Micó-Martínez P, García-Giménez J-L, Seco-Cervera M, López-Roldán A, Almiñana-Pastor P-J, Alpiste-Illueca F, Pallardó F-V
Dept. of Stomatology, Faculty of Medicine and Dentistry, University of Valencia, C/Gascó Oliag, 1, 46010 Valencia, Spain,
Med Oral Patol Oral Cir Bucal. 2018 May 1;23(3):e308-e314. doi: 10.4317/medoral.22329.
The study and identification of new biomarkers for periodontal disease, such as microRNAs (miRNAs), may give us more information about the location and severity of the disease and will serve as a basis for treatment planning and disease-monitoring. miRNAs are a group of small RNAs which are involved in gene regulation by binding to their messenger RNA target (mRNA). In this pilot study, the procedure for purifying miRNAs from gingival crevicular fluid (GCF) was, for the first time, described. In addition, the concentration of miRNAs in GCF was analyzed and compared between patients with moderate or severe chronic periodontitis (CP) and healthy controls.
GCF samples were collected from single-rooted teeth of patients with moderate or severe CP (n=9) and of healthy individuals (n=9). miRNAs were isolated from GCF using miRNeasy Serum/Plasma kit (Qiagen, CA. USA). Reverse transcription polymerase chain reaction (qRT-PCR) was used to determine the expression of a series of miRNAs candidates that are related to bone metabolism. The significance of differences in miRNA levels between both groups was determined using Mann-Whitney U test.
The results from this pilot study indicate that miRNAs can be isolated from GCF. Six different miRNAs were analyzed (miR-671, miR-122, miR-1306, miR-27a, miR-223, miR-1226), but only miR-1226 showed statically significant differences between the CP group and healthy controls (p<0.05). This miRNA was downregulated in patients with CP.
Within the limitations of the present study, it may be concluded that miR-1226 can be a promising biomarker for periodontal disease, adding relevant information to common clinical parameters used for diagnosis and prognosis of periodontitis.
对牙周病新生物标志物的研究与鉴定,如微小RNA(miRNA),可能会让我们更多地了解疾病的位置和严重程度,并为治疗方案制定和疾病监测提供依据。miRNA是一组小RNA,通过与信使RNA靶标(mRNA)结合参与基因调控。在这项初步研究中,首次描述了从龈沟液(GCF)中纯化miRNA的方法。此外,分析并比较了中度或重度慢性牙周炎(CP)患者与健康对照者龈沟液中miRNA的浓度。
从患有中度或重度CP的患者(n = 9)和健康个体(n = 9)的单根牙采集龈沟液样本。使用miRNeasy血清/血浆试剂盒(Qiagen,加利福尼亚州,美国)从龈沟液中分离miRNA。采用逆转录聚合酶链反应(qRT-PCR)来确定一系列与骨代谢相关的候选miRNA的表达。使用曼-惠特尼U检验确定两组之间miRNA水平差异的显著性。
这项初步研究的结果表明,可以从龈沟液中分离出miRNA。分析了六种不同的miRNA(miR-671、miR-122、miR-1306、miR-27a、miR-223、miR-1226),但只有miR-1226在CP组和健康对照之间显示出统计学上的显著差异(p < 0.05)。该miRNA在CP患者中表达下调。
在本研究的局限性范围内,可以得出结论,miR-1226可能是牙周病的一个有前景的生物标志物,为用于牙周炎诊断和预后的常见临床参数增添相关信息。