7 research outputs found
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
- Author
- Aldave Becerra Juan Carlos
- Belohradsky Bernd
- Blanche Stéphane
- Bousfiha Aziz
- Camcioglu Yildiz
- Casanova Jean-Laurent
- Dullaers Melissa
- Etzioni Amos
- Fouyssac Fanny
- Girisha Katta Mohan
- Grimbacher Bodo
- Haerynck Filomeen
- Hiller Julia
- Holland Steven
- Hoste Levi
- Kerns Leigh Ann
- Kisand Kai
- Kobayashi Masao
- Lagos Gomez Macarena
- Lilic Desa
- Marodi Laszlo
- Meyts Isabelle
- Milner Joshua D.
- Morio Tomohiro
- Okada Satoshi
- Oleastro Matias
- Ouachée-Chardin Marie
- Picard Capucine
- Puel Anne
- Reichenbach Janine
- Renner Ellen D.
- Rodriguez-Gallego Carlos
- Rosenzweig Sergio
- Toubiana Julie
- Traidl-Hoffmann Claudia
- van de Veerdonk Frank L.
- Van Montfrans Joris
- Publication venue
- 'American Society of Hematology'
- Publication date
- 01/01/2016
- Field of study
Since their discovery in patients with autosomal dominant (AD) chronic mucocutaneous candidiasis (CMC) in 2011, heterozygous STAT1 gain-of-function (GOF) mutations have increasingly been identified worldwide. The clinical spectrum associated with them needed to be delineated. We enrolled 274 patients from 167 kindreds originating from 40 countries from 5 continents. Demographic data, clinical features, immunological parameters, treatment, and outcome were recorded. The median age of the 274 patients was 22 years (range, 1-71 years); 98% of them had CMC, with a median age at onset of 1 year (range, 0-24 years). Patients often displayed bacterial (74%) infections, mostly because of Staphylococcus aureus (36%), including the respiratory tract and the skin in 47% and 28% of patients, respectively, and viral (38%) infections, mostly because of Herpesviridae (83%) and affecting the skin in 32% of patients. Invasive fungal infections (10%), mostly caused by Candida spp. (29%), and mycobacterial disease (6%) caused by Mycobacterium tuberculosis, environmental mycobacteria, or Bacille Calmette-Guérin vaccines were less common. Many patients had autoimmune manifestations (37%), including hypothyroidism (22%), type 1 diabetes (4%), blood cytopenia (4%), and systemic lupus erythematosus (2%). Invasive infections (25%), cerebral aneurysms (6%), and cancers (6%) were the strongest predictors of poor outcome. CMC persisted in 39% of the 202 patients receiving prolonged antifungal treatment. Circulating interleukin-17A-producing T-cell count was low for most (82%) but not all of the patients tested. STAT1 GOF mutations underlie AD CMC, as well as an unexpectedly wide range of other clinical features, including not only a variety of infectious and autoimmune diseases, but also cerebral aneurysms and carcinomas that confer a poor prognosis
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
- Author
- Aldave Becerra Juan Carlos
- Belohradsky Bernd
- Blanche Stéphane
- Bousfiha Aziz
- Camcioglu Yildiz
- Casanova Jean-Laurent
- Etzioni Amos
- Fouyssac Fanny
- Girisha Katta Mohan
- Grimbacher Bodo
- Hiller Julia
- Holland Steven
- Kerns Leigh Ann
- Kisand Kai
- Kobayashi Masao
- Lagos Gomez Macarena
- Lilic Desa
- Marodi Laszlo
- Meyts Isabelle
- Milner Joshua D
- Morio Tomohiro
- Okada Satoshi
- Oleastro Matias
- Ouachée-Chardin Marie
- Picard Capucine
- Puel Anne
- Reichenbach Janine
- Renner Ellen D
- Rodriguez-Gallego Carlos
- Rosenzweig Sergio
- Toubiana Julie
- Traidl-Hoffmann Claudia
- van de Veerdonk Frank L
- Van Montfrans Joris
- Publication venue
- 'American Society of Hematology'
- Publication date
- 01/06/2016
- Field of study
