The association between poor glycemic control and apical periodontitis: A systematic review and meta-analysis.

IF 2.2 3区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
X Wang, S Guo, X Yu, X Li, J Lai
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引用次数: 0

Abstract

Background: Diabetes mellitus (DM) is a common metabolic disorder, and persistent hyperglycemia may impair oral health through various immunological and inflammatory mechanisms, particularly by influencing the onset and healing of apical periodontitis (AP). This systematic review and meta-analysis aimed to evaluate whether poor glycemic control (PGC) is associated with the presence and progression of AP.

Material and methods: This study was conducted in accordance with the PRISMA 2020 guidelines. A comprehensive search of PubMed, Embase, Google Scholar, and Scopus was performed to identify relevant English-language studies published up to June 2025. Cross-sectional and longitudinal studies examining the association between glycemic control status-defined by glycated hemoglobin (HbA1c) levels-and AP-related outcomes were included. Data were synthesized using RevMan 5.3 software to calculate pooled odds ratios (ORs) and 95% confidence intervals (CIs). Heterogeneity and publication bias were also assessed.

Results: A total of 18 studies comprising approximately 51,070 patients were included. The relationship between PGC and AP was examined across three domains: AP prevalence, the persistence of apical periodontitis in root-filled teeth (AP-RFT), and alterations in local or systemic immune responses. Meta-analysis of AP prevalence (6 studies) revealed that individuals with PGC had a significantly increased risk of developing AP compared to controls (OR=2.38, 95% CI: 1.98-2.86, P<0.00001). Furthermore, meta-analysis of AP-RFT persistence (8 studies) showed that patients with PGC had a significantly higher risk of AP-RFT (OR=2.74, 95% CI: 2.03-3.70, P<0.0001). Several studies also reported elevated levels of inflammatory cytokines and bacterial load in patients with PGC.

Discussion: PGC appears to negatively influence both the development and healing of AP, possibly through immune-inflammatory pathways.

Conclusions: PGC is closely associated with the occurrence of AP and the failure of periapical healing following endodontic treatment. PGC may aggravate periapical tissue damage and inflammation through proinflammatory immune pathways. Clinicians should consider comprehensive evaluation and individualized management of DM patients during endodontic therapy to improve treatment outcomes and oral health.

血糖控制不良与根尖牙周炎之间的关系:一项系统综述和荟萃分析。
背景:糖尿病(DM)是一种常见的代谢性疾病,持续高血糖可通过多种免疫和炎症机制损害口腔健康,尤其是影响根尖牙周炎(AP)的发病和愈合。本系统综述和荟萃分析旨在评估血糖控制不良(PGC)是否与ap的存在和进展相关。材料和方法:本研究按照PRISMA 2020指南进行。我们对PubMed、Embase、b谷歌Scholar和Scopus进行了全面的检索,以确定截至2025年6月发表的相关英语研究。横断面和纵向研究检查了血糖控制状态(由糖化血红蛋白(HbA1c)水平定义)与ap相关结果之间的关系。采用RevMan 5.3软件对数据进行综合,计算合并优势比(or)和95%置信区间(ci)。异质性和发表偏倚也被评估。结果:共纳入18项研究,约51,070例患者。PGC和AP之间的关系从三个方面进行了研究:AP的患病率、根填充牙的根尖牙周炎(AP- rft)的持续性以及局部或全身免疫反应的改变。AP患病率的荟萃分析(6项研究)显示,与对照组相比,PGC患者发生AP的风险显著增加(OR=2.38, 95% CI: 1.98-2.86)。讨论:PGC似乎对AP的发展和愈合都有负面影响,可能是通过免疫炎症途径。结论:PGC与AP的发生及根管治疗后根尖周愈合失败密切相关。PGC可通过促炎免疫途径加重根尖周围组织损伤和炎症。临床医生应考虑在牙髓治疗期间对糖尿病患者进行综合评估和个体化管理,以改善治疗效果和口腔健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicina Oral Patologia Oral Y Cirugia Bucal
Medicina Oral Patologia Oral Y Cirugia Bucal DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.60
自引率
0.00%
发文量
52
审稿时长
3-8 weeks
期刊介绍: 1. Oral Medicine and Pathology: Clinicopathological as well as medical or surgical management aspects of diseases affecting oral mucosa, salivary glands, maxillary bones, as well as orofacial neurological disorders, and systemic conditions with an impact on the oral cavity. 2. Oral Surgery: Surgical management aspects of diseases affecting oral mucosa, salivary glands, maxillary bones, teeth, implants, oral surgical procedures. Surgical management of diseases affecting head and neck areas. 3. Medically compromised patients in Dentistry: Articles discussing medical problems in Odontology will also be included, with a special focus on the clinico-odontological management of medically compromised patients, and considerations regarding high-risk or disabled patients. 4. Implantology 5. Periodontology
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