Monfared Yousef Khazaei, Honardoost Maryam, Cea Michele, Gholami Soheyla, Mirzaei-Dizgah Iraj, Hashemipour Sima, Sarookhani Mohamad Reza, Farzam Seyed Amir
Dezful University of Medical Sciences, Dezful, Iran.
Dip. Di Chimica, Università Di Torino, Via P. Giuria 7, 10125 Turin, Italy.
J Diabetes Metab Disord. 2022 Jul 28;21(2):1469-1478. doi: 10.1007/s40200-022-01082-4. eCollection 2022 Dec.
Early-stage diagnosis of diabetes through non-invasive and diagnostic biofluid-like saliva has become a very popular approach to facilitate future preventive interventions and improve patient care. Meanwhile, the alteration of small non-coding RNA in human fluids has been suggested as a probable precedent for the early stages of diabetes.
In the present study, we checked the expression of miR-320a, 182-5p, 503, and 375 by using quantitative PCR in both stimulated and unstimulated saliva and blood samples of 40 adult patients with type-2 diabetes compared to 40 healthy individuals. In addition, we have sought to understand the possibility that miRNAs could provide new information about the status of type 2 diabetes in salivary samples beyond what can now be identified from blood samples and link their expression to the presence of clinically relevant risk factors. For this purpose, we have used a set of multivariate models.
The results showed that three miRNAs were more highly expressed in patients with type 2 diabetes, while miR-320-a was down-regulated in those patients compared to healthy subjects. Furthermore, the data showed that miR-320a was the most reliable predictor for distinguishing diabetic patients from healthy subjects, with AUCs of 0.997, 0.97, and 0.99 (97.4% sensitivity and 100% specificity, = 0.001) for serum, unstimulated, and stimulated saliva samples, respectively.
Interestingly, the results of this study indicated that the amount of four miRNAs expressed in stimulated saliva was the same as in serum samples, which could conclude that specific miR-320a and 503 in stimulated saliva may introduce credible, non-invasive, and diagnostic biomarkers that can be used to monitor diabetic patients' status, while there is a need to design more research studies to confirm these findings.
通过非侵入性且类似诊断生物流体的唾液对糖尿病进行早期诊断,已成为一种非常流行的方法,有助于未来的预防性干预并改善患者护理。与此同时,人体体液中小非编码RNA的改变被认为可能是糖尿病早期阶段的一个先兆。
在本研究中,我们使用定量PCR检测了40名成年2型糖尿病患者与40名健康个体的刺激唾液和非刺激唾液及血液样本中miR-320a、182-5p、503和375的表达。此外,我们试图了解miRNA是否有可能提供超出目前从血液样本中所能识别的关于唾液样本中2型糖尿病状态的新信息,并将它们的表达与临床相关危险因素的存在联系起来。为此,我们使用了一组多变量模型。
结果显示,三种miRNA在2型糖尿病患者中表达更高,而与健康受试者相比,miR-320-a在这些患者中表达下调。此外,数据表明,miR-320a是区分糖尿病患者和健康受试者最可靠的预测指标,血清、非刺激唾液和刺激唾液样本的曲线下面积分别为0.997、0.97和0.99(敏感性为97.4%,特异性为100%,P = 0.001)。
有趣的是,本研究结果表明,刺激唾液中表达的四种miRNA的量与血清样本中的相同,这可以得出结论,刺激唾液中的特定miR-320a和503可能会引入可靠的、非侵入性的诊断生物标志物,可用于监测糖尿病患者的状态,同时需要设计更多的研究来证实这些发现。