期刊文献+

阿托伐他汀对老年冠心病患者骨密度的影响 被引量:8

Effects of atorvastatin on bone mineral density in elderly coronary heart disease patients
原文传递
导出
摘要 目的:探讨常规剂量阿托伐他汀对老年冠心病患者骨密度的影响。方法:对冠状动脉造影检查确诊的冠心病患者94例,根据其血浆LDL-C水平给予阿托伐他汀10~20mg/d(平均13.65mg/d),治疗1年。对照组为87例同期在心血管病房住院的年龄及性别相匹配的其他患者。于入院时及随访1年后以数字式放射吸收测量法测定左手第2、3、4手指中节指骨的相对骨矿物质密度(BMD),并检测治疗前后血TC及LDL-C浓度。结果:1年后,治疗组患者血TC浓度降低25.86%[(5.22±0.97)mmol/L∶(3.87±0.42)mmol/L,P<0.01],LDL-C浓度均降低24.71%[(3.06±0.60)mmol/L∶(2.26±0.41)mmol/L,P<0.01],手指BMD增加5.78%[(0.588±0.061)g/cm2∶(0.622±0.046)g/cm2,P<0.01]。对照组患者血TC浓度[(4.37±1.03)mmol/L∶(4.67±0.49)mmol/L]及LDL-C浓度[(2.61±0.61)mmol/L∶(2.74±0.26)mmol/L,均差异无统计学意义,P>0.05],手指BMD降低0.13%[(0.596±0.062)g/cm2∶(0.585±0.047)g/cm2,P>0.05]。1年后BMD的变化2组相比差异有统计学意义(5.78%∶-0.13%,P<0.01)。结论:常规剂量的阿托伐他汀治疗降低血胆固醇水平的同时能增加老年冠心病患者BMD,改善患者的骨质疏松。 Objective:To investigate the effects of atorvastatin on bone mineral density (BMD) in elderly patients with CHD. Method:The total of 94 consecutive elderly patients (≥50 years with 68 men and 26 women ) with CHD, who have been diagnosed by coronary artery angiograph were treated for 12 months with 10--20 mg/ day atorvastatin(mean 13.65 mg/d) according to their baseline low-density lipoprotein cholesterol (LDL-C) levels and 87 age-and gender-matched patients without using statins provided control data. In all subjects, at baseline and after 1 year, plasma total cholesterol(TC) and LDL-C were measured in a fasting blood sample, while BMD was measured at the finge of left hang by dual energy x-ray absorpiometry (DEXA): Resuit:There were no significant differences between control and treatment groups in age, sex, body mass index, and baseline serum TC and LDL- C levels. In the group treated by atorvastatin, plasma TC levels reduced by 25.86% [(5.22±0.97) mmol/L : (3.87±0.42) mmol/L, P〈0.01] and LDL-C levels reduced by 24.71% [(3.06±0.60) mmol/L : (2.26±0.41) mmol/L, P〈0.01], while BMD showed a significant increase [(0. 588±0. 061) g/cm^2 : (0. 622±0. 046) g/cm^2, P〈 0. 01] during the 1-year follow-up period. In the controls grop, BMD showed a slight decrease [(0.596±0.062)g/cm^2 : (0.585±0.047) g/cm^2, P〉0.05] at the end of the study period. Percentage increments of BMD in the treatment group were significantly higher than in the control group(5.78% : -0.13%, P〈 0.01). Conclusion:This Study indicates that chronic administration of atorvastatin in old coronary heart disease patients exerts a beneficial effect on BMD.
出处 《临床心血管病杂志》 CAS CSCD 北大核心 2008年第2期103-105,共3页 Journal of Clinical Cardiology
关键词 冠状动脉疾病 阿托伐他汀 骨密度 胆固醇 Coronary disease Atorvastatin Bone mineral density Cholesterol
  • 相关文献

