Zainal Abidin Nurul Latifah, Latib Norjehan, Al-Bayaty Fouad Hussain, Hidayat Mohd Faizal Hafez
Centre of Periodontology Studies, University Technology MARA Sungai Buloh Campus, Jalan Hospital, Sungai Buloh, Malaysia.
Periodontic Unit, Kota Damansara Dental Clinic, Petaling Jaya, Malaysia.
Clin Exp Dent Res. 2025 Jun;11(3):e70044. doi: 10.1002/cre2.70044.
Peri-implant diseases (PID), specifically peri-implant mucositis and peri-implantitis, significantly jeopardize dental implant success. Traditional diagnostic methods, relying on periodontal probing and radiographs, have limitations in precisely diagnosing these conditions. Recent studies suggest that microRNA (miRNA) profiling might be a breakthrough in the early detection of PID. This study aimed to evaluate the expression levels of specific miRNAs-miR-98, miR-145, miR-146a, and let-7e-in individuals with peri-implant mucositis and peri-implantitis compared to a healthy control.
From January 2022 to October 2023, 19 participants with 38 dental implants were recruited according to established criteria. After clinical and radiographic evaluations, dental implants were grouped as peri-implant health (Group 1), peri-implant mucositis (Group 2), and peri-implantitis (Group 3). Subsequently, peri-implant crevicular fluid (PICF) samples were collected and analyzed through real-time quantitative polymerase chain reaction (qPCR).
Based on the findings, only let-7e biomarkers were consistently detected across all samples, with their expression increased eightfold in peri-implant mucositis and 94-fold in peri-implantitis cases. Kruskal-Wallis's test showed a statistically significant difference in relative gene expression of let-7e between the different groups, H(2) = 25.825, p ≤ 0.001.
Our study indicates that miRNA biomarkers, particularly let-7e, may play a significant role in the development and progression of PID, highlighting the need for further in-depth investigation, with PICF offering a practical, noninvasive sampling method.
种植体周围疾病(PID),特别是种植体周围黏膜炎和种植体周围炎,严重危及牙种植体的成功。传统的诊断方法依赖牙周探诊和X光片,在精确诊断这些病症方面存在局限性。最近的研究表明,微小RNA(miRNA)分析可能是PID早期检测的一项突破。本研究旨在评估与健康对照相比,种植体周围黏膜炎和种植体周围炎患者中特定miRNA——miR-98、miR-145、miR-146a和let-7e的表达水平。
从2022年1月至2023年10月,根据既定标准招募了19名有38颗牙种植体的参与者。经过临床和影像学评估后,将牙种植体分为种植体周围健康组(第1组)、种植体周围黏膜炎组(第2组)和种植体周围炎组(第3组)。随后,收集种植体周围龈沟液(PICF)样本,并通过实时定量聚合酶链反应(qPCR)进行分析。
基于研究结果,仅在所有样本中均一致检测到let-7e生物标志物,其表达在种植体周围黏膜炎病例中增加了8倍,在种植体周围炎病例中增加了94倍。Kruskal-Wallis检验显示,不同组之间let-7e的相对基因表达存在统计学显著差异,H(2) = 25.825,p≤0.001。
我们的研究表明,miRNA生物标志物,特别是let-7e,可能在PID的发生和发展中起重要作用,这突出了进一步深入研究的必要性,PICF提供了一种实用且无创的采样方法。