Aim: This study focused on the expression pattern of long non-coding RNA maternally expressed gene 3 (MEG3) and its value in ischemic stroke (IS).
Methods:The expression pattern and the roles of MEG3 in the development of IS were explored in mice IS model and human brain microvascular endothelial cells (hBMECs). A case-control study, including 215 IS patients and 153 controls, was also conducted to investigate its prognostic value.
Results:In vivo study showed that MEG3 increased significantly in the IS group (P 0.004), and its level remained stable within 3 to 48h after the onset of IS. Besides, the survival time of the mouse in the high MEG3 group was significantly lower than that in the low MEG3 group (P 0.042). In vitro study showed that oxygenglucose deprivation (OGD) treatment significantly up-regulated expressions of MEG3, Bax, and cleaved caspase-3, and further promoted apoptosis of hBMECs, while si-MEG3 blocked these effects. A human study showed that MEG3 increased markedly within 48h of IS onset and was positively associated with the National Institutes of Health Stroke Scale (r 0.347, P 0.001), modified Rankin Scale (r 0.385, P 0.001), high-sensitivity C-reactive protein (r 0.221, P 0.002) level, and infarct volume (r 0.201, P 0.006). Overall survival analysis showed that patients with higher MEG3 expression within 48h had a relatively poor prognosis (P 0.001). Meanwhile, multivariate analysis revealed that MEG3 was an independent prognostic marker for unfavorable functional outcome and death in IS patients.
Conclusions: This study suggested that MEG3 might be considered as an intervention point and potential prognostic indicator for IS.after ischemic stroke by computed tomography (CT), and CT is mainly used to quickly eliminate intracranial tumors or cerebral hemorrhage 2) . (2) Magnetic resonance imaging (MRI) has higher sensitivity and specificity than CT, but most medical institutions in China cannot conduct MRI examinations 2) . (3) A recent systematic review suggested that the survival rate of IS patients who can receive thrombolytic therapy within 6h of symptom onset can be increased by 46.0%, and the disability rate caused by IS can be reduced by 42.1% 3) . Unfortunately, only about 2% of