Evidence map›Paper›PMID 25691586›Full record

ArticlemBio2015

Dynamic changes in the subgingival microbiome and their potential for diagnosis and prognosis of periodontitis.

Baochen Shi, Michaela Chang, John Martin, Makedonka Mitreva, Renate Lux, Perry Klokkevold, Erica Sodergren, George M Weinstock, Susan K Haake, Huiying Li

Open access · goldAbstract read
In one paragraph

Article in mBio, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 4 pooled it
10.4field-weighted citation impact, top 1% 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

97 citing papers in PubMed, 4 syntheses or guidelines pooled it, 168 citations in OpenAlex.

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37 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Baochen ShiDepartment of Molecular and Medical Pharmacology, Crump Institute for Molecular Imaging, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
Michaela ChangSection of Periodontics, School of Dentistry, UCLA, Los Angeles, California, USA.
John MartinThe Genome Institute, Washington University, St. Louis, Missouri, USA.
Makedonka MitrevaThe Genome Institute, Washington University, St. Louis, Missouri, USA.
Renate LuxSection of Periodontics, School of Dentistry, UCLA, Los Angeles, California, USA.
Perry KlokkevoldSection of Periodontics, School of Dentistry, UCLA, Los Angeles, California, USA.
Erica SodergrenThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
George M WeinstockThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
Susan K HaakeSection of Periodontics, School of Dentistry, UCLA, Los Angeles, California, USA.
Huiying Lihuiying@mednet.ucla.edu.
University of California, Los Angeles · USInstitute for Molecular Medicine · USJackson Laboratory · USWashington University in St. Louis · US

Funding

Metagenomic Study of the Periodontal Microbiome in Healthy and Diabetic SubjectsR01DE021574 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HAAKE, SUSAN KINDER, LI, HUIYING · 2010 to 2013
$2.8M
Molecular signatures of the periodontitis metagenomeRC1DE020298 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HAAKE, SUSAN KINDER, LI, HUIYING · 2009 to 2010
$960k
NIDCR NIH HHS R01 DE021574NIDCR NIH HHS RC1 DE020298
6 · The paper itself

Abstract

unlabelledThe human microbiome influences and reflects the health or disease state of the host. Periodontitis, a disease affecting about half of American adults, is associated with alterations in the subgingival microbiome of individual tooth sites. Although it can be treated, the disease can reoccur and may progress without symptoms. Without prognostic markers, follow-up examinations are required to assess reoccurrence and disease progression and to determine the need for additional treatments. To better identify and predict the disease progression, we aim to determine whether the subgingival microbiome can serve as a diagnosis and prognosis indicator. Using metagenomic shotgun sequencing, we characterized the dynamic changes in the subgingival microbiome in periodontitis patients before and after treatment at the same tooth sites. At the taxonomic composition level, the periodontitis-associated microorganisms were significantly shifted from highly correlated in the diseased state to poorly correlated after treatment, suggesting that coordinated interactions among the pathogenic microorganisms are essential to disease pathogenesis. At the functional level, we identified disease-associated pathways that were significantly altered in relative abundance in the two states. Furthermore, using the subgingival microbiome profile, we were able to classify the samples to their clinical states with an accuracy of 81.1%. Follow-up clinical examination of the sampled sites supported the predictive power of the microbiome profile on disease progression. Our study revealed the dynamic changes in the subgingival microbiome contributing to periodontitis and suggested potential clinical applications of monitoring the subgingival microbiome as an indicator in disease diagnosis and prognosis. IMPORTANCE: Periodontitis is a common oral disease. Although it can be treated, the disease may reoccur without obvious symptoms. Current clinical examination parameters are useful in disease diagnosis but cannot adequately predict the outcome of individual tooth sites after treatment. A link between the subgingival microbiota and periodontitis was identified previously; however, it remains to be investigated whether the microbiome can serve as a diagnostic and prognostic indicator. In this study, for the first time, we characterized the subgingival microbiome of individual tooth sites before and after treatment using a large-scale metagenomic analysis. Our longitudinal study revealed changes in the microbiota in taxonomic composition, cooccurrence of subgingival microorganisms, and functional composition. Using the microbiome profiles, we were able to classify the clinical states of subgingival plaque samples with a high accuracy. Follow-up clinical examination of sampled sites indicates that the subgingival microbiome profile shows promise for the development of diagnostic and prognostic tools.

Indexed as

BiotaAdultGingivaHumansLongitudinal StudiesMetagenomicsMiddle AgedPeriodontitisPredictive Value of TestsSequence Analysis, DNATooth Root

Identifiers

PMID25691586
PMCPMC4337560
OpenAlexW2138854160

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.