高甘油三酯腰围表型冠心病患者冠状动脉病变特点及其危险因素的相关性研究
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摘要
目的:
     通过对高甘油三脂腰围表型(HTWP)的冠心病(CHD)患者冠脉病变积分(CAS)及其与CHD危险因素的相关性分析,探讨HTWP的CHD患者临床特征。
     方法:
     经选择性冠状动脉造影术确诊的CHD患者198人,其中男性151人,女性47人,年龄32~85岁(平均57.34±10.56岁)。所有患者均于入院3日内完成生化指标、炎症指标及体质指标等的采集,并计算体质指数(BMI)和腰围甘油三酯乘积指数(WTindex);计算CAS。根据患者是否同时存在腰围(WC)>90cm(男性)、85cm(女性)和血清甘油三酯水平(TG)≥1.7mmol/L将患者分为HTWP表型者(A组)共126例和非HTWP者(B组)共72例。对两组患者的相关指标进行对比分析,并对所有患者的CAS及各危险因素指标进行相关回归分析。
     结果:
     1、A组CAS显著高于B组(P<0.01)。
     2、与B组比较,A组患者的总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C),人纤维酶原激活物抑制物-1(PAI-1)、白细胞介素-6(IL-6)、收缩压(SBP)、舒张压(DBP)、 BMI、空腹血糖(FPG)、游离脂肪酸(FFA)、纤维蛋白原(Fib)、肿瘤坏死因子-a(TNF-a)和高敏C反应蛋白(hsCRP)的水平显著增高(P<0.05),而脂联素(APN)、高密度脂蛋白胆固醇(HDL-C)的水平明显降低(P<0.01)。
     3、所有入选的CHD患者的CAS与各危险因素相关及多元线性回归分析显示: CAS与WTindex、 hsCRP、 PAI-1、 TC呈显著正相关,与HDL-C、 APN呈显著负相关。
     4、 WTindex与FFA、 SBP呈显著正相关。
     结论:
     1、合并HTWP的CHD患者多个危险因素水平(如CAS、TC、 LDL-C、 PAI-1、 IL-6、 SBP、 DBP、 BMI、 FPG、 Fib、 TNF-α、 hsCRP和FFA等)均显著高于非HTWP的CHD患者,同时前者冠脉病变程度较后者严重。
     2、综合反映腹型肥胖和TG升高的新指标WTindex与冠状动脉病变的严重程度及部分CHD传统危险因素关系密切,因此WTindex可能是判断CHD风险的一个有用的指标,同时也可能成为CHD危险人群早期干预的靶点。
Objective:To investigate the relationship of abdominal obesity and coronary heart disease (CHD) by analyzing the hypertriglyceridemic waist phenotype, the risk factors of coronary heart disease and the conclusion of coronary angiography.
     Methods:We collected198CHD patients(male151and female47), aged from thirty two to eighty-five (mean age57.34-10.56years) in the hospital with suspected coronary heart disease during August2010to December2011. All patients'total cholesterol (TC), total triglyceride (TG), high density lipoprotein-cholesterol (HDL-C), low density lipoprotein—cholesterol (LDL-C), interleukin-6(IL6), hsCRP, fasting plasma glucose(FPG)and blood pressure were detected by the standard methods in3days after hospitalization. Body surveying index consisting of the patients'height, weight and waist circumference Was measured, waist circumferencextriglyceride index(WT index) and body mass index (BMI) were computed. According to the hypertriglyceridemic waist phenotype cut-off point, we enroll whose as abnormal hypertriglyceridemic waist phenotype group (n=126), the others normal hypertriglyceridemic waist phenotype group (n=72). Selected coronary angiography Was completed by special cardiac catheterization doctor to gain various vascular picture of the heart. All patients were calculated the coronary artery score (CAS). Date were pooled to analyze the level of blood lipids, inflammatory markers, FBG, blood pressure in normal hypertriglyceridemic waist phenotype group Versus (VS) hypertriglyceridemic waist phenotype group. Multiple linear correlation and regression analysis were applied to assess the correlationship between WT index, BMI and the aforementioned biochemical indicators, CAS.
