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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Association of circulating long non-coding RNA MALAT1 in diagnosis, disease surveillance, and prognosis of acute ischemic stroke
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Association of circulating long non-coding RNA MALAT1 in diagnosis, disease surveillance, and prognosis of acute ischemic stroke

机译:循环长期非编码RNA MALAT1在诊断,疾病监测和急性缺血性卒中预后的关联

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We aimed to investigate the association of long non-coding RNA metastasis-associated lung adenocarcinoma transcript 1 (lnc-MALAT1) with acute ischemic stroke (AIS), and its association with disease severity, inflammation, and recurrence-free survival (RFS) in AIS patients. One hundred and twenty AIS patients and 120 controls were recruited. Venous blood samples from AIS patients (within 24 h after symptoms onset) and controls (at entry to study) were collected to detect plasma lnc-MALAT1 expression by real-time quantitative polymerase chain reaction. AIS severity was assessed by the National Institutes of Health Stroke Scale (NIHSS) score. Plasma concentrations of inflammation factors (including C-reactive protein (CRP), tumor necrosis factor α (TNF-α), interleukin (IL)-6, IL-8, IL-10, IL-17, and IL-22) were measured and RFS was calculated. lnc-MALAT1 expression was decreased in AIS patients compared to controls, and it had a close correlation with AIS (AUC=0.791, 95% CI: 0.735-0.846). For disease condition, lnc-MALAT1 expression negatively correlated with NIHSS score and pro-inflammatory factor expression (including CRP, TNF-α, IL-6, IL-8, and IL-22), while it positively correlated with anti-inflammatory factor IL-10 expression. Furthermore, lnc-MALAT1 expression was elevated in AIS patients with diabetes. For prognosis, no statistical correlation of lnc-MALAT1 expression with RFS was found, while a trend for longer RFS was observed in patients with lnc-MALAT1 high expression compared to those with lnc-MALAT1 low expression.
机译:我们旨在探讨长期非编码RNA转移相关肺腺癌转录1(LNC-MALAT1)与急性缺血性卒中(AIS)的关联,及其与疾病严重程度,炎症和无复发存活(RFS)的关联AIS患者。招募了一百二十岁的AIS患者和120个对照。收集来自AIS患者(24小时后24小时内的静脉血液样本,并通过实时定量聚合酶链反应检测血浆LNC-MALAT1表达。 AIS严重程度被国家卫生卒中规模(NIHSS)得分评估。炎症因子的血浆浓度(包括C-反应蛋白(CRP),肿瘤坏死因子α(TNF-α),白细胞介素(IL)-6,IL-8,IL-10,IL-17和IL-22)是计算测量和RFS。与对照相比,AIS患者的LNC-MALAT1表达减少,与AIS(AUC = 0.791,95%CI:0.735-0.846)密切相关。对于疾病病症,LNC-MALAT1表达与NIHSS评分和促炎症因子表达呈负相关(包括CRP,TNF-α,IL-6,IL-8和IL-22),而其与抗炎因子呈正相关IL-10表达。此外,在AIS患有糖尿病患者中升高了LNC-MALAT1表达。对于预后,未发现LNC-MALAT1表达与RFS的统计相关性,而LNC-MALAT1高表达患者与LNC-MALAT1低表达的患者观察到较长RFS的趋势。

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