早发严重冠状动脉三支病变患者冠心病危险因素的分布及聚集
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
目的:近年来,冠心病(CHD)在我国的发病率呈迅速上升趋势,已成为威胁我国公众健康的重要疾病。现代生活方式的转变使CHD患者的发病年龄越来越早,冠脉病变程度越来越重。严重冠脉三支病变是导致终末期心力衰竭的主要原因,为个人和社会带来巨大的经济负担。目前关于早发严重冠脉三支病变危险因素的流行病学特点研究尚较少。本研究旨在探讨早发严重冠脉三支病变患者CHD危险因素的分布及聚集情况,对比不同性别CHD危险因素的差异并分析影响早发严重冠脉三支病变左室射血分数(LVEF)降低的因素,为年轻人防治冠脉严重病变提供依据。
     方法:连续筛选2009年3月-2011年3月天津医科大学第二医院心内科以CHD收入院并行冠脉造影检查的住院患者。根据冠脉造影结果筛选早发严重冠脉三支病变组(男性<55岁,女性<65岁;严重冠脉三支病变指按照定量冠脉造影法左前降支、左回旋支、右冠脉或左主干病变及右冠脉均有面积狭窄≥75%,病变组)339例和冠脉正常组(三支冠脉光滑、无狭窄或扩张,对照组)181例。对所有入选患者均记录性别、年龄,询问吸烟史、饮酒史、高血压史及病程、糖尿病(DM)史及病程、早发CHD家族史等。并计算体质量指数(BMI)=体重/身高2(kg/m2)。记录患者入院即刻抽血测定的血常规、凝血常规及肾功能。记录入选者空腹8小时次日清晨采取外周肘静脉血测定的肝功能、血脂、C反应蛋白(CRP)、肾素-血管紧张素-醛固酮等。常规行超声心动图检查评价心功能。采用SPSS11.5软件对数据进行统计处理。
     结果:1、两组间男性、吸烟史、高血压、DM、早发CHD家族史、代谢综合症比例及三酰甘油(TG)、高密度脂蛋白胆固醇(HDL-C)、BMI、尿酸(UA)、血小板(PLT)计数、白细胞(WBC)计数、纤维蛋白原(Fbg)、CRP水平差异有统计学意义(p<0.05)。多因素Logistic回归分析显示早发严重冠脉三支病变的危险因素有男性、早发CHD家族史、DM、肥胖、高TG血症、低HDL-C血症及高低密度脂蛋白胆固醇(LDL-C)血症。2、病变组与对照组相比危险因素分布存在差异,病变组危险因素个数>3的患者比例高于对照组(78.8%>25.4%,p<0.01),危险因素个数<3的患者比例低于对照组(2.6%<49.2%,p<0.01)。3、按性别行亚组分析显示男性病变与对照两组吸烟史、早发CHD家族史、BMI、HDL-C、LDL-C差异显著(p<0.05),女性病变与对照两组间早发CHD家族史、BMI、DM、高血压、TG、HDL-C差异显著(P<0.05)。病变组不同性别CHD危险因素比较时,男性组吸烟史、早发CHD家族史比例高于女性组(P<0.01),女性组DM、高TC血症及高TG血症比例高于男性组(p<0.05)。病变组男性危险因素个数>3的比例高于病变组女性(90.8%>38.5%)。4、病变组合并高血压、DM、吸烟或肥胖的患者TG水平高于对照组合并高血压、DM、吸烟或肥胖的患者,HDL-C水平低于对照组患者(P<0.01)。5、本研究亚组分析显示早发严重冠脉三支病变LVEF降低组(LVEF<50%) DM病程、BMI、CRP、PLT、肌酐(Scr)水平高于LVEF正常组(LVEF≥50%) (P<0.05),多因素logistic回归分析显示DM病程、肥胖及Scr是LVEF降低的影响因素。
     结论:1、早发严重冠脉三支病变的危险因素有男性、早发CHD家族史、DM、肥胖、高TG血症、低HDL-C血症及高LDL-C血症;2、早发严重冠脉三支病变患者存在多种CHD危险因素聚集现象,且3个以上危险因素聚集程度明显增加;3、不同性别早发严重冠脉三支病变患者CHD危险因素的分布及聚集存在差异。DM、高TG及高TC比例在女性早发严重冠脉三支病变患者中高,而吸烟史、早发CHD家族史比例在男性患者中高。男性早发严重冠脉三支病变危险因素聚集程度较女性强;4、无论合并高血压、DM、肥胖或吸烟,早发严重冠脉三支病变患者的TG水平较高而HDL-C水平较低;5、早发严重冠脉三支病变患者LVEF降低的相关因素有DM病程、肥胖及Scr水平。
Objective:In recent years, incidence of coronary heart disease (CHD) tends increasing trend. It has been a main disease threatening the public health. The onset of CHD is earlier and the extent of coronary artery lesions is severer with the changing of modern life style. Severe three-vessel coronary artery lesion is the main cause for the end-stage heart failure, which brings tremendous economic burden for the society and the individual. Studies about epidemiologic features of risk factors of premature severe three-vessel coronary artery lesions were fewer.This study is to analyze the contribution and clustering of the risk facors for the premature severe three-vessel coronary artery lesions, and to provide the evidence for prevention of the premature CHD patients.
