急性冠脉综合征介入前后中医证候要素演变规律及益气活血中药作用机制研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
1研究目的
     1.1研究急性冠脉综合征(acute coronary syndromes, ACS)患者介入治疗前中医证候要素的分布规律,探索中医证候要素与ACS危险分层的相关性,为中医药早期预防和干预ACS患者的不良预后提供临床依据。
     1.2观察ACS患者介入治疗后中医证候要素演变的规律,以及益气活血中药对中医证候要素演变的影响,为中医药临床治疗提供依据。
     1.3从炎症信号通路Toll样受体(toll-like receptors, TLRs) 2、4和下游促炎性细胞因子方面探讨益气活血中药联合缺血后适应干预大鼠急性心肌梗死再灌注损伤的作用机制,为中医药防治急性心肌梗死血运重建后再灌注损伤提供实验依据。
     2方法
     2.1临床证候要素规律研究
     本研究是一个前瞻性、随机、对照的多中心临床试验,将6家三级医院收集合格的241例ACS介入患者,随机分为益气活血干预组及对照组,对照组给予西医常规标准化治疗,益气活血干预组在西医常规标准化治疗基础上给予益气活血中药,分别对ACS介入患者入组前及入组后第3、6、12个月进行随访,具体
     方法包括:
     (1)通过横断面研究方法,对入组的241例ACS患者进行一般资料的频数分析,并对ACS患者进行全球急性冠状动脉事件注册(global registry of acute coronary event, GRACE)危险评分,基于GRACE危险评分的结果,采用多因子降维法和Logistic回归分析评价ACS高危患者的中医证候要素分布。
     (2)通过前瞻性调查研究方法,提取241例ACS患者入组后第3、6、12个月不同时间点的四诊信息,总结各个时间点的主要中医证候要素,观察ACS患者介入治疗后中医证候要素演变的规律,以及益气活血中药对中医证候要素演变的影响。
     2.2动物实验研究
     建立大鼠急性心肌梗死再灌注损伤模型,将SD大鼠随机分成假手术组、缺血再灌注组、缺血后适应组、益气活血+缺血后适应组以及福辛普利钠+缺血后适应组。通过血清心肌损伤标志物、心肌梗死面积、大体病理和超微结构的变化,观察益气活血中药联合缺血后适应辅助性治疗对再灌注损伤大鼠心肌的干预作用,并从TLR2.4及其下游促炎性细胞因子白细胞介素1β(interleukin-1β, IL-1β)、白细胞介素6(interleukin-6, IL-6)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)和单核细胞趋化蛋白-1(monocyte chemotactic protein-1, MCP-1)方面探讨其作用机理。
     3结果
     3.1临床证候要素规律研究
     3.1.1横断面研究分析的结果
     3.1.1.1241例ACS患者主要中医证候要素和证候要素组合
     241例ACS患者7个证候要素出现的比例由高到低依次为:血瘀(88.4%)>气虚(62.2%)>阴虚(32.8%)>痰浊偏寒(20.3%)>痰浊偏热(12.0%)>阳虚(8.7%)>气滞(0.8%),结果显示血瘀和气虚是ACS患者的主要证候要素;在具体中医证候分布中,2证候要素组合气虚+血瘀比例最高,占32%,其次是3证候要素组合气虚+阴虚+血瘀占11.6%,两者占241例ACS患者的43.6%。以本虚和标实证候要素组合的患者,所占比例为86.4%,表明ACS患者呈现的是“本虚标实,虚实夹杂”的特点。
     3.1.1.2 ACS高危患者中医证候要素分布
     对241例ACS患者进行GRACE危险评分,其中高危患者21人,中低危患者220人,基于GRACE评分结果,应用多因子降维法和Logistic回归分析ACS高危患者的中医证候要素分布,结果表明同时表现为血瘀、痰浊偏寒和阳虚证候要素的患者与不出现这复合中医证候要素的ACS患者相比,发生不良预后危险的比数比例为7.17,可以认为出现阳虚+血瘀+痰浊偏寒的ACS患者较不出现的患者6个月内可能发生全因死亡事件的百分比要高。
     3.1.2前瞻性研究分析的结果
     3.1.2.1 ACS介入后患者中医证候要素及其组合自然演变规律
     对照组患者西医常规治疗,血瘀、痰浊偏热在介入后显著降低,而气虚和阳虚逐渐增加,入组后12个月气虚和阳虚比例显著增加(共占63.8%);血瘀比例虽有所下降,但仍然占有较大比例,表明ACS介入后期中医证候以本虚为主,标实为辅的特征。
     中医证候要素组合在介入治疗前后也出现了显著的变化,介入治疗前中医证候要素组合形式以复合证候要素为主,2证候要素组合以上的比例占86%,随血运重建治疗后时间的延长,逐渐由较多证候组合类型向较少证候组合类型演变,到入组后第12月,单证候要素组合以下的比例占有54.2%,其中单证候要素中又以气虚和阳虚为主,表现出本虚的证候特征。
     3.1.2.2 ACS介入后患者中医证候要素及其组合在中药干预下的演变规律
     在西医常规治疗基础上,益气活血干预组的患者血瘀、气虚、阴虚和阳虚证候要素的百分比在四个时间点均有不同程度的下降,尤以血瘀和阴虚的降幅最大,痰浊偏寒在入组后第3月也有下降趋势,但在第6、12月出现波动未见明显下降,痰浊偏热整个病程变化不大,表明益气活血中药对痰浊的干预作用微弱。
     中医证候要素组合方面,2证候要素组合和3证候要素组合均在入组后第3个月显著减少,而无证候要素和单证候要素在入组后第3个月显著升高,至第12个月,有49例患者症状和舌脉好转,占益气活血干预组患者45.8%,单证候要素和2证候要素组合次之,分别占31.8%和16.8%,3证候要素组合和4证候要素组合少见。以上结果表明益气活血中药干预下,证候要素从复杂组合向简单组合的演变过程较对照组明显加快,ACS介入患者有向良好预后发展的趋势。3.1.2.3益气活血干预组和对照组患者中医证候要素各时间点的比较
     入组后第3、6、12个月各时间点的对照组和益气活血干预组进行单一证候要素的比较,结果显示益气活血干预组患者入组后第3、6个月时间点血瘀、气虚和阳虚显著下降,与对照组比较,差异有统计学意义(P<0.05,P<0.01),但是益气活血干预组中的痰浊与对照组比较未有显著差异;另外在第12个月的时间点,益气活血中药组患者血瘀和阳虚比例较对照组显著下降,差异有统计学意义(P<0.01),但气虚证候要素未见显著差异,这与益气活血中药仅干预ACS介入患者到入组后第6个月有一定的关系。
     另外,241例ACS患者共有16例患者发生心血管事件,其中12例是对照组,4例是益气活血干预组,两组进行卡方检验,χ2=4.137,P<0.05,差异有统计学意义。
     3.2动物实验研究
     3.2.1益气活血中药联合缺血后适应对再灌注损伤大鼠心肌的保护作用
     益气活血中药预处理联合缺血后适应能进一步减小缺血后适应心肌梗死面积,减少血清肌酸激酶同功酶(creatine kinase-MB, CK-MB)的含量(P<0.01);同时血清肌钙蛋白T(cardiac troponin T, cTnT)水平也较缺血后适应有所降低,但差异无统计学意义。大体病理和透射电镜观察结果也显示给予益气活血中药预处理联合缺血后适应后,心肌细胞内未见明显水肿,心肌肌原纤维排列尚规则,线粒体结构完整,无肿胀和空泡样变性,细胞核和核仁显示良好,未见明显胞核空洞样变及核固缩现象。
     3.2.2益气活血中药对缺血后适应心肌TLR2、4及下游促炎性细胞因子的影响
     与缺血后适应比较,益气活血中药预处理联合缺血后适应能进一步降低TLR2、4的表达(P<0.01);同时,缺血后适应基础上,应用益气活血中药能进一步降低缺血后适应心肌组织IL-1β、IL-6、TNF-α和MCP-1水平(P<0.05,P<0.01)。
     4结论
     4.1血瘀、气虚是ACS的主要证候要素,气虚血瘀是主要证候表现,高危ACS患者中医证候要素组合特点多表现为阳虚+血瘀+痰浊偏寒;
     4.2血瘀、气虚贯穿于ACS介入术后1年的整个病程,由实转虚,由繁化简是ACS介入术后中医证候要素的演变特点;
     4.3本研究进一步验证中医益气活血法是ACS介入术后患者的主要治法;
     4.4益气活血中药可加强缺血后适应对急性心肌梗死后再灌注损伤心肌的保护作用,其机制与抑制TLRs及其下游促炎性细胞因子有关。
1 Objectives
     1.1 To study distribution of TCM syndrome elements in patients with acute coronary syndromes (ACS) before percutaneous coronary intervention (PCI), and to explore the correlation of ACS risk stratification and TCM syndrome elements, so as to provide the clinical basis for early prevention and intervention of Chinese medicine from adverse outcome of ACS patients.
