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正畸治疗引起的牙龈肥大的临床、微生物学和免疫学因素。

Clinical, microbiologic, and immunologic factors of orthodontic treatment-induced gingival enlargement.

机构信息

Department of Stomatology, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Am J Orthod Dentofacial Orthop. 2011 Jul;140(1):58-64. doi: 10.1016/j.ajodo.2010.02.033.

Abstract

INTRODUCTION

The aim of this study was to investigate the microbiologic and immunologic factors related to orthodontic treatment-induced gingival enlargement (GE).

METHODS

Our study included 12 patients with GE undergoing fixed orthodontic treatment and 12 periodontally healthy controls. At baseline, periodontal variables, subgingival plaque samples, and gingival crevicular fluid (GCF) samples were taken from 2 preselected sites in both the GE and the control groups. The levels of Porphyromonas gingivalis, Aggregatibacter actinomycetemcomitans, Prevotella intermedia, Treponema denticola and Tannerella forsythia were determined by real-time polymerase chain reaction. GCF interleukin (IL)-1β and transforming growth factor-beta 1 (TGF-β1) were detected by enzyme-linked immunosorbent assay (Invitrogen, Camarillo, Calif). Periodontal therapy was given to the GE group, and all parameters were reassessed after 4 weeks.

RESULTS

At baseline, the GE group showed higher prevalences of the 5 periodontal pathogens than did the control group (P <0.05). IL-1β and TGF-β1 levels at the GE sites were also significantly higher than those at the control sites (P <0.05). Four weeks after periodontal therapy, the GE group showed significant improvements in the clinical parameters associated with significant reductions of P gingivalis, A actinomycetemcomitans, and T denticola. The levels of IL-1β decreased significantly compared with the baseline (P <0.05), whereas there was no significant change in TGF-β1 levels (P >0.05).

CONCLUSIONS

Periodontal pathogens might have a relationship with the initiation and development of orthodontic treatment-induced GE. Inflammatory cytokines (IL-1β and TGF-β1) can also be considered as contributing factors.

摘要

简介

本研究旨在探讨与正畸治疗相关性牙龈增生(GE)相关的微生物学和免疫学因素。

方法

本研究纳入了 12 名接受固定正畸治疗的 GE 患者和 12 名牙周健康对照者。在基线时,从 GE 组和对照组的 2 个预选位点采集牙周变量、龈下菌斑样本和龈沟液(GCF)样本。通过实时聚合酶链反应(PCR)检测牙龈卟啉单胞菌、伴放线放线杆菌、中间普氏菌、牙髓密螺旋体和福赛坦纳菌的水平。通过酶联免疫吸附试验(Invitrogen,加利福尼亚州卡马里洛)检测 GCF 白细胞介素(IL)-1β和转化生长因子-β1(TGF-β1)。给予 GE 组牙周治疗,4 周后重新评估所有参数。

结果

基线时,GE 组 5 种牙周病原体的流行率高于对照组(P<0.05)。GE 部位的 IL-1β 和 TGF-β1 水平也明显高于对照组(P<0.05)。牙周治疗 4 周后,GE 组与临床参数相关的各项参数均有显著改善,牙龈卟啉单胞菌、伴放线放线杆菌和牙髓密螺旋体的数量明显减少。与基线相比,IL-1β 水平显著降低(P<0.05),而 TGF-β1 水平无显著变化(P>0.05)。

结论

牙周病原体可能与正畸治疗相关性 GE 的发生和发展有关。炎症细胞因子(IL-1β 和 TGF-β1)也可被视为致病因素。

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