Since their discovery in patients with autosomal dominant (AD) chronic mucocutaneous candidiasis (CMC) in 2011, heterozygous STAT1 gain-of-function (GOF) mutations have increasingly been identified worldwide. The clinical spectrum associated with them needed to be delineated. We enrolled 274 patients from 167 kindreds originating from 40 countries from five continents. Demographic data, clinical features, immunological parameters, treatment, and outcome were recorded. The median age of the 274 patients was 22 years (range: 1 - 71 years); 98% of them had CMC, with a median age at onset of one year (range: 0 - 24 years). Patients often displayed bacterial (74%) infections, mostly due to Staphylococcus aureus (36%), including the respiratory tract and the skin in 47% and 28% of patients, respectively, and viral (38%) infections, mostly due to Herpesviridae (83%) and affecting the skin in 32% of patients. Invasive fungal infections (10%), mostly caused by Candida spp. (29%), and mycobacterial disease (6%) caused by Mycobacterium tuberculosis, environmental mycobacteria, or BCG vaccines, were less common. Many patients had autoimmune manifestations (37%), including hypothyroidism (22%), type 1 diabetes (4%), blood cytopenia (4%), and systemic lupus erythematosus (2%). Invasive infections (25%), cerebral aneurysms (6%), and cancers (6%) were the strongest predictors of poor outcome. CMC persisted in 39% of the 202 patients receiving prolonged antifungal treatment. Circulating IL-17A-producing T-cell count was low for most (82%) but not all of the patients tested. STAT1 GOF mutations underlie AD CMC, as well as an unexpectedly wide range of other clinical features, including not only a variety of infectious and autoimmune diseases, but also cerebral aneurysms and carcinomas that confer a poor prognosis.status: publishe
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
- Author
- Aldave Becerra Juan Carlos
- Belohradsky Bernd
- Blanche Stéphane
- Bousfiha Aziz
- Camcioglu Yildiz
- Casanova Jean-Laurent
- Etzioni Amos
- Fouyssac Fanny
- Girisha Katta Mohan
- Grimbacher Bodo
- Hiller Julia
- Holland Steven
- International STAT1 Gain-of-Function Study Group
- Kerns Leigh Ann
- Kisand Kai
- Kobayashi Masao
- Lagos Gomez Macarena
- Lilic Desa
- Marodi Laszlo
- Meyts Isabelle
- Milner Joshua D
- Morio Tomohiro
- Okada Satoshi
- Oleastro Matias
- Ouachée-Chardin Marie
- Picard Capucine
- Puel Anne
- Reichenbach Janine
- Renner Ellen D
- Rodriguez-Gallego Carlos
- Rosenzweig Sergio
- Toubiana Julie
- Traidl-Hoffmann Claudia
- van de Veerdonk Frank L
- van Montfrans Joris M.
- Publication venue
- Publication date
- 23/06/2016
- Field of study
Since their discovery in patients with autosomal dominant (AD) chronic mucocutaneous candidiasis (CMC) in 2011, heterozygous STAT1 gain-of-function (GOF) mutations have increasingly been identified worldwide. The clinical spectrum associated with them needed to be delineated. We enrolled 274 patients from 167 kindreds originating from 40 countries from 5 continents. Demographic data, clinical features, immunological parameters, treatment, and outcome were recorded. The median age of the 274 patients was 22 years (range, 1-71 years); 98% of them had CMC, with a median age at onset of 1 year (range, 0-24 years). Patients often displayed bacterial (74%) infections, mostly because of Staphylococcus aureus (36%), including the respiratory tract and the skin in 47% and 28% of patients, respectively, and viral (38%) infections, mostly because of Herpesviridae (83%) and affecting the skin in 32% of patients. Invasive fungal infections (10%), mostly caused by Candida spp. (29%), and mycobacterial disease (6%) caused by Mycobacterium tuberculosis, environmental mycobacteria, or Bacille Calmette-Guérin vaccines were less common. Many patients had autoimmune manifestations (37%), including hypothyroidism (22%), type 1 diabetes (4%), blood cytopenia (4%), and systemic lupus erythematosus (2%). Invasive infections (25%), cerebral aneurysms (6%), and cancers (6%) were the strongest predictors of poor outcome. CMC persisted in 39% of the 202 patients receiving prolonged antifungal treatment. Circulating interleukin-17A-producing T-cell count was low for most (82%) but not all of the patients tested. STAT1 GOF mutations underlie AD CMC, as well as an unexpectedly wide range of other clinical features, including not only a variety of infectious and autoimmune diseases, but also cerebral aneurysms and carcinomas that confer a poor prognosis
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
- Author
- Abel Laurent
- Abinum Mario
- Ailal Fatima
- Arkwright Peter D.