     1.2 To observe dynamic changes of TCM syndrome elements in ACS patients after PCI, and effect of Chinese herbs for nourishing qi and activating blood circulation (NQABC) on evolution of TCM syndrome element, so as to provide scientific basis for treatment of Chinese medicine.
     1.3 From aspects of toll-like receptor (TLR)2,4 and downstream pro-inflammatory cytokines, to observe mechanisms of Chinese herbs of NQABC combined with ischemic postconditioning (IPoC) on rat model of reperfusion injury after acute myocardial infarction, so as to provide experimental evidence for early prevention and treatment of Chinese medicine from reperfusion injury of acute myocardial infarction after revascularization.
     2 Methods
     2.1 Clinical investigation of syndrome element regularity
     This study is a prospective, randomized, controlled multicenter clinical trial, the 241 qualified ACS patients after PCI from six tertiary hospitals were randomly divided into NQABC intervention group and control group. The control group was treated by western medicine standardized therapy, and NQABC intervention group was treated by Chinese herbs of NQABC on the basis of western medicine standardized therapy, and then to follow up these ACS patients after PCI at four time points, which were respectively before enrolled into group and the 3rd,6th,12th month after enrolled into group. Detailed methods as follows:
     (1) By cross-sectional research method, to analyze general information of 241 ACS patients through frequency analysis, and to assess the prognosis of these patients through global registry of acute coronary event (GRACE) risk score. Based on the result of GRACE risk score, we assessed the distribution of TCM syndrome elements in ACS high-risk patients through multifactor dimensionality reduction (MDR) and Logistic regression analysis method.
     (2) By prospective research method, to investigate the four diagnostic information of ACS patients at different time points of 3rd,6th,12th after PCI, and to summarize the main TCM syndrome elements at each time point. At the same time, to observe the dynamic changes of TCM syndrome elements in ACS patients after PCI, and effect of Chinese herbs of NQABC on evolution of TCM syndrome elements. 2.2 Animal experiment research
     To established rat model of acute myocardial infarction reperfusion injury, SD rats were randomly divided into sham group, ischemic reperfusion group, IPoC group, NQABC+IPoC group and fosinopril sodium+IPoC group. By the changes of serum myocardial injury markers, myocardial infarction size, macropathology and ultrastructure changes, to observe the influence of Chinese herbs of NQABC combined with IPoC on rat myocardium with reperfusion injury, and to explore its possible mechanism from aspects of TLR2,4 and its downstream pro-inflammatory cytokines interleukin-1β(IL-1β), interleukin-6 (IL-6), tumor necrosis factor-a (TNF-a) and monocyte chemotactic protein-1 (MCP-1).
     3 Results
     3.1 Clinical investigation of syndrome element regularity
     3.1.1 Cross-sectional analytic results
     3.1.1.1 The main TCM syndrome elements and combination of syndrome elements in ACS patients
     The proportion of 7 TCM syndrome elements in ACS patients in order from high to low are blood stasis (88.4%)>qi deficiency (62.2%)>yin deficiency (32.8%)> turbid phlegm tending toward cold (20.3%)>turbid phlegm tending toward heat (12.0%)>yang deficiency (8.7%)>qi stagnation (0.8%), the results showed that blood stasis and qi deficiency are main syndrome elements of ACS patients. In the specific TCM syndromes, the proportion of combination of 2 syndrome elements blood stasis+qi deficiency was the highest, accounting for 32.0%, and the second is combination of 3 syndrome elements qi deficiency+yin deficiency+blood stasis, accounted for 11.6%, the two combinations accounted for 43.6% in 241 ACS patients. The proportion of combinations of syndrome elements which include root vacuity and tip repletion accounted for 86.4%, which demonstrated that the syndrome features of ACS patients are root vacuity and tip repletion and deficiency complicated with excess.
     3.1.1.2 The distribution of TCM syndrome elements in ACS high-risk patients
     241 ACS patients were evaluated by GRACE risk score, and 21 patients were high-risk,220 patients were low-risk and mediate-risk. Based on the results of GRACE risk score, the analytic results of MDR and Logistic regression analysis method demonstrated that the adverse outcomes of the patients with blood stasis, turbid phlegm tending toward cold and yang deficiency were 7.17 times as much as that of the patients without blood stasis, turbid phlegm tending toward cold and yang deficiency, so probability of all-cause death in the ACS patients with blood stasis, turbid phlegm tending toward cold and yang deficiency during six months were higher than that of the patients without blood stasis, turbid phlegm tending toward cold and yang deficiency.
     3.1.2 Prospective analytic results
     3.1.2.1 The natural dynamic changes of TCM syndrome elements and their combinations in ACS patients after PCI
     ACS patients in the control group were treated by western medicine standardized therapy method, blood stasis and turbid phlegm tending toward heat reduced significantly after PCI, qi deficiency and yang deficiency increased gradually, the proportion of qi deficiency and yang deficiency increased significantly at the 12th month, accounted for 63.8%, at the same time blood stasis decreased somewhat, but still accounted for a large proportion, which demonstrated that the feature of ACS patients in the later period after PCI was that deficiency syndrome is primary and repletion pattern is subordinate.
     The combinations of TCM syndrome elements before and after PCI also had a significant change, the main combinations of TCM syndrome elements before PCI was compound syndrome elements, the proportion of combination of 2 syndrome elements or more accounted for 86%. With the extension of revascularization time, the type of more combinations of syndrome elements turned to the type of less combinations of syndrome elements, the proportion of 1 syndrome element or less accounted for 54.2% at the 12th month, blood stasis and yang deficiency were main syndrome elements in the 1 syndrome element, which showed the feature of root deficiency syndrome.
     3.1.2.2 The dynamic changes of TCM syndrome elements and their combinations in ACS patients taking Chinese herbs after PCI
     On the basis of western medicine stantardized therapy, the proportion of the TCM syndrome elements blood stasis, qi deficiency, yin deficiency and yang deficiency in NQABC intervention group had different downward trends in four time points, particularly downward trends of blood stasis and yin deficiency were larger, the proportion of turbid phlegm tending toward heat also had a downward trend at the 3rd after enrolled into group, but had not significant downward trend at the 6th and the 12th. The proportion of turbid phlegm tending toward heat in the whole course of disease had not significant change, which demonstrated that the effect of Chinese herbs of NQABC on turbid phlegm is ineffective.