     Methods:Consecutive cases of hospitalized patients for CHD were collected at the Second Hospital of Tianjin Medical University during March 2009 to March 2011. All cases accepted coronary angiography. The criteria for premature severe three-vessel coronary artery lesions group included:(1) the onset age of CHD for male is less than 55 years old and for female is less than 65 years old; (2) severe three-vessel coronary artery lesions indicates the area stenosis of LAD, LCX, RCA or LM, RCA is more than 75 percent according to quantitative coronary angiography; The criteria for normal coronarography is that three coronary arteries are smooth without narrow or expansion; 339 cases for premature severe three-vessel coronary artery lesions and 181 cases for normal coronarography were included in the study. For all selected patients, medical history including gender, age, smoking, drinking alcohol, hypertention, diabetes mellitus (DM), positive family history (PFH) of CHD and so on were taken and body mass index (BMI) was measured. Routine blood cell test, blood coagulation and renal functions were measured at the moment of admission. At the next morning of admission peripheral venous blood was taken for the measurement of blood lipids, C reactive protein (CRP) and liver function. Routine examination of the echocardiography was performed. SPSS11.5 was used for statistical processing of data.
     Results:(1) There were significant difference in ratios of male, smoking, hypertension, DM, PFH of CHD, metabolic syndrome and the value of triglyceride, high-density-lipoprotein-cholesterol(HDL-C), BMI, uric acid, PLT, WBC, fibrinogen and CRP between groups(P< 0.05). Multiple logistic regression analysis showed that male, PFH, DM, obesity, low HDL-C level, high levels of low-density-lipoprotein-cholesterol (LDL-C) and triglyceride were risk factors for premature severe three-vessel coronary lesions. (2) The distribution of risk factors was different between disease group and control group. The ratio of patients with more than 3 risk factors was higher(78.8% vs 25.4%), and the ratio of patients with less than 3 risk factors was lower(2.6% vs 49.2%) in disease group than that in control group(P<0.01).(3) Subgroup analysis indicated that smoking, PFH, BMI, HDL-C, LDL-C were significantly different between male patients in disease group and male subjects in normal group. However, PFH, BMI, HDL-C, DM, hypertention, triglyceride were significantly different between female patients in disease group and female subjects in normal group(P< 0.05).Comparion of risk factors for two genders in the disease group showed that the ratios of smoking and PFH were higher in male disease group and the ratios of DM, hypercholesterolemia and hypertriglyceridemia were higher in female disease group(P<0.05).The proportion of risk factor number above three in male disease group was higher than female disease group(90.8% vs 38.5%).(4) Triglyceride level was higher and HDL-C level was lower in disease group with hypertention or DM or obesity or smoking than in control group with hypertention or DM or obesity or smoking(P<0.01).(5)Subgroup analysis showed that duration of diabetes, BMI, CRP, PLT and serum creatinine level was higher in LVEF reduction group(LVEF<50%) than LVEF normal group(LVEF≥50%) in patients of premature severe three-vessel coronary artery lesions(P<0.05). Multiple logistic regression analysis showed that duration of diabetes, obesity and serum creatinine level were predictors for LVEF reduction.
     Conclusion:(1) Male, PFH, DM, obesity, high LDL-C, low HDL-C and hypertriglyceridemia were independent risk factors for premature severe three-vessel coronary artery lesions. (2) Clustering of the main risk factors of CHD existed in the premature severe three-vessel coronary artery lesions and clustering extent of any three risk factors or more was significantly higher.(3) Risk factors were significantly different between two genders. DM, hypertriglyceridemia and hypercholesterolemia was significantly associated to female, while smoking and PFH was significantly associated to male. The clustering extent of risk factors was higher in male group.(4) The level of triglyceride was higher and the level of HDL-C was lower in patients with hypertention or DM or obesity or smoking of disease group than those subjects of normal group. (5) The risk factors associated with LVEF reduction in patients of premature severe three-vessel coronary artery lesions were duration of diabetes, obesity and high-creatinine.
引文
[1]De Backer G, Ambrosioni E, Borch-Johnsen K, et al.European guidelines on cardiovascular disease prevention in clinical practice. Third Joint Task Force of European and Other Societies on Cardiovascular Disease Prevention in Clinical Practice[J].Eur Heart J,2003,24(17):1601-1610.