- Ayvaz Deniz
- Badolato Raffaele
- Barbouche Ridha
- Barlogis Vincent
- Baumann Ulrich
- Bayart Sophie
- Becerra Macarena Lagos
- Belohradsky Leigh Ann
- Benmustapha Imen
- Bensaid Philippe
- Bezrodnik Liliana
- Blancas-Galicia Lizbeth
- Blanche Bernd
- Bodemer Christine
- Boisson-Dupuis Stéphanie
- Boiu Sorina
- Bondarenko Anastasia
- Boubidi Chahinez
- Bouchaib Jabir
- Bougnoux Marie-Elisabeth
- Bousfiha Stephane
- Boutboul David
- Buhl Timo
- Burgel Pierre-R´egis
- Bustamante Jacinta
- Bu´e M´elanie
- Camcioglu Joris
- Cant Andrew J.
- Casanova Steven
- Chernyshova Liudmyla
- Chopra Charu
- Church Joseph A.
- Cortina Mariana
- Cypowyj Anne
- Debr´e Marianne
- DEL GIACCO Stefano
- Depner Mark
- Desai Mukesh M.
- Dhalla Fatima
- Di Giovanni Daniela
- Drewe Elizabeth
- Drexel Barbara
- Dullaers Melissa
- Emmanuelgrimprel
- Español Teresa
- Etzioni Katta Mohan
- Eyerich Kilian
- Ferdman Ronald M.
- Fieschi Claire
- Firinu Davide
- Fischer Alain
- Fouyssac Marie
- Garcia-Martinez Juan-Miguel
- Gennery Andrew R.
- Gerst Talas Ulvi
- Giardino Giuliana
- Girisha Fanny
- Gomez Matias
- Grimbacher Sergio
- Haerynck Filomeen
- Haimi-Cohen Yishai
- Harrer Thomas
- Hayakawa Akira
- Henriet Stefanie
- Hermine Olivier
- Hiller Satoshi
- Hoernes Miriam
- Holland Joshua D.
- Hoste Levi
- Imai Kohsuke
- Jannier Sarah
- Jansson Annette F.
- Jeannetteboutros
- Jeannoel Guy-Patrick
- Karmochkine Marina
- Kerns Yildiz
- Kindle Gerhard
- Kisand Isabelle
- Kobayashi Tomohiro
- Kocacyk Dilara
- Korganow Anne-Sophie
- Lacuesta Gina
- Lanternier Fanny
- Leonard Stephanie
- Lesens Olivier
- Lilic Masao
- Logering Birgit
- Lortholary Olivier
- Marciano Beatriz E.
- MargaritaOrtega-Cisneros
- Marie-Cardine Aude
- Marodi Capucine
- Mekki Najla
- Mendoza David
- Mesdaghi Mehrnaz
- Meuwissen Hilaire
- Meyts Carlos
- Migaud Mélanie
- Milani Lili
- Milner Desa
- Miron Dan
- Mizoguchi Yoko
- Moens Leen
- Mohammadnabavi
- Morio Laszlo
- Moshous Despina
- Navarrete Carmen
- Netea Mihai G.
- Neven Benedicte
- Nikopensius Tiit
- Okada Julie
- Okawa Teppei
- Oleastro Julia
- Oswaldo Lugo Reyes Saul
- Ouachãe chardin Juan Carlos Aldave
- Ozaki Yusuke
- Pac Malgorzata
- Paillard Catherine
- Patel Smita Y.
- Peterson Part
- Picard Claudia
- Picco Paolo
- Pignata Claudio
- Polak Michel
- Puel Jean Laurent
- Reich Kristian
- Reichenbach Kai
- Remm Maido
- Renner Janine
- Revon-Rivire Gabriel
- Rezaei Nima
- Rodriguez gallego Aziz
- Roesler Joachim
- Roifman Chaim
- Rosenzweig Ellen D.
