7 research outputs found
HUMAN GENETICS The genetics of Mexico recapitulates Native American substructure and affects biomedical traits
- Author
- Acuna-Alonzo V
- Barquera-Lozano R
- Carnevale A
- Chapela R
- Contreras AV
- Eng C
- Estrada K
- Fernandez-Lopez JC
- Ford JG
- Galanter JM
- García-Herrera R
- Gignoux CR
- Granados-Arriola J
- Hidalgo-Miranda A
- Huntsman S
- Jimenez-Sanchez G
- Kenny EE
- London SJ
- Macin-Perez G
- Moreno-Estrada A
- Navarro BD
- Nuno-Arana I
- Ortiz-Tello P
- Robles V
- Rodriguez-Cintron W
- Rodriguez-Santana JR
- Romero-Hidalgo S
- Romieu I
- Ruiz-Linares A
- Sandoval K
- Sienra-Monge JJ
- Sikora M
- Soberon X
- Via M
- Zakharia F
- Publication venue
- 'American Association for the Advancement of Science (AAAS)'
- Publication date
- 01/01/2014
- Field of study
Stanford University; Department of Genetics; Federal Government of Mexico; Ministry of Health; Mexican Health Foundation (FUNSALUD); Gonzalo Rio Arronte Foundation; George Rosenkranz Prize for Health Care Research in Developing Countries; University of California San Francisco (UCSF) Chancellor's Research Fellowship; Dissertation Year Fellowship; NIH Training Grants [T32GM007175, T32HG000044]; Robert Wood Johnson Foundation Amos Medical Faculty Development Award; Sandler Foundation; American Asthma Foundation; CONACYT [129693]; BBSRC grant [BB/I021213/1]; National Institutes of Health (NIH) [R01GM090087, R01HG003229, ES015794, GM007546, GM061390, HL004464, HL078885, HL088133, HL111636, RR000083, P60MD006902, ZIA ES49019]; National Science Foundation [DMS-1201234]; Intramural Research Program of NIH, National Institute of Environmental Health Science
The genetics of Mexico recapitulates Native American substructure and affects biomedical traits
- Author
- A. Carnevale
- A. Hidalgo-Miranda
- A. Moreno-Estrada
- A. Ruiz-Linares
- A. V. Contreras
- Altshuler
- B. d. R. Navarro
- Bigham
- Browning
- Browning
- C. D. Bustamante
- C. Eng
- C. R. Gignoux
- Campbell
- E. E. Kenny
- E. G. Burchard
- F. Zakharia
- Fejerman
- G. Jimenez-Sanchez
- G. Macin-Perez
- Galanter
- Gorostiza
- H. Rangel-Villalobos
- Hancock
- HANKINSON
- Henn
- Henn
- Hey
- I. Nuno-Arana
- I. Romieu
- I. Silva-Zolezzi
- J. C. Fernandez-Lopez
- J. G. Ford
- J. Granados-Arriola
- J. J. Sienra-Monge
- J. M. Galanter
- J. R. Rodriguez-Santana
- Johnson
- K. Estrada
- K. Sandoval
- Kidd
- Lao
- Li
- Lisker
- M. Sikora
- M. Via
- Mao
- McVean
- Nalls
- Nalls
- Nelson
- Novembre
- P. Ortiz-Tello
- Peralta
- Pickrell
- Purcell
- R. Barquera-Lozano
- R. Chapela
- R. Garcia-Herrera
- Reich
- Romeo
- S. Canizales-Quinteros
- S. Huntsman
- S. J. London
- S. Romero-Hidalgo
- Salari
- Sandoval
- Stephens
- Stephens
- Tang
- To
- Torgerson
- Torgerson
- V. Acuna-Alonzo
- V. Robles
- W. Rodriguez-Cintron
- Wang
- Wang
- Wu
- X. Soberon
- Publication venue
- 'American Association for the Advancement of Science (AAAS)'
- Publication date
- 13/06/2014
- Field of study
