Evidence map›Paper›PMID 31860742›Full record

Trial reportJournal of clinical periodontology2020

Relationship between herpesviruses and periodontal disease progression.

Pinar Emecen-Huja, Robert J Danaher, Dolphus R Dawson, Chunmei Wang, Richard J Kryscio, Jeffrey L Ebersole, Craig S Miller

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical periodontology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
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 at 1 institution in 1 country.

Pinar Emecen-HujaDepartment of Oral Health Practice, University of Kentucky, Lexington, Kentucky.
Robert J DanaherDepartment of Oral Health Practice, University of Kentucky, Lexington, Kentucky.
Dolphus R DawsonDepartment of Oral Health Practice, University of Kentucky, Lexington, Kentucky.
Chunmei WangCenter for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, Kentucky.
Richard J KryscioDepartment of Statistics, College of Arts & Sciences, University of Kentucky, Lexington, Kentucky.
Jeffrey L EbersoleCenter for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, Kentucky.ORCID 0000-0002-9743-6585
Craig S MillerDepartment of Oral Health Practice, University of Kentucky, Lexington, Kentucky.ORCID 0000-0002-7657-4604
University of Kentucky · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
UKY DENTAL COBRE: POLYBACTERIAL PERIODONTITIS: N-3 PUFA AND ANTIOXIDANTSP20RR020145 · NCRR · UNIVERSITY OF KENTUCKY · PI EBERSOLE, JEFFREY L · 2004 to 2011
$18.3M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
NCATS NIH HHS UL1 TR000117NCATS NIH HHS UL1 TR001998NCRR NIH HHS P20 RR020145
6 · The paper itself

Abstract

aimTo investigate the role of Epstein-Barr virus (EBV), cytomegalovirus (CMV), and anaerobic bacteria in the progression of periodontitis.

methodsEighty-one adults with generalized moderate to severe periodontitis were randomly assigned to: oral hygiene or scaling and root planning ± placebo or polyunsaturated fatty acids fish oil. Subgingival plaque samples collected from three healthy and three disease sites at weeks 0, 16, and 28 and from sites demonstrating disease progression were analysed for EBV, CMV, P. gingivalis (Pg), T. forsythia (Tf), and T. denticola (Td) DNA using quantitative polymerase chain reaction.

resultsCytomegalovirus was detected in 0.3% (4/1454) sites. EBV was present in 12.2% of healthy sites (89/728) and 27.6% disease sites (201/726; p < .0001), but was in low copy number. Disease progression occurred in 28.4% of participants (23/81) and developed predominantly at sites identified as diseased (75/78; 96.2%). CMV and EBV were not associated with disease progression (p = .13) regardless of treatment. In contrast, disease sites were associated with higher levels of Pg, Td, Tf, and total bacteria, and sites that exhibited disease progression were associated with an abundance of Td and Tf (p < .04).

conclusionDisease progression was associated with Gram-negative anaerobic bacteria; not EBV or CMV.

Indexed as

HerpesviridaePeriodontitisAdultCytomegalovirusDisease ProgressionHerpesvirus 4, HumanHumanscytomegalovirusdisease progressionEpstein-Barr virus infectionsperiodontitis

Identifiers

PMID31860742
PMCPMC7096277
OpenAlexW2995594331

What OpenQuestion holds

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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.