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 inJournal of clinical periodontology Vol. 42; no. 6; pp. 506 - 512
Main Authors Gogeneni, Himabindu, Buduneli, Nurcan, Ceyhan-Öztürk, Banu, Gümüş, Pınar, Akcali, Aliye, Zeller, Iris, Renaud, Diane E., Scott, David A., Özçaka, Özgün
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.06.2015
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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.
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