Mexico harbors great cultural and ethnic diversity, yet fine-scale patterns of human genome-wide variation from this region remain largely uncharacterized. We studied genomic variation within Mexico from over 1,000 individuals representing 20 indigenous and 11 mestizo populations. We found striking genetic stratification among indigenous populations within Mexico at varying degrees of geographic isolation. Some groups were as differentiated as Europeans are from East Asians. Pre-Columbian genetic substructure is recapitulated in the indigenous ancestry of admixed mestizo individuals across the country. Furthermore, two independently phenotyped cohorts of Mexicans and Mexican Americans showed a significant association between sub-continental ancestry and lung function. Thus, accounting for fine-scale ancestry patterns is critical for medical and population genetic studies within Mexico, in Mexican-descent populations, and likely in many other populations worldwide
Cardiac Troponin T vs Other Biochemical Markers in Patients With Congestive Heart Failure
- Author
- Anand IS Florea VG, Fisher L
- Anand IS Kuskowski MA, Rector TS,
- Anand IS Latini R, Florea VG, Kusk
- Benjamin IJ Jalil JE, Tan LB, Cho
- Bhambi B Eghbali M
- Cohn JN Johnson GR, Shabetai R, Lo
- Cohn JN Levine TB, Olivari MT, Gar
- Crabos M Roth M, Hahn AW, Erne P
- Deswal A Peterson NJ, Feldman AM,
- Francis GS Cohn JN, Johnson G, Rec
- Koh E Nakamura T, Takahashi H
- Krown KA Page MT, Nguyen C, Zechne
- Maisel A
- Mann DL Kent RL, Parsons B, Cooper
- McAlister FA Ezekowitz J, Tonelli
- McMurray JJV Pfeffer MA
- Perna ER Macin SM, Canella JPC, Au
- Poulsen SH Host NB, Jensen SE, Egs
- Ryoji Taniguchi
- Sato Y Kataoka K, Matsumori A, Sas
- Sato Y Yamada T, Taniguchi R, Naga
- Satoshi Shizuta
- St John Sutton MG Sharpe N
- Takahiro Doi
- Takeshi Kimura
- Takeshi Morimoto
- Tan LB Jalil JE, Pick R, Janicki J
- Teiger E Dam T-V, Richard L
- Toru Kita
- Yukihito Sato
- Yukiko Nishio
- Zannad F Alla F, Dousset B, Perez
- Publication venue
- 'Japanese Circulation Society'
- Publication date
- 01/01/2007
- Field of study
Thrombin-receptor antagonist vorapaxar in acute coronary syndromes
- Author
- Aaberge L
- Aase O
- Abrahams L
- Adams M
- Addo T
- Adriaenssens T
- Agarwal H
- Aggarwal K
- Aguirre Salcedo J
- Ahn TH
- Ahsan A
- Ahsan C
- Airaksinen KE
- Akerblom A
- Albarran A
- Albertsson P
- Albirini A
- Allall O
- Altila T
- Alvarez P
- Alves AR Jr
- Ambrosio G
- Ambrosio G
- Ambrosio G
- Amlani M
- Anderson J
- Antoniucci D
- Appel KF
- Apro D
- Ardissino D
- Ardito W
- Ariani K
- Armaganijan L
- Armstrong PW
- Armstrong PW
- Armstrong PW
- Armstrong PW
- Aroney C
- Arstall M
- Asai T
- Ashraf R
- Assennato P
- Atar S
- Atassi K
- Auguadro C
- Aviles R
- Aylward PE
- Aylward PE
- Aylward PE
- Aylward PE
- Azrin M
- Bailey KR
- Baldus S
- Banchs H
- Barriales V
- Bata I
- Batchelor W
- Baumbach A
- Bayet G
- Bayon J
- Beernaert A
- Behrens S
- Beijerbacht HP
- Belchi J
- Belhassane A
- Bellenger N
- Beloscar J
- Bendermacher PE
- Bengtson J
