MMP13, TIMP2 and TGFB3 Gene Polymorphisms in Brazilian Chronic Periodontitis and Periimplantitis Subjects

Author:

Gonçalves Junior Roberto1,Pinheiro Aristides da Rosa2,Schoichet José Jorge1,Nunes Carlos Henrique Ramirez1,Gonçalves Rackel1,Bonato Leticia Ladeira1,Quinelato Valquiria1,Antunes Leonardo Santos1,Küchler Erika Calvano3,Lobo Julie1,Villas-Bôas Ricardo de Mello1,Vieira Alexandre Rezende4,Granjeiro José Mauro5,Casado Priscila Ladeira2

Affiliation:

1. Universidade Federal Fluminense, Brazil

2. Universidade Federal Fluminense, Brazil; Universidade Federal Fluminense, Brazil

3. University of São Paulo, Brazil

4. University of Pittsburgh, USA; University of Pittsburgh, USA

5. Universidade Federal Fluminense, Brazil; National Institute of Metrology, Brazil

Abstract

Abstract Subjects susceptible to chronic periodontitis (CP) show a high risk for the development of peiimplantitis (PI). Both diseases are multifactorial, presenting similarities in their pathophysiology and polygenic profile. MMP-13 (matrix metalloproteinases 13/ collagenase 3) is a collagenolytic enzyme, which expression is induced by TGF beta 3 (transforming growth factor type 3) in human gingival fibroblasts and inhibited by TIMP-2 (tissue inhibitor of metalloproteinase type 2). The aim of this study was to investigate the occurrence of peiimplantitis (PI) in subjects with history of chronic periodontitis (CP) and polymorphisms frequency in MMP13, TIMP2 and TGFB3 genes. One hundred and sixty-three volunteers received dental implant placement were submitted to oral and radiographic examination in order to identify past history of CP or presence of PI. Volunteers were divided into 4 groups: Control (without PI and CP, n=72), CP (with CP and without PI, n=28), PI (with PI and without CP, n=28) and diseased (with CP and PI, n=35). The chi-square test correlated genotypes in specific regions of MMP13 (rs2252070), TIMP2 (rs7501477) and TGFB3 (rs2268626) genes, considering the interaction between CP and PI. The results showed that volunteers with CP had 3.2 times more susceptibility to develop PI (p=0.0004) compared to those without CP. No significant association was observed in MMP13, TIMP2 and TGFB3 genes with CP or PI. CP is a risk factor to develop PI, however, there is no association of both diseases with polymorphisms in the MMP13, TIMP2 and TGFB3 genes.

Publisher

FapUNIFESP (SciELO)

Subject

General Dentistry

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