     Results:
     1、group A of CAS was significantly higher than group B (P<00.1).
     2、 Compared with group B, group A patients with total cholesterol (TC)、low density lipoprotein cholesterol (LDL-C)、human plasminogen activation inhibitor1(PAI-1)、interleukin-6(IL-6)、systolic blood pressure (SBP)、diastolic blood pressure (DBP)、 BMI、 fasting plasma glucose (FPG)、free fatty acid (FFA) fibrinogen (Fib)、tumor necrosis factor-alpha (TNF-a) and high-sensitivity C-reactive protein (hsCRP) levels were significantly higher (P<0.05); adiponectin (APN)、high density lipoprotein cholesterol (HDL-C) levels were significantly lower (P <0.01).
     3、CAS of all selected patients with CHD and multiple linear regression correlation analysis of the risk factors:WTindex、hsCRP、PAI-1and TC was significantly positively correlated with the CAS; HDL-C、 APN was significantly negatively correlated.
     4、WTindex with FFA、SBP was significantly positively related.
     Conclusion:
     1、Combined high triglycerides waist phenotype (HTWP) in patients with CHD risk factors levels (such as the CAS, the TC, LDL-C, PAI-1, IL-6, the SBP, DBP, and BMI, and of FPG, Fib, TNF-alpha, hsCRP and FFA etc.) were significantly higher than normal triglyceride waist phenotype in patients with CHD, while the former severe coronary lesions than the latter.
     2、Comprehensive report of abdominal obesity and elevated TG new index WTindex and the severity of coronary lesions and CHD traditional risk factors are closely related, so WTindex may be judged CHD risk is a useful indicator, also may be CHD populations at risk for early intervention targets.
引文
[1]Miller M, Cannon CP, Murphy SA, et al. PROVE-IT TIMI 22 Investigators, Impact of triglyceride levels beyond low-density lipoprotein cholesterol after acute coronary syndrome in the PROVE-IT TIMI 22 trial [J]. J Am Coll Cardiol,2008,51:724-730.
    [2]Fruchart JC, Sacks FM, et, al. The Residual Risk Reduction initiative:A call to action to reduce Residual vascular Risk in dyslipidemic patients. A condensed position paper by the Residual Risk Reduction initiation (R3j) [J]. Diabetes Vase Dis Res,2008,5:319-335.
    [3]Lemieux I, Pascot A, Couillard C, et al. Hypcrtriglyccridemic waist. A marker of the atherogenic metabolic triad (hyperinsulinemia. hyperapolipoprotcin B, small, dense LDL) in men [J]? Circulation 2000; 102:179-84.
    [4]中华医学会心血管病学分会,中华心血管病杂志编辑委员会.慢性稳定性心绞痛诊断与治疗指南[J].中华心血管病杂志,2007,35(3):195-206.
    [5]中华医学会心血管病学分会,中华心血管病杂志编辑委员会.不稳定性心绞痛和非ST段抬高心肌梗死诊断与治疗指南[J].中华心血管病杂志,2007,35(4):295-304.
    [6]Antman EM, Anbe DT Armstrong PW, et al. ACC/AHA Guidelines for the Management of Patients With ST-Elevation Infarction:A Report of the American college of cardiology/American heart Association Task Force on Practice Guidelines. Circulation,2004,10:e82-c293.)
    [7]中华医学会心血管病学分会,中华心血管病杂志编辑委员会,中国循环杂志编辑委员会.急性心肌梗死诊断和治疗指南[J].中华心血管病杂志,2001,29(12):710-725.
    [8]中国成人血脂异常防治指南制定委员会.中国成人血脂异常防治指南.中华心血管病杂志,2007,35(5):390-419.
    [9]中国高血压防治指南修订委员会.中国高血压指南(2005修订版)[J].高血压杂志,2005年,12(增):1-53.
    [10]Bernard JG, Eugene B, John DR. Chronic Coronary Artery Disease. Eugene Braunwald, cds. Heart Disease:A Textbook of Cardiovascular Medicine.5th cd. Philadelphia:W. B. Saundcrs, 1997:1289-1365.
