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可溶性ST2在心血管疾病中的临床应用及展望 被引量:3

Soluble ST2 and its prospects of clinical application in cardiovascular disease
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摘要 可溶性ST2(sST2)是白细胞介素-33(IL-33)的可溶性受体。当心肌细胞受到生物机械性拉伸时sST2和跨膜型ST2(ST2L)表达明显增高,尤其是sST2表达更为明显。大量sST2与IL-33结合,从而阻断IL-33与ST2L结合,继而削弱IL-33/ST2L信号通路的心血管保护作用。近年研究显示,sST2有望作为一种新的心力衰竭标志物应用于临床。血浆sST2对心力衰竭的诊断价值不及NT—proBNP,但可较好地预测呼吸困难、急性或慢性心力衰竭、心肌梗死患者的预后,尤其是中长期(1年及1年以上)预后。但是,需要更多的循证医学证据以证实血浆sST2对心血管疾病患者心力衰竭风险评估及预后的临床价值。(中华检验医学杂志,2014,37:969-972) Soluble ST2 (sST2) is a decoy receptor of IL-33 in blood, sST2and ST2L (receptor on cell membrane) seem to be markedly induced in mechanically overloaded cardiac myocytes, especially the expression of sST2. A large number of sST2 bind IL-33 thus subtracting IL-33 from the interaction with ST2L, potentially attenuating the cardioprotective effects of IL-33/ST2L pathway. Recently, sST2 has emerged as a novel for heart failure biomarker. Though sST2 was a less robust marker for the diagnosis of heart failure than NT-proBNP, it has been implicated in the prognostication of patients with acute dyspnea, acute or chronic heart failure and myocardial infarction, with particular value for mid- and long-term prognosis. However, further studies are needed in order to better point out the evidence for a routine use of sST2 evaluation in patients suffering from cardiovascular diseases. (Chin J Lab Med,2014 ,37 :969-972 )
作者 袁慧 马旭
出处 《中华检验医学杂志》 CAS CSCD 北大核心 2014年第12期969-972,共4页 Chinese Journal of Laboratory Medicine
关键词 心肌缺血 心力衰竭 受体 细胞表面 生物学标记 Myocardial ischemia Heart failure Receptors, cell surface Biological markers
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参考文献35

  • 1Ahem RM, Lozano R, Naghavi M, et al. Improving the public health utility of global cardiovascular mortality data: The rise of ischemic heart disease[J]. Popul Health Metr, 2011, 9: 8.
  • 2Schmitz J, Owyang A, Oldham E, et al. IL-33, an interleukin-1- like cytokine that signals via the IL-1 receptor related protein ST2 and induces T helper type 2-associated cytokines[ J]. Immunity, 2005, 23 : 479-490.
  • 3Sanada S, Hakuno D, Higgins LJ, et al. IL-33 and ST2 comprise a critical biomechanically induced and cardioprotective signaling system[ J~. J Clin Invest, 2007, 117 : 1538-1549.
  • 4Kakkar R, Lee RT. The IL-33/ST2 pathway: therapeutic target and novel biomarker[ J]. Nat Rev Drug Discov ,2008,7:827-840.
  • 5Zwaan L, Thijs A, Wagner C, et al. Does inappropriate selectivity in information use relate to diagnostic errors and patient harm? The diagnosis of patients with dyspnea[ Jl. Soc Sci Med, 2013, 91 : 32-38.
  • 6Januzzi JL Jr, Peacock WF, Maisel AS, et at. Measurement of the interleukin family member ST2 in patients with acute dyspnea: results from the PRIDE ( Pro-Brain Natriuretic Peptide Investigation of Dyspnea in the Emergency Department ) study [J]. J Am Coll Cardiol, 2007, 50: 607~513.
  • 7Januzzi JL Jr, Camargo CA, Anwaruddin S, et al. The N-terminal pro-BNP investigation of dyspnea in the emergency department (PRIDE) study[J]. Am J Cardiol, 2005, 95: 948-954.
  • 8Januzzi JL Jr, Sakhuja R, O'donoghue M, et al. Utility of amino- terminal pro-brain natriuretic peptide testing for prediction of 1- year mortality in patients with dyspnea treated in the emergency department[J]. Arch Intern Med, 2006, 166: 315-320.
  • 9Dieplinger B, Gegenhuber A, Kaar G, et at. Prognostic value of established and novel biomarkers in patients with shortness of breath attending an emergency department [ J ]. Clin Biochem, 2010, 43: 714-719.
  • 10Socrates T, deFilippi C, Reichlin T, et at. Interleukin family member ST2 and mortality in acute dyspnoea[ J]. J Interu Med, 2010, 268 : 493-500.

二级参考文献14

  • 1Bhardwaj A,Januzzi JL Jr. ST2 ; a novel biomarker for heartfailure[J]. Expert Rev Mol Diagn, 2010, 10:459464.
  • 2Kakkar R, Lee RT. The IL-33/ST2 pathway: therapeutic targetand novel biomarker [J] - Nat Rev Drug Discov, 2008 , 7: 827-840.
  • 3Rehman SU, Mueller T,Januzzi JL Jr. Characteristics of the NovelInterleukin Family Biomarker ST2 in Patients With Acute HeartFailure [J]. J Am Coll Cardiol, 2008 , 52 : 1458-1465.
  • 4Ky B, French B, McCloskey K, et al. High-Sensitivity ST2 forPrediction of Adverse Outcomes in Chronic Heart Failure[J]. CircHeart Fail,2011, 4: 180-187.
  • 5Boisot S, Beede J, Isakson S, et al. Serial Sampling of ST2Predicts 90-Day Mortality Following Destabilized Heart Failure[J]. J Card Fail, 2008,14: 732-738.
  • 6Dieplinger B, Januzzi JL Jr, Steinmair M, et al. Analytical andclinical evaluation of a novel high-sensitivity assay for measurementof soluble ST2- the Presage ST2 assay [J]. Clin Chim Acta.2009,409; 3340.
  • 7NCCLS. EP15-A User Demonstration of Performance for Precisionand Accuracy; Approved Guideline. Wayne, PA: NCCLS,2001.
  • 8NCCLS. EP6-A Evaluation of the Linearity of QuantitativeMeasurement Procedures : A Statistical Approach ; ApprovedGuideline. Wayne, PA; NCCLS,2003.
  • 9Januzzi JL Jr, Peacock WF, Maisel AS, et ai. Measurement of theinterleukin family member ST2 in patients with acute dyspnea :results from the PRIDE ( Pro-Brain Natriuretic PeptideInvestigation of Dyspnea in the Emergency Department) study [J].J Am Coll Cardiol, 2007,50: 607-613.
  • 10Kohli P, Bonaca MP, Kakkar R, et al. Role of ST2 in Non-ST-Elevation Acute Coronary Syndrome in the MERLIN-TIMI 36 Trial[J]. Clin Chem, 2012,58: 257-266.

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