- Salhi Aicha
- Sanal Ozden
- Sawalle-Belohradsky Julie
- Schaller Martin
- Schnopp Christina
- Sebnem Kilic Sara
- Shabashova Nadejda
- Simon Roherlich Pierre
- Soltesz Beata
- Sophie
- Spiegel Ronen
- Stephan Jean-Louis
- Tahuil Natalia
- Takeuchi Masato
- Taur Prasad
- Terance Benjamin Antony
- Teresa Martinez- Saavedra Maia
- Thomas Caroline
- Thumerelle Caroline
- Torres Lozano Carlos
- Toth Beata
- Toubiana
- Toulon Antoine
- Traidl hoffmann Frank L.
- Tucker Mark
- Van De Veerdonk Bodo
- Van Montfrans Amos
- Wallace Mark
- Warris Adilia
- Weiss Laurence
- Willis Mary
- Witte Torsten
- Yuenyongviwat Araya
- Zoghi Samaneh
- Publication venue
- 'American Society of Hematology'
- Publication date
- 01/01/2016
- Field of study
Since their discovery in patients with autosomal dominant (AD) chronic mucocutaneous candidiasis (CMC) in 2011, heterozygous STAT1 gain-of-function (GOF) mutations have increasingly been identified worldwide. The clinical spectrum associated with them needed to be delineated. We enrolled 274 patients from 167 kindreds originating from 40 countries from 5 continents. Demographic data, clinical features, immunological parameters, treatment, and outcome were recorded. The median age of the 274 patients was 22 years (range, 1-71 years); 98% of them had CMC, with a median age at onset of 1 year (range, 0-24 years). Patients often displayed bacterial (74%) infections, mostly because of Staphylococcus aureus (36%), including the respiratory tract and the skin in 47% and 28% of patients, respectively, and viral (38%) infections, mostly because of Herpesviridae (83%) and affecting the skin in 32% of patients. Invasive fungal infections (10%), mostly caused by Candida spp. (29%), and mycobacterial disease (6%) caused by Mycobacterium tuberculosis, environmental mycobacteria, or Bacille Calmette-Guérin vaccines were less common. Many patients had autoimmune manifestations (37%), including hypothyroidism (22%), type 1 diabetes (4%), blood cytopenia (4%), and systemic lupus erythematosus (2%). Invasive infections (25%), cerebral aneurysms (6%), and cancers (6%) were the strongest predictors of poor outcome. CMC persisted in 39% of the 202 patients receiving prolonged antifungal treatment. Circulating interleukin-17A-producing T-cell count was low for most (82%) but not all of the patients tested. STAT1 GOF mutations underlie AD CMC, as well as an unexpectedly wide range of other clinical features, including not only a variety of infectious and autoimmune diseases, but also cerebral aneurysms and carcinomas that confer a poor prognosis
Scedosporium and Lomentospora: an updated overview of underrated opportunists
- Author
- Accurso
- Adela Martin-Vicente
- Aitor Rementeria
- Aize Pellon
- Al-Laaeiby
- Alanio
- Alanio
- Albarrag
- Alvarez
- Ana Alastruey-Izquierdo
- Ananda-Rajah
- Andoni Ramirez-Garcia
- Anne Bernhardt
- April
- Bacconi
- Baddley
