Macrophage activity is associated with gingival inflammation: Soluble CD163 in an experimental gingivitis study.
Adult
Antigens, CD
/ immunology
Antigens, Differentiation, Myelomonocytic
/ immunology
Biomarkers
/ metabolism
Female
Gingival Crevicular Fluid
/ metabolism
Gingivitis
/ metabolism
Humans
Inflammation
/ metabolism
Macrophage Activation
/ physiology
Macrophages
/ metabolism
Male
Periodontal Index
Receptors, Cell Surface
/ immunology
Young Adult
Gingival inflammation
Gingivitis
Innate immunity
Macrophage
Macrophage activity
Periodontal diseases
sCD163
Journal
Cytokine
ISSN: 1096-0023
Titre abrégé: Cytokine
Pays: England
ID NLM: 9005353
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
received:
10
07
2019
revised:
08
11
2019
accepted:
09
12
2019
pubmed:
10
1
2020
medline:
19
8
2021
entrez:
10
1
2020
Statut:
ppublish
Résumé
This study aimed to investigate the association between gingival inflammation and levels of soluble CD163 (sCD163), a macrophage-specific marker associated to inflammation, in young adults participating in an experimental gingivitis study. Forty-two university students volunteered to participate in the study, which comprised three phases: a two-week Hygiene Phase (clinical examination and professional cleaning); a three-week Induction Phase (absence of oral hygiene); and a two-week Resolution Phase (reestablishment of oral hygiene). Clinical recordings of plaque (Modified Quigley and Hein Plaque Index) and gingival inflammation (Modified Gingival Index) were collected weekly during the Induction Phase, and after two weeks during the Resolution Phase. Levels of sCD163 from gingival crevicular fluid (GCF) were collected during Induction and Resolution Phases and measured by ELISA. Group-based-trajectory-modeling (GBTM) was used to model patterns of sCD163 throughout the Induction Phase. Mixed-effects multilevel models were used to estimate the effect of gingival inflammation on sCD163 over time. Levels of sCD163 increased steadily over time, however, sCD163 showed a lagged response to gingival inflammation. GBTM analysis identified two groups for sCD163: one with a "linear" trajectory of sCD163 over the Induction Phase (n = 35), and another with a "quadratic" (n = 7) increase of sCD163 at the end of the Induction Phase. Stratified analysis by the sCD163 groups revealed that "linear" sCD163 growth was associated with both GCF volume and gingival inflammation but lagged in time, while a "quadratic" growth was associated with gingival inflammation and time. Macrophage activity is associated with gingival inflammation and can be detected at early stages of gingivitis. However, while in most participants a "linear" trajectory of sCD163 over the development of gingival inflammation was observed, among few individuals an exacerbated increase of sCD163 levels in GCF was noticed particularly at the end of the Induction Phase.
Identifiants
pubmed: 31918162
pii: S1043-4666(19)30383-7
doi: 10.1016/j.cyto.2019.154954
pii:
doi:
Substances chimiques
Antigens, CD
0
Antigens, Differentiation, Myelomonocytic
0
Biomarkers
0
CD163 antigen
0
Receptors, Cell Surface
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
154954Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.