参考文献10

  • 1BALDINI V, MASTROPASQUA M, FRANCUCCI C M, et al. Cardiovascular disease and osteoporosis[J]. J Endocrinol Invest, 2005,28:69-72.
  • 2EDWARDS C J. SPECTOR T D. Statins as modulators of bone formation[J]. Arthritis Res, 2002,4 : 151-153.
  • 3葛晓娟,关振龙,刘蔚,马觉民.辛伐他汀在老年急性冠状动脉综合征早期应用的安全性及有效性[J].临床心血管病杂志,2006,22(4):203-205. 被引量:6
  • 4赵翠花,程冠昌,万琪琳,何瑞利.阿托伐他汀对急性心肌梗死患者内皮功能和斑块稳定性的影响[J].临床心血管病杂志,2006,22(4):200-202. 被引量:32
  • 5MUNDY G, GARRETT R, HARRIS S, et al. Stimulation of bone formation in vitro and in rodents by statins[J]. Science, 1999, 286:1946-1949.
  • 6PLOTKIN L I, WEINSTEIN R S, PARFITT A M, et al. Prevention of osteocyte and osteoblast apoptosis by bisphosphonates and calcitonin[J]. J Clin Invest, 1999, 104:1363-1374.
  • 7MEIER C R, SCHLIENGER R G, KRAENZLIN M E, et al. HMG-CoA reductase inhibitors and the risk of fractures[J]. JAMA, 2000, 283:3205-3210.
  • 8CHAN K A, ANDRADE S E, BOLES M, et al. Inhibitors of hydroxymethylglutaryl-coenzyme A reductase and risk of fracture among older women[J]. Lancet, 2000, 355:2185-2188.
  • 9EDWARDS C J, HART D J, SPECTOR T D. Oral statins and increased bone-mineral density in postmenopausal women[J]. Lancet, 2000, 355: 2218- 2219.
  • 10HATZIGEORGIOU C, JACKSON J L. Hydroxymethylglutaryl-coenzyme A reductase inhibitors and osteoporosis: a meta-analysis[J]. Osteoporos Int, 2005,16:990-998.

二级参考文献23

  • 1熊全庚,范木林,郭跃华.早期强化辛伐他汀治疗急性冠状动脉综合征的研究[J].临床心血管病杂志,2004,20(12):710-712. 被引量:25
  • 2KINLAY S, SELWYN A P, DELAGRANGE D, et al. Biological mechanisms for the clinical success of lipid-lowering in coronary artery disease and the use ofsurrogate end points [J]. Curr Opin Lipidol, 1996,7:389-397.
  • 3ALBEROLA AGUILAR A M, REVERT F, MOYA A, et al. Intravenous BQ-123 and phosphoramidon reduce ventricular ectopic beats and myocardial infarct size in dogs submitted to coronary occlusion and reperfusion[J]. Gen Pharmacol, 2000, 35 : 143- 147.
  • 4TRACY R P, LEMSITRE R N, PSATY B M, et al.Relationship of C-reactive protein to risk of cardiovascular disease in the elderly: results from the cardiovascular health study and the real health promotion project [J]. Arterioscler Thromb Vase Biol, 1997,17:1121-1126.
  • 5WATERS D D, AZAR R R. Should intensive cholesterol lowering play a role in the management of acute coronary syndromes [J]. Am J Cardiol, 2000, 86(8B): 35J-42J.
  • 6LIUZZO G, BIASUCCI L M, GALLIMORE J R, et al. The prognostic value of C-reactive protein and serum amyloid- A ptrotein in severe unstable angina [J].N Engl J Med, 1994, 331:417-424.
  • 7IGARASSHI M, TAKEDA Y, ISHIBASHI N, et al.Suppression of neointimal thickening by a newly developed HMG-CoA reductase inhibitor, BAYW6228,and its inhibitory effect on vascular smooth muscle cell growth[J]. Br J Pharmacs, 1997, 120:1172-1178.
  • 8KURIHARA H, YOSHIZUMI M, SUGIYAMA T,et al . The possible role of endothelin-1 in the pathogenesis of coronary vasospasm [J]. J Cardiovasc Pharmacol. 1989, 13(Suppl 5): S132-137.
  • 9LEA A P, McTAVISH D. Atorvastatin. a review of its pharmacolog and therapeutic potential in the management of hyperlipidemias [J]. Drugs, 1997, 53:828-847.
  • 10DIOMEDE L, ALBANI D, SOTTOCOMO M, et al.In vivo anti-inflammatory effect of statins is mediated by nonsterol mevalonate products[J]. Arterioscler Thromb Vasc Biol, 2001, 21:1327-1332.

共引文献36

同被引文献178

引证文献8

二级引证文献28

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部