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Darapladib for Preventing Ischemic Events in Stable Coronary Heart Disease

Identifieur interne : 000478 ( PascalFrancis/Corpus ); précédent : 000477; suivant : 000479

Darapladib for Preventing Ischemic Events in Stable Coronary Heart Disease

Auteurs : Harvey D. White ; Claes Held ; Ralph Stewart ; Elizabeth Tarka ; Rebekkah Brown ; Richard Y. Davies ; Andrzej Budaj ; Robert A. Harrington ; P. Gabriel Steg ; Diego Ardissino ; Paul W. Armstrong ; Alvaro Avezum ; Philip E. Aylward ; Alfonso Bryce ; HONG CHEN ; Ming-Fong Chen ; Ramon Corbalan ; Anthony J. Dalby ; Nicolas Danchin ; Robbert J. De Winter ; Stefan Denchev ; Rafael Diaz ; Moses Elisaf ; Marcus D. Flather ; Assen R. Goudev ; Christopher B. Granger ; Liliana Grinfeld ; Judith S. Hochman ; Steen Husted ; Hyo-Soo Kim ; WOLFGANG KOENIG ; Ales Linhart ; Eva Lonn ; José Lopez-Sendon ; Athanasios J. Manolis ; Emile R. Iii Mohler ; José C. Nicolau ; Prem Pais ; Alexander Parkhomenko ; Terje R. Pedersen ; Daniel Pella ; Marco A. Ramos-Corrales ; Mikhail Ruda ; Mátyás Sereg ; Saulat Siddique ; Peter Sinnaeve ; Peter Smith ; Piyamitr Sritara ; Henk P. Swart ; Rody G. Sy ; Tamio Teramoto ; Hung-Fat Tse ; David Watson ; W. Douglas Weaver ; Robert Weiss ; Margus Viigimaa ; Dragos Vinereanu ; JUNREN ZHU ; Christopher P. Cannon

Source :

RBID : Pascal:14-0105569

Descripteurs français

English descriptors

Abstract

BACKGROUND Elevated lipoprotein-associated phospholipase A2 activity promotes the development of vulnerable atherosclerotic plaques, and elevated plasma levels of this enzyme are associated with an increased risk of coronary events. Darapladib is a selective oral inhibitor of lipoprotein-associated phospholipase A2. METHODS In a double-blind trial, we randomly assigned 15,828 patients with stable coronary heart disease to receive either once-daily darapladib (at a dose of 160 mg) or placebo. The primary end point was the time to cardiovascular death, myocardial infarction, or stroke. Secondary end points included the components of the primary end point as well as major coronary events (death from coronary heart disease, myocardial infarction, or urgent coronary revascularization for myocardial ischemia) and total coronary events (death from coronary heart disease, myocardial infarction, hospitalization for unstable angina, or any coronary revascularization). RESULTS During a median follow-up period of 3.7 years, the primary end point occurred in 769 of 7924 patients (9.7%) in the darapladib group and 819 of 7904 patients (10.4%) in the placebo group (hazard ratio in the darapladib group, 0.94; 95% confidence interval [CI], 0.85 to 1.03; P=0.20).

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A06       @2 18
A08 01  1  ENG  @1 Darapladib for Preventing Ischemic Events in Stable Coronary Heart Disease
A11 01  1    @1 WHITE (Harvey D.)
A11 02  1    @1 HELD (Claes)
A11 03  1    @1 STEWART (Ralph)
A11 04  1    @1 TARKA (Elizabeth)
A11 05  1    @1 BROWN (Rebekkah)
A11 06  1    @1 DAVIES (Richard Y.)
A11 07  1    @1 BUDAJ (Andrzej)
A11 08  1    @1 HARRINGTON (Robert A.)
A11 09  1    @1 STEG (P. Gabriel)
A11 10  1    @1 ARDISSINO (Diego)
A11 11  1    @1 ARMSTRONG (Paul W.)
A11 12  1    @1 AVEZUM (Alvaro)
A11 13  1    @1 AYLWARD (Philip E.)
A11 14  1    @1 BRYCE (Alfonso)
A11 15  1    @1 HONG CHEN
A11 16  1    @1 CHEN (Ming-Fong)
A11 17  1    @1 CORBALAN (Ramon)
A11 18  1    @1 DALBY (Anthony J.)
A11 19  1    @1 DANCHIN (Nicolas)
A11 20  1    @1 DE WINTER (Robbert J.)
A11 21  1    @1 DENCHEV (Stefan)
A11 22  1    @1 DIAZ (Rafael)
A11 23  1    @1 ELISAF (Moses)
A11 24  1    @1 FLATHER (Marcus D.)
A11 25  1    @1 GOUDEV (Assen R.)
A11 26  1    @1 GRANGER (Christopher B.)
A11 27  1    @1 GRINFELD (Liliana)
A11 28  1    @1 HOCHMAN (Judith S.)
A11 29  1    @1 HUSTED (Steen)
A11 30  1    @1 KIM (Hyo-Soo)
A11 31  1    @1 WOLFGANG KOENIG
A11 32  1    @1 LINHART (Ales)
A11 33  1    @1 LONN (Eva)
A11 34  1    @1 LOPEZ-SENDON (José)
A11 35  1    @1 MANOLIS (Athanasios J.)
A11 36  1    @1 MOHLER (Emile R. III)
A11 37  1    @1 NICOLAU (José C.)
A11 38  1    @1 PAIS (Prem)
A11 39  1    @1 PARKHOMENKO (Alexander)
A11 40  1    @1 PEDERSEN (Terje R.)
A11 41  1    @1 PELLA (Daniel)
A11 42  1    @1 RAMOS-CORRALES (Marco A.)
A11 43  1    @1 RUDA (Mikhail)
A11 44  1    @1 SEREG (Mátyás)
A11 45  1    @1 SIDDIQUE (Saulat)
A11 46  1    @1 SINNAEVE (Peter)
A11 47  1    @1 SMITH (Peter)
A11 48  1    @1 SRITARA (Piyamitr)
A11 49  1    @1 SWART (Henk P.)
A11 50  1    @1 SY (Rody G.)
A11 51  1    @1 TERAMOTO (Tamio)
A11 52  1    @1 TSE (Hung-Fat)
A11 53  1    @1 WATSON (David)
A11 54  1    @1 WEAVER (W. Douglas)
A11 55  1    @1 WEISS (Robert)
A11 56  1    @1 VIIGIMAA (Margus)
A11 57  1    @1 VINEREANU (Dragos)
A11 58  1    @1 JUNREN ZHU
A11 59  1    @1 CANNON (Christopher P.)