    [11]David M. Lcaman MD, Ronald W, et a 1. Coronary artery atherosclerosis:severity of the disease, severity of angina pectoris and compromised left ventricular function [J]. Circulation, 1981-63:285-292.
    [12]中华人民共和国卫生部.2006中国卫生统计年鉴.北京:中国协和医科大学山版社,2006.
    [13]孔灵芝,胡承寿.中国心血管病报告2007.北京:中国大百科全书出版社,2009:4.)
    [14]孙宁玲.2004年中围高血压防治指南修订版的解读.高血.压杂志,2005,13:378-379.
    [15]王薇,赵冬,刘静,等.中国35~64岁人群血压水平与10年心血管病发病危险的前瞻性研究.中华内科杂志,2004。43:730-734.
    [16]Wiilet W, Creen A, Stampfer M, et al. Relative and absolute risks of coronary heart disease among women who smoke cigarettes. N Engl J Med,1987,317:1303-1309.
    [17]刘静,赵冬,秦兰萍,等.低密度脂蛋白胆固醇与心血.管病发病关系的前瞻性研究.中华心血管病杂志,2001,29:561-565.
    [18]周北凡,刘小清,武阳丰,等.我国中年人群糖尿病和空腹血糖异常对心血管病发病的预测价值.中华心血管病杂志,2003.31:226-230.
    [19]Executive Summary of the Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III) [J]. JAMA 2001; 285:2486-97.
    [20]Alberti KG, Zimmet P, Shaw J. The metabolic syndrome-a new worldwide definition. Lancet 2005;366:1059-62.
    [21]Grundy SM, Cleeman JI, Daniels SR, et al. Diagnosis and management of the metabolic syndrome:An American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement[J]. rculation 2005; 112:2735-52.
    [22]Gu DF, Gupm A, MunCitner P, et al. Prevalence of cardiovascular disease risk factor clustering among the adult population of China:results from the International Collaborative Study of Cardiovascular Disease in Asia (Inter Asia). Circulation,2005,112(5):658-665.
    [23]McNeiU AM, Resmond WD, Girman CJ, et al. the metabolic syndrome and 11-year risk of incident cardiovascular disease in the Atheroselerosis Risk in Communities Study. Diabetes Care.2005.28(2):385-390.
    [24]Grundy SM. Metabolic syndrome:Connecting and reconciling cardiovascular and diabetes world. J Am Coll Cardiol,2006,47(6):1093-1100.
    [25]Alexander CM, Landsman PB, Teutsch SM, et al. Third National Health and Nutrition Examination Survey (NHANESⅢ):NCEP-defined metabolic syndrome, diabetes, and prevalence of coronary heart disease among Nhanes III participants age 50 years and order. Diabetes.2003. 52(5).1210-1214.
    [26]Eckel RH, Kahn R, Robertson RM, et al. Preventing cardiovascular disease and diabetes: a call to action from the American Diabetes Association and the American Heart Association [J]. Circulation.2006.113:2943-2946.
    [27]Alberti K G, Zimmet P, Shaw J, et al. The metabolic syndrome-- new worldwide definition [J]. Lancel.2005,366(9491):1059-1062.)。
    [28]National Cholesterol Education Program (NCEP)Expert Panel on Detection, Evaluation and Treatment of High Blood Cholesterel in Adults(Adult Treatment Pancllll). Third Report of the National Cholesterol Education Program (NECP) Expert Panel on Detection, Evaluation and Treatment of High Blood Cholesterol in Adults (Adult Treatment PanelⅢ)final report. Circulation。2002,106(25):3143.
    [29]Balkan B, Charles MA, Drivsholm T, et al. European Group for the Study of Insulin Resistance(EGIR):frequency of the WHO metabolic syndrome in Europe an cohorts, and an alternative definition of an insulin resistance syndrome. Diabetes Metab,2002,28(5):364-376.
    [30]Alberti KGMM, Zimmet P, Shaw J, for the IDF Task Force Consensus Group. The metabolic syndrome--a new worldwide definition. Lancet,2005.366(9491):1059-1062.