- Berli M
- Berlowitz M
- Bertolami A
- Betriu A
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- Bettinotti M
- Bhagwat R
- Bhaktaram V
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- Blankenship J
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- Breedveld RW
- Brener S
- Brennan M
- Brilakis E
- Brill D
- Brodie B
- Brossoit R
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- Brunvand H
- Buerke M
- Burchenal JJ
- Burgess L
- Burkhardt W
- Butnaru A
- Butter C
- Calle G
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- Canaday D
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- Chang D
- Chang KC
- Chang M
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- Chen E
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- Weiss A
- Werner G
- Westendorp IC
- Westerhausen D
- Whellan DJ
- Whellan DJ
- Whellan DJ
- White H
- White HD
- White HD
- White HD
- White HD
- White JA
- White JK
- Widimsky P
- Widimsky P
- Wiedemann JY
- Wiemer M
- Wiering J
- Wilkins G
- Williams J
- Windecker S
- Wiseman A
- Wiseth R
- Wohns D
- Wolford T
- Wong A
- Wong G
- Wong L
- Wrestler J
- Wu CJ
- Yagi M
- Yamaguchi T
- Yamamoto E
- Yang Y
- Yeh HI
- Yigit Z
- Yildirir A
- Yilmaz M
- Yin WH
- Yoon JH
- Yovaniniz P
- Yu CM
- Yusof A
- Zadra R
- Zalewski J
- Zaman A
- Zambakides C
- Zapata G
- Zemanek D
- Zemour G
- Zenker G
- Zetterlund P
- Zeymer U
- Zhang F
- Zhao R
- Zheng Y
- Zhou C
- Ziada K
- Zouzoulas S
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2012
- Field of study
BACKGROUND
Vorapaxar is a new oral protease-activated–receptor 1 (PAR-1) antagonist that inhibits
thrombin-induced platelet activation.
METHODS
In this multinational, double-blind, randomized trial, we compared vorapaxar with
placebo in 12,944 patients who had acute coronary syndromes without ST-segment
elevation. The primary end point was a composite of death from cardiovascular causes,
myocardial infarction, stroke, recurrent ischemia with rehospitalization, or urgent
coronary revascularization.
RESULTS
Follow-up in the trial was terminated early after a safety review. After a median follow-up
of 502 days (interquartile range, 349 to 667), the primary end point occurred in 1031
of 6473 patients receiving vorapaxar versus 1102 of 6471 patients receiving placebo
(Kaplan–Meier 2-year rate, 18.5% vs. 19.9%; hazard ratio, 0.92; 95% confidence interval
[CI], 0.85 to 1.01; P = 0.07). A composite of death from cardiovascular causes,
myocardial infarction, or stroke occurred in 822 patients in the vorapaxar group
versus 910 in the placebo group (14.7% and 16.4%, respectively; hazard ratio, 0.89;
95% CI, 0.81 to 0.98; P = 0.02). Rates of moderate and severe bleeding were 7.2% in the
vorapaxar group and 5.2% in the placebo group (hazard ratio, 1.35; 95% CI, 1.16 to 1.58;
P<0.001). Intracranial hemorrhage rates were 1.1% and 0.2%, respectively (hazard
ratio, 3.39; 95% CI, 1.78 to 6.45; P<0.001). Rates of nonhemorrhagic adverse events
were similar in the two groups.
