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强化阿托伐他汀治疗对冠心病介入治疗患者颈动脉斑块的影响

朱军 王屹 王连生

朱军, 王屹, 王连生. 强化阿托伐他汀治疗对冠心病介入治疗患者颈动脉斑块的影响[J]. 分子影像学杂志, 2015, 38(1): 62-65. doi: 10.3969/j.issn.1674-4500.2015.01.19
引用本文: 朱军, 王屹, 王连生. 强化阿托伐他汀治疗对冠心病介入治疗患者颈动脉斑块的影响[J]. 分子影像学杂志, 2015, 38(1): 62-65. doi: 10.3969/j.issn.1674-4500.2015.01.19
Jun ZHU, Yi WANG, Liansheng WANG. Investigation of the effects of intensive atorvastatin treatment on carotid arterial plaque in the coronary artery disease patients receiving percutaneous coronary intervention[J]. Journal of Molecular Imaging, 2015, 38(1): 62-65. doi: 10.3969/j.issn.1674-4500.2015.01.19
Citation: Jun ZHU, Yi WANG, Liansheng WANG. Investigation of the effects of intensive atorvastatin treatment on carotid arterial plaque in the coronary artery disease patients receiving percutaneous coronary intervention[J]. Journal of Molecular Imaging, 2015, 38(1): 62-65. doi: 10.3969/j.issn.1674-4500.2015.01.19

强化阿托伐他汀治疗对冠心病介入治疗患者颈动脉斑块的影响

doi: 10.3969/j.issn.1674-4500.2015.01.19
详细信息
    作者简介:

    朱军,E-mail: zhujun555444@sina.com

Investigation of the effects of intensive atorvastatin treatment on carotid arterial plaque in the coronary artery disease patients receiving percutaneous coronary intervention

  • 摘要: 目的本研究在于探讨强化阿托伐他汀治疗对经皮冠状动脉介入治疗(percutaneous coronary intervention, PCI)的冠心病(coronary artery disease, CAD)患者颈动脉斑块的影响。方法选择在南京医科大学第一附属医院住院择期行PCI的CAD患者120例,随机分为常规治疗组60例,强化阿托伐他汀治疗组60例。在术前、术后1个月、术后6个月分别测定颈动脉内中膜厚度(intima media thickness, IMT)、斑块面积(plaque area, PA)。结果常规及强化他汀治疗组中的颈动脉IMT、PA比较有统计学差异[PCI术后1个月:IMT,OR=0.62,95%CI (0.13-3.05),P=0.015;PA,OR=0.78,95%CI (0.09-1.69),P=0.041;PCI术后6个月:IMT,OR=0.58,95%CI (0.10-2.90),P=0.013;PA,OR=0.70,95%CI (0.11-1.78),P=0.035]。结论PCI围手术期给予阿托伐他汀强化治疗减少了CAD患者颈动脉IMT及PA。

     

  • 表  1  所有受试者的基本资料(n=60)

    特征 A组 B组 P
    年龄 63.0±8.5 60.4±9.3 < 0.001
    性別(男),n(%) 42(70.0%) 39(65%) < 0.001
    体质量指数 24.0±2.9 23.5±3.0 0.180
    高血压病,n(%) 33(55%) 30(50.0%) 0.752
    糖尿病,n(%) 18(30.0%) 12(20.0%) 0.465
    高脂血症,n(%) 12(20.0%) 9(15%) 0.677
    吸烟,n(%) 21(35%) 18(30%) 0.736
    总胆固醇 4.41±1.12 4.26±1.19 0.205
    总卄油三脂 2.56±1.08 1.87±1.13 < 0.001
    高密度脂蛋白胆固醇 1.15±0.41 1.26±0.45 < 0.001
    低密度脂蛋白胆固醇 2.72±0.82 2.51±0.69 < 0.001
    年龄,总甘油三脂,总胆固醇,高密度脂蛋白胆固醇,低密度脂蛋白胆固醇(平均数±标准差)为非正态分布,使用Mann-Whitney U检验。体质量指数(平均数±标准差)是正态分布,使用独立样本t检验进行比较。其他数据表述为频率和百分比,并使用卡方检验。P < 0.05被认为是具有统计学差异;组A,常规治疗组;组B,强化他汀治疗组.
    下载: 导出CSV