     About the combinations of TCM syndrome elements, both the combination of 2 syndrome elements and the combination of 3 syndrome elements reduced significantly at the 3rd month after enrolled into group, while 0 syndrome element and 1 syndrome element increased significantly at the 3rd month after enrolled into group. At 12th month, symptoms as well as tongue and pulse presentations in 49 patient were improved, accounted for 45.8% in NQABC intervention group, the 1 syndrome element and the combination of 2 syndrome elements accounted for 31.8% and 16.8% respectively, the combination of 3 syndrome elements and the combination of 4 syndrome elements were rare. These results demonstrated that the evolutional time from more combinations of syndrome elements to less combinations of syndrome elements in NQABC intervention group is shorter than that of control group, and the ACS patients taking Chinese herbs of NQABC has the trend to good prognosis.
     3.1.2.3 The comparison of TCM syndrome elements in NQABC intervention group and control group at different time points
     Each syndrome element between two groups was compared at the 3rd,6th,12th month. The results show that the proportions of blood stasis, qi deficiency and yang deficiency were lower significantly in the NQABC intervention group than that of control group at the 3rd,6th month, the difference had statistical significance (P<0.05, P<0.01), but the turbid phlegm between two groups had not different significantly. At the 12th month, the proportions of blood stasis and yang deficiency were lower significantly in the NQABC intervention group than that of control group, the difference had statistical significance (P<0.01), but qi deficiency between two groups had not different significantly, which related to the intervention time of NQABC Chinese herbs.
     In addition,16 cases in 241 ACS patients had cardiovascular events, and there were 12 cases in the control group and 4 cases in the NQABC intervention group, the result of chi square test showed that the difference between two groups has statistical significance (χ2=4.137, P<0.05).
     3.2 Animal experiment research
     3.2.1 The effects of Chinese herbs of NQABC combined with IPoC protecting rat myocardium with reperfusion injury.
     Compared with IPoC group, NQABC plus IPoC further reduced infarction size and release of myocardial enzyme CK-MB (P<0.01), the content of serum cTNT was also lower in the NQABC+IPoC group than that of IPoC group, but the difference between two groups had not statistical significance. The results of macropathology and transmission electron microscope observations in the NQABC+IPoC group showed that there were not significant intracellular edema, myocardial fiber arrangement was still regular, mitochondrial structure was integrity, no swelling and vacuolation, nucleus and nucleolus were normal, no obvious nucleus cavity-like degeneration and nuclear pycnosis phenomenon.
     3.2.2 The effects Chinese herbs of NQABC combined with IPoC on TLR2.4 and downstream pro-inflammatory cytokines of rat myocardium with reperfusion injury.
     Compared with IPoC group, NQABC plus IPoC further decreased the expression of TLR2,4 (P<0.01). At the same time, Chinese herbs of NQABC on the basis of IPoC could further decrease the contents of IL-1β, IL-6, TNF-αand MCP-1 in rat myocardium with IPoC (P<0.05,P<0.01).
     4 Conclusions
     4.1 Blood stasis and qi deficiency were main syndrome elements of ACS patients, qi deficiency and blood stasis was main syndrome performance, the feature of TCM syndrome elements combinations in ACS high-risk patients mainly manifested yang deficiency+blood stasis+turbid phlegm tending toward cold.
     4.2 Blood stasis and qi deficiency run through the whole course of disease of ACS during one year after PCI, the evolutional features of TCM syndrome elements of ACS after PCI were from excess to deficiency and from complex to simple.
     4.3 This study further validated that NQABC might be the main therapy method of ACS after PCI.
     4.4 The pretreatment with Chinese herbs of NQABC enhanced the protective effect of IPoC on rat myocardial I/R injury, and its mechanism might be related to the inhibition of TLRs expression and the expression of the downstream proinflammatory cytokines.
引文
[1]Writing group members, Lloyd-Jones D, Adams RJ, et al. Heart disease and stroke statistics--2010 update:a report from the American Heart Association. Circulation, 2010,121(7):e46-e215.
    [2]Singh M, Rihal CS, Gersh BJ, et al. Twenty-five-year trends in in-hospital and long-term outcome after percutaneous coronary intervention:a single-institution experience. Circulation,2007,115(22):2835-2841.
    [3]Guo SK, Chen KJ, Yu FR, et al. Treatment of Acute Myocardial Infarction with AMI-Mixture Combined with Western Medicine. Planta Med,1983,48(5):63-64.
    [4]Xuhao, Chen Keji, Shi Dazhuo, et al. Clinical study of Xiongshao capsule in preventing restenosis after coronary intervention treatment. Chinese journal of integrative medicine,2002,8(3):162-166.
    [5]全国冠心病辨证论治研究座谈会.冠心病心绞痛、心肌梗死中医辨证试行标准.中医杂志,1980,21(8):46.
    [6]中国中西医结合学会心血管学会.冠心病中医辨证标准.中西医结合杂志,1991,11(5):257.
    [7]郑筱萸.中药新药临床研究指导原则.北京:中国医药科技出版社,2002:69-70.
    [8]肖政.127例急性冠脉综合征的中医证候回顾研究.中华实用中西医杂志,2007,7(20):553-554.
    [9]马晓昌,尹太英,陈可冀,等.冠心病中医辨证分型与冠状动脉造影所见相关性比较研究.中国中西医结合杂志,2001,21(9):654-656.
    [10]魏丹霞,刘明,庞永诚,等.111例冠心病患者中医证型分布规律研究.云南中医中 药杂志,2008,29(7):7-8.
    [11]王玲,刘红旭,邹志东.北京地区中医医院急性心肌梗死住院病人中医证候特征研究.中西医结合心脑血管病杂志,2008,6(4):379-380.
    [12]农一兵,林谦,王薇,等.急性心肌梗死中医辨证论治现状的研究-基于北京288例患者的横断面调查.北京中医,2007,26(7):387-388.
    [13]陈力,肖政.急性冠脉综合征中医证候回顾研究.广州中医药大学学报,2008,25(3):248-250.
    [14]高铸烨,苗阳,雷燕,等.西苑医院中西医结合诊治急性心肌梗死的回顾分析.辽宁中医杂志,2006,33(7):769-771.
    [15]衷敬柏.178例急性冠脉综合征证候要素应证组合的回顾分析.北京中医药,2008,27(9):675-677.
    [16]黄汉超.温阳法治疗冠心病不稳定型心绞痛述评.中医研究,2006,19(1):53-55.
    [17]衷敬柏,王阶.178例急性冠脉综合征临床特点的调查分析.上海中医药大学学报,2005,19(4):16-17.
    [18]卢笑晖.论热毒在急性冠脉综合征发病中的作用.中国中医急症,2005,14(8):750-751.
    [19]肖政,陈力.黄春林教授治疗真心痛经验介绍.新中医,2007,39(9):16-17.
    [20]夏宝泉.温阳益肾法在急性冠脉综合征治疗中的运用初探.四川中医,2007,25(7):24-25.
    [21]陈全福,刘敏雯.急性冠脉综合征与中医“风”的关系.辽宁中医学院学报,2004,6(6):457.
    [22]王阶,邢雁伟,陈建新,等.1069例冠心病患者冠状动脉造影与中医证候特点.中西医结合学报,2008,6(2):148-152.
    [23]石磊,陈晓虎,李莲静,等.冠心病症状分析指导中医辨证分型客观化.现代中西医结合杂志,2008,17(31):4815-4816.
    [24]高铸烨,徐浩,史大卓,等.急性心肌梗死中医四诊信息的聚类分析.中华中医药学刊,2007,25(9):1855-1857.
