Evidence map›Paper›PMID 30543027›Full record

ArticleClinical oral investigations2019

Subgingival lipid A profile and endotoxin activity in periodontal health and disease.

Alexander Strachan, Zoe Harrington, Clare McIlwaine, Matthew Jerreat, Louise A Belfield, Aniko Kilar, Simon K Jackson, Andrew Foey, Svetislav Zaric

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Article in Clinical oral investigations, 2019. 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
1.3field-weighted citation impact, top 19% 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, 15 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Alexander StrachanFaculty of Medicine and Dentistry, University of Plymouth, Plymouth, PL4 8AA, UK.
Zoe HarringtonFaculty of Medicine and Dentistry, University of Plymouth, Plymouth, PL4 8AA, UK.
Clare McIlwaineFaculty of Medicine and Dentistry, University of Plymouth, Plymouth, PL4 8AA, UK.
Matthew JerreatFaculty of Medicine and Dentistry, University of Plymouth, Plymouth, PL4 8AA, UK.
Louise A BelfieldFaculty of Medicine and Dentistry, University of Plymouth, Plymouth, PL4 8AA, UK.
Aniko KilarMedical School, Institute of Bioanalysis, University of Pécs, Pécs, Hungary.
Simon K JacksonFaculty of Medicine and Dentistry, University of Plymouth, Plymouth, PL4 8AA, UK.
Andrew FoeyFaculty of Medicine and Dentistry, University of Plymouth, Plymouth, PL4 8AA, UK.
Svetislav ZaricFaculty of Medicine and Dentistry, University of Plymouth, Plymouth, PL4 8AA, UK. svetislav.zaric@plymouth.ac.uk.ORCID http://orcid.org/0000-0003-4127-0253
University of Plymouth · GBUniversity of Pecs · HU

Funding

British Society for Oral and Dental Research GSK Research Grant ProgrammeDowager Countess Eleanor Peel Trust 219New National Excellence Program of the Hungarian Ministry of Human Capacities NKFIH K-125275New National Excellence Program of the Hungarian Ministry of Human Capacities UNKP-17-4-III
6 · The paper itself

Abstract

objectivesRegulation of lipopolysaccharide (LPS) chemical composition, particularly its lipid A domain, is an important, naturally occurring mechanism that drives bacteria-host immune system interactions into either a symbiotic or pathogenic relationship. Members of the subgingival oral microbiota can critically modulate host immuno-inflammatory responses by synthesizing different LPS isoforms. The objectives of this study were to analyze subgingival lipid A profiles and endotoxin activities in periodontal health and disease and to evaluate the use of the recombinant factor C assay as a new, lipid A-based biosensor for personalized, point-of-care periodontal therapy. MATERIALS AND

methodsSubgingival plaque samples were collected from healthy individuals and chronic periodontitis patients before and after periodontal therapy. Chemical composition of subgingival lipid A moieties was determined by ESI-Mass Spectrometry. Endotoxin activity of subgingival LPS extracts was assessed using the recombinant factor C assay, and their inflammatory potential was examined in THP-1-derived macrophages by measuring TNF-α and IL-8 production.

resultsCharacteristic lipid A molecular signatures, corresponding to over-acylated, bi-phosphorylated lipid A isoforms, were observed in diseased samples. Healthy and post-treatment samples were characterized by lower m/z peaks, related to under-acylated, hypo-phosphorylated lipid A structures. Endotoxin activity levels and inflammatory potentials of subgingival LPS extracts from periodontitis patients were significantly higher compared to healthy and post-treatment samples.

conclusionsThis is the first study to consider structure-function-clinical implications of different lipid A isoforms present in the subgingival niche and sheds new light on molecular pathogenic mechanisms of subgingival biofilm communities. CLINICAL RELEVANCE: Subgingival endotoxin activity (determined by lipid A chemical composition) could be a reliable, bacterially derived biomarker and a risk assessment tool for personalized periodontal care.

Indexed as

Chronic PeriodontitisDental PlaqueEndotoxinsMicrobiotaPeriodontitisBacteriaHumansLipid AEndotoxinsLipid ABiomarkerLipid ALipopolysaccharidePeriodontal diseasesSubgingival microbiota

Identifiers

PMID30543027
OpenAlexW2905573605

What OpenQuestion holds

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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.