    [2]Khawaja FJ, Rihal CS, Lennon RJ, et al.Temporal trends (over 30 years), clinical characteristics, outcomes, and gender in patients≤50 years of age having percutaneous coronary intervention[J].Am J Cardiol,2011,107(5):668-674.
    [3]E L, Fragakis N, Ioannidou E, et al. Increased levels of proinflammatory cytokines in children with family history of coronary artery disease[J].Clin Cardiol,2010,33(4):E6-10.
    [4]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(4):450-458.
    [5]Hausenloy DJ, Yellon DM.Targeting residual cardiovascular risk:raising high-density lipoprotein cholesterol levels[J].Heart,2008,94:706-714
    [6]Carey VJ, Bishop L, Laranjo N, et al. Contribution of high plasma triglycerides and low high-density lipoprotein cholesterol to residual risk of coronary heart disease after establishment of low-density lipoprotein cholesterol control [J]. Am J Cardiol,2010,106(6):757-763.
    [7]Das B, Daga MK, Gupta SK, et al. Lipid Pentad Index:A novel bioindex for evaluation of lipid risk factors for atherosclerosis in young adolescents and children of premature coronary artery disease patients in India[J].Clin Biochem,2007,40(1-2):18-24.
    [8]Lloyd-Jones DM, Nam BH, D'Agostino RB Sr, et al. Parental cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults:a prospective study of parents and offspring[J]. JAMA,2004,291(18):2204-2211.
    [9]Myers RH, Kiely DK, Cupples LA,et al. Parental history is an independent risk factor for coronary artery disease:the Framingham Study[J]. Am Heart J,1990,120(4):963-969.
    [10]Saghafi H, Mahmoodi MJ, Fakhrzadeh H, et al.Cardiovascular risk factors in first-degree relatives of patients with premature coronary artery disease[J].Acta Cardiol,2006,61(6):607-613.
    [11]Brown BD, Nsengimana J, Barrett JH, et al. An evaluation of inflammatory gene polymorphisms in sibships discordant for premature coronary artery disease:the GRACE-IMMUNE study[J]. BMC Med,2010,13;8:5.
    [12]van der Net JB, van Etten J, Yazdanpanah M, et al.Gene-load score of the renin-angiotensin-aldosterone system is associated with coronary heart disease in familial hypercholesterolaemia[J]. Eur Heart J,2008,29(11):1370-1376.
    [13]Iribarren C, Go AS, Husson G, et al. Metabolic syndrome and early-onset coronary artery disease:is the whole greater than its parts?[J]. J Am Coll Cardiol,2006,48(9):1800-1807.
    [14]Kalantzi K, Korantzopoulos P, Tzimas P, et al.The relative value of metabolic syndrome and cardiovascular risk score estimates in premature acute coronary syndromes[J]. Am Heart J,2008,155(3):534-540.
    [15]陶红,米树华,赵全明,等.青中年冠心病患者代谢综合征危险因素的分布与聚集状况分析[J].临床,心血管病杂志,2005,21(7):387-389.
    [16]占亚平,卓伟明.女性冠状动脉性心脏病危险因素分析[J].岭南心血管病杂志,2009,15(5):384-386.
    [17]Mazza A, Tikhonoff V, Schiavon L, et al. Triglycerides+high-density-lipoprotein-cholesterol dyslipidaemia, a coronary risk factor in elderly women:the Cardiovascular Study in the Elderly[J]. Intern Med J,2005,35(10):604-610.
    [18]Huxley R, Barzi F, Woodward M, et al. Excess risk of fatal coronary heart disease associated with diabetes in men and women:meta-analysis of 37 prospective cohort studies[J]. BMJ,2006,332(7533):73-78.
    [19]Acharjee S, Qin J, Murphy SA, et al. Distribution of traditional and novel risk factors and their relation to subsequent cardiovascular events in patients with acute coronary syndromes(from the PROVE IT-TIMI 22 trial) [J]. Am J Cardiol,2010,105(5):619-623.
    [20]刘志远,李纲,李玉尔,等.早发CHD患者冠状动脉病变特点及危险因素的临床研究[J].中国心血管病研究,2008,6(9):657-659.
    [21]刘晓宁,张春玲,武文,等.年轻人冠心病危险因素分布及聚集状况[J].中华心血管病杂志,2003,31(2):87-90.
    [22]田学增.早发冠心病患者危险因素的临床研究[J].中国保健,2010,6:150-151.
    [23]李岩,张志寿.冠心病三支病变54例危险因素的临床分析[J].血管康复医学杂志,2005,14(2):111-113.
    [24]李晟,林捷,黄伟剑,等.冠心病三支病变与易患因素关系的临床观察[J].心脑血管病防治,2001,1(3):47.