    [25]王阶,何庆勇,李海霞,等.815例不稳定型心绞痛中医证候的因子分析.中西医结合学报,2008,6(8):788-791.
    [26]王阶,邢雁伟,陈建新,等.复杂系统熵聚堆方法对1069例冠心病心绞痛证候要素提取和应证组合规律研究.中国中医基础医学杂志,2008,14(3):211-213.
    [27]]丁邦晗,吕强,张敏州,等.胸痹心痛的中医危险证型-附375例聚类分析.中国中医急症,2004,13(5):298-300.
    [28]丁邦晗,刘涛,罗翌,等.胸痹心痛危险证型的回归分析.中国中医急症,2004,13(4):225-226.
    [29]洪永敦,黄衍寿,吴辉,等.冠心病中医证候与炎症因子关系的临床研究.广州中医药大学学报,2005,22(2):81-86.
    [30]洪永敦,张智琳,李小兵,等.急性冠脉综合征痰瘀证候若干炎症因子的临床研究.新中医,2007,39(7):18-20.
    [31]王强,张双旗.急性冠脉综合征中医证型与IL-18、 hs-CRP的相关性临床探讨.河南中医学院学报,2007,22(128):55-56.
    [32]缪灿铭,陈翊,麦美琪.急性冠脉综合征中医证型与冠脉病变及C反应蛋白相关性的临床探讨.光明中医,2009,24(8):1423-1424.
    [33]王剑,严灿,吴丽丽,等.“无形之痰”实质假想.中国中医基础医学杂志.1999,21(10):44-46.
    [34]王阶,何庆勇,施展,等.冠心病证候要素组合与心功能及血脂的相关性.中西医结合学报,2008,6(9):897-901.
    [35]张继东,崔红燕,傅善基.冠心病中医证型与血清高半胱氨酸水平关系的临床研究.山东中医药大学学报,2000,24(3):207.
    [36]严卉,胡晓晟,陈君柱,等.血浆同型半胱氨酸和冠状动脉粥样硬化严重程度与中医证型的关系.中国中西医结合杂志,2002,22(11):813.
    [37]张保亭,颜乾麟,颜德馨,等.急性冠状动脉综合征不同证候病变血管数、血管狭窄程度、Braunwald积分比较及相关性研究.中国中医急症,2005,14(2):147-149.
    [38]缪灿铭,陈翊,麦美琪.急性冠脉综合征中医证型与冠脉病变及C反应蛋白相关性的临床探讨.光明中医,2009,24(8):1423-1424.
    [39]史海波,陈晓虎.真心痛中医辨证分型与冠状动脉造影结果相关性研究.南京中医药大学学报,2009,25(3):174-175.
    [40]农一兵,林谦,王旭升,等.冠心病中医证候与冠状动脉造影的相关性研究.北京 中医,2006,25(12):707-708.
    [41]刘红旭,王振裕,彭伟,等.113例冠状动脉造影患者中医证候与造影特点分析.中日友好医院学报,2006,20(1):35-37.
    [42]张敏州,邹旭,李新梅,等.胸痹心痛证冠状动脉造影100例临床分析.浙江中西医结合杂志,2001,11(8):472-473.
    [43]薛增明,李长生,宁美芳,等.42例冠心病患者冠状动脉支架植入术前后中医证型的演变.山东中医杂志,2005,24(12):719-720.
    [44]丁邦晗,杨敏,周珂,等.胸痹心痛患者心电图改变与中医证型的关系.中国中西医结合急救杂志,2008,15(1):31-33.
    [45]丁邦晗,周珂,李俊,等.305例胸痹心痛患者超声心动图改变及其与中医证型的关系及其与中医证型的关系.中国中医药信息杂志,2008,15(1):19-21.
    [1]Writing group members, Lloyd-Jones D, Adams RJ, et al. Heart disease and stroke statistics--2010 update:a report from the American Heart Association. Circulation, 2010,121(7):e46-e215.
    [2]Kume T, Okura H, Yamada R, et al. Frequency and spatial distribution of thin-cap fibroatheroma assessed by 3-vessel intravascular ultrasound and optical coherence tomography:an ex vivo validation and an initial in vivo feasibility study. Circ J,2009, 73(6):1086-1091.
    [3]Libby P, Okamoto Y, Rocha VZ, et al. Inflammation in atherosclerosis:transition from theory to practice. Circ J,2010,74(2):213-220.
    [4]Monaco C, Andreakos E, Kiriakidis S, et al. T cell-mediated signalling in immune, inflammatory and angiogenic processes:the cascade of events leading to inflammatory diseases. Curr Drug Targets Inflamm Allergy,2004,3(1):35-42.
    [5]Van der Wal AC, Becker AE, van der Loos CM, et al. Site of intimal rupture or erosion of thrombosed coronary atherosclerotic plaques is characterized by an inflammatory process irrespective of the dominant plaque morphology. Circulation, 1994,89(1):36-44.
    [6]Meuwissen M, van der Wal AC, Koch KT, et al. Association between complex coronary artery stenosis and unstable angina and the extent of plaque inflammation. Am J Med,2003,114(7):521-527.
    [7]Hosono M, de Boer OJ, van der Wal AC, et al. Increased expression of T cell activation markers (CD25, CD26, CD40L and CD69) in atherectomy specimens of patients with unstable angina and acute myocardial infarction. Atherosclerosis,2003, 168(1):73-80.
    [8]Paulsson G, Zhou X, Tornquist E, et al. Oligoclonal T cell expansions in atherosclerotic lesions of apolipoprotein E-deficient mice. Arterioscler Thromb Vasc Biol,2000,20(1):10-17.
    [9]Hansson GK, Libby P, Schonbeck U,et al. Innate and adaptive immunity in the pathogenesis of atherosclerosis. Circ Res,2002,91(4):281-291.
    [10]Hansson GK. Inflammation, atherosclerosis, and coronary artery disease. N Engl J Med,2005,352(16):1685-1695.
    [11]Veillard NR, Kwak B, Pelli G, et al. Antagonism of RANTES receptors reduces atherosclerotic plaque formation in mice. Circ Res,2004,94(2):253-261.
    [12]Lutters BC, Leeuwenburgh MA, Appeldoorn CC, et al. Blocking endothelial adhesion molecules:a potential therapeutic strategy to combat atherogenesis. Curr Opin Lipidol,2004,15(5):545-52.
    [13]Mestas J, Ley K. Monocyte-endothelial cell interactions in the development of atherosclerosis. Trends Cardiovasc Med,2008,18(6):228-232.
    [14]Peiser L, Mukhopadhyay S, Gordon S. Scavenger receptors in innate immunity. Curr Opin Immunol,2002,14(1):123-128.
    [15]Silverstein RL. Inflammation, atherosclerosis, and arterial thrombosis:role of the scavenger receptor CD36. Cleve Clin J Med.2009,76(Suppl 2):S27-S30.
    [16]Febbraio M, Podrez EA, Smith JD, et al. Targeted disruption of the Class B scavenger receptor, CD36, protects against atherosclerotic lesion development in mice. J Clin Invest,2000,105(8):1049-1056.
    [17]Xu Q. Role of heat shock proteins in atherosclerosis. Arterioscler Thromb Vasc Biol,2002,22(10):1547-1559.
    [18]Miller YI, Chang MK, Binder CJ, et al. Oxidized low density lipoprotein and innate immune receptors. Curr Opin Lipidol,2003,14(5):437-445.
    [19]Edfeldt K, Swedenborg J, Hansson GK, et al. Expression of toll-like receptors in human atherosclerotic lesions:a possible pathway for plaque activation. Circulation, 2002,105(10):1158-1161.
