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急性毛细支气管炎并心衰患儿血小板活化因子,血小板源生长因子的表达及临床意义
引用本文:马少春,蓝峻峰,张元凤,蒋玉红.急性毛细支气管炎并心衰患儿血小板活化因子,血小板源生长因子的表达及临床意义[J].生物磁学,2011(15):2885-2887.
作者姓名:马少春  蓝峻峰  张元凤  蒋玉红
作者单位:[1]山东青岛妇女儿童医院,山东青岛266011 [2]青岛卫生学校,山东青岛266021
摘    要:目的:探讨血小板活化因子(PAF)、肿瘤坏死因子-α(TNF-α)及血小板源生长因子(PDGF)水平变化在毛细支气管炎并急性心衰的变化,探讨它们在该病的发病中的作用。方法:58例心衰组患儿分别于治疗前和临床症状消失后采用双抗体夹心ABC.ELISA法检测PAF、TNF-α及PDGF血清含量,设正常对照组40例比较。结果:心衰组PAF治疗前为370.57±23.6ng/L,明显高于对照组的56.78±19.6ng/L,组间比较差异具有非常显著性意义(t=15.95,P〈0.001);治疗后恢复至49.63±14.5ng/L,与正常对照差异不明显;治疗前后比较,差异具有非常显著性意义(t=3.70,P〈0.001)。TNF-α治疗前为457.4±40.5ng/L,明显高于对照组的148.8±21.6ng/L,组间比较差异具有显著性意义(t=2.135,P〈0.05);治疗后恢复至162.6±37.61ng/L,与正常对照差异不明显;治疗前后比较,差异具有非常显著性意义(t=7.25,P〈0.01)。PDGF治疗前为596.23±199.43)ng/L,较对照组259.76±69.58ng/L增高,组间比较,差异具有非常显著性意义(t=-25.52,P〈0.01);治疗后降为272.83±116.96ng/L,较治疗前明显恢复,组间比较差异均具有显著性意义(t=7.66,P〈0.01)。结论:结果表明,PAF、TNF-α、PDGF作为炎症介质不仅参与心衰的发病过程,还提示细胞外基质的异常在心衰发病学中的重要地位。

关 键 词:血小板活化因子(PAY)  坏死因子-α(TNF-α)  血小板源生长因子(PDGF)

Expression of Platelet-activating Factor and Platelet-derived Growth Factor in Bronchiolitis with Acute Heart Failure and Their Clinical Significance
MA Shao-chun,LAIN Jun-feng,ZHANG Yuan-feng,JIANG Yu-hong.Expression of Platelet-activating Factor and Platelet-derived Growth Factor in Bronchiolitis with Acute Heart Failure and Their Clinical Significance[J].Biomagnetism,2011(15):2885-2887.
Authors:MA Shao-chun  LAIN Jun-feng  ZHANG Yuan-feng  JIANG Yu-hong
Institution:1 Women and Children Hospital, Qingdao, Shandong, 266000)
Abstract:Objective: The present study was designed to study the level changes and effects of platelet-activating factor, tumor necrosis factor-a and platelet-derived growth factor in Bronchiolitis with acute heart failure. Methods: Set heart failure group (n=58 cases), and healthy control group (n=40 cases). Collect the patients' blood samples before treatment and after clinical symptoms disappeared. The levels of serum PAF, TNF-a and PDGF were detected by ABC-ELISA method. Results: Before treatment, PAF of heart failure group was significantly higher than healthy control group. The difference between groups was statistically significant (t=3.70, P〈0. 001). After clinical symptoms disappeared, PAF of heart failure group had no statistically significant difference with healthy control group. Before and after treatment, the difference was statistically significant (t=3.70, P〈0.001). TNF-α of heart failure group was significantly higher than healthy control group. The difference between groups was statistically significant (t=2.135, P〈0.05). After clinical symptoms disappeared, TNF-a of heart failure group had no statistically significant difference with healthy control group. Before and after treatment, the difference was statistically significant (t=7.25, P〈0.01). PDGF of heart failure group was significantly higher than healthy control group. The difference between groups was statistically significant (t=-25.52, P 〈0.01). Before and after treatment, the difference was statistically significant (t=7.66, P 〈0.01). Conclusion: As inflammatory mediators, platelet-activating factor, tumor necrosis factor-α and platelet-derived growth factor involved in the pathogenesis of heart failure, and abnormal extracellular matrix has an important part in the pathogenesis of heart failure.
Keywords:Platelet-activating factor(PAF)  Tumor necrosis factor-α(TNF-α)  Platelet-derived growth factor(PDGF)
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