    [25]Murabito JM, Pencina MJ, Nam BH, et al. Sibling cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults[J].JAMA,2005,294(24):3117-3123.
    [26]Konnov MV, Dobordzhginidze LM, Deev AD, et al.Own and parental predictors of arterial prehypertension and hypertension in children of persons with premature coronary heart disease[J]. Kardiologiia,2010,50(3):22-25.
    [27]Sivapalaratnam S, Boekholdt SM, Trip MD, et al.Family history of premature coronary heart disease and risk prediction in the EPIC-Norfolk prospective population study[J]. Heart,2010,96(24):1985-1989.
    [28]De Sutter J, De Bacquer D, Kotseva K, et al. Screening of family members of patients with premature coronary heart disease; results from the EUROASPIRE Ⅱ family survey[J].Eur Heart J,2003,24(3):249-257.
    [29]Hopkins PN, Hunt SC, Schreiner PJ, et al.Lipoprotein(a) interactions with lipid and non-lipid risk factors in patients with early onset coronary artery disease: results from the NHLBI Family Heart Study[J].Atherosclerosis,1998,141(2):333-345.
    [30]Michos ED, Nasir K, Rumberger JA, et al. Relation of family history of premature coronary heart disease and metabolic risk factors to risk of coronary arterial calcium in asymptomatic subjects[J]. Am J Cardiol,2005,95(5):655-657.
    [31]Palmieri V, Bella JN, Arnett DK, et al. Effect of type 2 diabetes mellitus on left ventricular geometry and systolic function in hypertensive subjects:Hypertension Genetic Epidemiology Network (HyperGEN) study[J]. Circulation,2001,103(1):102-107.
    [32]Babar GS, Zidan H, Widlansky ME, et al. Impaired endothelial function in preadolescent children with type 1 diabetes[J].Diabetes Care,2011,34(3):681-685.
    [33]Liu J, Grundy SM, Wang W, et al.Ten-year risk of cardiovascular incidenee related to diabetes,prediabetos,and the metabolic syndrome[J].Am Heart J,2007,153(4):552-558.
    [34]Fruchart JC, Sacks F, Hermans MP, et al. The Residual Risk Reduction Initiative: a call to action to reduce residual vascular risk in patients with dyslipidemia[J]. Diab Vasc Dis Res,2008,5(4):319-335.
    [35]Tonkin AM, Chen L. Effects of combination lipid therapy in the management of patients with type 2 diabetes mellitus in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial[J].Circulation,2010,122(8):850-852.
    [36]Lyons TJ, Jenkins AJ, Zheng D, et al. Diabetic retinopathy and serum lipoprotein subclasses in the DCCT/EDIC cohort[J]. Invest Ophthalmol Vis Sci,2004,45(3):910-918.
    [37]Qiao Q, Tuomilto J, Borch-Johnsen K, et al. Post-challenge hyperglycaemia is associated with premature death and macrovascular complications[J].Diabetologia,2003,46:M 17-21.
    [38]Sever PS, Dahlof B, Poulter NR, et al. Prevention of coronary and stroke events with atorvastatin in hypertensive patients who have average or lower-than-average cholesterol concentrations, in the Anglo-Scandinavian Cardiac Outcomes Trial-Lipid Lowering Arm (ASCOT-LLA):a multicentre randomised controlled trial[J]. Lancet,2003,361 (9364):1149-1158.
    [39]Pedersen TR, Faergeman O, Kastelein JJ, et al. High-dose atorvastatin vs usual-dose simvastatin for secondary prevention after myocardial infarction:the IDEAL study:a randomized controlled trial[J]. JAMA,2005,294(19):2437-2445.
    [40]Baigent C, Keech A, Kearney PM, et al. Efficacy and safety of cholesterol-lowering treatment:prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins[J]. Lancet,2005,366(9493):1267-1278.
    [41]Grundy SM, Cleeman JI, Merz CN, et al. Implications of recent clinical trials for the National Cholesterol Education Program Adult Treatment Panel Ⅲ guidelines[J], Circulation,2004,110(2):227-239.
    [42]LaRosa JC, Grundy SM, Waters DD, et al. Intensive lipid lowering with atorvastatin in patients with stable coronary disease[J]. N Engl J Med,2005,352(14):1425-1435.
    [43]Gordon T, Castelli WP, Hjortland MC, et al. High density lipoprotein as a protective factor against coronary heart disease. The Framingham Study[J]. Am J Med,1977,62(5):707-714.
    [44]Sharrett AR, Ballantyne CM, Coady SA, et al. Coronary heart disease prediction from lipoprotein cholesterol levels, triglycerides, lipoprotein(a), apolipoproteins A-I and B, and HDL density subfractions:The Atherosclerosis Risk in Communities (ARIC) Study[J].Circulation,2001,104(10):1108-1113.