    [20]Bjorkbacka H, Kunjathoor VV, Moore KJ, et al. Reduced atherosclerosis in MyD88-null mice links elevated serum cholesterol levels to activation of innate immunity signaling pathways. Nat Med,2004,10(4):416-421.
    [21]Stemme S, Faber B, Holm J, et al. T lymphocytes from human atherosclerotic plaques recognize oxidized low density lipoprotein. Proc Natl Acad Sci U S A,1995, 92(9):3893-3897.
    [22]van der Wal AC, Houtkamp MA, Ossewaarde JM, et al. Unstable atherosclerotic plaques contain T-cells that respond to Chlamydia pneumoniae. Cardiovasc Res,2000, 48(3):402-408.
    [23]Szabo SJ, Sullivan BM, Peng SL, et al. Molecular mechanisms regulating Thl immune responses. Annu Rev Immunol,2003,21:713-758.
    [24]Frostegard J, Ulfgren AK, Nyberg P, et al. Cytokine expression in advanced human atherosclerotic plaques:dominance of proinflammatory (Thl) and macrophage-stimulating cytokines. Atherosclerosis,1999,145(1):33-43.
    [25]Ovchinnikova O, Robertson AK, Wagsater D, et al. T-cell activation leads to reduced collagen maturation in atherosclerotic plaques of Apoe(-/-) mice. Am J Pathol, 2009,174(2):693-700.
    [26]Whitman SC, Ravisankar P, Daugherty A. IFN-gamma deficiency exerts genderspecific effects on atherogenesis in apolipoprotein E-/- mice. J Interferon Cytokine Res,2002,22(6):661-670.
    [27]Laurat E, Poirier B, Tupin E, et al. In vivo downregulation of T helper cell 1 immune responses reduces atherogenesis in apolipoprotein E-knockout mice. Circulation,2001,104(2):197-202.
    [28]Binder CJ, Hartvigsen K, Chang MK, et al. IL-5 links adaptive and natural immunity specific for epitopes of oxidized LDL and protects from atherosclerosis. J Clin Invest,2004,114(3):427-37.
    [29]Shimizu K, Shichiri M, Libby P, et al. Th2-predominant inflammation and blockade of IFN-gamma signaling induce aneurysms in allografted aortas. J Clin Invest,2004,114(2):300-308.
    [30]Tupin E, Nicoletti A, Elhage R, et al. CD1d-dependent activation of NKT cells aggravates atherosclerosis. J Exp Med,2004,199(3):417-422.
    [31]Hansson GK. Inflammatory mechanisms in atherosclerosis. J Thromb Haemost, 2009,7(Suppl 1):328-331.
    [32]Ludewig B, Freigang S, Jaggi M, et al. Linking immune-mediated arterial inflammation and cholesterol-induced atherosclerosis in a transgenic mouse model. Proc Natl Acad Sci U S A,2000,97(23):12752-12757.
    [33]van Wanrooij EJ, de Jager SC, van Es T, et al. CXCR3 antagonist NBI-74330 attenuates atherosclerotic plaque formation in LDL receptor-deficient mice. Arterioscler Thromb Vasc Biol,2008,28(2):251-257.
    [34]Mach F, Schoenbeck U, Bonnefoy JY, et al. Activation of monocyte/macrophage functions related to acute atheroma complication by ligation of CD40:Induction of collagenase, stromelysin,and tissue factor. Circulation,1997,96(2):396-399.
    [35]Yilmaz A, Lochno M, Traeg F et al. Emergence of dendritic cells in rupture-prone regions of vulnerable carotid plaques. Atherosclerosis,2004,176(1): 101-110.
    [36]Yilmaz A, Weber J, Cicha I, et al. Decrease in circulating myeloid dendritic cell precursors in coronary artery disease. J Am Coll Cardiol,2006,48(1):70-80.
    [37]Ranjit S, Dazhu L, Qiutang Z, et al. Differentiation of dendritic cells in monocyte cultures isolated from patients with unstable angina. Int J Cardiol,2004,97(3): 551-555.
    [38]Trinchieri G. Interleukin-12 and the regulation of innate resistance and adaptive immunity. Nat Rev,2003,3(2):133-146.
    [39]Hoshino K, Kaisho T, Iwabe T, et al. Differential involvement of IFN-beta in Toll-like receptor-stimulated dendritic cell activation. Int Immunol,2002,14(10): 1225-1231.
    [40]Zhang D, Zhang G, Hayden MS, et al. A toll-like receptor that prevents infection by uropathogenic bacteria. Science,2004,303(5663):1522-2526.
    [41]Akira S, Takeda K, Kaisho T. Toll-like receptors:critical proteins linking innate and acquired immunity. Nat Immunol,2001,2(8):675-680.
    [42]Vitseva OI, Tanriverdi K, Tchkonia TT, et al. Inducible Toll-like receptor and NF-kappaB regulatory pathway expression in human adipose tissue. Obesity(Silver Spring),2008,16(5):932-937.
    [43]Liu Y, Yu H, Zhang Y, et al. TLRs are important inflammatory factors in atherosclerosis and may be a therapeutic target. Med Hypotheses,2008,70(2): 314-316.
    [44]Castrillo A, Joseph SB, Vaidya SA, et al. Crosstalk between LXR and toll-like receptor signaling mediates bacterial and viral antagonism of cholesterol metabolism. Mol Cell,2003,12(4):805-816.
    [45]Michelsen KS, Wong MH, Shah PK, et al. Lack of Toll-like receptor 4 or myeloid differentiation factor 88 reduces atherosclerosis and alters plaque phenotype in mice deficient in apolipoprotein E. Proc Natl Acad Sci U S A,2004,101(29): 10679-10684.
    [46]Bjorkbacka H, Kunjathoor VV, Moore KJ, et al. Reduced atherosclerosis in MyD88-null mice links elevated serum cholesterol levels to activation of innate immunity signaling pathways. Nat Med,2004,10(4):416-421.
    [47]Wang L, Li D, Yang K, et al. Toll-like receptor-4 and mitogen-activated protein kinase signal system are involved in activation of dendritic cells in patients with acute coronary syndrome. Immunology,2008,125(1):122-130.
    [48]Shiraki R, Inoue N, Kobayashi S, et al. Toll-like receptor 4 expressions on peripheral blood monocytes were enhanced in coronary artery disease even in patients with low C-reactive protein. Life Sci,2006,80(1):59-66.
    [49]Fukushima R, Soejima H, Fukunaga T, et al. Expression levels of Toll-like receptor genes in coronary atherosclerotic lesions of patients with acute coronary syndrome or stable angina pectoris. Circ J,2009,73(8):1479-1484.
    [50]Rattazzi M, Puato M, Faggin E, et al. C-reactive protein and interleukin-6 in vascular disease:culprits or passive bystanders? J Hypertens,2003,21(10): 1787-1803.
    [51]Huber SA, Sakkinen P, Conze D, et al. Interleukin-6 exacerbates early atherosclerosis in mice. Arterioscler Thromb Vasc Biol,1999,19(10):2364-2367.
    [52]Kerr R, Stirling D, Ludlam CA. Interleukin 6 and haemostasis. Br J Haematol, 2001,115(1):3-12.
    [53]Rus HG, Vlaicu R, Niculescu F. Interleukin-6 and interleukin-8 protein and gene expression in human arterial atherosclerotic wall. Atherosclerosis,1996,127(2): 263-271.
    [54]Schieffer B, Schieffer E, Hilfiker-Kleiner D, et al. Expression of angiotensin II and interleukin 6 in human coronary atherosclerotic plaques:potential implications for inflammation and plaque instability. Circulation,2000,101(12):1372-1378.