A14 01      @1 Green Lane Cardiovascular Service, Auckland City Hospital and University of Auckland @2 Auckland @3 NZL @Z 1 aut. @Z 3 aut.
A14 02      @1 Department of Medical Sciences, Cardiology, Uppsala University, and Uppsala Clinical Research Center @2 Uppsala @3 SWE @Z 2 aut.
A14 03      @1 Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKline, King of Prussia @2 PA @3 USA @Z 4 aut. @Z 6 aut.
A14 04      @1 Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKlineResearch Triangle Park @2 North Carolina @3 USA @Z 5 aut. @Z 47 aut. @Z 53 aut.
A14 05      @1 Duke University Medical Center @2 Durham, North Carolina @3 USA @Z 26 aut.
A14 06      @1 Postgraduate Medical School, Grochowski Hospital @2 Warsaw @3 POL @Z 7 aut.
A14 07      @1 Department of Medicine, Stanford University @2 Stanford, CA @3 USA @Z 8 aut.
A14 08      @1 INSERM Unité 1148, Assistance Publique-Hôpitaux de Paris, Département Hospitalo-Universitaire FIRE, Hôpital Bichat @2 Paris @3 FRA @Z 9 aut.
A14 09      @1 Université Paris-Diderot, Sorbonne-Paris Cité @2 Paris @3 FRA @Z 9 aut.
A14 10      @1 Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, INSERM Unité 970 and Université Paris Descartes @2 Paris @3 FRA @Z 19 aut.
A14 11      @1 NHLI Imperial College, ICMS, Royal Brompton Hospital @2 London @3 GBR @Z 9 aut.
A14 12      @1 Azienda Ospedaliero-Universitaria di Parma @2 Parma @3 ITA @Z 10 aut.
A14 13      @1 Canadian VIGOUR Centre, University of Alberta @2 Edmonton @3 CAN @Z 11 aut.
A14 14      @1 Department of Medicine and Population Health Research Institute, McMaster University @2 Hamilton, ON @3 CAN @Z 33 aut.
A14 15      @1 Dante Pazzanese Institute of Cardiology @2 São Paulo @3 BRA @Z 12 aut.
A14 16      @1 Heart Institute (InCor), University of São Paulo Medical School @2 São Paulo @3 BRA @Z 37 aut.
A14 17      @1 South Australian Health and Medical Research Institute, Flinders University and Medical Centre @2 Adelaide, SA @3 AUS @Z 13 aut.
A14 18      @1 Cardiogolf/Clinica El Golf @2 Lima @3 PER @Z 14 aut.
A14 19      @1 Department of Cardiology, Peking University People's Hospital @2 Beijing @3 CHN @Z 15 aut.
A14 20      @1 Department of Internal Medicine, National Taiwan University Hospital @2 Taipei @3 TWN @Z 16 aut.
A14 21      @1 Cardiovascular Division Pontificia Universidad Catolica de Chile @2 Santiago @3 CHL @Z 17 aut.
A14 22      @1 Milpark Hospital @2 Johannesburg @3 ZAF @Z 18 aut.
A14 23      @1 Department of Cardiology, Academic Medical Center, University of Amsterdam @2 Amsterdam @3 NLD @Z 20 aut.
A14 24      @1 Clinic of Cardiology, University Hospital Alexandrovska @2 Sofia @3 BGR @Z 21 aut.
A14 25      @1 Cardiology Department, Queen Giovanna University Hospital @2 Sofia @3 BGR @Z 25 aut.
A17 01  1    @1 STABILITY Investigators @3 INC
A20       @1 1702-1711
A21       @1 2014
A23 01      @0 ENG
A43 01      @1 INIST @2 6013 @5 354000500437940060
A44       @0 0000 @1 © 2014 INIST-CNRS. All rights reserved.
A45       @0 22 ref.
A47 01  1    @0 14-0105569
A60       @1 P
A61       @0 A
A64 01  1    @0 The New England journal of medicine
A66 01      @0 USA
C01 01    ENG  @0 BACKGROUND Elevated lipoprotein-associated phospholipase A2 activity promotes the development of vulnerable atherosclerotic plaques, and elevated plasma levels of this enzyme are associated with an increased risk of coronary events. Darapladib is a selective oral inhibitor of lipoprotein-associated phospholipase A2. METHODS In a double-blind trial, we randomly assigned 15,828 patients with stable coronary heart disease to receive either once-daily darapladib (at a dose of 160 mg) or placebo. The primary end point was the time to cardiovascular death, myocardial infarction, or stroke. Secondary end points included the components of the primary end point as well as major coronary events (death from coronary heart disease, myocardial infarction, or urgent coronary revascularization for myocardial ischemia) and total coronary events (death from coronary heart disease, myocardial infarction, hospitalization for unstable angina, or any coronary revascularization). RESULTS During a median follow-up period of 3.7 years, the primary end point occurred in 769 of 7924 patients (9.7%) in the darapladib group and 819 of 7904 patients (10.4%) in the placebo group (hazard ratio in the darapladib group, 0.94; 95% confidence interval [CI], 0.85 to 1.03; P=0.20).