    表  2  强化阿托伐他汀和常规治疗组中患者PCI术后1个月颈动脉IMT、PA比较

    组別 IMI (mm) PA (mm2) HDL-C (mmol/l) LDL-C (mmol/l)
    治疗前 治疗后1个月 治疗前 治疗后1个月 治疗前 治疗后1个月 治疗前 治疗后1个月
    A组 1.19±0.17 1.08±0.21 15.99±1.20 15.99±1.20 1.15±0.41 1.20±0.40 2.72±0.82 2.45±0.79
    B组 1.33±0.26 1.20±0.32 15.13±1.53 15.13±1.53 1.26±0.45 1.32±0.31 2.51±0.69 2.13±0.58
    P 0.015 0.041 0.040 < 0.05
    P < 0.05.
    下载: 导出CSV

    表  3  强化阿托伐他汀和常规治疗组中患者PCI术后6个月颈动脉IMT、PA比较

    组別 IMI (mm) PA (mm) HDL-C (mmol/l) LDL-C (mmol/l)
    治疗前 治疗后6个月 治疗前 治疗后6个月 治疗前 治疗后6个月 治疗前 治疗后6个月
    A组 1.19±0.17 1.00±0.18 15.99±1.20 12.70±1.28 1.15±0.41 1.24±0.43 2.72±0.82 2.30±0.75
    B组 1.33±0.26 1.13±0.26 15.13±1.53 11.06±1.32 1.26±0.45 1.35±0.41 2.51±0.69 2.01±0.43
    P 0.013 0.035 0.048 < 0.05
    P < 0.05.
    下载: 导出CSV
  • [1] Ozben B, Erdogan O. The role of inflammation and allergy in acute coronary syndromes[J]. Inflamm Allergy Drug Targets, 2008, 7(3): 136-44. doi: 10.2174/187152808785748128
    [2] Brener SJ, Ellis SG, Schneider J, et al. Frequency and long-term impact of myonecrosis after coronary stenting[J]. Eur Heart J, 2002, 23(11): 869-76. doi: 10.1053/euhj.2001.2976
    [3] Briguori C, Colombo A, Airoldi F, et al. Statin administration before percutaneous coronary intervention: Impact on periprocedural myocardial infarction [J]. Eur Heart J, 2004, 94(6A, S): 112E. http://eurheartj.oxfordjournals.org/content/25/20/1822.short
    [4] Zhao XQ, Krasuski RA, Baer J, et al. Effects of combination lipid therapy on coronary stenosis progression and clinical cardiovascular events in coronary disease patients with metabolic syndrome: a combined analysis of the familial atherosclerosis treatment study (FATS), the HDL-Atherosclerosis treatment study (HATS), and the armed forces regression study (AFREGS) J]. Am J Cardiol, 2009, 104(11): 1457-64. doi: 10.1016/j.amjcard.2009.07.035
    [5] Di Sciascio G, Patti G, Pasceri V, et al. Efficacy of atorvastatin reload in patients on chronic statin therapy undergoing percutaneous coronary intervention: results of the ARMYDA-RECAPTURE (Atorvastatin for Reduction of Myocardial Damage During Angioplasty) Randomized Trial[J]. J Am Coll Cardiol, 2009, 54(6): 558-65. doi: 10.1016/j.jacc.2009.05.028
    [6] Jia XW, Fu XH, Zhang J, et al. Intensive cholesterol lowering with statin improves the outcomes of percutaneous coronary intervention in patients with acute coronary syndrome[J]. Chin Med J (Engl), 2009, 122(6): 659-64. http://med.wanfangdata.com.cn/Paper/Detail?id=PeriodicalPaper_zhcmj200906013
    [7] van Kuilenburg J, Lappegard KT, Sexton JA, et al. Persisting thrombin activity in elderly patients with atrial fibrillation on oral anticoagulation is decreased by anti-inflammatory therapy with intensive cholesterol-lowering treatment[J]. J Clin Lipidol, 2011, 5 (4): 273-80. doi: 10.1016/j.jacl.2011.05.003
    [8] Nesar HV, Yosef NK. Short-term therapy with high dose atorvastatin in patients with coronary artery disease can reduce inflammatory process[J]. Acta Med Iran, 2010, 48(4): 218-21. http://www.oalib.com/paper/2256401
    [9] Mitsutake R, Miura SI, Okamura KA, et al. Successful intensive lipid-lowering therapy using atorvastatin stabilizes coronary artery plaque as assessed by multi-detector row computed tomography[J]. Intern Med, 2007, 46(12): 859-63. doi: 10.2169/internalmedicine.46.6434
