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논문 기본 정보

자료유형
학술저널
저자정보
Ana Luiza Cabral de Ávila Andrade (Pontifical Catholic University of Minas Gerais) Yasmin Dias de Almeida Pinto (Pontifical Catholic University of Minas Gerais) Bernardo Emerenciano Barros Maia (Pontifical Catholic University of Minas Gerais) Joice Dias Corrêa (Pontifical Catholic University of Minas Gerais) Diogo de Azevedo Miranda (Pontifical Catholic University of Minas Gerais) Flávio Ricardo Manzi (Pontifical Catholic University of Minas Gerais) Izabella Lucas de Abreu Lima (Pontifical Catholic University of Minas Gerais)
저널정보
대한치과교정학회 대한치과교정학회지 대한치과교정학회지 제54권 제5호
발행연도
2024.9
수록면
284 - 302 (19page)

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초록· 키워드

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Objective: External apical root resorption (EARR) is characterized by permanent loss of dental structure at the root apex. This study aimed to systematically review gene polymorphisms associated with EARR in orthodontic patients. Methods: Electronic database searches were performed across several databases. Results: This systematic review included 21 studies. Outcome measures were based on tooth dimensions observed on radiographs obtained before and after treatment. Polymorphisms in the following genes were genotyped using polymerase chain reaction-restriction fragment length polymorphism analysis: purinergic-receptor-P2X, ligand-gated ion channel 7 (P2RX7), caspase-1/ interleukin-converting enzyme (CASP1/ICE), caspase-5 (CASP5), IL-1beta (IL1B), IL-1alpha (IL1A), interleukin-1 receptor antagonist gene (IL1RN), tissue nonspecific alkaline phosphatase (TNSALP), tumor necrosis factor-alpha (TNFα), tumor necrosis factor receptor superfamily gene member 11a (TNFRSF11A), secreted phosphoprotein 1 (SPP1), tumor necrosis factor receptor superfamily gene member 11b (TNFRSF11B), interleukin 17A (IL17), interleukin 6 (IL6), receptor activator of nuclear factor-kappa B (RANK), osteoprotegerin (OPG), stromal antigen 2 (STAG2), vitamin D receptor (VDR), cytochrome P450 family 24 subfamily A member 1 (CYP24A1), cytochrome P450 family 27 subfamily B (CYP27B1), group-specific component (GC), and interleukin-1 receptor-associated kinases 1 (IRAK1). Conclusions: Almost all studies suggested that IL1 gene is associated with EARR. Additionally, P2RX7 may be an important factor contributing to the etiopathogenesis of EARR. TNFRSF11A, SPP1, IL1RN, IL6, TNFRSF11B, STAG2, VDR, IRAK1, IL-17, CASP1/ICE and CASP5 have been identified in isolated studies. Further observational studies are needed to better explain the association between these genes and EARR.

목차

INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
CONCLUSIONS
REFERENCES

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