CONCLUSIONS
In patients with acute coronary syndromes, the addition of vorapaxar to standard
therapy did not significantly reduce the primary composite end point but significantly
increased the risk of major bleeding, including intracranial hemorrhage
Ezetimibe added to statin therapy after acute coronary syndromes
- Author
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- Aambakk MB
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- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2015
- Field of study
BACKGROUND: Statin therapy reduces low-density lipoprotein (LDL) cholesterol levels and the risk of cardiovascular events, but whether the addition of ezetimibe, a nonstatin drug that reduces intestinal cholesterol absorption, can reduce the rate of cardiovascular events further is not known. METHODS: We conducted a double-blind, randomized trial involving 18,144 patients who had been hospitalized for an acute coronary syndrome within the preceding 10 days and had LDL cholesterol levels of 50 to 100 mg per deciliter (1.3 to 2.6 mmol per liter) if they were receiving lipid-lowering therapy or 50 to 125 mg per deciliter (1.3 to 3.2 mmol per liter) if they were not receiving lipid-lowering therapy. The combination of simvastatin (40 mg) and ezetimibe (10 mg) (simvastatin-ezetimibe) was compared with simvastatin (40 mg) and placebo (simvastatin monotherapy). The primary end point was a composite of cardiovascular death, nonfatal myocardial infarction, unstable angina requiring rehospitalization, coronary revascularization ( 6530 days after randomization), or nonfatal stroke. The median follow-up was 6 years. RESULTS: The median time-weighted average LDL cholesterol level during the study was 53.7 mg per deciliter (1.4 mmol per liter) in the simvastatin-ezetimibe group, as compared with 69.5 mg per deciliter (1.8 mmol per liter) in the simvastatin-monotherapy group (P<0.001). The Kaplan-Meier event rate for the primary end point at 7 years was 32.7% in the simvastatin-ezetimibe group, as compared with 34.7% in the simvastatin-monotherapy group (absolute risk difference, 2.0 percentage points; hazard ratio, 0.936; 95% confidence interval, 0.89 to 0.99; P = 0.016). Rates of pre-specified muscle, gallbladder, and hepatic adverse effects and cancer were similar in the two groups. CONCLUSIONS: When added to statin therapy, ezetimibe resulted in incremental lowering of LDL cholesterol levels and improved cardiovascular outcomes. Moreover, lowering LDL cholesterol to levels below previous targets provided additional benefit
Rivaroxaban with or without aspirin in stable cardiovascular disease
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- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