- Barreto-Bergter
- Barreto-Bergter
- Barreto-Bergter
- Belanger
- Berenguer
- Berenguer
- Bernhard
- Bernhardt
- Bernhardt
- Bertrand
- Bertrand
- Bhagavatula
- Bhat S
- Biswas
- Bittencourt
- Blatzer
- Blyth
- Blyth
- Borghi
- Borish
- Brakhage
- Brown
- Bryan
- Buldain
- Buonfrate
- Buzina
- Caira
- Carsten Schwarz
- Casadevall
- Casadevall
- Castanheira
- Castiglioni
- Chen
- Chen
- Cimon
- Cooley
- Cooney
- Cortez
- Coulibaly
- Cowen
- Cowen
- Crous
- Cuenca-Estrella
- Da Silva
- da Silva
- De Gannes
- de Hoog GS
- Debeljak
- Defontaine
- Delhaes
- Denton
- Doligalski
- Eliana Barreto-Bergter
- Elizur
- Fernanado
- Fernandez Guerrero
- Fernando L Hernando
- Figari
- Figueiredo
- Figueiredo
- Fraczek
- Galgóczy
- Garzoni
- Geiger
- Gelabert-González
- Ghamrawi
- Gil-Lamaignere
- Gil-Lamaignere
- Gil-Lamaignere
- Gil-Lamaignere
- Gilgado
- Gilgado
- Gompels
- Gorin
- Gosbell
- Gottardi
- Gottardi
- Gottardi
- Gottardi
- Green
- Grenouillet
- Grisham
- Gruber
- Gu
- Guarro
- Güngör
- Harun
- Harun
- Hata
- Hawksworth
- Heath
- Hennebert
- Holle
- Homa
- Horré
- Horré
- Horré
- Howden
- Husain
- Idigoras
- Idoia Buldain
- Irinyi
- Jabado
- Janda-Ulfig
- Jardel Vieira de Meirelles
- Javier Capilla
- Javier Peman
- Jean-Philippe Bouchara
- Johannes Rainer
- Johnson
- Johnson
- Jose Cano-Lira
- Kaltseis
- Kaltseis
- Kantarcioglu
- Kathrin Tintelnot
- Katragkou
- Kaur
- Kelly
- Kennedy
- Kiffer-Moreira
- Kim
- Kimura
- Kooijman
- Krasny
- Kuroda
- Lackner
- Lackner
- Lackner
- Lackner
- Lackner
- Lackner
- Lamaris
- Lamaris
- Lamaris
- Larcher
- Laszlo Irinyi
- Leyre M López-Soria
- Li
- Lima
- Lopes
- Lu
- Marcinkiewicz
- Maria Teresa Martin-Gomez
- Mariana Ingrid D S Xisto
- Markus Nagl
- Martin-Vicente
- Martin-Vicente
- Martinez
- Matray
- Mcneill
- Meletiadis
- Meletiadis
- Metzgar
- Michaela Lackner
- Mina
- Mina
- Miyazaki
- Montagna
- Montejo
- Morio
- Musk
- Mylonakis
- Nagl
- Nakamura
- Neofytos
- Netea
- Nishimori
- Novak
- Novák
- Ochi
- Odabasi
- Oliveira
- Oliver
- Ong
- Ortoneda
- Ortoneda
- Ortoneda
- Osherov
- Padoan
- Panackal
- Pappas
- Patrick Vandeputte
- Paugam
- Pellon
- Pellon
- Pellon
- Pellon
- Pereira
- Perfect
- Pfaller
- Pfaller
- Pfaller
- Pihet
- Pinto
- Pinto
- Pinto
- Pluhacek
- Prichystal
- Queiroz-Telles
- Rainer
- Rainer
- Rainer
- Ravikumar
- Regamey
- Richardson
- Robbins
- Rodrigo Rollin-Pinheiro
- Rodrigues
- Rodriguez-Tudela
- Rodriguez-Tudela
- RodrÃguez
- Roilides
- Roilides
- Rolfe
- Rollin-Pinheiro
- Romani
- Romão
- Rougeron
- Russell
- Sahi
- Sandrine Giraud
- Santos
- Santos
- Sarvat
- Sayah
- Schwarz
- Schwienbacher
- Sedlacek
- Sedlacek
- Selbmann
- Sharon Chen
- Shin
- Shoham
- Silva
- Silva
- Simitsopoulou
- Sitterlé
- Sleiman
- Song
- Steinbach
- Steinbach
- Stensvold
- Stephane Ranque
- Studahl
- Sybren de Hoog
- Taj-Aldeen
- Tammer
- Thomas
- Thomson
- Thornton
- Thornton
- Tintelnot
- Tintelnot
- Tong
- Tortorano
