血清MicroRNA-122作为脓毒症诊断特异性标志物的研究

邓 婕,王慧娟,苏龙翔,张 鑫,肖 坤,贾艳红,解立新

武警医学 ›› 2013, Vol. 24 ›› Issue (5) : 383-386.

武警医学 ›› 2013, Vol. 24 ›› Issue (5) : 383-386.
论著

血清MicroRNA-122作为脓毒症诊断特异性标志物的研究

  • 邓 婕1,王慧娟2,苏龙翔2,张 鑫1,肖 坤1,贾艳红1,解立新1
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Serum microRNA-122 as a specific marker of sepsis diagnosis

  • DENG Jie1,WANG Huijuan2,SU Longxiang2,ZHANG Xin1,XIAO Kun1,JIA Yanhong1,and XIE Lixin1
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摘要

目的 观察脓毒症患者血清中miRNA-122的表达量在病程中的动态变化情况,并探讨其与脓毒症严重程度的关系。方法 选择52例脓毒症患者,其中一般脓毒症23例,重症脓毒症29例,23例健康人作为对照。采用荧光定量 PCR(qRT-PCR) 检测研究对象在入组第1,3,5,7,10,14天血清中 miRNA- 122表达量,并记录患者的基本临床信息。结果 在脓毒症患者入组后14 d的病程中,52例脓毒症患者和23例健康人群血清中的miRNA-122表达量在每个时间点比较,前者均比后者显著下降(P<0.01)。用入组第1天的miRNA表达量做ROC诊断分析得出,miRNA-122诊断脓毒症的特异性是95.7%,敏感性是53.8%。重症脓毒症组的血清miRNA-122表达量水平高于一般脓毒症组,并且在各个观测时间点两组表达量具有统计学差异(P<0.01)。结论 血清中miRNA-122可能作为脓毒症诊断的特异性标志物,具有潜在的临床价值,并且miRNA-122在预警脓毒症患者疾病严重程度方面具有积极的临床意义。

Abstract

Objective To study the dynamic changes in serum miRNA-122 levels during sepsis and the correlation between serum miRNA-122 and sepsis severity. Methods Fifty-two sepsis patients (including 23 non-severe septic patients and 29 severe septic patients)and 23 healthy controls were recruited in the study. The expression levels of serum miRNA-122 were quantified by quantitative reverse transcriptase polymerase chain reaction assays (qRT-PCR).Levels of serum miRNA-122 were detected on the 1 st, 3 rd, 5 th, 7 th, 10 th and 14 th day after their admissions in intensive care unit. All the patients clinical information was also recorded. Results After comparison, levels of serum miRNA-122 in sepsis patients on every observation time point were all significantly lower than those in healthy controls (P<0.01). The receiver operating characteristic curve was obtained and the area under curve was calculated on the levels of serum miRNA-122 on the first day of their admissions. When the cut-off point was set at 0.710, miRNA-122 had a specificity of 95.7% and a sensitivity of 53.8%. The expression levels of serum miRNA-122 in severe sepsis group were significantly higher than in sepsis group on each observation time point (P<0.01). Conclusions Serum miRNA-122 can used as a specific biomarker for diagnosis of sepsis. And miRNA-122 might be correlated with the organ injuries of septic patients.

关键词

脓毒症 / 微小RNA-122 / 微小RNA / 诊断

Key words

sepsis / microRNA-122 / microRNA / diagnosis

引用本文

导出引用
邓 婕,王慧娟,苏龙翔,张 鑫,肖 坤,贾艳红,解立新. 血清MicroRNA-122作为脓毒症诊断特异性标志物的研究[J]. 武警医学. 2013, 24(5): 383-386
DENG Jie,WANG Huijuan,SU Longxiang,ZHANG Xin,XIAO Kun,JIA Yanhong,and XIE Lixin. Serum microRNA-122 as a specific marker of sepsis diagnosis[J]. Medical Journal of the Chinese People Armed Police Forces. 2013, 24(5): 383-386
中图分类号: R593.9   

参考文献

[1] Levy M M, Fink M P, Marshall J C, et al. Ramsay G: 2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference[J]. Crit Care Med, 2003, 31(4):1250-1256.

[2] Wang H, Zhang P, Chen W, et al. Evidence for serum miR-15a and miR-16 levels as biomarkers that distinguish sepsis from systemic inflammatory response syndrome in human subjects[J]. Clin Chem Lab Med, 2012, 50(8): 1423-1428.

[3] Wang H, Meng K, Chen W J, et al. Serum miR-574-5p: a prognostic predictor of sepsis patients [J]. Shock, 2012, 37(3): 263-267.

[4] Bone R C, Balk R A, Cerra F B, et al. Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. The ACCP/SCCM Consensus Conference Committee. American College of Chest Physicians/Society of Critical Care Medicine[J]. Chest ,1992, 101(6):1644-1655.

[5] Ambros V. The functions of animal microRNAs [J]. Nature, 2004, 431: 350–355.

[6] Vasilescu C, Rossi S, Shimizu M, et al. MicroRNA fingerprints identify miR-150 as a plasma prognostic marker in patients with sepsis [J]. PLoS One, 2009, 4(10): e7405.

[7] Wang Jiafeng, Yu Manli, Yu Guang, et al. Serum miR-146a and miR-223 as potential new biomarkers for sepsis[J]. Biochem Biophys Res Commun, 2010, 394(1): 184-188.

[8] Wang Huijuan, Zhang Pengjun, Chen Weijun, et al. Serum MicroRNA Signatures Identified by Solexa Sequencing Predict Sepsis Patients’ Mortality: A Prospective Observational Study [J]. PLoS One, 2012, 7(6): e38885.

[9] Hotchkiss R S, Nicholson D W. Apoptosis and caspases regulate death and inflammation in sepsis?[J]. Nat Rev Immunol, 2006, 6: 813-822.

[10] Hotchkiss R S, Tinsley K W, Swanson P E, et al. Sepsis-induced apoptosis causes progressive profound depletion of B and CD4+ T lymphocytes in humans[J]. Immunol,2001,166: 6952–6963.

[11] Hotchkiss R S, Tinsley K W, Swanson P E, et al. Depletion of dendritic cells, but not macrophages, in patients with sepsis[J]. Immunol, 2002,168: 2493–2500.

[12] Jia Y X, Pan C S, Yang J H, et al. Altered L-arginine/nitric oxide synthase/nitric oxide pathway in the vascular adventitia of rats with sepsis[J]. Clin Exp Pharmacol Physiol, 2006, 33(12):1202-1208.

[13] Chang J, Nicolas E, Marks D,et al. miR-122, a mammalian liver-specific microRNA, is processed from her mRNA and may downregulate the high affinity cationic amino acid transporter CAT-1 [J]. RNA Biol, 2004, 1(2): 106-113.

基金

国家自然科学基金(81170008);军队十二五面上课题(CWS11J094)


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