C02 01  X    @0 002B01
C02 02  X    @0 002B12A03
C03 01  X  FRE  @0 Ischémie @5 01
C03 01  X  ENG  @0 Ischemia @5 01
C03 01  X  SPA  @0 Isquemia @5 01
C03 02  X  FRE  @0 Cardiopathie coronaire @5 02
C03 02  X  ENG  @0 Coronary heart disease @5 02
C03 02  X  SPA  @0 Cardiopatía coronaria @5 02
C03 03  X  FRE  @0 Darapladib @2 FR @5 04
C03 03  X  ENG  @0 Darapladib @2 FR @5 04
C03 03  X  SPA  @0 Darapladib @2 FR @5 04
C03 04  X  FRE  @0 Prévention @5 07
C03 04  X  ENG  @0 Prevention @5 07
C03 04  X  SPA  @0 Prevención @5 07
C03 05  X  FRE  @0 Médecine @5 08
C03 05  X  ENG  @0 Medicine @5 08
C03 05  X  SPA  @0 Medicina @5 08
C07 01  X  FRE  @0 Pathologie de l'appareil circulatoire @5 37
C07 01  X  ENG  @0 Cardiovascular disease @5 37
C07 01  X  SPA  @0 Aparato circulatorio patología @5 37
C07 02  X  FRE  @0 Inhibiteur de la phospholipase A2 @4 INC @5 86
N21       @1 139
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 14-0105569 INIST
ET : Darapladib for Preventing Ischemic Events in Stable Coronary Heart Disease
AU : WHITE (Harvey D.); HELD (Claes); STEWART (Ralph); TARKA (Elizabeth); BROWN (Rebekkah); DAVIES (Richard Y.); BUDAJ (Andrzej); HARRINGTON (Robert A.); STEG (P. Gabriel); ARDISSINO (Diego); ARMSTRONG (Paul W.); AVEZUM (Alvaro); AYLWARD (Philip E.); BRYCE (Alfonso); HONG CHEN; CHEN (Ming-Fong); CORBALAN (Ramon); DALBY (Anthony J.); DANCHIN (Nicolas); DE WINTER (Robbert J.); DENCHEV (Stefan); DIAZ (Rafael); ELISAF (Moses); FLATHER (Marcus D.); GOUDEV (Assen R.); GRANGER (Christopher B.); GRINFELD (Liliana); HOCHMAN (Judith S.); HUSTED (Steen); KIM (Hyo-Soo); WOLFGANG KOENIG; LINHART (Ales); LONN (Eva); LOPEZ-SENDON (José); MANOLIS (Athanasios J.); MOHLER (Emile R. III); NICOLAU (José C.); PAIS (Prem); PARKHOMENKO (Alexander); PEDERSEN (Terje R.); PELLA (Daniel); RAMOS-CORRALES (Marco A.); RUDA (Mikhail); SEREG (Mátyás); SIDDIQUE (Saulat); SINNAEVE (Peter); SMITH (Peter); SRITARA (Piyamitr); SWART (Henk P.); SY (Rody G.); TERAMOTO (Tamio); TSE (Hung-Fat); WATSON (David); WEAVER (W. Douglas); WEISS (Robert); VIIGIMAA (Margus); VINEREANU (Dragos); JUNREN ZHU; CANNON (Christopher P.)
AF : Green Lane Cardiovascular Service, Auckland City Hospital and University of Auckland/Auckland/Nouvelle-Zélande (1 aut., 3 aut.); Department of Medical Sciences, Cardiology, Uppsala University, and Uppsala Clinical Research Center/Uppsala/Suède (2 aut.); Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKline, King of Prussia/PA/Etats-Unis (4 aut., 6 aut.); Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKlineResearch Triangle Park/North Carolina/Etats-Unis (5 aut., 47 aut., 53 aut.); Duke University Medical Center/Durham, North Carolina/Etats-Unis (26 aut.); Postgraduate Medical School, Grochowski Hospital/Warsaw/Pologne (7 aut.); Department of Medicine, Stanford University/Stanford, CA/Etats-Unis (8 aut.); INSERM Unité 1148, Assistance Publique-Hôpitaux de Paris, Département Hospitalo-Universitaire FIRE, Hôpital Bichat/Paris/France (9 aut.); Université Paris-Diderot, Sorbonne-Paris Cité/Paris/France (9 aut.); Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, INSERM Unité 970 and Université Paris Descartes/Paris/France (19 aut.); NHLI Imperial College, ICMS, Royal Brompton Hospital/London/Royaume-Uni (9 aut.); Azienda Ospedaliero-Universitaria di Parma/Parma/Italie (10 aut.); Canadian VIGOUR Centre, University of Alberta/Edmonton/Canada (11 aut.); Department of Medicine and Population Health Research Institute, McMaster University/Hamilton, ON/Canada (33 aut.); Dante Pazzanese Institute of Cardiology/São Paulo/Brésil (12 aut.); Heart Institute (InCor), University of São Paulo Medical School/São Paulo/Brésil (37 aut.); South Australian Health and Medical Research Institute, Flinders University and Medical Centre/Adelaide, SA/Australie (13 aut.); Cardiogolf/Clinica El Golf/Lima/Pérou (14 aut.); Department of Cardiology, Peking University People's Hospital/Beijing/Chine (15 aut.); Department of Internal Medicine, National Taiwan University Hospital/Taipei/Taïwan (16 aut.); Cardiovascular Division Pontificia Universidad Catolica de Chile/Santiago/Chili (17 aut.); Milpark Hospital/Johannesburg/Afrique du Sud (18 aut.); Department of Cardiology, Academic Medical Center, University of Amsterdam/Amsterdam/Pays-Bas (20 aut.); Clinic of Cardiology, University Hospital Alexandrovska/Sofia/Bulgarie (21 aut.); Cardiology Department, Queen Giovanna University Hospital/Sofia/Bulgarie (25 aut.)
DT : Publication en série; Niveau analytique
SO : The New England journal of medicine; ISSN 0028-4793; Coden NEJMAG; Etats-Unis; Da. 2014; Vol. 370; No. 18; Pp. 1702-1711; Bibl. 22 ref.
LA : Anglais
EA : BACKGROUND Elevated lipoprotein-associated phospholipase A2 activity promotes the development of vulnerable atherosclerotic plaques, and elevated plasma levels of this enzyme are associated with an increased risk of coronary events. Darapladib is a selective oral inhibitor of lipoprotein-associated phospholipase A2. METHODS In a double-blind trial, we randomly assigned 15,828 patients with stable coronary heart disease to receive either once-daily darapladib (at a dose of 160 mg) or placebo. The primary end point was the time to cardiovascular death, myocardial infarction, or stroke. Secondary end points included the components of the primary end point as well as major coronary events (death from coronary heart disease, myocardial infarction, or urgent coronary revascularization for myocardial ischemia) and total coronary events (death from coronary heart disease, myocardial infarction, hospitalization for unstable angina, or any coronary revascularization). RESULTS During a median follow-up period of 3.7 years, the primary end point occurred in 769 of 7924 patients (9.7%) in the darapladib group and 819 of 7904 patients (10.4%) in the placebo group (hazard ratio in the darapladib group, 0.94; 95% confidence interval [CI], 0.85 to 1.03; P=0.20).
