a decreasing positive correlation with glycemic parameters in the order of plasma, glandular saliva, and whole saliva, suggesting systemic-to-oral migration and subsequent microbial consumption. Saccharide migration was more pronounced in participants with dental caries and plaque accumulation, coinciding with shifts in supragingival microbiota, including depletion of Streptococcus sanguinis, Corynebacterium durum, and Rothia aeria, and enrichment of Streptococcus mutans, Veillonella parvula, and Actinomyces sp. oral taxon 448. Glycolytic potential increased at the community level. Improved glycemic control reduced fructose migration and mitigated dysbiosis, decreasing fructose phosphotransferase abundance and shifting the S. mutans-S. sanguinis balance. Experimental validation demonstrated that fructose promotes S. mutans dominance over S. sanguinis in dual-species biofilms.

conclusionsThis study establishes saccharide migration as a metabolic driver of supragingival dysbiosis in T2D. The findings highlight the role of both glucose and fructose in caries pathogenesis and suggest that glycemic control could serve as an effective strategy as part of caries control. Video Abstract.

Indexed as

Diabetes Mellitus, Type 2FructoseGingivaGlucoseMicrobiotaSalivaAdultAgedBacteriaBiofilmsDental CariesFemaleHumansMaleMetabolomicsMetagenomicsFructoseGlucoseDental cariesGlycemic controlOral microbiomeSaccharide migrationSalivary metabolomicsShotgun metagenomicsSupragingival biofilmType 2 diabetes

Identifiers

PMID41345979
PMCPMC12849494

What Socratic holds

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LicenceCC BY
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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 Socratic graph.