    [31]中华医学会糖尿病学分会代谢综合征研究协作组.中华医学会糖尿病学分会关于代谢综合征的建议.中华糖尿病杂志,2004,12(3):156—160.
    [32]中华医学会糖尿病学分会.空腹血糖受损下限诊断切割点的建议.中华医学杂志,2005,85(28):1947—1950.)
    [33]陈蕾,贾伟平,陈俊茜,等.上海市成人“代谢综合征”流行调查.中华心血管病杂志,2003,31(12):909-912.)
    [34]Miller M, Stone NJ, Balinntyne C, et al. Triglycerides and cardiovascular disease:a scientific statement from the American Heart Association. Circulation,2011。Epub ahead of print].
    [35]Girt AK。 Drexel J, Ferrieres J, et al. High prevalence of dyslipidcmia in 18.574 patients treated with statins in Europe and Canada:results of the dyslipidcmia international study. Eur Heart J,2009,30(suppll):303.
    [36]中华人民共和国卫生部.中国居民营养与健康现状.中国心血管病研究杂志,2004,2:919-922.
    [37]王森,王薇,赵冬,等.北京地区青年人群心血管病危险因素10年变化趋势.心肺血管病杂志,2005,24:65-67.
    [38]Assmann G, Schulte H, Cullen P, et al. Assessing risk of myocardial infarction and stroke: new data from the prospective cardiovascular Munster (PROCAM) study. Eur J clin Invst,2007, 37:925-932.
    [39]Vine DF, Takechi R, Russell JC, et al. Impaired postprandial apolipoprotein-B48 metabolism in the obsess, insulin-resistant JCR:LA-cp rat:increased atherogenicity for the metabolic syndrome [J]. Atherosderosis.2007.190:282-290.)。
    [40]Weinstein MM, Yin L, Tu Y, et al. Chylomicmnemia elicits atheroscderosis in mice-brief report[J]. Arteroscler Thromb Vase Biol,2010.30:20-23.
    [41]LinL,Wen T, Zheng XY, et al. Remnant—ike particles accelerate endothelial progenitor cells senescence and induce cellular dysfunction via an oxidative mechanism[J]. Athemsclermis, 2009,202:405-414.
    [42]Assmann G, Schulte H, Seedorf U. Cardiovascular risk assessment in the metabolic syndrome. Results from the Prospective Cardiovascular Munster (PROCAM) study [J]. Tnt J Obes,2008, 32:S11-S16.
    [43]Sarwar N, Danesh J, Eiriksdottir G, et al. Triglycerides and the risk of coronary heart disease: 10,158 Incident cases among 262,525 participants in 29 Western prospective studies [J]. Circulation,2007,115:450-458.
    [44]Jeppesen J, Hein HO, Suadicani P, et al. Triglyceride concentration and ischemic heart disease:an eight-year follow-up in the Copenhagen Male Study [J]. Circulation,1998,97: 1029-1036.
    [45]Tirosh A, Rudich A, Shochat T, et al. Changes in triglyceride levels and risk for coronary heart disease in young men. Ann Tntem Med,2007,147:377-385.)
    [46]Abdel-Maksoud MF, Hokanson JE. The complex role of triglycerides in cardiovascular disease [J]. Semin Vase Med,2002,2:325-333.
    [47]Borge G. Nordestgaard; Marianne Benn; Peter Schnohr; et al. Nonfasting Teiglycerides and Risk of Myocardial infarction, Ischemic Heart Disease, and Death in Men and Women. JAMA. 2007;298(3):299-308.
    [48]Atar lA, Atar l, Aydinalp A, et al. Is there any relationship betweet coronary disease and postprandial triglyceride levels?2011; 11 (3):201-6.
    [49]武阳丰,马冠生,胡永华,等.中国居民的超重和肥胖流行现状[J].中华预防医学杂志.2005,39:316-320.
    [50]Hubert HB, Feiuleib M, MeNamam I'M, et al. Obesity as an independent risk factor for cardiovascular disease:a 26-year follow-up of participants in the Framingham heart study. Circulation,1983,67:968-977.