    [45]Hausenloy DJ, Yellon DM. Targeting residual cardiovascular risk:raising high-density lipoprotein cholesterol levels[J]. Heart,2008,94(6):706-714.
    [46]Natarajan P, Ray KK, Cannon CP, et al. High-density lipoprotein and coronary heart disease:current and future therapies[J]. J Am Coll Cardiol,2010,55(13):1283-1299.
    [47]Grundy SM.Hypertriglyceridemia, atherogenic dyslipidemia, and the metabolic syndrome[J]. Am J Cardiol,1998,81 (4A):18B-25B.
    [48]Assmann G, Cullen p, Schulte H, et al. The Muenster Heart Study (PROCAM). Results of follow up at 8 years[J].Eur Heart J,1998,19(Suppl A):A2-A11.
    [49]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(11):1029-1036.
    [50]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(4):450-458.
    [51]Shepherd J, Betteridge J, Van Gaal L, et al. Nicotinic acid in the management of dyslipidaemia associated with diabetes and metabolic syndrome:a position paper developed by a European consensus panel [J].Curr Med Res Opin, 2005,21(5):665-682.
    [52]Assmann G, Schulte H. Relation of high-density lipoprotein cholesterol and triglycerides to incidence of atherosclerotic coronary artery disease (the PROCAM experience) [J]. Am J Cardiol,1992,70(7):733-737.
    [53]Farnier M, Ducobu J, Bryniarski L, et al. Efficacy and safety of adding fenofibrate 160 mg in high-risk patients with mixed hyperlipidemia not controlled by pravastatin 40 mg monotherapy[J]. Am J Cardiol,2010,106(6):787-792.
    [54]Fazio S, Guyton JR, Polis AB, et al. Long-term safety and efficacy of triple combination ezetimibe/simvastatin plus extended-release niacin in patients with hyperlipidemia[J]. Am J Cardiol,2010,105(4):487-494.
    [55]Zhu W, Huang X, He J, et al. Arterial intima-media thickening and endothelial dysfunction in obese Chinese children[J].Eur J Pediatr.2005,164(6):337-344.
    [56]Ramhamadany E, Dasgupta P, Brigden G, et al.Cardiovascular changes in obese subjects on very low calorie diet[J].Int J Obes,1989;13 Suppl 2:95-99.
    [57]Longo-Mbenz B, Luila EL, Mbete P, et al.Is hyperuricemia a risk factor of stroke and coronary heart disease among Africans[J].Int J Cardiol,1999,71(1):17-22.
    [58]潘广杰,常学伟,谷云飞,等.血清胆红素及尿酸水平与冠状动脉易损斑块的相关性研究[J].中国全科医学,2010,19(30):3370-3372.
    [59]Bickel C, Rupprecht HJ, Blankenberg S, et al.Serum uric acid as an independent predictor of mortality in pafien with angiographically prove coronary artery disease[J].Am J Cardiol,2002,89(1):12-17.
    [60]Schwertner HA, Jackson WG, Tolan G, et al. Association of low serum concentration of bilirubin with increased risk of coronary artery disease[J]. Clin Chem,1994,40(1):18-23.
    [61]Allen LA, Felker GM, Pocock S, et al. Liver function abnormalities and outcome in patients with chronic heart failure:data from the Candesartan in Heart Failure: Assessment of Reduction in Mortality and Morbidity (CHARM) program [J]. Eur J Heart Fail,2009,11(2):170-177.
    [62]Mennander A, Kuukasjarvi P, Laurikka J, et al.Diagnostic performance of plasma high sensitive C-reactive protein in detecting three-vessel coronary artery disease:modification by apolipoprotein E genotype[J].Scand J Clin Lab Invest,2008,68(8):714-719.
    [63]Weber M, McNicoll S, Marcil M, et al. Metabolic factors clustering, lipoprotein cholesterol, apolipoprotein B, lipoprotein (a) and apolipoprotein E phenotypes in premature coronary artery disease in French Canadians[J].Can J Cardiol,1997,13(3):253-260.
    [64]吴兆苏,姚崇华,赵冬,等.11省市队列人群心血管病发病前瞻性研究II.个体危险因素聚集与心血管病发病的关系[J].中华心血管病杂志,2001,29(4):246-250.
    [65]Chen W, Srinivasan SR, Li S, et al.Metabolic syndrome variables at low levels in childhood are beneficially associated with adulthood cardiovascular risk:the Bogalusa Heart Study[J].Diabetes Care,2005,28(1):126-131.