BACKGROUND: We evaluated whether rivaroxaban alone or in combination with aspirin would be more effective than aspirin alone for secondary cardiovascular prevention. METHODS: In this double-blind trial, we randomly assigned 27,395 participants with stable atherosclerotic vascular disease to receive rivaroxaban (2.5 mg twice daily) plus aspirin (100 mg once daily), rivaroxaban (5 mg twice daily), or aspirin (100 mg once daily). The primary outcome was a composite of cardiovascular death, stroke, or myocardial infarction. The study was stopped for superiority of the rivaroxaban-plus-aspirin group after a mean follow-up of 23 months. RESULTS: The primary outcome occurred in fewer patients in the rivaroxaban-plus-aspirin group than in the aspirin-alone group (379 patients [4.1%] vs. 496 patients [5.4%]; hazard ratio, 0.76; 95% confidence interval [CI], 0.66 to 0.86; P<0.001; z=−4.126), but major bleeding events occurred in more patients in the rivaroxaban-plus-aspirin group (288 patients [3.1%] vs. 170 patients [1.9%]; hazard ratio, 1.70; 95% CI, 1.40 to 2.05; P<0.001). There was no significant difference in intracranial or fatal bleeding between these two groups. There were 313 deaths (3.4%) in the rivaroxaban-plus-aspirin group as compared with 378 (4.1%) in the aspirin-alone group (hazard ratio, 0.82; 95% CI, 0.71 to 0.96; P=0.01; threshold P value for significance, 0.0025). The primary outcome did not occur in significantly fewer patients in the rivaroxaban-alone group than in the aspirin-alone group, but major bleeding events occurred in more patients in the rivaroxaban-alone group. CONCLUSIONS: Among patients with stable atherosclerotic vascular disease, those assigned to rivaroxaban (2.5 mg twice daily) plus aspirin had better cardiovascular outcomes and more major bleeding events than those assigned to aspirin alone. Rivaroxaban (5 mg twice daily) alone did not result in better cardiovascular outcomes than aspirin alone and resulted in more major bleeding events
A Survey of Empirical Results on Program Slicing
- Author
- ABAT MARC EVANS
- ABDUL RAHIM AIZAI AZAN
- ABE MITSUNORI
- ABIB JR EDUARDO
- ABOLA MARIA TERESA
- Aboyans Victor
- ABOYANS VICTOR
- ABRANTES JOSE ANTONIO
- ABU HASSAN MUHAMMAD RADZI
- ACCINI MENDOZA JOSE LUIS
- ADLER FREDRIC
- AHUAD GUERRERO RODOLFO ANDRES
- AKATSUKA YUTAKA
- AKO JUNYA
- AL-KHALILI FARIS
- AL-QOOFI FAISAL
- ALBERTSSON PER
- ALBISU DI GENNERO JUAN PABLO
- ALCARAZ JOHN DENNIS
- Alings Marco
- ALINGS MARCO
- ALMROTH HENRIK
- ALVAREZ MOIRA
- AMERENA JOHN
- Anand Sonia S
- ANDERSSON TOMMY
- ANDO KENJI
- ANONUEVO JOHN
- APPEL KARL-FRIEDRICH
- ARCOS EDGAR
- ARIMIE RALUCA
- AROCA GUSTAVO
- ARSENESCU CATALINA
- ATAR SHAUL
- AUSHEVA AZA
- AUSTIN DAVID
- AVERKOV OLEG
- Avezum Alvaro A
- BABAPULLE MOHAN
- BACHARACH J MICHAEL
- BAE JANG-HO
- BAI XIAO JUAN
- BAINEY KEVIN
- BAJNOK LASZLO
- BAKAEEN FAISAL
- BAKAI JUDIT
- BALDIN MARIA GRAZIA
- BANERJEE SUBHASH
- Bangdiwala Shrikant I
- BARBARASH OLGA
- BARBIERI MARIA
- BARTELS GERARD
- BARTOLACCI INES PALMIRA
- BARTON JOHN
- BAZYLEVYCH ANDRIY
- BEDWELL NOEL
- BENEDEK IMRE
- BENESOVA MIROSLAVA
- BERLINGIERI JOSEPH
- BERNARDINANGELI MARINO
- BHARGAVA RAKESH
- Bhatt Deepak L
- BIRDI INDERPAUL
- BITTNER VERA
- BLACK ROBERT
- BLOMBERY PETER
- BOBESCU ELENA
- BOCCARA FRANCK
- BODA ZOLTAN
- BOENELYKKE SOERENSEN VIBEKE
- BORDONAVA ANSELMO PAULINO
- Bosch Jackie
- BOSI STEFANO
- BOTELHO ROBERTO
- BOURGEOIS RONALD
- BOYLE ANDREW
- BRAILE MARIA