CC : 002B01; 002B12A03
FD : Ischémie; Cardiopathie coronaire; Darapladib; Prévention; Médecine
FG : Pathologie de l'appareil circulatoire; Inhibiteur de la phospholipase A2
ED : Ischemia; Coronary heart disease; Darapladib; Prevention; Medicine
EG : Cardiovascular disease
SD : Isquemia; Cardiopatía coronaria; Darapladib; Prevención; Medicina
LO : INIST-6013.354000500437940060
ID : 14-0105569

Links to Exploration step

Pascal:14-0105569

Le document en format XML

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<name sortKey="Steg, P Gabriel" sort="Steg, P Gabriel" uniqKey="Steg P" first="P. Gabriel" last="Steg">P. Gabriel Steg</name>
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<name sortKey="Ardissino, Diego" sort="Ardissino, Diego" uniqKey="Ardissino D" first="Diego" last="Ardissino">Diego Ardissino</name>
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<name sortKey="Armstrong, Paul W" sort="Armstrong, Paul W" uniqKey="Armstrong P" first="Paul W." last="Armstrong">Paul W. Armstrong</name>
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<name sortKey="Avezum, Alvaro" sort="Avezum, Alvaro" uniqKey="Avezum A" first="Alvaro" last="Avezum">Alvaro Avezum</name>
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<name sortKey="Aylward, Philip E" sort="Aylward, Philip E" uniqKey="Aylward P" first="Philip E." last="Aylward">Philip E. Aylward</name>
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<name sortKey="Bryce, Alfonso" sort="Bryce, Alfonso" uniqKey="Bryce A" first="Alfonso" last="Bryce">Alfonso Bryce</name>
<affiliation>
<inist:fA14 i1="18">
<s1>Cardiogolf/Clinica El Golf</s1>
<s2>Lima</s2>
<s3>PER</s3>
<sZ>14 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hong Chen" sort="Hong Chen" uniqKey="Hong Chen" last="Hong Chen">HONG CHEN</name>
<affiliation>
<inist:fA14 i1="19">
<s1>Department of Cardiology, Peking University People's Hospital</s1>
<s2>Beijing</s2>
<s3>CHN</s3>
<sZ>15 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Chen, Ming Fong" sort="Chen, Ming Fong" uniqKey="Chen M" first="Ming-Fong" last="Chen">Ming-Fong Chen</name>
<affiliation>
<inist:fA14 i1="20">
<s1>Department of Internal Medicine, National Taiwan University Hospital</s1>
<s2>Taipei</s2>
<s3>TWN</s3>
<sZ>16 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Corbalan, Ramon" sort="Corbalan, Ramon" uniqKey="Corbalan R" first="Ramon" last="Corbalan">Ramon Corbalan</name>
<affiliation>
<inist:fA14 i1="21">
<s1>Cardiovascular Division Pontificia Universidad Catolica de Chile</s1>
<s2>Santiago</s2>
<s3>CHL</s3>
<sZ>17 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Dalby, Anthony J" sort="Dalby, Anthony J" uniqKey="Dalby A" first="Anthony J." last="Dalby">Anthony J. Dalby</name>
<affiliation>
<inist:fA14 i1="22">
<s1>Milpark Hospital</s1>
<s2>Johannesburg</s2>
<s3>ZAF</s3>
<sZ>18 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Danchin, Nicolas" sort="Danchin, Nicolas" uniqKey="Danchin N" first="Nicolas" last="Danchin">Nicolas Danchin</name>
<affiliation>
<inist:fA14 i1="10">
<s1>Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, INSERM Unité 970 and Université Paris Descartes</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="De Winter, Robbert J" sort="De Winter, Robbert J" uniqKey="De Winter R" first="Robbert J." last="De Winter">Robbert J. De Winter</name>
<affiliation>
<inist:fA14 i1="23">
<s1>Department of Cardiology, Academic Medical Center, University of Amsterdam</s1>
<s2>Amsterdam</s2>
<s3>NLD</s3>
<sZ>20 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Denchev, Stefan" sort="Denchev, Stefan" uniqKey="Denchev S" first="Stefan" last="Denchev">Stefan Denchev</name>
<affiliation>
<inist:fA14 i1="24">
<s1>Clinic of Cardiology, University Hospital Alexandrovska</s1>
<s2>Sofia</s2>
<s3>BGR</s3>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Diaz, Rafael" sort="Diaz, Rafael" uniqKey="Diaz R" first="Rafael" last="Diaz">Rafael Diaz</name>
</author>
<author>
<name sortKey="Elisaf, Moses" sort="Elisaf, Moses" uniqKey="Elisaf M" first="Moses" last="Elisaf">Moses Elisaf</name>
</author>
<author>
<name sortKey="Flather, Marcus D" sort="Flather, Marcus D" uniqKey="Flather M" first="Marcus D." last="Flather">Marcus D. Flather</name>
</author>
<author>
<name sortKey="Goudev, Assen R" sort="Goudev, Assen R" uniqKey="Goudev A" first="Assen R." last="Goudev">Assen R. Goudev</name>
<affiliation>
<inist:fA14 i1="25">
<s1>Cardiology Department, Queen Giovanna University Hospital</s1>
<s2>Sofia</s2>
<s3>BGR</s3>
<sZ>25 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Granger, Christopher B" sort="Granger, Christopher B" uniqKey="Granger C" first="Christopher B." last="Granger">Christopher B. Granger</name>
<affiliation>
<inist:fA14 i1="05">
<s1>Duke University Medical Center</s1>
<s2>Durham, North Carolina</s2>
<s3>USA</s3>
<sZ>26 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Grinfeld, Liliana" sort="Grinfeld, Liliana" uniqKey="Grinfeld L" first="Liliana" last="Grinfeld">Liliana Grinfeld</name>
</author>
<author>
<name sortKey="Hochman, Judith S" sort="Hochman, Judith S" uniqKey="Hochman J" first="Judith S." last="Hochman">Judith S. Hochman</name>
</author>
<author>
<name sortKey="Husted, Steen" sort="Husted, Steen" uniqKey="Husted S" first="Steen" last="Husted">Steen Husted</name>
</author>
<author>
<name sortKey="Kim, Hyo Soo" sort="Kim, Hyo Soo" uniqKey="Kim H" first="Hyo-Soo" last="Kim">Hyo-Soo Kim</name>
</author>
<author>
<name sortKey="Wolfgang Koenig" sort="Wolfgang Koenig" uniqKey="Wolfgang Koenig" last="Wolfgang Koenig">WOLFGANG KOENIG</name>
</author>
<author>
<name sortKey="Linhart, Ales" sort="Linhart, Ales" uniqKey="Linhart A" first="Ales" last="Linhart">Ales Linhart</name>
</author>
<author>
<name sortKey="Lonn, Eva" sort="Lonn, Eva" uniqKey="Lonn E" first="Eva" last="Lonn">Eva Lonn</name>
<affiliation>
<inist:fA14 i1="14">
<s1>Department of Medicine and Population Health Research Institute, McMaster University</s1>
<s2>Hamilton, ON</s2>
<s3>CAN</s3>
