首页> 外文期刊>Journal of clinical laboratory analysis. >Association of circulating long non‐coding RNA HULC expression with disease risk, inflammatory cytokines, biochemical index levels, severity‐assessed scores, and mortality of sepsis
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Association of circulating long non‐coding RNA HULC expression with disease risk, inflammatory cytokines, biochemical index levels, severity‐assessed scores, and mortality of sepsis

机译:与疾病 风险 ,炎性 细胞因子, 生化指标 水平 ,严重程度 , 评估 评分, 和脓毒病 的 死亡 循环 长的非 编码RNA HULC 表达 的 关联

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Background The present study aimed to explore the correlation of long non‐coding RNA highly up‐regulating in liver cancer (lncRNA HULC) with disease risk, inflammatory cytokines, biochemical indexes, disease severity, infective features, and 28‐day mortality of sepsis. Methods Totally 174 sepsis patients and 100 controls were enrolled. Peripheral blood samples were collected from sepsis patients after diagnosis and from controls at enrollment, respectively, and further for separation of peripheral blood mononuclear cell (PBMC) and serum samples. PBMC samples were for lncRNA HULC detection, and serum samples were for inflammatory cytokine detection. Results LncRNA HULC expression was increased in sepsis patients compared with controls. Moreover, lncRNA HULC was positively associated with TNF‐α, IL‐6, IL‐17, intercellular adhesion molecule 1, vascular cell adhesion molecule 1, serum creatinine, white blood cell, and C‐reactive protein in sepsis patients, but not in controls. Furthermore, in sepsis patients, lncRNA HULC expression was positively correlated with acute physiology and chronic health evaluation II score and sequential organ failure assessment score, but not correlated with primary infection sites or primary infection organisms; meanwhile, lncRNA HULC expression was increased in deaths compared with survivors; subsequent receiver operating characteristic curve indicated that lncRNA HULC presented good value in predicting increased 28‐day mortality (AUC: 0.785, 95% CI: 0.713–0.857), and its independent predictive value for mortality was also verified by multivariate analysis. Conclusion LncRNA HULC is correlated with higher disease risk, severity, and inflammation and serves as an independent factor for predicting increased mortality, suggesting its potential in promoting accuracy of prognostic prediction for sepsis management.
机译:背景技术本研究旨在探讨肝癌(LNCRNA Hulc)的长期非编码RNA高度上调与疾病风险,炎症细胞因子,生化指标,疾病严重程度,感染性特征和败血症28天死亡率的相关性。方法共于174例败血症患者和100种对照。在诊断后从败血症患者和注册的对照中收集外周血样品,进一步用于分离外周血单核细胞(PBMC)和血清样品。 PBMC样品用于LNCRNA Hulc检测,血清样品用于炎症细胞因子检测。结果与对照组相比,败血症患者中的LNCRNA Hulc表达增加。此外,LNCRNA Hulc与TNF-α,IL-6,IL-17,细胞间粘附分子1,血管细胞粘附分子1,血清肌酐,白细胞和在败血症患者中的C反应蛋白质呈正相关,但不在控制。此外,在败血症患者中,LNCRNA Hulc表达与急性生理学和慢性健康评估II得分和顺序器官衰竭评分呈正相关,但与原发性感染网站或原发性感染生物无关;同时,与幸存者相比,LNCRNA Hulc表达增加死亡;随后的接收器操作特征曲线表明,LNCRNA Hulc在预测增加的28天死亡率(AUC:0.785,95%CI:0.713-0.857)中呈现了良好的价值,并且通过多变量分析还验证了其对死亡率的独立预测值的影响。结论LNCRNA Hulc与疾病风险,严重程度和炎症相关,作为预测死亡率增加的独立因素,表明其促进败血症管理预后预测准确性的潜力。

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