- Branch Kelley
- BRANCH KELLEY
- BRANNY MARIAN
- BRAT RADIM
- BRAUN-DULLAEUS RUEDIGER
- BREEDVELD ROB
- BRONCEL MARLENA
- BROWN CRAIG
- BRTKO MIROSLAV
- BRULOTTE STEEVE
- CACCAVO ALBERTO
- CALVERT JOHN
- CAMP ALAN
- CAMPEAU JEAN
- CANADYOVA JULIA
- CARDONA MARCELO
- CARMINE DE MATTEIS
- CARROLL PATRICK
- CARTASEGNA LUIS
- CARTER JUSTIN
- CASTILLO HENRY
- CAYLA GUILLAUME
- CHA JAMES
- CHACON CAROLINA
- CHANDRA LOKESH
- Chen Edmond
- CHEN XIAO PING
- CHEN XIN
- CHILTON ROBERT
- CHIONCEL OVIDIU
- CHUA PHILIP
- CINTEZA MIRCEA
- CIRRINCIONE VINCENZO
- COBOS JORGE LEONARDO
- COLQUHOUN DAVID
- COMAN IOAN
- COMEROTA ANTHONY
- COMMERFORD PATRICK
- Commerford Patrick J
- CONNOLLY DEREK
- Connolly Stuart J
- CORBALAN RAMON
- COSMI FRANCO
- COSTABEL JUAN PABLO
- COSTELLO FREDERICK
- COTTON JAMES
- COUFAL ZDENEK
- CREAN PETER
- CRUZ JOSEFINA
- CUADRADO JESUS
- CUERVO MILLAN FRANCISCO
- CUNEO CARLOS
- CURTIN RONAN
- CZARNECKA DANUTA
- CZARNECKI WLODZIMIERZ
- DAGENAIS FRANCOIS
- DAGENAIS GILLES R
- DAGHER GEORGE
- DAIDA HIROYUKI
- DARIUS HARALD
- DAVEY PATRICK
- DAVIERWALA PIROZE
- DE CARVALHO CANTARELLI MARCELO JOSE
- DE GROOT MARC ROBERT
- DE VRIES KEES-JAN
- DEBONNAIRE PHILIPPE
- DEL PILAR JOSE CARLO
- DELLA SIEGA ANTHONY
- DELLBORG MIKAEL
- DEMPSEY STEPHEN
- DEN HARTOG FRANK
- DI BIASE MATTEO
- DI PASQUALE GIUSEPPE
- DIAZ ARIEL
- Diaz Rafael
- DIMULESCU DOINA
- DINNEEN SEAN
- DIXEN ULRIK
- DOBREANU DAN
- DOMAE HIROSHI
- DONG YUGANG
- DONNELLY PATRICK
- DORSEL THOMAS
- DRAN RICARDO DARIO
- DROZDAKOVA ERIKA
- DUARTE YAN CARLOS
- DUENGEN HANS-DIRK
- DUJARDIN KARL
- DUTRA OSCAR
- EBO GERALDINE
- ECTOR BAVO
- EFREMUSHKINA ANNA
- Eikelboom John W
- ELEGEERT IVAN
- ENGELBRECHT JAN
- FAGGIANO POMPILIO
- FELL DAVID
- FERRARI EMILE
- FERRE PACORA FREDY ANTONI
- FIELDS RONALD
- FLORIAN JINDRICH
- FOLTYNOVA CAISOVA LENKA
- Fox Keith A A
- FREMES STEPHEN
- FRENCH WILLIAM
- FU GUOSHENG
- FUJII KENSHI
- GAITA DAN
- GAJOS GRZEGORZ
- GALVANI MARCELLO
- GARCIA DURAN RUBEN OMAR
- GARCIA HENRY
- GARCIA LUIS HERNANDO
- GARRIDO MARCELO
- GASPAR LUDOVIT
- GE JUNBO
- GIBSON KATHLEEN
- GILLESPIE EVE
- GISLASON GUNNAR
- GLANZ ANTHONY
- GOGIA HARINDER
- GOMEZ VILAMAJO OSCAR
- GOMEZ JUAN
- GONZALEZ COLASO PATRICIA DEL CARMEN
- GOSSELIN GILBERT
- GOSSELINK MARCEL
- GRENA PAUL
- GRINFELD DIEGO
- GROENEMEIJER BJORN
- GUEROCAK OSMAN
- GULIZIA MICHELE MASSIMO
- GURBEL PAUL
- GUZIK TOMASZ
- GUZMAN LUIS
- GUZMAN RANDOLPH
- HA JONG-WON
- HAKAS JOSEPH
- HALABI MAJDI
- HAMMETT CHRISTOPHER
- HAMROFF GLENN
- HARRISON ROBERT
- Hart Robert G
- HARTLEIB MICHAEL
- HASBANI EDUARDO
- HASHIMOTO TETSUO
- HATALOVA KATARINA
- HEFFERNAN MICHAEL
- HEIMAN MARK
- HERNANDES MAURO
- HERRMAN JEAN PAUL
- HIGASHINO YORIHIKO
- HIGASHIUE SHINICHI
- HIGUCHI YOSHIHARU
- HII CHRIS
- HILL LAURIE
- HILTON THOMAS
- HIMI TOSHIHARU
- HIRAYAMA ATSUSHI
- HIROKAMI MITSUGU
- HIRSCH GREGORY
- HISAMATSU YUJI
- HOEKSTRA EDUARD
- HOFFER ETIENNE
- HOMINAL MIGUEL ANGEL
- HOMZA MIROSLAV
- HOOGSLAG PIETER
- HORAK ADRIAN
- HOSOKAWA SHINOBU
- HOULIND KIM
- HRABAR ADRIAN
- HRANAI MARIAN
- HU TAO HONG
- HUANG WEIJIAN
- HUNTER JOHN J.