    [51]中国肥胖问题工作组数据汇总分析协作组.中国成人体重指数和腰围对相关疾病危险因素异常的预测价值:适宜体重指数和腰围切点的研究.中华流行病学杂志,2002,23(1):5—10.
    [52]周北凡,武阳丰,李莹,等.中国成人代谢综合征腰围切点的研究.中华心血管病杂志,2005,33(1):81-85.
    [53]中华人民共和国卫生部控制司.中国成人超重和肥胖症预防与控制指南.北京:人民卫生出版社,2006.
    [54]中国成人超重和肥胖症预防控制指南//陈春明,孔灵芝主编.北京:人民卫生出版社.2006.
    [55]Pouliot MC, Despres JP, Lemieux S, et al. Waist circumference and abdominal sagittal diameter:Best simple anthropometric indexes of abdominal visceral adipose tissue accumulation and related cardiovascular risk in men and women [J]. Am J Cardiol.1994;73:460-8.
    [56]Li TY, Rana JS, Manson JE, et al. Obesity as compared with physical activity in predicting risk of coronary heart disease in women. Circulation [J].2006; 113:499-506.
    [57]Lau DCW, Dhillon B, Yan H, et al. Adipokines:molecular links between obesisty and atheresclerosis. Am J Physiol,2005,288:H2031-H 141.
    [58]Berg AH, Scherer PE. Adipose tissue, inflammation, and cardiovascular disease. Circ Res,2005,96:939-949.
    [59]Matsuzawa Y. Therapy insight:adipocytokines in metabolic syndrome and related cardiovascular disease. Nature Clin Pract Cardiovasc Med,2006.3:3542.
    [60]Kahn SE, Hull RL, Utzschneider KM. Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature.2006,444:840-846.
    [61]Wajchenberg B. Subcutaneous and visceral adipose tissue:their relation to the metabolic syndrome. Endocr Rcv 。2000。21:697-738.
    [62]Cart MC, Brunsell JD. Abdominal obesity and dyslipidemia in the metabolic syndrome: importance of type 2 diabetes and familial combined hypeflipidemia in coronary artery disease risk. J Clin Endocrinol Metab,2004.89:2601-2607.
    [63]祝之明,主编.代谢综合征.病因探索与临床实践.北京:人民军医出版社,2005,308-323.
    [64]Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III) [J]. JAMA 2001; 285:2486-97.
    [65]Alberti KG. Zimmet P, Shaw J. The metabolic syndrome-a new worldwide definition. Lancet,2005,366:1059-1062.
    [66]潘长玉.代谢综合征的认识和防治的新进展-评《国际糖尿病联盟关于代谢综合征定义的全球共识》.中华内分泌代谢杂志,2005,21:298-300.
    [67]Despres JP, Lemieux I, Bergeron J, et al. Abdominal obesity and the metabolic syndrome: contribution to global cardio-metabolic risk. Arterioscler Thromb Vase Biol,2008,28:1039-1049.
    [68]Yusuf S, Hawken S, Ounpuu S, et al. Obesity and the risk of myocardial infarction in 27,000 participants from 52 countries:A case-control study [J]. Lancet 2005; 366:1640-9.
    [69]Manson JE, Willett WC, Stampfer MJ, et al. Body weight and mortality among women. N Engl J Med 1995; 333:677-85.
    [70]Colditz GA, Willett WC, Rotnitzky A, Manson JE. Weight gain as a risk factor for clinical diabetes mellitus in women. Ann Intern Med 1995; 122:481-6.
    [71]Lemieux S, Prud'homme D, Bouchard C, Tremblay A, Despres JP. A single threshold value of waist girth identifies normal-weight and overweight subjects with excess visceral adipose tissue[J]. Am J Clin Nutr.1996; 64:685-93.
    [72]何洪波,赵志钢,蒲云飞,等.腹型肥胖的类型与代谢综合征发生的风险[J].中华医学杂志,2008,88(18):1251—1254.
    [73]Nicklas BJ, Penninx BW, Cesari M, et al. Association of visceral adipose tissue with incident myocardial infarction in older men and women:The Health, Aging and Body Composition Study [J]. Am J Epidemiol.2004; 160:741-9.