<sZ>33 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Lopez Sendon, Jose" sort="Lopez Sendon, Jose" uniqKey="Lopez Sendon J" first="José" last="Lopez-Sendon">José Lopez-Sendon</name>
</author>
<author>
<name sortKey="Manolis, Athanasios J" sort="Manolis, Athanasios J" uniqKey="Manolis A" first="Athanasios J." last="Manolis">Athanasios J. Manolis</name>
</author>
<author>
<name sortKey="Mohler, Emile R Iii" sort="Mohler, Emile R Iii" uniqKey="Mohler E" first="Emile R. Iii" last="Mohler">Emile R. Iii Mohler</name>
</author>
<author>
<name sortKey="Nicolau, Jose C" sort="Nicolau, Jose C" uniqKey="Nicolau J" first="José C." last="Nicolau">José C. Nicolau</name>
<affiliation>
<inist:fA14 i1="16">
<s1>Heart Institute (InCor), University of São Paulo Medical School</s1>
<s2>São Paulo</s2>
<s3>BRA</s3>
<sZ>37 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Pais, Prem" sort="Pais, Prem" uniqKey="Pais P" first="Prem" last="Pais">Prem Pais</name>
</author>
<author>
<name sortKey="Parkhomenko, Alexander" sort="Parkhomenko, Alexander" uniqKey="Parkhomenko A" first="Alexander" last="Parkhomenko">Alexander Parkhomenko</name>
</author>
<author>
<name sortKey="Pedersen, Terje R" sort="Pedersen, Terje R" uniqKey="Pedersen T" first="Terje R." last="Pedersen">Terje R. Pedersen</name>
</author>
<author>
<name sortKey="Pella, Daniel" sort="Pella, Daniel" uniqKey="Pella D" first="Daniel" last="Pella">Daniel Pella</name>
</author>
<author>
<name sortKey="Ramos Corrales, Marco A" sort="Ramos Corrales, Marco A" uniqKey="Ramos Corrales M" first="Marco A." last="Ramos-Corrales">Marco A. Ramos-Corrales</name>
</author>
<author>
<name sortKey="Ruda, Mikhail" sort="Ruda, Mikhail" uniqKey="Ruda M" first="Mikhail" last="Ruda">Mikhail Ruda</name>
</author>
<author>
<name sortKey="Sereg, Matyas" sort="Sereg, Matyas" uniqKey="Sereg M" first="Mátyás" last="Sereg">Mátyás Sereg</name>
</author>
<author>
<name sortKey="Siddique, Saulat" sort="Siddique, Saulat" uniqKey="Siddique S" first="Saulat" last="Siddique">Saulat Siddique</name>
</author>
<author>
<name sortKey="Sinnaeve, Peter" sort="Sinnaeve, Peter" uniqKey="Sinnaeve P" first="Peter" last="Sinnaeve">Peter Sinnaeve</name>
</author>
<author>
<name sortKey="Smith, Peter" sort="Smith, Peter" uniqKey="Smith P" first="Peter" last="Smith">Peter Smith</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKlineResearch Triangle Park</s1>
<s2>North Carolina</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>47 aut.</sZ>
<sZ>53 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Sritara, Piyamitr" sort="Sritara, Piyamitr" uniqKey="Sritara P" first="Piyamitr" last="Sritara">Piyamitr Sritara</name>
</author>
<author>
<name sortKey="Swart, Henk P" sort="Swart, Henk P" uniqKey="Swart H" first="Henk P." last="Swart">Henk P. Swart</name>
</author>
<author>
<name sortKey="Sy, Rody G" sort="Sy, Rody G" uniqKey="Sy R" first="Rody G." last="Sy">Rody G. Sy</name>
</author>
<author>
<name sortKey="Teramoto, Tamio" sort="Teramoto, Tamio" uniqKey="Teramoto T" first="Tamio" last="Teramoto">Tamio Teramoto</name>
</author>
<author>
<name sortKey="Tse, Hung Fat" sort="Tse, Hung Fat" uniqKey="Tse H" first="Hung-Fat" last="Tse">Hung-Fat Tse</name>
</author>
<author>
<name sortKey="Watson, David" sort="Watson, David" uniqKey="Watson D" first="David" last="Watson">David Watson</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKlineResearch Triangle Park</s1>
<s2>North Carolina</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>47 aut.</sZ>
<sZ>53 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Weaver, W Douglas" sort="Weaver, W Douglas" uniqKey="Weaver W" first="W. Douglas" last="Weaver">W. Douglas Weaver</name>
</author>
<author>
<name sortKey="Weiss, Robert" sort="Weiss, Robert" uniqKey="Weiss R" first="Robert" last="Weiss">Robert Weiss</name>
</author>
<author>
<name sortKey="Viigimaa, Margus" sort="Viigimaa, Margus" uniqKey="Viigimaa M" first="Margus" last="Viigimaa">Margus Viigimaa</name>
</author>
<author>
<name sortKey="Vinereanu, Dragos" sort="Vinereanu, Dragos" uniqKey="Vinereanu D" first="Dragos" last="Vinereanu">Dragos Vinereanu</name>
</author>
<author>
<name sortKey="Junren Zhu" sort="Junren Zhu" uniqKey="Junren Zhu" last="Junren Zhu">JUNREN ZHU</name>
</author>
<author>
<name sortKey="Cannon, Christopher P" sort="Cannon, Christopher P" uniqKey="Cannon C" first="Christopher P." last="Cannon">Christopher P. Cannon</name>
</author>
</titleStmt>
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<idno type="wicri:source">INIST</idno>
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<idno type="RBID">Pascal:14-0105569</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000478</idno>
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<title xml:lang="en" level="a">Darapladib for Preventing Ischemic Events in Stable Coronary Heart Disease</title>
<author>
<name sortKey="White, Harvey D" sort="White, Harvey D" uniqKey="White H" first="Harvey D." last="White">Harvey D. White</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Green Lane Cardiovascular Service, Auckland City Hospital and University of Auckland</s1>
<s2>Auckland</s2>
<s3>NZL</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Held, Claes" sort="Held, Claes" uniqKey="Held C" first="Claes" last="Held">Claes Held</name>
<affiliation>
<inist:fA14 i1="02">
<s1>Department of Medical Sciences, Cardiology, Uppsala University, and Uppsala Clinical Research Center</s1>
<s2>Uppsala</s2>
<s3>SWE</s3>
<sZ>2 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Stewart, Ralph" sort="Stewart, Ralph" uniqKey="Stewart R" first="Ralph" last="Stewart">Ralph Stewart</name>
<affiliation>
<inist:fA14 i1="01">
<s1>Green Lane Cardiovascular Service, Auckland City Hospital and University of Auckland</s1>
<s2>Auckland</s2>
<s3>NZL</s3>
<sZ>1 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Tarka, Elizabeth" sort="Tarka, Elizabeth" uniqKey="Tarka E" first="Elizabeth" last="Tarka">Elizabeth Tarka</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKline, King of Prussia</s1>
<s2>PA</s2>
