氨氯地平对高血压患者颈动脉粥样硬化的影响
Effects of Amlodipine on Carotid Atherosclerosis in Patients with Hypertension
DOI: 10.12677/ACM.2019.911195, PDF,   
作者: 杜芯瑜, 崔 鹏, 张 锐, 赵海蓉*:青岛市海慈医疗集团全科医学科(高血压门诊),山东 青岛;潘金鹏:青岛市第九人民医院心内科,山东 青岛
关键词: 高血压氨氯地平颈动脉粥样硬化Hypertension Amlodipine Carotid Atherosclerosis
摘要: 目的:进一步探讨氨氯地平对颈动脉粥样硬化的影响,为患者临床用药的选择提供理论依据。方法入选120名患者,实验组(60例服用氨氯地平5 mg/日)和对照组(60例,服用安慰剂5 mg/日),分别测量初始、6个月、12个月患者的颈动脉超声情况。结果:1) 实验组与对照组比较,在性别、年龄、现在吸烟情况、体重指数(BMI)、总胆固醇(TC)、低密度脂蛋白(LDL)、高密度脂蛋白(HDL)、甘油三酯(TG)、空腹血糖、收缩压、舒张压、动脉粥样硬化斑块体积、劲动脉斑块厚度无统计学差异(p < 0.05);2) 实验组颈动脉硬化斑块体积6个月(706.12 ± 90.08 mm3, p = 0.012)到12个月(427.84 ± 69.62 mm3, p < 0.001),差异有统计学意义;相反,对照组中颈动脉硬化斑块体积6个月(793.63 ± 118.17 mm3, p = 0.964)到12个月(690.52 ± 136.57 mm3, p = 0.088),差异无统计学意义;3) 实验组颈动脉硬化斑块厚度6个月(1.28 ± 0.13 mm, p = 0.379)到12个月(1.00 ± 0.13 mm, p < 0.000);相反,对照组中颈动脉硬化斑块厚度6个月1.33 ± 0.12 mm, p = 0.652)到12个月(1.31 ± 0.13 mm3, p = 0.715),差异无统计学意义。结论:发现氨氯地平在不影响血压的情况下,可降低劲动脉粥样硬化的发生。
Abstract: Objective: To further explore the effect of amlodipine on carotid atherosclerosis, and to provide a theoretical basis for the selection of clinical medication for patients. Methods: 120 patients were enrolled in the experimental group (60 patients taking amlodipine at 5 mg/day) and the control group (60 patients taking placebo at 5 mg/day). Carotid ultrasound was measured at the beginning, 6 months and 12 months, respectively. Results: 1) The experimental group compared with control group, now in gender, age, smoking, body mass index (BMI), total cholesterol (TC), low density lipo-protein (LDL), high-density lipoprotein (HDL), triglyceride (TG), fasting blood glucose, systolic pressure, diastolic blood pressure, atherosclerosis plaque volume, and the artery plaque thickness has no statistical difference (p < 0.05); 2) The carotid plaque volume in the experimental group ranged from 6 months (706.12 ± 90.08 mm3, p = 0.012) to 12 months (427.84 ± 69.62 mm3, p < 0.001), and the difference was statistically significant. In contrast, carotid plaque volume in the control group ranged from 6 months (793.63 ± 118.17 mm3, p = 0.964) to 12 months (690.52 ± 136.57 mm3, p = 0.088), with no statistically significant difference; 3) The thickness of carotid plaque in the experimental group ranged from 6 months (1.28 ± 0.13 mm, p = 0.379) to 12 months (1.00 ± 0.13 mm, p < 0.000). In contrast, carotid plaque thickness in the control group ranged from 1.33 ± 0.12 mm (p = 0.652) to 12 months (1.31 ± 0.13 mm3, p = 0.715), with no statistically significant difference. Conclusion: Amlodipine can reduce the incidence of atherosclerosis without affecting blood pressure.