- Troke
- Uenotsuchi
- Uno
- Verweij
- Vladimir Havlicek
- Wakabayashi
- Waldorf
- Waldorf
- Walsh
- Warris
- Wiederhold
- Wieland Meyer
- Winn
- Wood
- Wüthrich
- Xisto
- Xisto
- Yamamoto
- Yohann Le Govic
- Yustes
- Zeng
- Ziesing
- Zouhair
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- Field of study
Analysis of Outcomes in Ischemic vs Nonischemic Cardiomyopathy in Patients With Atrial Fibrillation A Report From the GARFIELD-AF Registry
- Author
- A'Court Christine
- Abdel-Qader Muwafeg
- Abe Masahiko
- Abe Masatake
- Abe Mitsunori
- Abe Sumihisa
- Abe Yukihiko
- Abhayaratna Walter
- Accogli Michele
- Adachi Susumu
- Adachi Toru
- Adak Dhriti
- Adam Matthew
- Adriaansen Henk
- Aegerter Emanuel
- Ageta Masato
- Aggarwala Anil
- Agnelli Giancarlo
- AgnieszkaMetzgier-Gumiela AgnieszkaMetzgier-Gumiela
- Ahlmark Hakan
- Ahmad Kamran
- Ahmad Shahid
- Ahmed Fayzal
- Ahn Jung Joo
- Akers Lori
- Akiyama Masahiro
- Al Mahmeed Wael
- Al-Khalili Faris
- Alberts Mark
- Alborough Elizabeth
- Aldegather Jehad
- Aleksandrova Elena
- Alexandre Almeida Carlos
- Ali Amar
- Ali Gholam
- Alia Pilar Montero
- Allasia Bartolomeo
- Alonso Carmela
- Alonso Concepcion
- Altun Armagan
- Alunni Massimo
- Alvarez Garcia Pere
- Alvarez Douglas
- Alvarez Miguel
- Alzogaray Maria Fernanda
- Amarenco Pierre
- Amaro Marisol
- Ambicka Monika
- Ambrosino Pasquale
- Ambrosio Giuseppe
- Amin Joseph
- Amrhein Diana
- Amstutz Daniela
- An Hae Jung
- Andere Natalia
- Andersson Agneta
- Andersson Lisbeth
- Ando Hiroshi
- Ando Shinichi
- Andrzejewski Dariusz
- Angaran Paul
- Ansoult Nadege
- Antonova Petra
- Antonsen Hege
- Aoki Kenji
- Aoyama Takuma
- Appleby Nigel
- Appleby Nigel
- Aracil Villar Joaquin
- Arai Hidekazu
- Araminowicz Joanna
- Aras Funda
- Arcocha Torres Maria Fe
- Argena Antonio
- Arima Shinichi
- Armangau Pauline
- Arstall Margaret
- Asafu-Adjaye Nana
- Asano Hiroshi
- Asano Taku
- Ashraf M. Javed
- Assagay Maharajh S.
- Assouline Serge
- Astridge Penny
- Atar Dan
- Atar Dan
- Ausen Karin
- Austria Aileen
- Aves Theresa
- Avinc Gamze
- Avinc Gamze
- Avinc Gamze
- Axthelm Christoph
- Ayar Ozge
- Aydinlar Ali
- Ayres Bronte
- Azakami Shiro
- Aziz Michael
- Azuma Junya
- Baba Takao
- Babjakova Zuzana
- Babyesiza Adyeri
- Bae Sang Cheol
- Baek Ae Lee
- Baglioni Gregorio
- Bai Chunlin
- Baksh Farisha
- Balaraju Swathi
- Ball Kelly
- Bamungpong Panthipa
- Banfi Elena
- Barbarash Olga
- Barbeira Pablo Saleta
- Barkowski Timothy
- Barnes Dylan
- Barnes Dylan
- Baron Esquivias Gonzalo
- Barraquer Feu Edelmira
- Barreau Angeline
- Barreda Maria
- Barretto Antonio Carlos Pereira
- Barrow Susan
- Barry Lisa
- Bartkowiak Radoslaw
- Bartlett Melialoha
- Bartnik Jerzy
- Basiak Marcin
- Basily Wagdy
- Bassand Jean-Pierre
- Bassand Jean-Pierre
- Bassand Jean-Pierre
- Bassand Jean-Pierre
- Bastani Lisa
- Baszak Jacek
- Batalov Roman
- Batlle Javier
- Batta Claire
- Batta Claire
- Baumbach Sylvia
