dc.contributor.authors |
Yilmaz, Neslihan; Polat, Recep; Gursoy, Mervi; Kaman, Wendy; Aydin, Elif Gul; Fteita, Dareen; Yilmaz, Dogukan; Bikker, Floris; Gursoy, Ulvi Kahraman |
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dc.date.accessioned |
2024-02-23T11:13:56Z |
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dc.date.available |
2024-02-23T11:13:56Z |
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dc.date.issued |
2023 |
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dc.identifier.issn |
0022-3492 |
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dc.identifier.uri |
http://dx.doi.org/10.1002/JPER.22-0314 |
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dc.identifier.uri |
https://hdl.handle.net/20.500.12619/101941 |
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dc.description |
Bu yayının lisans anlaşması koşulları tam metin açık erişimine izin vermemektedir. |
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dc.description.abstract |
BackgroundThis cross-sectional study aimed to evaluate salivary concentrations of macrophage activation-related chemokines and mitogen-activated kinase kinase (MAPKK)-degrading proteolytic activity in children and adolescents with and without type 1 diabetes mellitus (T1DM). MethodsA total of 122 children and adolescents (65 T1DM patients, 50.8% female, mean age:10.9 years; 57 systemically healthy controls, 36.8% female, mean age: 9.5 years) were included in the study. Salivary concentrations of interferon gamma inducible protein-10 (IP-10), monocyte chemoattractant protein (MCP)-1, MCP-2, MCP-3, MCP-4, macrophage-derived chemokine (MDC), macrophage migration inhibitory factor (MIF), monokine induced by interferon gamma (MIG), and macrophage inflammatory protein-1 alpha (MIP-1 & alpha;) were quantified using a bead-based technique. MAPKK-degrading proteolytic activity was detected using fluorescent peptide substrates. ResultsThe T1DM group had higher plaque index (PI%, p = 0.032) and bleeding on probing (BOP%, p = 0.045) scores, and lower decayed, missing, filled teeth (dmft/DMFT, p = 0.002) index scores compared to the healthy controls. Compared to the controls, salivary MCP-1 (p = 0.007), MCP-3 (p < 0.001), MIG (p = 0.007), and MIP-1 & alpha; (p = 0.033) concentrations were elevated whereas MCP-4 concentrations decreased (p < 0.001) in the T1DM group. After adjusting for age, PI%, BOP%, and dmft/DMFT scores, significant differences in salivary concentrations of MIG (p = 0.033) and MIP-1 & alpha; (p = 0.017) were observed between the groups. Moreover, protease activities directed to the cleavage sites of MEK23-18 (p = 0.001), MKK6b7-22 (p = 0.007), MKK451-66 (p = 0.005), MKK7b37-52 (p = 0.034), and MKK7b69-84 (p = 0.009) were elevated in the T1DM group. ConclusionT1DM disrupts the salivary macrophage activation-related chemokine profile and dysregulates proteolytic MAPKK cleavage. These findings can be an outcome of the impaired systemic immune response in T1DM. |
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dc.language.iso |
English |
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dc.relation.isversionof |
10.1002/JPER.22-0314 |
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dc.subject |
PERIODONTAL-DISEASE |
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dc.subject |
CHILDREN |
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dc.subject |
COMPLICATIONS |
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dc.subject |
ADOLESCENTS |
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dc.subject |
BIOMARKERS |
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dc.subject |
PATTERNS |
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dc.subject |
HEALTH |
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dc.title |
Salivary macrophage activation-related chemokines and mitogen-activated kinase kinase-degrading proteolytic activity in type 1 diabetes mellitus |
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dc.type |
Article |
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dc.contributor.authorID |
Bikker, Floris/0000-0002-9453-4630 |
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dc.contributor.authorID |
Yilmaz, Neslihan/0000-0001-7939-9525 |
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dc.contributor.authorID |
polat, recep/0000-0002-3786-0739 |
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dc.contributor.authorID |
Gursoy, Ulvi Kahraman/0000-0002-1225-5751 |
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dc.contributor.authorID |
Yilmaz, Dogukan/0000-0003-2576-0885 |
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dc.identifier.volume |
94 |
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dc.identifier.startpage |
896 |
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dc.identifier.endpage |
904 |
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dc.relation.journal |
J PERIODONTOL |
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dc.identifier.issue |
7 |
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dc.identifier.doi |
10.1002/JPER.22-0314 |
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dc.identifier.eissn |
1943-3670 |
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dc.contributor.author |
Yilmaz, N |
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dc.contributor.author |
Polat, R |
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dc.contributor.author |
Gürsoy, M |
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dc.contributor.author |
Kaman, W |
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dc.contributor.author |
Aydin, EG |
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dc.contributor.author |
Fteita, D |
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dc.contributor.author |
Yilmaz, D |
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dc.contributor.author |
Bikker, F |
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dc.contributor.author |
Gürsoy, UK |
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dc.relation.publicationcategory |
Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı |
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