<s3>USA</s3>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Brown, Rebekkah" sort="Brown, Rebekkah" uniqKey="Brown R" first="Rebekkah" last="Brown">Rebekkah Brown</name>
<affiliation>
<inist:fA14 i1="04">
<s1>Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKlineResearch Triangle Park</s1>
<s2>North Carolina</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>47 aut.</sZ>
<sZ>53 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Davies, Richard Y" sort="Davies, Richard Y" uniqKey="Davies R" first="Richard Y." last="Davies">Richard Y. Davies</name>
<affiliation>
<inist:fA14 i1="03">
<s1>Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKline, King of Prussia</s1>
<s2>PA</s2>
<s3>USA</s3>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Budaj, Andrzej" sort="Budaj, Andrzej" uniqKey="Budaj A" first="Andrzej" last="Budaj">Andrzej Budaj</name>
<affiliation>
<inist:fA14 i1="06">
<s1>Postgraduate Medical School, Grochowski Hospital</s1>
<s2>Warsaw</s2>
<s3>POL</s3>
<sZ>7 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Harrington, Robert A" sort="Harrington, Robert A" uniqKey="Harrington R" first="Robert A." last="Harrington">Robert A. Harrington</name>
<affiliation>
<inist:fA14 i1="07">
<s1>Department of Medicine, Stanford University</s1>
<s2>Stanford, CA</s2>
<s3>USA</s3>
<sZ>8 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Steg, P Gabriel" sort="Steg, P Gabriel" uniqKey="Steg P" first="P. Gabriel" last="Steg">P. Gabriel Steg</name>
<affiliation>
<inist:fA14 i1="08">
<s1>INSERM Unité 1148, Assistance Publique-Hôpitaux de Paris, Département Hospitalo-Universitaire FIRE, Hôpital Bichat</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="09">
<s1>Université Paris-Diderot, Sorbonne-Paris Cité</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
<affiliation>
<inist:fA14 i1="11">
<s1>NHLI Imperial College, ICMS, Royal Brompton Hospital</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>9 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Ardissino, Diego" sort="Ardissino, Diego" uniqKey="Ardissino D" first="Diego" last="Ardissino">Diego Ardissino</name>
<affiliation>
<inist:fA14 i1="12">
<s1>Azienda Ospedaliero-Universitaria di Parma</s1>
<s2>Parma</s2>
<s3>ITA</s3>
<sZ>10 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Armstrong, Paul W" sort="Armstrong, Paul W" uniqKey="Armstrong P" first="Paul W." last="Armstrong">Paul W. Armstrong</name>
<affiliation>
<inist:fA14 i1="13">
<s1>Canadian VIGOUR Centre, University of Alberta</s1>
<s2>Edmonton</s2>
<s3>CAN</s3>
<sZ>11 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Avezum, Alvaro" sort="Avezum, Alvaro" uniqKey="Avezum A" first="Alvaro" last="Avezum">Alvaro Avezum</name>
<affiliation>
<inist:fA14 i1="15">
<s1>Dante Pazzanese Institute of Cardiology</s1>
<s2>São Paulo</s2>
<s3>BRA</s3>
<sZ>12 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Aylward, Philip E" sort="Aylward, Philip E" uniqKey="Aylward P" first="Philip E." last="Aylward">Philip E. Aylward</name>
<affiliation>
<inist:fA14 i1="17">
<s1>South Australian Health and Medical Research Institute, Flinders University and Medical Centre</s1>
<s2>Adelaide, SA</s2>
<s3>AUS</s3>
<sZ>13 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Bryce, Alfonso" sort="Bryce, Alfonso" uniqKey="Bryce A" first="Alfonso" last="Bryce">Alfonso Bryce</name>
<affiliation>
<inist:fA14 i1="18">
<s1>Cardiogolf/Clinica El Golf</s1>
<s2>Lima</s2>
<s3>PER</s3>
<sZ>14 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Hong Chen" sort="Hong Chen" uniqKey="Hong Chen" last="Hong Chen">HONG CHEN</name>
<affiliation>
<inist:fA14 i1="19">
<s1>Department of Cardiology, Peking University People's Hospital</s1>
<s2>Beijing</s2>
<s3>CHN</s3>
<sZ>15 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Chen, Ming Fong" sort="Chen, Ming Fong" uniqKey="Chen M" first="Ming-Fong" last="Chen">Ming-Fong Chen</name>
<affiliation>
<inist:fA14 i1="20">
<s1>Department of Internal Medicine, National Taiwan University Hospital</s1>
<s2>Taipei</s2>
<s3>TWN</s3>
<sZ>16 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Corbalan, Ramon" sort="Corbalan, Ramon" uniqKey="Corbalan R" first="Ramon" last="Corbalan">Ramon Corbalan</name>
<affiliation>
<inist:fA14 i1="21">
<s1>Cardiovascular Division Pontificia Universidad Catolica de Chile</s1>
<s2>Santiago</s2>
<s3>CHL</s3>
<sZ>17 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Dalby, Anthony J" sort="Dalby, Anthony J" uniqKey="Dalby A" first="Anthony J." last="Dalby">Anthony J. Dalby</name>
<affiliation>
<inist:fA14 i1="22">
<s1>Milpark Hospital</s1>
<s2>Johannesburg</s2>
<s3>ZAF</s3>
<sZ>18 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Danchin, Nicolas" sort="Danchin, Nicolas" uniqKey="Danchin N" first="Nicolas" last="Danchin">Nicolas Danchin</name>
<affiliation>
<inist:fA14 i1="10">
<s1>Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, INSERM Unité 970 and Université Paris Descartes</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>19 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="De Winter, Robbert J" sort="De Winter, Robbert J" uniqKey="De Winter R" first="Robbert J." last="De Winter">Robbert J. De Winter</name>
<affiliation>
<inist:fA14 i1="23">
<s1>Department of Cardiology, Academic Medical Center, University of Amsterdam</s1>
<s2>Amsterdam</s2>
<s3>NLD</s3>
<sZ>20 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Denchev, Stefan" sort="Denchev, Stefan" uniqKey="Denchev S" first="Stefan" last="Denchev">Stefan Denchev</name>
<affiliation>
<inist:fA14 i1="24">
<s1>Clinic of Cardiology, University Hospital Alexandrovska</s1>
<s2>Sofia</s2>
<s3>BGR</s3>
<sZ>21 aut.</sZ>
</inist:fA14>
</affiliation>
</author>
<author>
<name sortKey="Diaz, Rafael" sort="Diaz, Rafael" uniqKey="Diaz R" first="Rafael" last="Diaz">Rafael Diaz</name>
</author>
<author>
<name sortKey="Elisaf, Moses" sort="Elisaf, Moses" uniqKey="Elisaf M" first="Moses" last="Elisaf">Moses Elisaf</name>
</author>
<author>
<name sortKey="Flather, Marcus D" sort="Flather, Marcus D" uniqKey="Flather M" first="Marcus D." last="Flather">Marcus D. Flather</name>
</author>
<author>
