Harbood Omer Mohammed, Abbas Raghad Fadhil
Department of Periodontology, College of Dentistry, University of Baghdad, Baghdad, Iraq.
Int J Dent. 2024 Apr 1;2024:3007148. doi: 10.1155/2024/3007148. eCollection 2024.
The chemokine "Fractalkine" (CX3CL1) and its corresponding receptor (CX3CR1), chemokine belonging to the CX3C family, have an essential role in developing several systemic inflammatory disorders. Accordingly, the proliferation, adhesion, and migration of inflammatory cells are all affected by it. In light of this, the present study attempts to address the following questions: (1) Is the salivary level of fractalkine and its receptor associated with periodontitis patients with different severities? (2) Is it possible to distinguish periodontitis from periodontally healthy subjects?
This study included 30 individuals who had been considered controls, having healthy periodontium, and 90 patients with varying stages of periodontitis. The patients were equally divided into three groups: those with Stage I, Stage II, and Stage III. After each subject's saliva was collected, periodontal markers including bleeding on probing (BOP), probing pocket depth (PPD), and clinical attachment loss (CAL) were recorded. Enzyme-linked immunosorbent assays (ELISA) were used to detect the protein levels of salivary CX3CL1 and CX3CR1.
In comparison to the control group, patients with periodontitis had statistically increased salivary concentrations of CX3CL1 and CX3CR1 ( < 0.001). Additionally, all clinical periodontal indicators (BOP, PPD, and CAL) had a strong association with salivary CX3CL1 and CX3CR1 levels. Furthermore, by using the ROC (receiver operating characteristic), both biomarkers showed a good ability to differentiate periodontitis from periodontally healthy subjects, and an excellent ability to distinguish Stage I and Stage III periodontitis from periodontally healthy subjects. The AUC for salivary CX3L1 and its receptors, CX3R, was 0.93 and 0.8, respectively, to distinguish Stage I from patients with good periodontal health. In contrast, the biomarkers' AUC for separating individuals with Stage III periodontitis from those in healthy periodontal conditions was 1.
Fractalkine and its receptor are linked to periodontitis and may distinguish between periodontitis and healthy periodontal tissues, suggesting its role as a possible part of periodontal disease pathogenesis.
趋化因子“Fractalkine”(CX3CL1)及其相应受体(CX3CR1)属于CX3C趋化因子家族,在多种全身性炎症性疾病的发生发展中起重要作用。因此,炎症细胞的增殖、黏附和迁移均受其影响。鉴于此,本研究试图解决以下问题:(1)Fractalkine及其受体的唾液水平与不同严重程度的牙周炎患者是否相关?(2)能否将牙周炎患者与牙周健康受试者区分开来?
本研究纳入30名牙周健康的对照个体以及90例不同阶段牙周炎患者。患者被平均分为三组:I期、II期和III期。收集每位受试者的唾液后,记录包括探诊出血(BOP)、探诊袋深度(PPD)和临床附着丧失(CAL)在内的牙周指标。采用酶联免疫吸附测定(ELISA)法检测唾液中CX3CL1和CX3CR1的蛋白水平。
与对照组相比,牙周炎患者唾液中CX3CL1和CX3CR1的浓度在统计学上显著升高( < 0.001)。此外,所有临床牙周指标(BOP、PPD和CAL)均与唾液中CX3CL1和CX3CR1水平密切相关。此外,通过使用ROC(受试者工作特征)曲线,两种生物标志物均显示出良好的区分牙周炎患者与牙周健康受试者的能力,以及出色的区分I期和III期牙周炎患者与牙周健康受试者的能力。唾液CX3L1及其受体CX3R区分I期患者与牙周健康良好者的AUC分别为0.93和0.8。相比之下,区分III期牙周炎患者与牙周健康者的生物标志物AUC为1。
Fractalkine及其受体与牙周炎有关,可能有助于区分牙周炎和健康的牙周组织,提示其可能参与牙周疾病发病机制。