    [74]杨明,贾伟平,包玉倩,等.性别、年龄及体脂参数与静息能量消耗的关系.中华内分泌代谢杂志,2004,20:20-22.
    [75]Gustafsson F, Kragelund CB, Torp-Pedersen C, et al. Efect of obesity and being overweight on long term mortality in congestive heart failure:influence of left ventrieular systolic function. Eur Heat J,2005,26:58-64.
    [76]Kadowaki T, Yamauchi T, Kubota N. et al. Adiponectin and adiponectin receptors in insulin resistance, diabetes。 and the metabolic syndrome. J Clin Invest,2006,116:1784.1792.
    [77]祝之明.代谢综合征:研究进展与面临的挑战[J].中国实用内科杂志,2008,28(11):905—906.
    [78]Taskinen MR, Adiels M, Westerbacka J, et al. Dual metabolic defects arc required to produce hypertriglyceridemia in obese subjects. Artcrioscler Thromb Vase Biol[J].2011 sep; 31(9): 1946-8.
    [79]Despres JP, Lemieux 1. Abdominal obesity and metabolic syndrome [J].Nature 2006; 444:881-7.
    [80]Lemieux I, Pascot A, Couillard C, et al. Hypertriglyceridemic waist. A marker of the atherogenic metabolic triad (hyperinsulinemia, hyperapolipoprotein B, small, dense LDL) in men [J]? Circulation 2000; 102:179-84.
    [81]Lamarche B, Tchernof A, Mauriege P, et al. Fasting insulin and apolipoprotein B levels and low-density lipoprotein particle size as risk factors for ischemic heart disease [J]. JAMA 1998; 279:1955-61.
    [82]Lemieux I, Almeras N, Mauriege P, et al. Prevalence of" hypertriglyceridemic waist" in men who participated in the Quebec Health Survey:Association with atherogenic and diabetogenic metabolic risk factors[J]. Can J Cardiol 2002; 18:725-32.
    [83]LaMonte MJ, Ainsworth BE, DuBose KD, et al. The hypertriglyceridemic waist phenotype among women [J]. Atherosclerosis 2003; 171:123-30.
    [84]Solati M, Ghanbarian A, Rahmani M, Sarbazi N, Allahverdian S, Azizi F. Cardiovascular risk factors in males with hypertriglycemic waist (Tehran Lipid and Glucose Study[J]). Int J Obes Relat Metab Disord 2004; 28:706-9.
    [85]St-Pierre J, Lemieux I, Vohl MC, et al. Contribution of abdominal obesity and hypertriglyceridemia to impaired fasting glucose and coronary artery disease. Am J Cardiol 2002; 90:15-8.
    [86]Blackburn P, Lamarche B, Couillard C, et al. Postprandial hyperlipidemia:Another correlate of the "hypertriglyceridemic waist" phenotype in men [J]. Atherosclerosis 2003; 171:327-36.
    [87]Czernichow S, Bruckert E, Bertrais S, et al. Hypertriglyceridemic waist and 7.5-year prospective risk of cardiovascular disease in asymptomatic middle-aged men[J]. Int J Obes (Lond) 2006.
    [88]Tanko LB, Bagger YZ, Qin G, et al. Enlarged waist combined with elevated triglycerides is a strong predictor of accelerated atherogenesis and related cardiovascular mortality in postmenopausal women [J]. Circulation 2005; 111:1883-90.
    [89]Kahn HS, Valdez R. Metabolic risks identified by the combination of enlarged waist and elevated triacylglycerol concentration [J]. Am J Clin Nutr 2003; 78:928-34.
    [90]Gazi IF, Filippatos TD, Tsimihodimos V, et al. The hypertriglyceridemic waist phenotype is a predictor of elevated levels of small, dense LDL cholesterol [J]. Lipids 2006; 41:647-54.
    [91]Hiura Y, Acklin F, Newman J, et al. Hypertriglyceridemic waist as a screening tool for CVD risk in indigenous Australian women[J]. Ethn Dis 2003; 13:80-4.
