Gender differences in immunological response of African-American juveniles with Grade C molar incisor pattern periodontitis

Tamara T. Tavakoli, Fatemeh Gholami, Hong Huang, Patricia Furtado Gonçalves, Alejandro Villasante-Tezanos, Ikramuddin Aukhil, Rubelisa C.G. de Oliveira, Niki Hovencamp, Shannon Wallet, Efthimia Ioannidou, Luciana M. Shaddox

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Background: Prevalence of Grade C molar incisor periodontitis (C/MIP) in females (F) and males (M) is controversial, although some studies suggest higher prevalence in females. The objective of this study was to evaluate differences in clinical parameters, and levels of cyto/chemokines in gingival crevicular fluid (GCF) and peripheral blood response. Methods: GCF and blood were collected from 79 C/MIP African-American participants (53F and 26 M) and healthy controls (58F and 38 M), aged 5 to 23. Blood was stimulated with ultrapure LPS from Escherichia coli (Ec) and Porphyromonas gingivalis (Pg) and we quantified levels of 14 cyto/chemokines. Clinical parameters were collected before and 12 months following treatment. Results: No clinical parameters or age differences were found between males and females, although age was negatively correlated with response to treatment. GCF levels of TNFα, IFNγ, MIP1α, and MCP1 from diseased and sites and healthy sites IFNγ levels were higher in M (P < 0.05). C/MIP females presented higher Pg and Ec LPS induced levels of Eotaxin, IFNγ, and GMCSF (P < 0.05), whereas healthy males presented higher Ec LPS induced levels of Eotaxin and IFNγ (P < 0.05). Inflammatory profiles were also different among genders in disease (P = 0.004). Conclusions: Although males seemed to present few elevated inflammatory markers in the GCF in disease and in health, females presented an elevated systemic inflammatory response to LPS in disease, which indicates a possible differential susceptibility to inflammation. Future studies need to determine if sex hormones have a role in the peripheral host response and in the pathogenesis of C/MIP.

Original languageEnglish
Pages (from-to)392-402
Number of pages11
JournalJournal of Periodontology
Volume93
Issue number3
DOIs
StatePublished - Mar 2022

Bibliographical note

Publisher Copyright:
© 2021 American Academy of Periodontology

Funding

The authors acknowledge the financial support from NIH/NIDCR (R01DE019456) and the assistance from Drs. Peter Harrison and Theodora Kompotiati for assistance with examinations and sample collections and also the doctors and staff at the different clinical centers of this study: Drs Zapert and Bidwell from Leon County Health Department, Drs Varnado from Jacksonville Health Department, FL and the Pediatrics and Periodontology Department at U. Florida for cases referrals. This study was supported by NIH/NIDCR R01DE019456.

FundersFunder number
National Institutes of Health (NIH)
National Institute of Dental and Craniofacial ResearchR01DE019456

    Keywords

    • active immune response
    • aggressive periodontitis
    • cytokines
    • epidemiology
    • therapy

    ASJC Scopus subject areas

    • Periodontics

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