Expression of matrix metalloproteinases 2 and 9 in replanted teeth with external root resorption: a cross-sectional study

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Objective: To evaluate matrix metalloproteinase (MMP) expression in replanted permanent teeth with external root resorption (ERR). Design: The present cross-sectional study included 42 patients with replanted permanent teeth, presenting with progressive forms of ERR, and referred for extraction according to the rehabilitation treatment plan or due to root fractures. The control group consisted of 12 healthy premolars, from 5 patients with good periodontal health and no radiographic evidence of root resorption, referred for extraction for orthodontic reasons. Root fragments were processed soon after extraction, and the supernatant was collected to measure matrix metalloproteinase 2/tissue inhibitor of metalloproteinase 2 (MMP-2/TIMP-2) and matrix metalloproteinase 9/tissue inhibitor of metalloproteinases 2 (MMP-9/TIMP-2) complexes through a double-ligand enzyme-linked immunosorbent assay (ELISA). Results: Case groups with external inflammatory root resorption (EIRR) or external replacement root resorption (ERRR) showed significantly higher levels of MMP-2/TIMP-2 and MMP-9/TIMP-2 complexes than the control group. Additionally, comparisons between the case groups demonstrated that the MMP-2/TIMP-2 complex also had significantly higher levels in the ERRR group (p < 0.001). Conclusions: Our results suggest that MMP-2 and MMP-9 participate in the pathobiology of both types of ERR. In addition, the higher levels of MMP-2/TIMP-2 complex in the ERRR group support common modulation mechanisms with physiological bone turnover.

Abstract

Assunto

Matrix metalloproteinase 2, Matrix metalloproteinase 9, Matrix metalloproteinases, Tooth avulsion, Tooth replantation, Tissue inhibitor of metalloproteinase-2, Evaluation study

Palavras-chave

External root resorption, MMP-2, MMP-9, Matrix metalloproteinase, Tooth avulsion, Tooth replantation

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https://www.sciencedirect.com/science/article/pii/S0003996921001576?via%3Dihub

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