    [66]Parry DJ, Grant PJ, Scott DJ, et al. Atherothrombotic risk factor clustering in healthy male relatives of male patients with intermittent claudication[J].J Vasc Surg,2004,40(5):891-898.
    [67]Lewandowski K, Swierczynska A, Kwasnikowski P, et al. The prevalence of C807T mutation of glycoprotein la gene among young male survivors of myocardial infarction:a relation with coronary angiography results[J].Kardiol Pol,2005,63(2):107-113.
    [68]Brown BD, Nsengimana J, Barrett JH, et al. An evaluation of inflammatory gene polymorphisms in sibships discordant for premature coronary artery disease:the GRACE-IMMUNE study[J].BMC Med,2010 Jan 13;8:5.
    [69]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[J].Circulation,2000,101 (12): 1372-1378.
    [70]Critchley JA, Capewell S. Mortality risk reduction associated with smoking cessation in patients with coronary heart disease:a systematic review[J].JAMA,2003,290(1):86-97.
    [71]Austin MA. Plasma triglyceride as a risk factor for cardiovascular disease[J]. Can J Cardiol,1998 May; 14 Suppl B:14B-17B.
    [72]Lin HF, Liu CK, Liao YC, et al.The risk of the metabolic syndrome on carotid thickness and stiffness:sex and age specific effects[J]. Atherosclerosis,2010,210(1):155-159.
    [73]Tonstad S, Sandvik E, Larsen PG, et al.Gender differences in the prevalence and determinants of the metabolic syndrome in screened subjects at risk for coronary heart disease[J].Metab Syndr Relat Disord,2007,5(2):174-182.
    [74]Lubiszewska B, Skora E, Kruk M, et al. Prevalence of classical risk factors in Polish women with premature coronary artery disease[J].Kardiol Pol, 2010,68(9):1032-1037.
    [75]Patel MJ, de Lemos JA, Philips B, et al. Implications of family history of myocardial infarction in young women[J].Am Heart J,2007,154(3):454-460.
    [76]Mautner SL, Lin F, Mautner GC, et al. Comparison in women versus men of composition of atherosclerotic plaques in native coronary arteries and in saphenous veins used as aortocoronary conduits [J].J Am Coll Cardiol,1993,21(6):1312-1318.
    [77]Hoehner-Celnikier D, Manor O, Gotnnan O, et al. Gender gap in coronary artery disease:comparison of the extent, severity and risk racers in men and women aged 45-65 years[J].Cardiology,2002,97(1):18-23.
    [78]杨跃进.心力衰竭预后的预测因素[J].中华心血管病杂志,2002,30(10):637-639.
    [79]邓晓莉,张福春,赵月,等.血运重建方式对冠心病三支病变患者预后的影响[J].中国介入心脏病学杂志,2007,15(6):317-320.
    [80]Dzau VJ.Tissure angiotensin and pathobiology of vascular disease:a unifying hypothesis[J].Hypertension,2001,37(4):1047-1052.
    [81]胡大一.促进心血管健康,实现心血管疾病预防战略前移[J].中华心血管病杂志,2010,38(4):290-291.
    [1]Backer G D, Ambrosioni E, Knut B J, et al.European guidelines on cardiovascular disease prevention in clinical practice:Third Joint Task Force of European and other Societies on Cardiovascular Disease Prevention in Clinical Practice[J]. Eur J Cardiovasc Prev Rehabil,2003,10(4):S1-S10.
    [2]Jousilahti P, Vartiainen E, Tuomilehto J, et al. Sex,age,cardiovascular risk factors and coronary heart disease:a prospective follow-up study of 14768 middle-aged men and women in Finland[J]. Crculation,1999,99(9):1165-1172.
    [3]李岩,张志寿.冠心病三支病变54例危险因素的临床分析[J].血管康复医学杂志,2005,14(2):111-113.
    [4]李晟,林捷,黄伟剑,等.冠心病三支病变与易患因素关系的临床观察[J].,心脑血管病防治,2001,1(3):47.
    [5]Berry C, Hamilton CA, Brosnan J, et al. Investigation into the sources of superoxide in human blood vessels:angiotensin II increases superoxide production in human internal mammary arteries[J]. Circulation,2000,101(18):2206-2212.
    [6]Tonkin AM, Chen L. Effects of combination lipid therapy in the management of patients with type 2 diabetes mellitus in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial[J]. Circulation,2010,122(8):850-852.
    [7]Enas EA, Mohan V, Deepa M, et al. The metabolic syndrome and dyslipidemia among Asian Indians:a population with high rates of diabetes and premature coronary artery disease[J]. J Cardiometab Syndr,2007,2 (4):267-275.
    [8]Wilson PW, D'Agostino RB, Levy D, et al. Prediction of coronary heart disease using risk factor categories[J]. Circulation,1998,97(18):1837-1847.
