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. 2020 Sep 11;15(9):e0239101.
doi: 10.1371/journal.pone.0239101. eCollection 2020.

Association of IL16 polymorphisms with periodontitis in Brazilians: A case- control study

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Association of IL16 polymorphisms with periodontitis in Brazilians: A case- control study

Victor Hugo Souza et al. PLoS One. .

Abstract

Periodontitis (PD) is a chronic inflammatory process resulting from the relationship of the immune response with the components in dental plaque. Cytokines and their genetic polymorphisms seem to be involved in the immunopathogenesis of this disease. This study aimed to evaluate the correlation of IL16 polymorphism with PD. A case-control study was conducted in a sample of individuals from southern Brazil. The genotyping of IL16, rs11556218 T>G, rs4072111 C>T e rs4778889 T>C, was performed using the PCR-RFLP methodology. The serum level of IL-16 was determined using an IL-16 ELISA kit for humans. SNPStats and OpenEpi software and Wilcoxon's U test were used to perform statistical analysis. IL16 rs11556218 polymorphism was significantly associated to PD in nonsmoking patients: individuals with G/G genotype were less likely to develop PD compared to the T/T genotype (OR = 0.10; Pc = 0.019, codominant model). In addition, the TTT haplotype was associated with a high risk for PD (OR = 2.45; P = 0.01). A low IL-16 serum level was observed among individuals with PD when compared to controls (P = 0.027). Thus, the IL16 rs16556218 polymorphism and the serum levels of IL-16 were associated with periodontitis in a Brazilian sample, and this was influenced by environmental factors such as smoking.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Serum levels of IL-16 in nonsmoking PD patients and controls.
(A) Comparison of IL-16 serum level between PD and controls; (B) between periodontitis groups; (C) between men and women with periodontitis; (D) among patients with and without G allele variant of rs11556218 for IL16; (E) among patients with and without the C allele variant of rs4778889 for IL16; and (F) among patients with and without the variant allele T of rs4072111 for IL16.

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