Implementation of a predictive strategy in the diagnosis of inflammatory periodontal diseases

O. V. Eremin, L. Ostrovskaya, N. Zakharova, L. S. Kathanova, V. M. Morgunova, J. Kobzeva, M. Barulina, V. A. Tsitronov, D. Domenyuk
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Abstract

Relevance. The diagnosis of periodontal diseases, considering their severity, prevalence, progression, and staging, can be achieved by determining the levels of biomarkers or molecular imaging biomarkers in biofluids such as crevicular or sulcular fluid (GCF or GSF), saliva, and oral fluid. GCF is currently regarded as one of the diagnostically significant biological fluids for assessing the condition of periodontal tissues, not only in clinical diagnostic laboratories but also in dental offices. The implementation of sensitive, highly accurate, non-invasive, and specific methods for rapid GCF diagnosis, based on the qualitative analysis of biomarkers of cytokine imbalance, immunological disorders, changes in non-specific defence factors, and biophysical indicators, will allow for an objective assessment of the condition of periodontal tissues.Purpose. To improve the efficiency of periodontitis prevention using a developed mathematical model for personalized prediction of the course of inflammatory periodontal diseases based on the investigated biomarkers in GCF.Material and methods. The study included 101 patients: Group I consisted of 22 patients diagnosed with K05.10 (gingivitis), Group II included 31 patients diagnosed with K05.31 (mild periodontitis), and Group III comprised 18 patients diagnosed with K05.31 (moderate periodontitis). The comparison group consisted of 30 individuals with clinically healthy periodontium. All subjects underwent clinical and instrumental examination, determination of periodontal indices, GCF collection, and quantitative analysis of immune regulatory mediators (IL-1β, IL-6, TNF-α, IL-8, MCP-1, IL-17, VEGF, IL-1RA).Results. The study of immune regulatory mediators confirmed the significance of increased levels of pro- and anti-inflammatory cytokines/chemokines, as well as the reduction of the anti-inflammatory biomarker IL-1RA in GCF at the early stages of inflammatory changes in periodontal tissues. This is accompanied by the appearance of signs indicating the destruction of the dentogingival junction. Using logistic regression and training a multiclass classifier based on the support vector machine method, a model was developed to predict the risk of dentogingival junction loss in patients, potentially leading to periodontitis.Conclusion. The results of logistic regression modelling and training a multiclass classifier based on the support vector machine method demonstrate that in diagnosing the initial stages of periodontal tissue damage with the loss of the dentogingival junction (DGJ), the most effective approach is the comprehensive use of inflammatory process biomarkers and the development of multi-marker algorithms based on a computer program.
在牙周炎症性疾病诊断中实施预测策略
相关性。考虑到牙周疾病的严重程度、患病率、进展和分期,牙周疾病的诊断可以通过测定生物液体(如缝隙液或沟液(GCF 或 GSF)、唾液和口腔液)中的生物标志物或分子成像生物标志物的水平来实现。GCF 目前不仅在临床诊断实验室,而且在牙科诊所都被视为评估牙周组织状况的重要诊断生物液体之一。根据对细胞因子失衡、免疫紊乱、非特异性防御因子变化和生物物理指标等生物标志物的定性分析,采用灵敏、高度准确、非侵入性和特异性的 GCF 快速诊断方法,可以对牙周组织的状况进行客观评估。根据所研究的 GCF 中的生物标志物,利用所开发的数学模型对炎症性牙周病的病程进行个性化预测,从而提高牙周炎预防的效率。研究包括 101 名患者:第一组包括 22 名确诊为 K05.10(牙龈炎)的患者,第二组包括 31 名确诊为 K05.31(轻度牙周炎)的患者,第三组包括 18 名确诊为 K05.31(中度牙周炎)的患者。对比组包括 30 名临床牙周健康的患者。所有受试者均接受了临床和仪器检查、牙周指数测定、GCF 采集以及免疫调节介质(IL-1β、IL-6、TNF-α、IL-8、MCP-1、IL-17、VEGF、IL-1RA)的定量分析。对免疫调节介质的研究证实,在牙周组织发生炎症变化的早期阶段,GCF 中促炎症和抗炎症细胞因子/凝血因子水平的升高以及抗炎症生物标志物 IL-1RA 的降低具有重要意义。与此同时,还出现了牙龈交界处被破坏的迹象。利用逻辑回归和基于支持向量机方法的多类分类器训练,建立了一个模型来预测患者牙龈交界处脱落的风险,这有可能导致牙周炎。逻辑回归建模和基于支持向量机方法的多类分类器训练的结果表明,在诊断牙龈交界处(DGJ)缺失的牙周组织损伤初期阶段,最有效的方法是综合利用炎症过程生物标志物和开发基于计算机程序的多标志物算法。
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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