    [9]Sacks FM.The role of high-density lipoprotein (HDL) cholesterol in the prevention and treatment of coronary heart disease:expert group recommendations[J]. Am J Cardiol,2002,90(2):139-143.
    [10]Natarajan P, Ray KK, Cannon CP, et al. High-density lipoprotein and coronary heart disease:current and future therapies[J]. J Am Coll Cardiol,2010,55(13):1283-1299.
    [11]孙彩琴,陈忠,马根山,等.合并不同高密度脂蛋白胆固醇水平早发冠心病患者临床类型及冠状动脉病变关系分析[J].临床急诊杂志,2008,9(3):164-165.
    [12]Assmann G, Schulte H. Relation of high-density lipoprotein cholesterol and triglycerides to incidence of atherosclerotic coronary artery disease (the PROCAM experience) [J]. Am J Cardiol,1992,70(7):733-737.
    [13]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(4):450-458.
    [14]Farnier M, Ducobu J, Bryniarski L, et al. Efficacy and safety of adding fenofibrate 160 mg in high-risk patients with mixed hyperlipidemia not controlled by pravastatin 40mg monotherapy [J]. Am J Cardiol,2010,106(6):787-792.
    [15]Fazio S, Guyton JR, Polis AB, et al. Long-term safety and efficacy of triple combination ezetimibe/simvastatin plus extended-release niacin in patients with hyperlipidemia[J]. Am J Cardiol,2010,105(4):487-494.
    [16]Nordestgaard BG, Chapman MJ, Ray K, et al. Lipoprotein(a) as a cardiovascular risk factor:current status[J]. Eur Heart J,2010,31(23):2844-2853.
    [17]陈军,郭志刚,胡威,等.男性早发冠心病冠状动脉病变特点和危险因素的研究[J].第三军医大学学报,2009,31(11):1091-1094.
    [18]占亚平,卓伟明.女性冠状动脉性心脏病危险因素分析[J].岭南心血管病杂志,2009,15(5):384-386.
    [19]Huxley R, Barzi F, Woodward M, et al. Excess risk of fatal coronary heart disease associated with diabetes in men and women:meta-analysis of 37 prospective cohort studies[J]. BMJ,2006,332(7533):73-78.
    [20]Mazza A, Tikhonoff V, Schiavon L, et al. Triglycerides+high-density-lipoprotein-cholesterol dyslipidaemia, a coronary risk factor in elderly women:the Cardiovascular Study in the Elderly[J].Intern Med J,2005,35(10):604-610.
    [21]Zimmerman FH, Cameron A, Fisher LD, et al. Myocardial infarction in young adults:angiographic characterization, risk factors and prognosis (Coronary Artery Surgery Study Registry)[J]. J Am Coll Cardiol,1995,26(3):654-661.
    [22]Guthikonda S, Sinkey C, Barenz T, et al. Xanthine oxidase inhibition reverses-endothelial dysfunction in heavy smokers[J]. Circulation,2003,107(3):416-421.
    [23]Critchley JA, Capewell S. Mortality risk reduction associated with smoking cessation in patients with coronary heart disease:a systematic review[J].JAMA,2003,290(1):86-97.
    [24]Saghafi H, Mahmoodi MJ, Fakhrzadeh H, et al.Cardiovascular risk factors in first-degree relatives of patients with premature coronary artery disease[J].Acta Cardiol,2006,61 (6):607-613.
    [25]Mottillo S, Filion KB, Genest J.et al. The metabolic syndrome and cardiovascular risk a systematic review and meta-analysis[J].J Am Coll Cardiol,2010,56(14):1113-1132.
    [26]Murabito JM, Pencina MJ, Nam BH, et al. Sibling cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults[J].J AMA,2005,294(24):3117-3123.
    [27]Hurrell C, Wietlisbach V, Jotterand V, et al. High prevalence of major cardiovascular risk factors in first-degree relatives of individuals with familial premature coronary artery disease--the GENECARD project[J].Atherosclerosis,2007,194(1):253-264.
    [28]Gaeta G, De Michele M, Cuomo S,et al. Arterial abnormalities in the offspring of patients with premature myocardial infarction[J].N Engl J Med,2000,343(12):840-846.
    [29]Sivapalaratnam S, Boekholdt SM, Trip MD, et al. Family history of premature coronary heart disease and risk prediction in the EPIC-Norfolk prospective population study[J]. Heart,2010,96(24):1985-1989.
    [30]Konnov MV, Dobordzhginidze LM, Deev AD, et al. Own and parental predictors of arterial prehypertension and hypertension in children of persons with premature coronary heart disease[J]. Kardiologiia,2010,50(3):22-25.
    [31]E L, Fragakis N, loannidou E, et al. Increased levels of proinflammatory cytokines in children with family history of coronary artery disease[J].Clin Cardiol,2010,33(4):E6-10.