    [10] Mega JL, Morrow DA, Cannon CP, et al. Cholesterol, C-reactive protein, and cerebrovascular events following intensive and moderate statin therapy[J]. J Thromb Thrombolysis, 2006, 22(1): 71-6. doi: 10.1007/s11239-006-8081-0
    [11] Kadoglou N, Gerasimidis T, Moumtzouoglou A, et al. Intensive lipid-lowering therapy ameliorates novel calcification markers and GSM score in patients with carotid stenosis[J]. Eur J Vasc Endovasc Surg, 2008, 35(6): 661-8. doi: 10.1016/j.ejvs.2007.12.011
    [12] Krasinski A, Chiu B, Spence JD, et al. Three-dimensional ultrasound quantification of intensive statin treatment of carotid atherosclerosis[J]. Ultrasound Med Biol, 2009, 35(11): 1763-72. doi: 10.1016/j.ultrasmedbio.2009.05.017
    [13] Tzou WS, Korcarz CE, Aeschlimann SE. Use of hand-held ultrasound by a nonsonographer clinician to measure carotid intima-media thickness[J]. J Am Soc Echocardiogr, 2006, 19(10): 1286-92. doi: 10.1016/j.echo.2006.04.038
    [14] Nicholls SJ, Tuzcu EM, Schoenhagen P, et al. Effect of atorvastatin (80 mg/day) versus pravastatin (40 mg/day) on arterial remodeling at coronary branch points (from the REVERSAL study) J]. Am J Cardiol, 2005, 96(12): 1636-9. doi: 10.1016/j.amjcard.2005.07.085
    [15] Yu CM, Zhang Q, Lam L, et al. Comparison of intensive and low-dose atorvastatin therapy in the reduction of carotid intimal-medial thickness in patients with coronary heart disease[J]. Heart, 2007, 93(8): 933-9. doi: 10.1136/hrt.2006.102848
    [16] Kini A, Baber U, Kooacic JC, et al. Changes in plaque lipid content after short-term intensive versus standard statin therapy[J]. J Am Coll Cardiol, 2013, 62(1): 21-9. doi: 10.1016/j.jacc.2013.03.058
    [17] Yang JM, Guo XH, Yu X. Long-term intensive glycemic and lipid control ameliorates the carotid intima medial thickness in type 2 diabetes mellitus[J]. Beijing Da Xue Xue Bao, 2007, 39(6): 649-52. http://cn.bing.com/academic/profile?id=2385018597&encoded=0&v=paper_preview&mkt=zh-cn
    [18] Martinez-Hervas S, Priego A, Lorente RA, et al. Subclinical carotid atherosclerosis in patients with familial combined hyperlipidemia. Two years follow-up after treatment with high doses of atorvastatin[J]. Med Clin (Barc), 2012, 138(1): 1-6. doi: 10.1016/j.medcli.2010.12.009
    [19] Yokoi H, Nohara R, Daida H, et al. Change in carotid Intima-Media thickness in a High-Risk group of patients by intensive Lipid-Lowering therapy with rosuvastatin subanalysis of the JART study[J]. Int Heart J, 2014, 55(2): 146-52. doi: 10.1536/ihj.13-216
    [20] Yamasaki T, Iwashimay, Iesmins, et al. Comparison of efficacy of intensive versus mild pitavastatin therapy on lipid and inflammation biomarkers in hypertensive patients with dyslipidemia [J]. PLoS One, 2014, 9(2): e89057. doi: 10.1371/journal.pone.0089057
    [21] Prahl U, Wikstrand J, Bergstrom GM, et al. Slightly elevated High-Sensitivity C-Reactive protein (hsCRP) concentrations are associated with carotid atherosclerosis in women with varying degrees of glucose tolerance[J]. Angiology, 2010, 61(8): 793-801. doi: 10.1177/0003319710370959
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  • 收稿日期:  2014-10-09
  • 刊出日期:  2015-05-15

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