Monfared Yousef Khazaei, Mirzaii-Dizgah Mohammad-Reza, Khodabandehloo Elham, Sarookhani Mohamad Reza, Hashemipour Sima, Mirzaii-Dizgah Iraj
Cellular and Molecular Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Dip. Di Chimica, Università di Torino, Via P. Giuria 7, 10125 Torino, Italy.
J Diabetes Metab Disord. 2021 Oct 28;20(2):1631-1638. doi: 10.1007/s40200-021-00914-z. eCollection 2021 Dec.
Emerging of miRNAs have illustrated the new mechanistic layer to regulate type 2 diabetes process and suggests a possible role of these RNAs in this defect. Thus, we designed this study to improve our understanding of salivary miRNA-126 and 135a expression utility as an easy of collection and non-invasive way in diabetic patients instead of blood sample.
This case-control study was done on TD (n = 40) and healthy individuals (n = 40). The level of biochemical parameters were determined by enzymatic methods as well as glycosylated hemoglobin (HbA1c) was measured by immunoturbidimetry. We used the pooled whole stimulated saliva sample from cases and controls to assess the differentiation expression of miRNA 126 and 135-a with quantitative RT-PCR method. Unpaired Student's t test, Pearson's correlation coefficient and Receiver Operating Characteristic (ROC) analysis were used.
A correlation was observed between the level of HbA1c, glucose and lipid profiles (TG, TC, and LDL) in serum and whole stimulated saliva samples in TD patients compared to control (p < 0.001). miR-135a expression was considerably higher by 4.7-fold in TD compared to the control group (1.8-fold) (p < 0.001) while the miR126 expression was significantly decreased by 3.9-fold in TD compared to the controls (6.3-fold) (p < 0.001).
The results of this case and control study showed that miR-135a and miR126 expression in saliva fluid as a reliable biomarkers and non-invasive approach in combination by change of lipid profiles, glucose and HbA1c may be used to monitor diabetic and non-diabetic patients, while further research is needed to investigate the relationship of these salivary miRNAs (miR135a, miR126) levels change on shifting the levels of clinical laboratory outcomes.
微小RNA(miRNA)的出现揭示了调控2型糖尿病进程的新机制层面,并提示这些RNA在这一病症中可能发挥的作用。因此,我们开展本研究,旨在更好地理解唾液中miRNA - 126和135a的表达效用,以便能以一种易于采集且非侵入性的方式,替代血液样本用于糖尿病患者的检测。
本病例对照研究选取了40例2型糖尿病(TD)患者和40例健康个体。通过酶法测定生化参数水平,采用免疫比浊法测定糖化血红蛋白(HbA1c)。我们使用病例组和对照组的混合全刺激唾液样本,通过定量逆转录聚合酶链反应(RT - PCR)方法评估miRNA 126和135 - a的差异表达。采用非配对学生t检验、Pearson相关系数和受试者工作特征(ROC)分析。
与对照组相比,TD患者血清和全刺激唾液样本中的HbA1c、血糖和血脂水平(甘油三酯、总胆固醇和低密度脂蛋白)之间存在相关性(p < 0.001)。与对照组(1.8倍)相比,TD组中miR - 135a的表达显著升高4.7倍(p < 0.001),而与对照组(6.3倍)相比,TD组中miR126的表达显著降低3.9倍(p < 0.001)。
本病例对照研究结果表明,唾液中miR - 135a和miR126的表达作为可靠的生物标志物以及非侵入性方法,结合血脂、血糖和HbA1c的变化,可用于监测糖尿病和非糖尿病患者,不过还需要进一步研究来探讨这些唾液miRNA(miR135a、miR126)水平变化与临床实验室检测结果水平变化之间的关系。