Increased infection with key periodontal pathogens during gestational diabetes mellitus
Aim Gestational diabetes mellitus (GDM), gingivitis, infection with specific periodontal pathogens and systemic inflammation each increase the risk for poor pregnancy outcome. We set out to monitor the interactions of gingivitis and GDM with respect to oral infection and the systemic inflammatory bu...
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Published in | Journal of clinical periodontology Vol. 42; no. 6; pp. 506 - 512 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.06.2015
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Subjects | |
Online Access | Get full text |
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Summary: | Aim
Gestational diabetes mellitus (GDM), gingivitis, infection with specific periodontal pathogens and systemic inflammation each increase the risk for poor pregnancy outcome. We set out to monitor the interactions of gingivitis and GDM with respect to oral infection and the systemic inflammatory burden.
Materials and Methods
Four case–control groups (n = 117) were recruited, (1) No gingivitis, No GDM (n = 27); (2) Gingivitis, No GDM (n = 31); (3) No gingivitis, GDM (n = 21); and (4) Gingivitis, GDM (n = 38). Oral infection with three key periodontal pathogens was determined by PCR. Systemic inflammation was determined by quantification of CRP by EIA.
Results
Gingivitis during pregnancy was associated with oral infection with Porphyromonas gingivalis, Filifactor alocis and Treponema denticola and combinations thereof (all p < 0.01). GDM was also associated with increased infection with individual and multiple oral pathogens (all p < 0.05). Gingivitis during pregnancy led to a 325% increase in systemic CRP (mean, 2495 versus 8116 ng/ml, p < 0.01).
Conclusions
Diabetes and gingivitis act in concert to increase risk biomarkers for poor pregnancy outcome. |
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Bibliography: | ark:/67375/WNG-P6CW73S1-M ArticleID:JCPE12418 NIDCR - No. RO1 DE019826 istex:61E0459422BE4896E9346AB4FD09538316EC5CBB Ege University Research Foundation - No. 2013 DIS 026 This study was funded, in part, by NIDCR (Grant # RO1 DE019826, DAS) and the Ege University Research Foundation (Project No: 2013 DIS 026). The authors have no conflict of interest. Conflict of interest and source of funding statement ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0303-6979 1600-051X |
DOI: | 10.1111/jcpe.12418 |