    [55]Schieffer B, Selle T, Hilfiker A, et al. Impact of interleukin-6 on plaque development and morphology in experimental atherosclerosis. Circulation,2004, 110(22):3493-3500.
    [56]Maier W, Altwegg LA, Corti R, et al. Inflammatory markers at the site of ruptured plaque in acute myocardial infarction:locally increased interleukin-6 and serum amyloid A but decreased C-reactive protein. Circulation,2005,111(11): 1355-1361.
    [57]Biasucci LM, Liuzzo G, Fantuzzi G, et al. Increasing levels of interleukin (IL)-1Ra and IL-6 during the first 2 days of hospitalization in unstable angina are associated with increased risk of in-hospital coronary events. Circulation,1999, 99(16):2079-2084.
    [58]Ridker PM, Rifai N, Stampfer MJ, et al. Plasma concentration of interleukin-6 and the risk of future myocardial infarction among apparently healthy men. Circulation,2000,101(15):1767-1772.
    [59]Tan J, Hua Q, Gao J, et al. Clinical implications of elevated serum interleukin-6, soluble CD40 ligand, metalloproteinase-9, and tissue inhibitor of metalloproteinase-1 in patients with acute ST-segment elevation myocardial infarction. Clin Cardiol,2008, 31(9):413-418.
    [60]Jones CB, Sane DC, Herrington DM. Matrix metalloproteinases:a review of their structure and role in acute coronary syndrome. Cardiovasc Res,2003,59(4):812-823.
    [61]Galis ZS, Sukhova GK, Lark MW, et al. Increased expression of matrix metalloproteinases and matrix degrading activity in vulnerable regions of human atherosclerotic plaques. J Clin Invest,1994,94(6):2493-2503.
    [62]Inokubo Y, Hanada H, Ishizaka H, et al. Plasma levels of matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 are increased in the coronary circulation in patients with acute coronary syndrome. Am Heart J,2001, 141(2):211-217.
    [63]Eckart RE, Uyehara CF, Shry EA, et al. Matrix metalloproteinases in patients with myocardial infarction and percutaneous revascularization. J Interv Cardiol,2004, 17(1):27-31.
    [64]Blankenberg S, Rupprecht HJ, Poirier O, et al. AtheroGene Investigators. Plasma concentrations and genetic variation of matrix metalloproteinase 9 and prognosis of patients with cardiovascular disease. Circulation,2003,107(12):1579-1585.
    [65]Konstantino Y, Nguyen TT, Wolk R, et al. Potential implications of matrix metalloproteinase-9 in assessment and treatment of coronary artery disease. Biomarkers,2009,14(2):118-129.
    [66]Dhillon OS, Khan SQ, Narayan HK, et al. Matrix metalloproteinase-2 predicts mortality in patients with acute coronary syndrome. Clin Sci (Lond),2009,118(4): 249-257.
    [67]Celik T, Iyisoy A, Kardesoglu E, et al. Matrix metalloproteinases in acute coronary syndromes:a new therapeutic target? Int J Cardiol,2009,134(3):402-404.
    [68]Nelken NA, Coughlin SR, Gordon D, et al. Monocyte chemoattractant protein-1 in human atheromatous plaques. J Clin Invest,1991,88(4):1121-1127.
    [69]Cushing SD, Berliner JA, Valente AJ, et al. Minimally modified low density lipoprotein induces monocyte chemotactic protein 1 in human endothelial cells and smooth muscle cells. Proc Natl Acad Sci U S A,1990,87(13):5134-5138.
    [70]. Gu L, Okada Y, Clinton SK, et al. Absence of monocyte chemoattractant protein-1 reduces atherosclerosis in low density lipoprotein receptor-deficient mice. Mol Cell,1998,2(2):275-281.
    [71]Dawson TC, Kuziel WA, Osahar TA, et al. Absence of CC chemokine receptor-2 reduces atherosclerosis in apolipoprotein E-deficient mice. Atherosclerosis,1999, 143(1):205-211.
    [72]Ni W, Egashira K, Kitamoto S, et al. New anti-monocyte chemoattractant protein-1 gene therapy attenuates atherosclerosis in apolipoprotein E-knockout mice. Circulation,2001,103(16):2096-2101.
    [73]Robinson SC, Scott KA, Balkwill FR. Chemokine stimulation of monocyte matrix metalloproteinase-9 requires endogenous TNF-alpha. Eur J Immunol,2002, 32(2):404-412.
    [74]Lutgens E, Faber B, Schapira K, et al. Gene profiling in atherosclerosis reveals a key role for small inducible cytokines:validation using a novel monocyte chemoattractant protein monoclonal antibody. Circulation,2005,111(25):3443-3452.
    [75]Inoue S, Egashira K, Ni W, et al. Anti-monocyte chemoattractant protein-1 gene therapy limits progression and destabilization of established atherosclerosis in apolipoprotein E-knockout mice. Circulation,2002,106(21):2700-2706.
    [76]Nishiyama K, Ogawa H, Yasue H, et al. Simultaneous elevation of the levels of circulating monocyte chemoattractant protein-1 and tissue factor in acute coronary syndromes. Jpn Circ J,1998,62(9):710-712.
    [77]Aukrust P, Berge RK, Ueland T, et al. Interaction between chemokines and oxidative stress:possible pathogenic role in acute coronary syndromes. J Am Coll Cardiol,2001,37(2):485-491.
    [78]Kervinen H, Manttari M, Kaartinen M, et al. Prognostic usefulness of plasma monocyte/macrophage and T-lymphocyte activation markers in patients with acute coronary syndromes. Am J Cardiol,2004,94(8):993-996.
    [79]de Lemos JA, Morrow DA, Blazing MA, et al. Serial measurement of monocyte chemoattractant protein-1 after acute coronary syndromes:results from the A to Z trial. J Am Coll Cardiol,2007,50(22):2117-2124.
    [80]Aukrust P, Halvorsen B, Yndestad A, et al. Chemokines and Cardiovascular Risk. Arterioscler Thromb Vase Biol,2008,28(11):1909-1919.
    [81]Aukrust P, Yndestad A, Smith C, et al. Chemokines in cardiovascular risk prediction. Thromb Haemost,2007,97(5):748-754.
    [82]Gonzalez-Quesada C, Frangogiannis NG Monocyte chemoattractant protein-1/CCL2 as a biomarker in acute coronary syndromes. Curr Atheroscler Rep, 2009,11(2):131-138.
    [83]Schonbeck U, Libby P. CD40 signaling and plaque instability. Circ Res,2001, 89(12):1092-1103.
    [84]Schonbeck U, Gerdes N, Varo N, et al. Oxidized low-density lipoprotein augments and 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors limit
    CD40 and CD40L expression in human vascular cells. Circulation,2002,106(23): 2888-2893.
    [85]Schonbeck U, Sukhova GK, Shimizu K, et al. Inhibition of CD40 signaling limits evolution of established atherosclerosis in mice. Proc Natl Acad Sci U S A,2000, 97(13):7458-7463.
    [86]Aukmst P, Muller F, Ueland T, et al. Enhan ced levels of soluble and membrane-bound CD40 ligand in patients with unstable angina:possible reflection of T lymphocyte and platelet involvement in the pathogenesis of acute coronary syndromes. Circulation,1999,100(6):614-620.
    [87]Blake GJ, Ostfeld RJ, Yucel EK, et al. Soluble CD40 ligand levels indicate lipid accumulation in carotid atheroma:an in vivo study with high-resolution MRI. Arterioscler Thromb Vasc Biol,2003,23(1):ell-e14.
    [88]Fouad HH, Al-Dera H, Bakhoum SW, et al. Levels of sCD40 Ligand in Chronic and Acute Coronary Syndromes and its Relation to Angiographic Extent of Coronary Arterial Narrowing. Angiology.2010 Mar 19. [Epub ahead of print].
