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16篇 您的检索式:作者名="Jacques Genest"
    题名 作者 年代 出处 被引量
1Urotensin II differentially regulates macrophage and hepatic cholesterol homeostasis显示文摘Robert S. Kiss Zhipeng You Jacques Genest David J. Behm Adel Giaid 2011Peptides2011,,5:2
22009 Canadian Cardiovascular Society/Canadian guidelines for the diagnosis and treatment of dyslipidemia and prevention of cardiovascular disease in the adult – 2009 recommendations显示文摘Jacques Genest Ruth McPherson Jiri Frohlich Todd Anderson Norm Campbell André Carpentier Patrick Couture Robert Dufour George Fodor Gordon A. Francis Steven Grover Milan Gupta Robert A. Hegele David C. Lau Lawrence Leiter Gary F. Lewis Eva Lonn G.B. John 2009Canadian Journal of Cardiology2009,,10:2
3Circulating levels of the vasoactive peptide urotensin II in patients with Acute Coronary Syndrome and Stable Coronary Artery Disease显示文摘Hamood Al-Kindi Anouar Hafiane Zhipeng You Isabella Albanese Louise Pilote Jacques Genest Adel Schwertani 2014Peptides2014,,:1
4The Genetics of Dilated Cardiomyopathy: A Prioritized Candidate Gene Study of LMNA , TNNT2 , TCAP , and PLN显示文摘Marika Hirtle‐Lewis Katia Desbiens Isabelle Ruel Nicholas Rudzicz Jacques Genest James C. Engert Nadia Giannetti 2013Clin Cardiol2013,,10:1
5Familial lipoprotein disorders and premature coronary artery disease 显示文摘Schaefer Ernst J Genest Jacques J Ordovas Jose M 1993Current Opinion in Lipidology1993,4,4:1
6Inflammtion modulation and cardiovascular disease prevention显示文摘Zuhier Awan Jacques Genest 2014European Jouranl of Preventive Cradiology2014,3,1:1
7Low density lipoprotein size and coronary artery disease显示文摘 Jacques J Genest J 1992Arterioscler Thromb1992,12,:1
8The Metabolic Syndrome and Cardiovascular Risk显示文摘Mottillo Salvatore Filion Kristian B Genest Jacques 2010Journal of the American College of Cardiology2010,56,14:1
9Clinical Comparison of Acoustic and Electronic Stethoscopes and Design of a New Electronic Stethoscope 显示文摘Grenier MC Katerie Gagnon ID Jacques Genest M 1998Am J Cardiol1998,81,5:1
10Familial Lipoprotein Disorders in Patients With Premature Coronary Artery Disease显示文摘Jacques J. Genest Sarah S. Martin-Munley Judith R. McNamara Jose M. Ordovas Jennifer Jenner Richard H. Myers Steven R. Silberman Peter W.F. Wilson Deeb N. Salem Ernst J. Schaefer 1992Circulation1992,,6:1
112012 Update of the Canadian Cardiovascular Society Guidelines for the Diagnosis and Treatment of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult显示文摘Todd J. Anderson Jean Grégoire Robert A. Hegele Patrick Couture G.B. John Mancini Ruth McPherson Gordon A. Francis Paul Poirier David C. Lau Steven Grover Jacques Genest André C. Carpentier Robert Dufour Milan Gupta Richard Ward Lawrence A. Leiter Eva Lon 2013Canadian Journal of Cardiology2013,,:1
12The Metabolic Syndrome and Cardiovascular Risk显示文摘Salvatore Mottillo Kristian B. Filion Jacques Genest Lawrence Joseph Louise Pilote Paul Poirier Stéphane Rinfret Ernesto L. Schiffrin Mark J. Eisenberg 2010Journal of the American College of Cardiology2010,,14:1
13Effect of Obesity on High -density Lip- oprotein Metabolism显示文摘Shirya Rashid Jacques Genest 2007OBESITY2007,15,12:1
14The Metabolic Syndrome and Cardiovascular Risk显示文摘Salvatore Mottillo Kristian B. Filion Jacques Genest Lawrence Joseph Louise Pilote Paul Poirier Stéphane Rinfret Ernesto L. Schiffrin Mark J. Eisenberg 2010Journal of the American College of Cardiology2010,,14:1
15Metaelliptical copulas and their use in frequency analysis of multivariate hydrological data显示文摘Genest C Favre AC Be'liveau J Jacques C 2007Water Resources Research2007,43,:1
16瑞舒伐他汀治疗后c反应蛋白、LDL胆固醇及心血管事件率的降低:JUPITER试验的一项前瞻性研究显示文摘背景他汀类药物可降低高敏c反应蛋白(hsCRP)和胆固醇的浓度,而假设生成分析提示,若予以他汀类药物治疗后能使hsCRP浓度〈2mg/L同时LDL胆固醇浓度〈1.8mmol/L(〈7mg/L),则患者的临床结局可得到改善。然而,对他汀类药物治疗使LDL胆固醇和hsCRP同时降低的临床益处仍存有争议。该研究旨在前瞻性验证这一假设。方法在对JUPITER试验的15548例(占全部队列的87%)初始健康的个体进行的分析中,前瞻性评估瑞舒伐他汀20mg与安慰剂相对比的疗效。按治疗时LDL胆固醇浓度(〈1.8mmol/L、≥1.8mmol/L)和hsCRP浓度(〈2mg/L、〉/2mv2L)划分,以非致死性心肌梗死率、非致死性卒中率、因不稳定型心绞痛入院率、动脉血运重建率、心血管性死亡率(预设终点)为指标进行疗效评价。该研究最长随访时间为5年(M=1.9)。将随机分组后发生的所有事件均纳入。该试验在Clinical Trails.gov的注册编号为NCT00239681。结果与安慰剂组相比,瑞舒伐他汀治疗组中达到LDLJ胆固醇〈1.8mmol/L人群的血管事件减少了55%[事件发生率1.11/100(人·年)US0.51/100(人·年);HR0.45,95%C10.34~0.60,P〈0.0001],达到hsCRP〈2mg/L.h.群的血管事件减少了62%[事件发生率0.42/100(人·年);HR0.38,95%CI0.26~0.56,P〈0.0001]。虽然对于患者个体而言,LDL胆固醇与hsCRP的降低仅有微弱相关(r〈0.15),但研究发现,瑞舒伐他汀治疗组中同时达到LDL)胆固醇〈1.8mmol/L和hsCRP〈2mg/L人群的血管事件减少了65%[事件发生率0.38/100(人·年);校正HR0.35,95%CI0.23~0.54],而仅达到其中一项或两项均未达到的人群的血管事件仅减少了33%[事件发生率0.74/100(人·年);HR0.67,95%CI0.52~0.87](治疗组间P〈0.0001)。在达到LDL胆固醇〈1.8mmol/L和hsCRP〈1mg/L的人群中,血管事件减少了79%[事件发生率0.24/100(人·年);HR0.21,95%CI0.09~0.52]。无论选用何种脂质检测项目(包括载脂蛋白B/载脂蛋白AI比)作为终点,所达到的hsCRP浓度均为事件发生率的预测指标。结论对于选择开始进行药物预防的人群,LDL胆固醇和hsCRP浓度同时降低可作为瑞舒伐他汀治疗成功的指标。Paul M Ridker Eleanor Danielson Francisco A H Fonseca Jacques Genest Antonio M Gotto Jr John J P Kastelein Wolfgang Koenig Peter Libby Alberto J Lorenzatti Jean G MocFadyen Barge G Nordestgaard James Shepherd James T Willerson Robert J Glynn 徐斌(译) 2009世界临床医学2009,,10:0
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