    [92]Esmaillzadeh A, Mirmiran P, Azizi F. Clustering of metabolic abnormalities in adolescents with the hypertriglyceridemic waist phenotype [J]. Am J Clin Nutr 2006;83:36-46;quiz 183-4. [93] Bell D, McAuley KA, Mann J, Murphy E, Williams S. The hypertriglyceridaemic waist in New Zealand Maori [J]. Asia Pac J Clin Nutr 2004; 13:74-7.
    [94]Esmaillzadeh A, Mirmiran P, Azadbakht L, Azizi F. Prevalence of the hypertriglyceridemic waist phenotype in Iranian adolescents[J].Am J Prev Med 2006;30:52-8.
    [95]Esmaillzadeh A, Mirmiran P, Azizi F. Whole-grain intake and the prevalence of hypertriglyceridemic waist phenotype in Tehranian adults[J]. Am J Clin Nutr 2005;81:55-63.
    [96]Arsenault BJ, Lemieux I, Despres JP, et al. The Hypertriglyceridemic-waist phenotype and the risk of coronary artery disease:results from the EPIC-Norfolk prospective population study[J]. CMAJ,2010,182(13):1396-1398.
    [97]Ford ES, Mokdad AH, Giles WH. Trends in waist circumference among U.S[J]. adults. Obes Res 2003; 11:1223-31.
    [1]Willige S, Standeven KF, Philippou H, et al. The pleiotropic role of the fibrinogen γ'chain in hemostasis [J]. Blood,2009,5 (11):114 (19):3994-4001.
    [2]Hellenthal FA, Buurman WA, Wodzig WK, et al. Biomarkers of AAA progression. Part 1: extracellular matrix degeneration[J]. Nat Rev Cardiol,2009,6(7):464-474.
    [3]Papageorgiou N, Tousoulis D, Siasos G, et al. Is fibrinogen a marker of inflammation in coronary artery disease? Hellenic J Cardiol [J]. Hellenic J Cardiol,2010,51(1):1-9.
    [4]Lominadze D, Dean WL, Tyagi SC, et al. Mechanisms of fibrinogen-induced microvascular dysfunction during cardiovascular disease [J]. Acta Physiol (Oxf),2010,198(1):1-13.
    [5]De Luca G, Verdoia M, Cassetti E, et al. Novara atherosclerosis study group(NAS).high fibrinogen level is an Independent predictor of presence and extent of coronary artery disease among Italian population [J]. J Thromb Thrombolysis,2011,31(4):458-463.
    [6]Lau DH, Huynh LT, Chew DP, et al. Prognostic impact of types of atrial fibrillation in acute coronary syndromes [J].Am J Cardiol,2009,104(10):1317-1323.
    [7]Luo BJ, Yu DQ, Chen JY, et al. Correlation of microalbuminuria and fibrinogen to the severity of coronary artery lesions in patients with metabolic syndrome [J]. Nan Fang Yi Ke Da Xue Xue Bao,2010,30(11):2459-2462.
    [8]Khalil A,Mandal K,KhaliI S,et aI.Homocysteine,fibrinogen and Iipid profiIe in children of young adults with coronary artery disease[J].Indian Pediatr,2011,48(2):156-157.
    [9]Kafle DR,Shrestha P. Study of fibrinogen in pati'ents with diabetes mellitus[J].Nepal Med Coll J,20l0 3,12(1):34-37.
    [10]Tousoulis D,Papageorgiou N,et al.Fibrinogen and cardiovascular disease:genetics and biomarkers.Blood Rev[Z],201111;25(6).239-45.
    [11]Lau DH,Huynh LT,Chew DP,et al.Prognostic impact oftypes ofatrial fibrillation in acute coronary syndromes[J].Am J Cardiol,2009,104(1):1317-1323.
    [12]Fragoso-Lona JM, Ramirez-Bello J, Cruz-Robles D, et al.Pro-inflammatory and anti-innammatory markers in coronary artery disease and acute ischemic coronary syndrome[J] Arch Cardiol Mex,2009,79(1):54-62.
    [13]Radovic VV Predictive value of inflammation and myocardial necrosis markers in acute coronary syndrome[z],Med Pregl.2010v63n9-l0.662-667.
