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Sökning: WFRF:(Zwicker A.) > (2019) > MMP-12 and S100s in...

MMP-12 and S100s in saliva reflect different aspects of periodontal inflammation

Björnfot Holmström, Sofia (författare)
Center for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden; Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Stockholm, Sweden
Lira-Junior, Ronaldo (författare)
Karolinska Institutet
Zwicker, Stephanie (författare)
Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Stockholm, Sweden
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Majster, Mirjam (författare)
Karolinska Institutet
Gustafsson, Anders (författare)
Karolinska Institutet
Åkerman, Sigvard (författare)
Malmö universitet,Odontologiska fakulteten (OD)
Klinge, Björn (författare)
Karolinska Institutet,Malmö universitet,Odontologiska fakulteten (OD),Division of Oral Diseases, Department of Dental Medicine, Karolinska Institutet, Stockholm, Sweden
Svensson, Mattias (författare)
Center for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden
Boström, Elisabeth A (författare)
Karolinska Institutet
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 (creator_code:org_t)
Academic Press, 2019
2019
Engelska.
Ingår i: Cytokine. - : Academic Press. - 1043-4666 .- 1096-0023. ; 113, s. 155-161
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Matrix metalloproteinase (MMP)-12, S100A8/A9, and S100A12 are involved in innate immune responses. We addressed whether different aspects of oral health and non-disease-related covariates influence their levels in saliva. 436 participants were clinically examined, completed a health questionnaire, and provided stimulated saliva. Salivary levels of MMP-12, S100A8/A9, and S100A12 were determined by enzyme-linked immunosorbent assays. Lower MMP-12 levels were observed in individuals 40-64years old (yo) compared to < 40yo, and higher S100A8/A9 levels were found in individuals > 64yo compared to 40-64yo. Smokers exhibited lower MMP-12 and S100A12 levels compared to non-smokers. All three proteins were elevated in individuals with bleeding on probing (BOP)>20% compared to those with BOP/= 10% gingival pocket depths (PPD)>/=4mm compared to the ones with shallow pockets < 4mm. The extent of alveolar bone loss or presence of manifest caries did not alter any of the markers. MMP-12, S100A8/A9, and S100A12 levels were higher in participants with high periodontal inflammatory burden. All three proteins correlated positively to BOP, PPD, and to several inflammatory mediators. The explanatory variables for MMP-12 in saliva were age, smoking, presence of any tumor, and percentage of PPD>/=4mm. The determinant of salivary S100A8/A9 was percentage of BOP, while S100A12 levels were associated with percentage of BOP and presence of any tumor. Taken together, MMP-12 and the S100/calgranulin levels in saliva reflect different aspects of periodontal inflammation. Smoking and age should be taken into account in further investigation of these proteins as biomarker candidates of periodontal disease.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Odontologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dentistry (hsv//eng)

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  • Cytokine (Sök värdpublikationen i LIBRIS)

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