    [89]Heeschen C, Dimmeler S, Hamm CW, et al. Soluble CD40 ligand in acute coronary syndromes. N Engl J Med,2003,348(12):1104-1111.
    [90]Nerea V, James A, Lemos D, et al. Soluble CD40L risk prediction after acute coronary syndromes. Circulation,2003,108(9):1049-1053.
    [1]中华医学会心血管病学分会.不稳定性心绞痛和非ST段抬高心肌梗死诊断与治疗指南.中华心血管病杂志,2007,35(4):295-304.
    [2]Armstrong, EricR.Bates, LeeA.Green, et al.2007 Focused Update of the ACC/AHA 2004 Guidelines for the Management of Patients With ST-Elevation Myocardial Infaretion. JACC,2008,51(2):210-247.
    [3]Eagle KA, Lim MJ, Dabbous OH, et al. A validated prediction model for all forms of acute coronary syndrome:estimating the risk of 6-month postdischarge death in an international registry.JAMA,2004,291(22):2727-2733.
    [4]Fox KA, Dabbous OH, Goldberg RJ, et al. Prediction of risk of death and myocardial infarction in the six months after presentation with acute coronary syndrome:prospective multinational observational study (GRACE). BMJ,2006, 333(7578):1091-1097.
    [5]Ferreira-Gonzalez I, Permanyer-Miralda G, Heras M, et al. Patterns of use and effectiveness of early invasive strategy in non-ST-segment elevation acute coronary syndromes:an assessment by propensity score. Am Heart J,2008,156(5):946-953.
    [6]Elbarouni B, Goodman SG, Yan RT, et al. Validation of the Global Registry of Acute Coronary Event (GRACE) risk score for in-hospital mortality in patients with acute coronary syndrome in Canada. Am Heart J,2009,158(3):392-399.
    [7]中国中西医结合学会心血管病学会.冠心病中医诊断标准.中西医结合杂志,1991,11(5):257.
    [8]Singh M, Rihal CS, Gersh BJ, et al. Twenty-five-year trends in in-hospital and long-term outcome after percutaneous coronary intervention:a single-institution experience. Circulation,2007,115(22):2835-2841.
    [9]金明娟,刘冰,张爽爽,等.多因子降维法在人群散发性结直肠癌交互作用分析中的应用.中华流行病学杂志,2008,29(6):535-539.
    [10]李佳圆,龙启明,陶萍,等.基于多因子降维法模型的代谢酶易感基因多态性与乳腺癌患病风险的交互作用研究.四川大学学报(医学版),2008,39(5):780-783.
    [11]Braunwald E, Antman EM, Beasley JW, et al. ACC/AHA guideline update for the management of patients with unstable angina and non-ST-segment myocardial infarction:a report of the American College of Cardiology/American heart Association Task Force on practice Guidelines (Committee on the Management of Patients with Unstable Angina). J Am Coll Cardio,2002,40(7):1366-1374.
    [12]Yagi H, Komukai K, Hashimoto K, et al. Difference in risk factors between acute coronary syndrome and stable angina pectoris in the Japanese:Smoking as a crucial risk factor of acute coronary syndrome. J Cardiol.2010, [Epub ahead of print]
    [13]王玲,刘红旭,邹志东.北京地区中医医院急性心肌梗死住院病人中医证候特征研究.中西医结合心脑血管病杂志,2008,6(4):379-380.
    [14]Timoteo AT, Toste A, Ramos R, et al. Does admission NT-proBNP increase the prognostic accuracy of GRACE risk score in the prediction of short-term mortality after acute coronary syndromes? Acute Card Care,2009,11(4):236-242.
    [15]Correia LC, Rocha MS, Bittencourt AP, et al. Does acute hyperglycemia add prognostic value to the GRACE score in individuals with non-ST elevation acute coronary syndromes? Clin Chim Acta,2009,410(1-2):74-78.
    [16]Jedrzkiewicz S, Goodman SG, Yan RT, et al. Temporal trends in the use of invasive cardiac procedures for non-ST segment elevation acute coronary syndromes according to initial risk stratification. Can J Cardiol,2009,25(11):e370-e376.
    [17]Nallamothu B, Fox KA, Kennelly BM, et al. Relationship of treatment delays and mortality in patients undergoing fibrinolysis and primary percutaneous coronary intervention. The Global Registry of Acute Coronary Events. Heart,2007,93(12): 1552-1555.
    [18]Ritchie MD, Hahn LW. Roodi N, et al. Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. Am J Hum Genet,2001,69(1):138-147.
    [19]Coffey CS, Hebert PR, Ritchie MD, et al. An application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene interactions on risk of myocardial infarction:the importance of model validation. BMC Bioinformatics,2004,5:49-58.
    [20]Williams SM, Ritchie MD, Phillips JA 3rd, et al. Multilocus analysis of hypertension:a hierarchical approach. Hum Hered,2004,57(1):28-38.
    [21]Agirbasli D, Agirbasli M, Williams SM, et al. Interaction among 5,10 methylenetetrahydrofolate reductase, plasminogen activator inhibitor and endothelial nitric oxide synthase gene polymorphisms predicts the severity of coronary artery disease in Turkish patients. Coron Artery Dis,2006,17(5):413-417.
    [22]Hsieh CH, Liang KH, Hung YJ, et al. Analysis of epistasis for diabetic nephropathy among type 2 diabetic patients. Hum Mol Genet,2006,15(18): 2701-2708.
    [23]Oestergaard MZ, Tyrer J, Cebrian A, et al. Interactions between genes involved in the antioxidant defence system and breast cancer risk. Br J Cancer,2006,95(4): 525-531.
    [24]骆常好,刘桂芬,张爱莲.多因子降维法和Logistic回归交互效应分析对比研究.中国药物与临床,2008,8(10):777-779.
    [1]Guo SK, Chen KJ, Yu FR, et al. Treatment of Acute Myocardial Infarction with AMI-Mixture Combined with Western Medicine. Planta Med,1983,48(5):63-64.
    [2]侯霄雷,李白翎,赵雷,等.血府逐瘀胶囊对急性心肌梗死再灌注后心肌及内皮素-1、一氧化氮/一氧化氮合酶体系影响的实验研究.中西医结合学报,2008,6(4):381-386.
    [3]贺运河,古继红,陈光贤,等.益气活血法对大鼠心肌缺血再灌注损伤保护作用的实验研究.中西医结合心脑血管病杂志.2007;5(8):707-708.
    [4]Zhao ZQ, Corvera JS, Halkos ME, et al. Inhibition of myocardial injury by ischemic postconditioning during reperfusion:comparison with ischemic preconditioning. Am J Physiol Heart Circ Physiol,2003,285(2):H579-H588.
    [5]Thibault H, Piot C, Staat P, et al. Long-Term Benefit of Postconditioning. Circulation,2008,117(8):1037-1044.
    [6]Laskey WK, Yoon S, Calzada N, et al. Concordant improvements in coronary flow reserve and ST-segment resolution during percutaneous coronary intervention for acute myocardial infarction:a benefit of postconditioning. Catheter Cardiovasc Interv,2008,72(2):212-220.
    [7]Zatta AJ, Kin H, Lee Q et al. Vinten-Johansen J. Infarct-sparing effect of myocardial postconditioning is dependent on protein kinase C signalling. Cardiovasc Res,2006,70(2):315-324.
    [8]梁日欣,黄璐琦,刘菊福,等.药对川芎和赤芍对高脂血症大鼠降脂、抗氧化及血管内皮功能的实验观察.中国实验方剂学杂志,2002,8(1):43-45.
