دورية أكاديمية

Effects of Anacetrapib in Patients with Atherosclerotic Vascular Disease

التفاصيل البيبلوغرافية
العنوان: Effects of Anacetrapib in Patients with Atherosclerotic Vascular Disease
المؤلفون: Bowman L, Hopewell Jc, Chen F, Wallendszus K, Stevens W, Collins R, Wiviott Sd, Cannon Cp, Braunwald E, Sammons E, Landray M.J. Jiang L, Armitage J, Haynes R, Maggioni Ap, Angermann Ce, Ertl G, Wanner C, Pedersen T, Goto S, Teramoto T, Baigent C, Barter P, Chen Y, Chen Z, Gray A, Mihaylova B, Sleight P, Tobert J, Blaustein R, Delucca P, Mitchel Y, Van Leijenhorst G, Sandercock P, Demets D, Kjekshus J, Neuberger J, Tonkin A, Emberson J, Granger C, Colhoun H, Barton J, Bray C, Dayanandan R, Knott C, Lay M, Murphy K, Wincott E, Achiri P, Barry S, Bateman S, Brewster A, Briggs S, Brown R, Burke A, Butler E, Cobb L, Collet A, Crowther J, Cureton L, Danesh-pour S, Fathers S, Fletcher L, Frederick K, Gordon T, Gray M, Heineman J, Howard S, Jackson D, Lam N, Lee R, Machin O, Madgwick Z, Matthewson M, Nolan J, Nunn M, Panicker A, Pank L, Pearson-burton E, Pickworth S, Qiao Y, Radley A, Roby K, Sayer J, Shah S, Taylor K, Thorne H, Timadjer A, Vandenberg K, Wickman M, Willett M, Woods J, Yu H, Aung T, Bulbulia R, Clarke R, Herrington W, Judge P, Lewis D, Llewellyn-bennett R, Mafham M, Preiss D, Reith C, Storey B, Tomson J, Waters E, Baxter A, GOODENOUGH, OLIVER RAMSDELL, Ait-sadi R, Arnold M, Barton I, Berry C, Blower G, Booth J, Brown E, Bu Y, Cleverley P, Coates G, Cox J, Craig M, Cui G, Dalton P, Danel L, Daniels C, Dawe C, Field A, Gilbert S, Harding P, Jayne K, Kurien R, Lancaster G, Maskill A, Mcdougall A, Mostefai Y, Mulay S, Munday A, Murawska A, Prajapati N, Ramesh S, Reid R, Syed S, Todd H, Young A, ZHU, WANGQIN, Parish S, Valdes-marquez E, Hill M, Clark S, Emmens K, Mcclean G, Radley M, Wintour J, Allworth M, Beneat Am, Bird C, Boggs L, CASEY, MAEVE ANN, Chavagnon T, Chung K, Chung R, Cockram L, Cox R, Douglas J, Finnegan L, French H, Goodwin N, Gordon A, Gordon J, Guest C, Hazim S, Hill J, Hrusecka R, Lacey M, Luker N, Mulligan S, Obrero Me, Plunkett N, Sansom L, Shellard R, Taylor J, Taylor P, Tyler J, Weaving L, Wheeler J, Williams T, Yeung M, Beebe S, Bowsher-brown K, Dabrowski J, Henderson J, James J, Lochhead H, Toghill V, Wright L, Young L, Hundei W, Liu J, Qu J, Zhang H, Dai H, Feng F, Hou L, Li J, Ma L, Niu S, Tang R, WANG, SHIYANG, WEI, XICHUN, Xie M, YAN, XIAOTING, Yang M, Zhang Y, Zhang L, Zhang A, Zhang S, Zhao L, Zhong H, Chen L, Gao Y, Li L, YANG, HEE JUNG, Zhang J, Brenner S, Heldmann M, Kraus B, Meyer B, Fajardo-moser M, Hartner C, Knoppe A, Pop-marschall D, Renner J, Saemann U, FABBRI, GIORGIO, Lorimer A, Lucci D, Bartolomei Mecatti B, Ceseri M, Baldini E, Benoni S, Bianchini, Filippo, Ferruzzi P, Miccoli M, Musio S, Ramani F, Gorini M, Orsini G, Kato E, Tawara K, Tomita A, Kitamura S, Saitoh Y, Shimizu M, Shiozaki S, Soeda K, Tanaka A, Eisen A, Steen D, Fish P, Macdonnell S, Kent J, Mccagg A, Greene E, Klements D, Washington K, Davis A, Goeres M, Joyce J, Koen J, Colicchia J, Domercant J, Foster V, Fox C, Gennusa C, Hollis R, Kassa Y, Kelley A, Magloire V, Owens C, Yeh N, Arnesson K, Mosegaard S, Andersen K, Haywood S, Osmanagic A, Pilgaard Madsen C, Rebnord E, Serup-hansen K, Tarras Wahlberg M, Hannibal K, Johansen T, Rasmussen L, Sloth A, Kiuru P, 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Qi G, Jia Z, Meng Y, Wu C, Liu B, Bian X, Li W, Jing J, Sun Y, Wu S, XU, DAN YI, Lv F, Guo C, Long J, Huang Z, Fu X, Yao H, Zheng Y, LIU, CHUNRONG, Tong Q, Wang G, Cheng Y, Gang X, Guo W, He G, Han Q, Bian H, Duan