- HUYNH THAO
- I-HSUAN TSAI PETER
- IANCU ADRIAN
- IBANEZ SAGGIA LUZ MARIA
- ILIESIU ADRIANA
- IMAMAKI MIZUHO
- INDIO DO BRASIL CLARISSE
- INGARAMO ADRIAN
- INOKO MORIAKI
- IZUKAWA NILO
- JANION MARIANNA
- JANO GABRIEL
- JANSEN SHIRLEY
- JANSKY PETR
- JARAI ZOLTAN
- JARNERT CHRISTINA
- JESERICH MICHAEL
- JIA KAIYING
- JOHANSSON LARS
- JOHNSTON JAMES
- JOO SEUNGJAE
- JUNGMAIR WOLFGANG
- KADEL CHRISTOPH
- Kakkar Ajay K
- KALETOVA MARKETA
- KAMIYA HARUO
- KANNO TAKAYASU
- KANTOLA ILKKA
- KARPENKO OLEKSANDR
- KASIM SAZZLI
- KATZ AMOS
- KAWAKAMI HIDEO
- KE YUANNAN
- Keltai Katalin
- KEMENY VENDEL
- KHAYKIN YAARIV
- KIAII BOB
- KIM CHEOLHO
- KIM CHONG-JIN
- KIM DONG-SOO
- KIM JANG YOUNG
- KIM YONG JIN
- KIM YOUNG-KWON
- KIMURA KAZUO
- KINOSHITA NORIYUKI
- KIS ERNO
- KLAINMAN ELIEZER
- KLUG ERIC
- KOBAYASHI HIROO
- KOBER LARS
- KONG YE
- KONONENKO LYUDMYLA
- KORANYI LASZLO
- KORETSUNE YUKIHIRO
- KOSHY N. MATHEW
- KOSTIS JOHN B.
- KOVAL OLENA
- KOVAL VALENTYNA
- KRAGTEN HANS
- KRYZA RADIM
- KUKREJA NEVILLE
- KURAMOCHI TAKEHIKO
- LADER ELLIS
- LAM ANDY
- LAMY ANDRE
- LASZLO ZOLTAN
- LEAES PAULO
- LECLERCQ FLORENCE
- Leong Darryl P
- LEROY JEAN
- LEWIS BASIL
- Lewis Basil S
- LI CHUNJIAN
- LI JIANPING
- LI JUNXIA
- LIGHEZAN DANIEL
- LINDNER JAROSLAV
- LITVAK BRUNO MARCOS RAUL
- LIU BO
- LIU SHAO WEN
- LO WINGCHI
- LOK DIRK
- LONN EVA
- LOPEZ JOSE
- Lopez-Jaramillo Patricio
- LOYOLA ALDRIN
- LUBANDA JEAN-CLAUDE
- LUCIARDI HECTOR LUCAS
- LUPOVITCH STEVEN
- LUQUEZ HUGO
- MABIN THOMAS
- MACHIDA MASAHARU
- MACIN STELLA MARIS
- MACKINNON IGNACIO J.
- MACNEILL BRIAIN
- MAFFEI LAURA ELENA
- MAGA PAWEL
- Maggioni Aldo P
- MAHON NIALL
- MAIA LILIA
- MAJUL CLAUDIO RODOLFO
- MAKOTOKO ELLEN MAKONLI
- MALHOTRA VINAY
- MALY JIRI
- MALY MARTIN
- MALYNOVSKY YAROSLAV
- MANDORLA SARA
- MANENTI EULER
- MANITA MAMORU
- MANZUR J FERNANDO
- MARCIAN PAVEL
- MARCINEK GABRIEL
- MARMOL RICARDO
- MATUSKA JIRI
- MCADAM BRENDAN
- MCCORMICK MATTHEW
- MCGUINN WILLIAM
- MEDINA MARCELO
- MEHTA PRAVINSAGAR
- MEHTA RAJENDRA
- MERALI FATIMA
- MESSAS EMMANUEL
- MICHAELSON STEPHEN
- MILHOUS JOHANNES GERT-JAN
- MINELLI CESAR
- MISMETTI PATRICK
- Misselwitz Frank
- MITA TERUAKI
- MIYAMOTO NAOMASA
- MIZUTOMI KAZUAKI
- MOCCETTI TIZIANO
- MOHAMED ZAID
- MOHD ZAMRIN DIMON
- MOLINA DE SALAZAR DORA INES
- MONTANA OSCAR
- MOOE THOMAS
- MORALES DANTE
- MORAN MICHAEL
- MORENO SILGADO GUSTAVO ADOLFO
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- WILLEMS FRANK
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- YAMADA YUTAKA
- YANG PING
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- YIN PENGFEI
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- YU LITIAN
- YUSOFF KHALID
- Yusuf Salim
- ZABOWKA MACIEJ
- ZAIDMAN CESAR
- ZATEYSHCHIKOV DMITRY
- ZEGERS ERWIN
- ZELTSER DAVID
- ZEUTHEN ELISABETH
- ZHANG JIWEI
- ZHANG RUIYAN
- ZHENG YANG
- ZHENG ZHE
- ZHOU XINMIN
- Zhu Jun
- ZIDKOVA EVA
- ZIMLICHMAN REUVEN
- ZIMLICHMAN REUVEN
- ZIMMERMANN SERGIO LUIZ
- ZOET-NUGTEREN STIENEKE
- ZSARY ANDRAS
- Publication venue
- Publication date
- 01/01/2004
- Field of study