    [9]李立志,刘剑刚,马鲁波,等.芍芍胶囊对兔动脉粥样硬化模型脂质代谢及血小板聚集的影响.中国中西医结合杂志,2008,28(12):1100-1103.
    [10]阮金兰,赵钟祥,曾庆忠,等.赤芍化学成分和药理作用的研究进展.中国药理学通报,2003,19(9):965-970.
    [11]CHEN Ke-ji, SHI Da-zhuo, XU Hao, et al. XS0601 reduces the incidence of restenosis:a Prospective study of 335 Patients undergoing Percutaneous coronary intervention in China. Chinese Medical Journal,2006,119(1):6-13.
    [12]丁涛,徐惠波,孙晓波,等.西洋参茎叶总皂苷对心肌缺血的保护作用.中药药理与临床,2002,18(4):14-16.
    [13]王承龙,史大卓,殷惠军,等.西洋参茎叶总皂苷对急性心肌梗死大鼠心肌VEGF、 bFGF表达及血管新生的影响.中国中西医结合杂志,2007,27(4):331-334.
    [14]王承龙,缪宇,殷惠军,等.西洋参茎叶总皂苷对急性心肌梗死大鼠心肌能量代谢的影响.中华老年心脑血管病杂志,2005,7(5):341-343.
    [15]王承龙,殷惠军,史大卓,等.西洋参茎叶皂苷心血管药理研究概述.中药新药与临床药理,2006,17(1):76-78.
    [16]Ozer MK, Sahna E, Birincioglu M, et al. Effects of captopril and losartan on myocardial ischemia-reperfusion induced arrhythmias and necrosis in rats. Pharmacol Res,2002,45(4):257-263.
    [17]Dogan R, Farsak B, Isbir S, et al. Protective effect of lisinopril against ischemia-reperfusion injury in isolated guinea pig hearts. Cardiovasc Surg (Torino), 2001,42(1):43-48.
    [18]Li K, Chen X. Protective effects of captopril and enalapril on myocardial ischemia and reperfusion damage of rat. J Mol Cell Cardiol,1987,19(9):909-915.
    [19]Dogan R, Farsak B, Isbir S, et al. Protective effect of lisinopril against ischemia-reperfusion injury in isolated guinea pig hearts. Cardiovasc Surg (Torino), 2001,42(1):43-48.
    [20]Li K, Chen X. Protective effects of captopril and enalapril on myocardial ischemia and reperfusion damage of rat. J Mol Cell Cardiol,1987,19(9):909-915.
    [21]Wang LX, Ideishi M, Yahiro E, et al. Mechanism of the cardioprotective effect of inhibition of the renin-angiotensin system on ischemia/reperfusion-induced myocardial injury. Hypertens Res,2001,24(2):179-187.
    [22]Sun HY, Wang NP, Kerendi F, et al. Hypoxic postconditioning reduces cardiomyocyte loss by inhibiting ROS generation and intracellular Ca2+ overload. Am J Physiol,2005,288:H1900-H1908.
    [23]Dow J, Bhandari A, Kloner RA. The mechanism by which ischemic postconditioning reduces reperfusion arrhythmias in rats remains elusive. J Cardiovasc Pharmacol Ther,2009,14(2):99-103.
    [24]Brener SJ, Ellis SG, Schneider J, et al. Frequency and long-term impact of myonecrosis after coronary stenting. Eur Heart J,2002,23(11):869-876.
    [25]Kazmi KA, Iqbal SP, Bakr A, et al. Admission creatine kinase as a prognostic marker in acute myocardial infarction. J Pak Med Assoc,2009,59(12):819-822.
    [26]Miller WL, Garratt KN, Burritt MF, et al. Baseline troponin level:key to understanding the importance of post-PCI troponin elevations. Eur Heart J,2006, 27(9):1061-1069.
    [27]Setiadi BM, Lei H, Chang J. Troponin not just a simple cardiac marker: prognostic significance of cardiac troponin. Chin Med J (Engl),2009,122(3): 351-358.
    [28]Eagle KA, Lim MJ, Dabbous OH, et al. A validated prediction model for all forms of acute coronary syndrome:estimating the risk of 6-month postdischarge death in an international registry. JAMA,2004,291(22):2727-2733.
    [29]Boyd JH, Mathur S, Wang Y, et al. Toll-like receptor stimulation in cardiomyoctes decreases contractility and initiates an NF-kappaB dependent inflammatory response. Cardiovasc Res,2006,72(3):384-393.
    [30]Yang J, Yang J, Ding JW, et al. Sequential expression of TLR4 and its effects on the myocardium of rats with myocardial ischemia-reperfusion injury. Inflammation, 2008,31(5):304-312.
    [31]Shimamoto A, Chong AJ, Yada M, et al. Inhibition of Toll-like receptor 4 with eritoran attenuates myocardial ischemia-reperfusion injury. Circulation,2006,114(1): 1270-1274.
    [32]Oyama J, Blais C Jr, Liu X, et al. Reduced myocardial ischemia-reperfusion injury in toll-like receptor 4-deficient mice. Circulation,2004,109(6):784-789.
    [33]Riad A, Jager S, Sobirey M, et al. Toll-like receptor-4 modulates survival by induction of left ventricular remodeling after myocardial infarction in mice. J Immunol,2008,180(10):6954-6961.
    [34]Sakata Y, Dong JW, Vallejo JG, et al. Toll-like receptor 2 modulates left ventricular function following ischemia-reperfusion injury. Am J Physiol Heart Circ Physiol,2007,292(1):H503-H509.
    [35]Chamorro A. Role of inflammation in stroke and atherothrombosis. Cerebrovasc Dis 2004,17(Suppl3):1-5.
    [36]Frangogiannis NG. Chemokines in ischemia and reperfusion. Thromb Haemost, 2007,97(5):738-747.
    [37]李拥军,丁文惠,高炜,等.白介素-1受体拮抗剂对缺血再灌注心肌的保护作用及其机制探讨.中华医学杂志,2004,84(7):546-553.
    [38]Herskowitz A, Choi S, Ansari AA, et al. Cytokine mRNA expression in postischemic/reperfused myocardium. Am J Pahtol,1995,146(2):419-428.
    [39]Yoshimoto T. The expression of ICAM-1 and Cytokines in the reperfusional state. Hokkaido Igakuzasshi,1997,72(1):137-140.
    [40]Frangogiannis N G. The immune system and cardiac repair [J]. Pharmacol Res, 2008,58(2):88-111.
    [41]Dewald O, Ren G, Duerr GD, et al. Of mice and dogs:species-specific differences in the inflammatory response following myocardial infarction. Am J Pathol,2004,164(2):665-677.
    [42]Finkel MS, Oddis CV, Jacob TD, et al. Negative inotropic effects of cytokines on the heart mediated by nitric oxide. Science,1992,257(5068):387-389.
    [43]Engel D, Peshock R, Armstong RC, et al. Cardiac myocyte apoptosis provokes adverse cardiac remodeling in transgenic mice with targeted TNF overexpression. Am J Physiol Heart Circ Physiol,2004,287:H1303-H1311.
    [44]Hayasaki T, Kaikita K, Okuma T, et al. CC chemokine receptor-2 deficiency attenuates oxidative stress and infarct size caused by myocardial ischemia-reperfusion in mice. Circ J,2006,70(3):342-351.
    [45]Kajihara N, Morita S, Nishida T, et al. Transfection with a dominant-negative inhibitor of monocyte chemoattractant protein-1 gene improves cardiac function after 6 hours of cold preservation. Circulation,2003,108(Suppl 1):Ⅱ213-Ⅱ218.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700