文章引用:杜芯瑜, 崔鹏, 潘金鹏, 张锐, 赵海蓉. 氨氯地平对高血压患者颈动脉粥样硬化的影响[J]. 临床医学进展, 2019, 9(11): 1261-1265. https://doi.org/10.12677/ACM.2019.911195

参考文献

[1] Underhill, H.R., Yuan, C., Yarnykh, V.L., et al. (2010) Predictors of Surface Disruption with MR Imaging in Asymp-tomatic Carotid Artery Stenosis. American Journal of Neuroradiology, 31, 487-493. [Google Scholar] [CrossRef
[2] Lorenz, M.W., Polak, J.F., Kavousi, M., et al. (2012) Carotid Inti-ma-Media Thickness Progression to Predict Cardiovascular Events in the General Population (the PROG-IMT Collabo-rative Project): A Meta-Analysis of Individual Participant Data. The Lancet, 379, 2053-2062. [Google Scholar] [CrossRef
[3] Nambi, V., Chambless, L., He, M., et al. (2012) Common Carotid Artery Intima-Media Thickness Is as good as Carotid Intima-Media Thickness of All Carotid Artery Segments in Improving Prediction of Coronary Heart Disease Risk in the Atherosclerosis Risk in Communities (ARIC) Study. Euro-pean Heart Journal, 55, 183-190. [Google Scholar] [CrossRef] [PubMed]
[4] Mathiesen, E.B., Joakimsen, O., BØNaa, K.H. (2001) Prevalence of and Risk Factors Associated with Carotid Artery Stenosis: The Tromsø Study. Cerebrovascular Diseases, 12, 44-51. [Google Scholar] [CrossRef] [PubMed]
[5] Prasad, K. (2015) Pathophysiology and Medical Treatment of Carotid Ar-tery Stenosis. International Journal of Angiology, 24, 158-172. [Google Scholar] [CrossRef] [PubMed]
[6] Cuspidi, C., Negri, F., Giudici, V., et al. (2009) Effects of Antihy-pertensive Drugs on Carotid Intima-Media Thickness: Focus on Angiotensin II Receptor Blockers. A Review of Ran-domized, Controlled Trials. Integrated Blood Pressure Control, 2009, 1-8. [Google Scholar] [CrossRef
[7] Nissen, S.E., Tuzcu, E.M., Libby, P., et al. (2004) Effect of Antihyper-tensive Agents on Cardiovascular Events in Patients with Coronary Disease and Normal Blood Pressure: The CAMELOT Study: A Ran-Domized Controlled Trial. JAMA, 292, 2217-2225. [Google Scholar] [CrossRef] [PubMed]
[8] Dahlöf, B., Sever, P.S., Poulter, N.R., et al. (2005) Prevention of Cardiovascular Events with an Antihypertensive Regimen of Amlodipine Adding Perindopril as Required versus Atenolol Adding Bendroflumethiazide as Required, in the Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BPLA): A Multicentre Randomised Controlled Trial. The Lancet, 366, 895-906. [Google Scholar] [CrossRef
[9] Weiss, D. and Taylor, W.R. (2008) Deoxycorticosterone Ac-etate Salt Hypertension in Apolipoprotein E−/− Mice Results in Accelerated Atherosclerosis: The Role of Angiotensin II. Hypertension, 51, 218-224. [Google Scholar] [CrossRef
[10] Chen, X.F., Rateri, D.L., Howatt, D.A., et al. (2013) Amlodipine Reduces AngII-Induced Aortic Aneurysms and Atherosclerosis in Hypercholesterolemic Mice. PLoS ONE, 8, e81743. [Google Scholar] [CrossRef] [PubMed]
[11] Doran, D.E., Weiss, D., Zhang, Y., Griendling, K.K. and Taylor, W.R. (2007) Differential Effects of AT1 Receptor and Ca2+ Channel Blockade Onatherosclerosis, In-flammatory Gene Expression, and Production of Reactive Oxygen Species. Atherosclerosis, 195, 39-47. [Google Scholar] [CrossRef] [PubMed]
[12] Nakandakare, E.R., Charf, A.M. and Quintão, E.C.R. (2008) Dietary Salt Restriction Increases Plasma Lipoprotein and Inflammatory Marker Concentrations in Hypertensive Patients. Atherosclerosis, 200, 410-416. [Google Scholar] [CrossRef] [PubMed]
[13] Kayamori, H., Shimizu, I., Yoshida, Y., et al. (2018) Amlodipine Inhibits Vascular Cell Senescence and Protects Against Atherogenesis through the Mechanism Independent of Calcium Channel Blockade. International Heart Journal, 59, 607-613. [Google Scholar] [CrossRef] [PubMed]