Rechenberg Dan-Krister, Galicia Johnah C, Peters Ove A
Department of Preventive Dentistry, Periodontology and Cariology, Center of Dental Medicine, University of Zürich, Zürich, Switzerland.
Department of Endodontics, Arthur A. Dugoni School of Dentistry, University of the Pacific, San Francisco, California, United States of America.
PLoS One. 2016 Nov 29;11(11):e0167289. doi: 10.1371/journal.pone.0167289. eCollection 2016.
Pulpitis is mainly caused by an opportunistic infection of the pulp space with commensal oral microorganisms. Depending on the state of inflammation, different treatment regimes are currently advocated. Predictable vital pulp therapy depends on accurate determination of the pulpal status that will allow repair to occur. The role of several players of the host response in pulpitis is well documented: cytokines, proteases, inflammatory mediators, growth factors, antimicrobial peptides and others contribute to pulpal defense mechanisms; these factors may serve as biomarkers that indicate the status of the pulp. Therefore, the aim of this systematic review was to evaluate the presence of biomarkers in pulpitis.
The electronic databases of MEDLINE, EMBASE, Scopus and other sources were searched for English and non-English articles published through February 2015. Two independent reviewers extracted information regarding study design, tissue or analyte used, outcome measures, results and conclusions for each article. The quality of the included studies was assessed using a modification of the Newcastle-Ottawa-Scale.
From the initial 847 publications evaluated, a total of 57 articles were included in this review. In general, irreversible pulpitis was associated with different expression of various biomarkers compared to normal controls. These biomarkers were significantly expressed not only in pulp tissue, but also in gingival crevicular fluid that can be collected non-invasively, and in dentin fluid that can be analyzed without extirpating the entire pulpal tissue. Such data may then be used to accurately differentiate diseased from healthy pulp tissue. The interplay of pulpal biomarkers and their potential use for a more accurate and biologically based diagnostic tool in endodontics is envisaged.
牙髓炎主要由口腔共生微生物对牙髓腔的机会性感染引起。根据炎症状态,目前提倡不同的治疗方案。可预测的牙髓活力保存治疗取决于对牙髓状态的准确判定,从而实现牙髓修复。宿主反应中的多种因素在牙髓炎中的作用已有充分记载:细胞因子、蛋白酶、炎症介质、生长因子、抗菌肽等参与牙髓防御机制;这些因素可作为指示牙髓状态的生物标志物。因此,本系统评价的目的是评估牙髓炎中生物标志物的存在情况。
检索MEDLINE、EMBASE、Scopus等电子数据库,查找截至2015年2月发表的英文和非英文文章。两名独立评审员提取每篇文章的研究设计、所用组织或分析物、结局指标、结果和结论等信息。采用纽卡斯尔-渥太华量表的改良版评估纳入研究的质量。
在最初评估的847篇出版物中,本综述共纳入57篇文章。总体而言,与正常对照相比,不可逆性牙髓炎与多种生物标志物的不同表达相关。这些生物标志物不仅在牙髓组织中显著表达,而且在可无创采集的龈沟液以及无需切除整个牙髓组织即可分析的牙本质液中也有显著表达。这些数据可用于准确区分病变牙髓组织与健康牙髓组织。设想了牙髓生物标志物之间的相互作用及其在牙髓病学中用于更准确且基于生物学的诊断工具的潜在用途。