<name sortKey="Goudev, Assen R" sort="Goudev, Assen R" uniqKey="Goudev A" first="Assen R." last="Goudev">Assen R. Goudev</name>
<affiliation>
<inist:fA14 i1="25">
<s1>Cardiology Department, Queen Giovanna University Hospital</s1>
<s2>Sofia</s2>
<s3>BGR</s3>
<sZ>25 aut.</sZ>
</inist:fA14>
</affiliation>
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<author>
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<name sortKey="Junren Zhu" sort="Junren Zhu" uniqKey="Junren Zhu" last="Junren Zhu">JUNREN ZHU</name>
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<series>
<title level="j" type="main">The New England journal of medicine</title>
<title level="j" type="abbreviated">N. Engl. j. med.</title>
<idno type="ISSN">0028-4793</idno>
<imprint>
<date when="2014">2014</date>
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<title level="j" type="main">The New England journal of medicine</title>
<title level="j" type="abbreviated">N. Engl. j. med.</title>
<idno type="ISSN">0028-4793</idno>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Coronary heart disease</term>
<term>Darapladib</term>
<term>Ischemia</term>
<term>Medicine</term>
<term>Prevention</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Ischémie</term>
<term>Cardiopathie coronaire</term>
<term>Darapladib</term>
<term>Prévention</term>
<term>Médecine</term>
</keywords>
</textClass>
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<front>
<div type="abstract" xml:lang="en">BACKGROUND Elevated lipoprotein-associated phospholipase A
<sub>2</sub>
activity promotes the development of vulnerable atherosclerotic plaques, and elevated plasma levels of this enzyme are associated with an increased risk of coronary events. Darapladib is a selective oral inhibitor of lipoprotein-associated phospholipase A
<sub>2</sub>
. METHODS In a double-blind trial, we randomly assigned 15,828 patients with stable coronary heart disease to receive either once-daily darapladib (at a dose of 160 mg) or placebo. The primary end point was the time to cardiovascular death, myocardial infarction, or stroke. Secondary end points included the components of the primary end point as well as major coronary events (death from coronary heart disease, myocardial infarction, or urgent coronary revascularization for myocardial ischemia) and total coronary events (death from coronary heart disease, myocardial infarction, hospitalization for unstable angina, or any coronary revascularization). RESULTS During a median follow-up period of 3.7 years, the primary end point occurred in 769 of 7924 patients (9.7%) in the darapladib group and 819 of 7904 patients (10.4%) in the placebo group (hazard ratio in the darapladib group, 0.94; 95% confidence interval [CI], 0.85 to 1.03; P=0.20).</div>
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<s1>Department of Medicine and Population Health Research Institute, McMaster University</s1>
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<s1>Dante Pazzanese Institute of Cardiology</s1>
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<s1>South Australian Health and Medical Research Institute, Flinders University and Medical Centre</s1>
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<s1>Department of Cardiology, Peking University People's Hospital</s1>
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<s1>Department of Internal Medicine, National Taiwan University Hospital</s1>
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<s1>Cardiology Department, Queen Giovanna University Hospital</s1>
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<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>The New England journal of medicine</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>BACKGROUND Elevated lipoprotein-associated phospholipase A
<sub>2</sub>
activity promotes the development of vulnerable atherosclerotic plaques, and elevated plasma levels of this enzyme are associated with an increased risk of coronary events. Darapladib is a selective oral inhibitor of lipoprotein-associated phospholipase A
<sub>2</sub>
. METHODS In a double-blind trial, we randomly assigned 15,828 patients with stable coronary heart disease to receive either once-daily darapladib (at a dose of 160 mg) or placebo. The primary end point was the time to cardiovascular death, myocardial infarction, or stroke. Secondary end points included the components of the primary end point as well as major coronary events (death from coronary heart disease, myocardial infarction, or urgent coronary revascularization for myocardial ischemia) and total coronary events (death from coronary heart disease, myocardial infarction, hospitalization for unstable angina, or any coronary revascularization). RESULTS During a median follow-up period of 3.7 years, the primary end point occurred in 769 of 7924 patients (9.7%) in the darapladib group and 819 of 7904 patients (10.4%) in the placebo group (hazard ratio in the darapladib group, 0.94; 95% confidence interval [CI], 0.85 to 1.03; P=0.20).</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B01</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002B12A03</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Ischémie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Ischemia</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Isquemia</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Cardiopathie coronaire</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Coronary heart disease</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Cardiopatía coronaria</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Darapladib</s0>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Darapladib</s0>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Darapladib</s0>
<s2>FR</s2>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Prévention</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Prevention</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Prevención</s0>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Médecine</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Medicine</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Medicina</s0>