    [32]Taraboanta C, Wu E, Lear S, et al. Subclinical atherosclerosis in subjects with family history of premature coronary artery disease[J].Am Heart J,2008,155(6):1020-1026.
    [33]Lewandowski K, Swierczynska A, Kwasnikowski P, et al. The prevalence of C807T mutation of glycoprotein la gene among young male survivors of myocardial infarction:a relation with coronary angiography results[J].Kardiol Pol,2005,63(2):107-113.
    [34]Brown BD, Nsengimana J, Barrett JH, et al. An evaluation of inflammatory gene polymorphisms in sibships discordant for premature coronary artery disease:the GRACE-IMMUNE study[J].BMC Med,2010 Jan 13;8:5.
    [35]Schaefer EJ, Santos RD, Asztalos BF, et al. Marked HDL deficiency and premature coronary heart disease[J]. Curr Opin Lipidol,2010,21(4):28.9-297.
    [36]Kunicki TJ, Nugent DJ. The genetics of normal platelet reactivity[J].Blood,2010,116(15):2627-2634.
    [37]van der Net JB, van Etten J, Yazdanpanah M, et al. Gene-load score of the renin-angiotensin-aldosterone system is associated with coronary heart disease in familial hypercholesterolaemia[J]. Eur Heart J,2008,29(11):1370-1376.
    [38]Brown BD, Nsengimana J, Barrett JH, et al. An evaluation of inflammatory gene polymorphisms in sibships discordant for premature coronary artery disease:the GRACE-IMMUNE study[J]. BMC Med,2010 Jan 13;8:5.
    [39]刘志远,李纲,李玉东,等.早发CHD患者冠状动脉病变特点及危险因素的临床研究[J].中国心血管病研究杂志,2008,6(9):657-659.
    [40]Wang MH, Lee WL, Wang KY, et a 1.Short-term follow-up results of drug-eluting stenting in premature coronary artery disease patients with multiple atherosclerotic risk factors[J].J Chin Med Assoc,2008,71(7):342-346.
    [41]李昌繁,江时森.CHD危险因素聚集与冠状动脉狄窄的关系研究[J].中国微循 环,2007,11(2):122-124.
    [42]Krishaswami S, Joseph G. Lack of correlation between coronary risk factor and CAD severity[J]. Int J Cardiol,1994,47(1):37-43.
    [43]黄聪,张政红,曹辉,等.冠状动脉狭窄程度与冠心病危险因素的关系[J].第二军医大学学报,2003,24(9):1034-1036.
    [44]方瑛,陈忠,马根山,等.早发急性心肌梗死患者的临床和冠状动脉病变特点[J].现代医学,2009,37(2):129-132.
    [45]Reaven G, Metablie syndrome:Pathophysiology and implications for the management of cardiovascular disease[J].Circulation,2002,106(3):286-288.
    [46]刘晓宁,张春玲,武文君,等.年轻人CHD危险因素分布及聚集状况[J].中华心血管病杂志,2003,31(2):87-89.
    [47]Dallongeville J, Grupposo MC, Cottel D, et al. Association between the metabolic syndrome and parental history of premature cardiovascular disease[J].Eur Heart J,2006,27(6):722-728.
    [48]Acharjee S, Qin J, Murphy SA, et al. Distribution of traditional and novel risk factors and their relation to subsequent cardiovascular events in patients with acute coronary syndromes(from.the PROVE IT-TIMI 22 trial)[J].Am J Cardiol,2010,105(5):619-623.
    [49]Shanker J, Perumal G, Rao VS, et al.Genetic studies on the APOA1-C3-A5 gene cluster in Asian Indians with premature coronary artery disease[J].Lipids Health Dis,2008 Sep 19;7:33.
    [50]Lubiszewska B, Skora E, Kruk M, et al. Prevalence of classical risk factors in Polish women with premature coronary artery disease[J].Kardiol Pol,2010,68(9):1032-1037.
    [51]胡大一.促进心血管健康,实现心血管疾病预防战略前移[J].中华心血管病杂志,2010,38(4):290-291.
    [52]陈忠,马根山,黄峻,等.早发冠心病患者颈动脉内膜中膜厚度特点及其预测价位[J].中国动脉硬化杂志,2004,12(1):81-83.
    [53]张录站,陈忠,马根山,等.早发冠心病患者血浆MCP-1水平检测及其临床意义[J].现代医学,2008,36(3):170-173.
    [54]Hippisley-Cox J, Coupland C, Robson J, et al. Derivation, validation, and evaluation of a new QRISK model to estimate lifetime risk of cardiovascular disease:cohort study using QResearch database[J].BMJ,2010,341:c6624.

© 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