L, Jin C, Xing W, Xu J, Jin Y, Lin Y, ZHOU, XINGYU, Li Y, Guan X, Liu H, PAN, HUA QIONG, Fan P, Ma R, WANG, PENG FEI, Cui R, Sun G, Xie R, Qu P, Li G, Mei J, WANG, FLORIAN LIFAN, Yang Q, Zhang C, Yu B, Cao W, Du W, Luan Y, Wang W, Zhu Y, Jiao H, Qu Y, Yang Z, Du N, Liang B, WANG, DAJIAN, Zhao P, Xu B, Zong D, Tang X, Zong C, Mo Z, Jin P, Xiong J, Cong H, Guo X, Liang R, ZHOU, JUAN, Liu Y, Sun Z, Wan Z, Bian B, ZHANG, WEN, Yao Z, Wang R, Chen G, Ma C, Jiang J, Ni L, Yan H, Su X, Cai J, Ma J, Zhong R, Gu Y, Hu L, Wu X, Feng J, Huang H, Ouyang F, ZHOU, YINGYUAN, Yang T, Deng X, Peng L, Su S, Fu Q, Zong X, Shang Y, SUN, HENGYU, Guo S, He Y, Cha L, Lu Y, Egstrup K, Berg Schmidt E, Dinesen P, Gammelmark A, NIELSEN, MARCELLO, Rix T, Vadmann H, Christensen B, Hessing Kobbelgaard L, 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سنة النشر: 2017
المجموعة: IRIS UNIPV (Università degli studi di Pavia)
مصطلحات موضوعية: lipoprotein, CETP inhibitor, cardiovascular outcomes
الوصف: BACKGROUND: Patients with atherosclerotic vascular disease remain at high risk for cardiovascular events despite effective statin-based treatment of low-density lipoprotein (LDL) cholesterol levels. The inhibition of cholesteryl ester transfer protein (CETP) by anacetrapib reduces LDL cholesterol levels and increases high-density lipoprotein (HDL) cholesterol levels. However, trials of other CETP inhibitors have shown neutral or adverse effects on cardiovascular outcomes. METHODS: We conducted a randomized, double-blind, placebo-controlled trial involving 30,449 adults with atherosclerotic vascular disease who were receiving intensive atorvastatin therapy and who had a mean LDL cholesterol level of 61 mg per deciliter (1.58 mmol per liter), a mean non-HDL cholesterol level of 92 mg per deciliter (2.38 mmol per liter), and a mean HDL cholesterol level of 40 mg per deciliter (1.03 mmol per liter). The patients were assigned to receive either 100 mg of anacetrapib once daily (15,225 patients) or matching placebo (15,224 patients). The primary outcome was the first major coronary event, a composite of coronary death, myocardial infarction, or coronary revascularization. RESULTS: During the median follow-up period of 4.1 years, the primary outcome occurred in significantly fewer patients in the anacetrapib group than in the placebo group (1640 of 15,225 patients [10.8%] vs. 1803 of 15,224 patients [11.8%]; rate ratio, 0.91; 95% confidence interval, 0.85 to 0.97; P=0.004). The relative difference in risk was similar across multiple prespecified subgroups. At the trial midpoint, the mean level of HDL cholesterol was higher by 43 mg per deciliter (1.12 mmol per liter) in the anacetrapib group than in the placebo group (a relative difference of 104%), and the mean level of non-HDL cholesterol was lower by 17 mg per deciliter (0.44 mmol per liter), a relative difference of -18%. There were no significant between-group differences in the risk of death, cancer, or other serious adverse events. CONCLUSIONS: Among patients ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: STAMPA
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28847206; info:eu-repo/semantics/altIdentifier/wos/WOS:000411838100005; volume:377; issue:13; firstpage:1217; lastpage:1227; numberofpages:11; journal:NEW ENGLAND JOURNAL OF MEDICINE; https://hdl.handle.net/11571/1203906Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85030329600
DOI: 10.1056/NEJMoa1706444
الإتاحة: https://doi.org/10.1056/NEJMoa1706444Test
https://hdl.handle.net/11571/1203906Test
رقم الانضمام: edsbas.1CDA76
قاعدة البيانات: BASE