International audienceBACKGROUND:Patients with peripheral artery disease have an increased risk of cardiovascular morbidity and mortality. Antiplatelet agents are widely used to reduce these complications.METHODS:This was a multicentre, double-blind, randomised placebo-controlled trial for which patients were recruited at 602 hospitals, clinics, or community practices from 33 countries across six continents. Eligible patients had a history of peripheral artery disease of the lower extremities (previous peripheral bypass surgery or angioplasty, limb or foot amputation, intermittent claudication with objective evidence of peripheral artery disease), of the carotid arteries (previous carotid artery revascularisation or asymptomatic carotid artery stenosis of at least 50%), or coronary artery disease with an ankle-brachial index of less than 0·90. After a 30-day run-in period, patients were randomly assigned (1:1:1) to receive oral rivaroxaban (2·5 mg twice a day) plus aspirin (100 mg once a day), rivaroxaban twice a day (5 mg with aspirin placebo once a day), or to aspirin once a day (100 mg and rivaroxaban placebo twice a day). Randomisation was computer generated. Each treatment group was double dummy, and the patient, investigators, and central study staff were masked to treatment allocation. The primary outcome was cardiovascular death, myocardial infarction or stroke; the primary peripheral artery disease outcome was major adverse limb events including major amputation. This trial is registered with ClinicalTrials.gov, number NCT01776424, and is closed to new participants.FINDINGS:Between March 12, 2013, and May 10, 2016, we enrolled 7470 patients with peripheral artery disease from 558 centres. The combination of rivaroxaban plus aspirin compared with aspirin alone reduced the composite endpoint of cardiovascular death, myocardial infarction, or stroke (126 [5%] of 2492 vs 174 [7%] of 2504; hazard ratio [HR] 0·72, 95% CI 0·57-0·90, p=0·0047), and major adverse limb events including major amputation (32 [1%] vs 60 [2%]; HR 0·54 95% CI 0·35-0·82, p=0·0037). Rivaroxaban 5 mg twice a day compared with aspirin alone did not significantly reduce the composite endpoint (149 [6%] of 2474 vs 174 [7%] of 2504; HR 0·86, 95% CI 0·69-1·08, p=0·19), but reduced major adverse limb events including major amputation (40 [2%] vs 60 [2%]; HR 0·67, 95% CI 0·45-1·00, p=0·05). The median duration of treatment was 21 months. The use of the rivaroxaban plus aspirin combination increased major bleeding compared with the aspirin alone group (77 [3%] of 2492 vs 48 [2%] of 2504; HR 1·61, 95% CI 1·12-2·31, p=0·0089), which was mainly gastrointestinal. Similarly, major bleeding occurred in 79 (3%) of 2474 patients with rivaroxaban 5 mg, and in 48 (2%) of 2504 in the aspirin alone group (HR 1·68, 95% CI 1·17-2·40; p=0·0043).INTERPRETATION:Low-dose rivaroxaban taken twice a day plus aspirin once a day reduced major adverse cardiovascular and limb events when compared with aspirin alone. Although major bleeding was increased, fatal or critical organ bleeding was not. This combination therapy represents an important advance in the management of patients with peripheral artery disease. Rivaroxaban alone did not significantly reduce major adverse cardiovascular events compared with asprin alone, but reduced major adverse limb events and increased major bleeding