<s5>08</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Pathologie de l'appareil circulatoire</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Cardiovascular disease</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Aparato circulatorio patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Inhibiteur de la phospholipase A2</s0>
<s4>INC</s4>
<s5>86</s5>
</fC07>
<fN21>
<s1>139</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 14-0105569 INIST</NO>
<ET>Darapladib for Preventing Ischemic Events in Stable Coronary Heart Disease</ET>
<AU>WHITE (Harvey D.); HELD (Claes); STEWART (Ralph); TARKA (Elizabeth); BROWN (Rebekkah); DAVIES (Richard Y.); BUDAJ (Andrzej); HARRINGTON (Robert A.); STEG (P. Gabriel); ARDISSINO (Diego); ARMSTRONG (Paul W.); AVEZUM (Alvaro); AYLWARD (Philip E.); BRYCE (Alfonso); HONG CHEN; CHEN (Ming-Fong); CORBALAN (Ramon); DALBY (Anthony J.); DANCHIN (Nicolas); DE WINTER (Robbert J.); DENCHEV (Stefan); DIAZ (Rafael); ELISAF (Moses); FLATHER (Marcus D.); GOUDEV (Assen R.); GRANGER (Christopher B.); GRINFELD (Liliana); HOCHMAN (Judith S.); HUSTED (Steen); KIM (Hyo-Soo); WOLFGANG KOENIG; LINHART (Ales); LONN (Eva); LOPEZ-SENDON (José); MANOLIS (Athanasios J.); MOHLER (Emile R. III); NICOLAU (José C.); PAIS (Prem); PARKHOMENKO (Alexander); PEDERSEN (Terje R.); PELLA (Daniel); RAMOS-CORRALES (Marco A.); RUDA (Mikhail); SEREG (Mátyás); SIDDIQUE (Saulat); SINNAEVE (Peter); SMITH (Peter); SRITARA (Piyamitr); SWART (Henk P.); SY (Rody G.); TERAMOTO (Tamio); TSE (Hung-Fat); WATSON (David); WEAVER (W. Douglas); WEISS (Robert); VIIGIMAA (Margus); VINEREANU (Dragos); JUNREN ZHU; CANNON (Christopher P.)</AU>
<AF>Green Lane Cardiovascular Service, Auckland City Hospital and University of Auckland/Auckland/Nouvelle-Zélande (1 aut., 3 aut.); Department of Medical Sciences, Cardiology, Uppsala University, and Uppsala Clinical Research Center/Uppsala/Suède (2 aut.); Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKline, King of Prussia/PA/Etats-Unis (4 aut., 6 aut.); Metabolic Pathways and Cardiovascular Therapeutic Area, GlaxoSmithKlineResearch Triangle Park/North Carolina/Etats-Unis (5 aut., 47 aut., 53 aut.); Duke University Medical Center/Durham, North Carolina/Etats-Unis (26 aut.); Postgraduate Medical School, Grochowski Hospital/Warsaw/Pologne (7 aut.); Department of Medicine, Stanford University/Stanford, CA/Etats-Unis (8 aut.); INSERM Unité 1148, Assistance Publique-Hôpitaux de Paris, Département Hospitalo-Universitaire FIRE, Hôpital Bichat/Paris/France (9 aut.); Université Paris-Diderot, Sorbonne-Paris Cité/Paris/France (9 aut.); Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, INSERM Unité 970 and Université Paris Descartes/Paris/France (19 aut.); NHLI Imperial College, ICMS, Royal Brompton Hospital/London/Royaume-Uni (9 aut.); Azienda Ospedaliero-Universitaria di Parma/Parma/Italie (10 aut.); Canadian VIGOUR Centre, University of Alberta/Edmonton/Canada (11 aut.); Department of Medicine and Population Health Research Institute, McMaster University/Hamilton, ON/Canada (33 aut.); Dante Pazzanese Institute of Cardiology/São Paulo/Brésil (12 aut.); Heart Institute (InCor), University of São Paulo Medical School/São Paulo/Brésil (37 aut.); South Australian Health and Medical Research Institute, Flinders University and Medical Centre/Adelaide, SA/Australie (13 aut.); Cardiogolf/Clinica El Golf/Lima/Pérou (14 aut.); Department of Cardiology, Peking University People's Hospital/Beijing/Chine (15 aut.); Department of Internal Medicine, National Taiwan University Hospital/Taipei/Taïwan (16 aut.); Cardiovascular Division Pontificia Universidad Catolica de Chile/Santiago/Chili (17 aut.); Milpark Hospital/Johannesburg/Afrique du Sud (18 aut.); Department of Cardiology, Academic Medical Center, University of Amsterdam/Amsterdam/Pays-Bas (20 aut.); Clinic of Cardiology, University Hospital Alexandrovska/Sofia/Bulgarie (21 aut.); Cardiology Department, Queen Giovanna University Hospital/Sofia/Bulgarie (25 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>The New England journal of medicine; ISSN 0028-4793; Coden NEJMAG; Etats-Unis; Da. 2014; Vol. 370; No. 18; Pp. 1702-1711; Bibl. 22 ref.</SO>
<LA>Anglais</LA>
<EA>BACKGROUND Elevated lipoprotein-associated phospholipase A
<sub>2</sub>
activity promotes the development of vulnerable atherosclerotic plaques, and elevated plasma levels of this enzyme are associated with an increased risk of coronary events. Darapladib is a selective oral inhibitor of lipoprotein-associated phospholipase A
<sub>2</sub>
. METHODS In a double-blind trial, we randomly assigned 15,828 patients with stable coronary heart disease to receive either once-daily darapladib (at a dose of 160 mg) or placebo. The primary end point was the time to cardiovascular death, myocardial infarction, or stroke. Secondary end points included the components of the primary end point as well as major coronary events (death from coronary heart disease, myocardial infarction, or urgent coronary revascularization for myocardial ischemia) and total coronary events (death from coronary heart disease, myocardial infarction, hospitalization for unstable angina, or any coronary revascularization). RESULTS During a median follow-up period of 3.7 years, the primary end point occurred in 769 of 7924 patients (9.7%) in the darapladib group and 819 of 7904 patients (10.4%) in the placebo group (hazard ratio in the darapladib group, 0.94; 95% confidence interval [CI], 0.85 to 1.03; P=0.20).</EA>
<CC>002B01; 002B12A03</CC>
<FD>Ischémie; Cardiopathie coronaire; Darapladib; Prévention; Médecine</FD>
<FG>Pathologie de l'appareil circulatoire; Inhibiteur de la phospholipase A2</FG>
<ED>Ischemia; Coronary heart disease; Darapladib; Prevention; Medicine</ED>
<EG>Cardiovascular disease</EG>
<SD>Isquemia; Cardiopatía coronaria; Darapladib; Prevención; Medicina</SD>
<LO>INIST-6013.354000500437940060</LO>
<ID>14-0105569</ID>
</server>
</inist>
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