    [14]Lobbes MB,Kooi ME,Lutgens E,et al.Myeloperoxidase,and pregnancy-associated plasma protein a as biomarkers for cardiovascular disease:towards a multi-biomarker approach[Z]. IntJ Vasc Med.2010:2010:726207.
    [15]Shi Y,Wu Y,Bian C,et al.Predictive valuc ofplasma fibrinogen levels in patients admitted for acute coronary syndrome[J].Tex Heart Inst J,2010,37(2):178-183.
    [16]Brien SE, Ronksley PE,Turner BJ,et al.Effect of alcohol consumption On biological markers associated with risk of coronary heart disease:systematic review and meta-analysis of interventional studies[Z],BMJ.2011:222:342:d636.
    [17]Mad rid-Miller A,Moreno-Ruiz LA,Borrayo-sanchez G,et al.Ipact of bezafibrate treatment in patients with hyPerfibrinogenemia and ST-elevation acute myocardial infarction:a randomized clinical trial [J].Cir Cir,2010,78(3):229-237.
    [18]Sobel BE, Hardjson RM, Genuth S, et al. Profibrinolytic, antithrombotic,and antiinflammatory cfiects of an insulin-sensitizing strategy in patients in the bypass angioplasty revascularization investigation 2 diabetes (BARI 2D)trials[J].Circulation,2011,124(6): 695.703.
    [19]Chudy P,Kotulicova D,stasko J,et al.The relationship among TAFI,t-PA,PAI-I and F1+2 in type 2 diabetic patients with normoalbuminuria and microalbuminuria [J]. Blood Coagul Fibrinolysis,2011,22(6):493-498.
    [20]McBane RD 2D. Hardison RM,Sobel BE; BARI 2D Study Group. Compairson of plasminogen activator inhibitor-1, tissue type plasminogen activator antigen, fibrinogen and D-dimer levels in various age decades in patients with type 2 diabetes mellitus and stable coronary artery disease (from the BARI 2D trial) [J]. Am J Cardiol.2010 11; 105(1):17-24.
    [21]Figueras J, Monasterio J, Domingo E, et al. Prothrombotic profile in patients with vasospastic or non vasospastic angina and non significant coronary stenosis [Z].Thromb J.2011 5 27; 9:10.
    [22]Walter T, Szabo S, Suselbeck T, et al. Effect of atorvastatin on haemostasis, fibrinolysis and inflammation in normocholesterolaemic patients with coronary artery disease:a post hoc analysis of data from a prospective, randomized, double-blind study [J]. Clin Drug Investig,2010, 30(7):453-460.
    [23]Pal'tseva EM, Rodina AV, Andreev DA, et al. Urokinase-type plasminogen activator and its inhibitor type 1 in the diagnosis of evolving complications in coronary heart disease. Klin Lab Dign [J].2010,6(6):51-55.
    [24]Ha H, Oh EY, Lee HB. The role of plasminogen activator inhibitor 1 in renal and cardiovascular diseases [J]. Nat Rev Nephrol,2009,5(4):203-211.
    [25]Abboud N, Ghazouani L, Saidi S. Association of PAI-1 4G/5G and-844G/A gene polymorphisms and changes in PAI-1/tissue plasminogen activator levels in myocardial infarction:a case-control study [J].Genet Test Mol Biomarkers,20102,14(1):23-27.
    [26]Satra M, Samara M, Wozniak G, et al. Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion[J]. Pharmacogenomics,2011 2,12(2):195-203.
    [27]Ahmed W, Malik M, Saeed I, et al. Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarction [J]. Mol Biol Rep,20114,38(4): 2541-2548.
    [28]Suzuki J, Ogawa M, Muto S, et al. Effects of specific chemical suppressors of plasminogen activator inhibitor-1 in cardiovascular diseases [J]. Expert Opin Investig Drugs,2011 2,20(2): 255-264.
    [29]Huang K.W, Guo JW, Chen JM, et al. Effects of erigeron breviscapus injection on TNF-alpha, PAI-1 and tPA in rats with acute myocardial infarction [J]. Zhong Yao Cai,201010, 33(10):1592-1595.