- Baumgartner Philipp
- Baweja Paramdeep
- Bayat Junaid
- Beattie Andre
- Becerra Munoz Victor
- Begum Haseena
- Bekieszczuk Ewa
- Belenkova Yulia
- Belenky Dmitry
- Bengtsberg Daniel
- Bennett James
- Berardi Mario
- Berg-Johansen Berg-Johansen
- Berge Eivind
- Berge Trude
- Berit Anne
- Berman Sofia Graciela
- Bernat Lukasz
- Berneau Jean-Baptiste
- Best Peggy
- Beton Osman
- Betsuyaku Tetsuo
- Beveridge Rosemary
- Bezrodna Larysa
- Bhargava Kartikeya
- Biagioli Viviana
- Bianchi Alfredo
- Biedrzycka Malgorzata
- Biedrzycka Malgorzata
- Biedrzycki Lukasz
- Biernacka Anita
- Bigcanoe Julie
- Bignell Nanci
- Bilas Roman
- Bilecen Sinan
- Billger Annelie
- Bindig Hans-Walter
- Binnekamp Maurits
- Bird Nigel
- Bireciklioglu Mustafa Fehmi
- Birhan MEHMET BÄ°RHAN
- Bitakova Fatima
- Black Andrew
- Blenkhorn Adam
- Blinkova Marina
- Blombery Peter
- Blumberg Edwin
- Bockova Lucie
- Boda Zoltan
- Boehme Stefanie
- Boen Rigmor
- Boersma Misannia
- Boggian Giulio
- Bonet Jorge
- Bongaerts Maarten
- Bongiorni Maria Grazia
- Bonin Kerstin
- Bonkowski Grzegorz
- Bonner Michelle
- Bonnetain Anne
- Boon Jannie
- Boonyapisit Warangkana
- Boos Laura
- Booysen Maria
- Borjesson Ulf
- Borras Ana Domenech
- Boshoff Cecilia
- Bosman Femmy
- Bosschaert Mike
- Bossolasco Pierdomenico
- Botha Margo
- Bottarelli Maria Luisa
- Bouzamayor Maria Belen Lage
- Bowen-Simpkins Emma
- Bowers Suzanne
- Boys Janice
- Bradshaw Colin
- Braham Simon
- Brauer Gunter
- Bray Bryan
- Breakwell Lynn
- Bremmelgaard Arne
- Breschi Marco
- Breukel Laura
- Briceno Hinojo Ana
- Brimley Jennifer
- Broad Oulton
- Brodmann Marianne
- Bronisz Marek
- Broton Elzbieta
- Brotons Cuixart Carles
- Browne Debbie
- Bruegger Jasmine
- Brugnaux Jean Philippe
- Bruin Sandra
- Brusorio Stefania
- Bruun Michael
- Bruun Michael
- Brzustowska Malgorzata
- Buckley Elizabeth
- Buiks Paul
- Bulla Claudio
- Bultas Jan
- Bunyapipat Thanita
- Burdeina Liudmyla
- Burke Elizabeth
- Burns Stephen
- Busch Florian
- Butter Keith
- Cabrera Ramos Mercedes
- Cabrini Romina
- Caimi Teresa Maria
- Calcagnoli Francesca
- Cameron Alex
- Camm A. John
- Camm A. John
- Camm A. John
- Camm A. John
- Campagna Giuseppe
- Campo Moreno Mariela
- Campo Monica
- Cancho Corchado Gema
- Cannon Claire
- Canosa Roddy
- Canova Michaela
- Cao Shiping
- Cap Austl
- Cappelli Roberto
- Capucci Alessandro
- Carlton Lesley
- Carpenedo Monica
- Carroll Lisa
- Carroll Patrick
- Cartasegna Luis Rodolfo
- Cartwright Simon
- Casanova Gil Miguel
- Casassus Frederic
- Caspar Andreas
- Cassidy Doran
- Cassimjee Soraya
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- Turpie Alexander G. G.
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- Tybura Sebastian
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- Wang Yong
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- Yamasawa Masanori
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- Yamazoe Masahiro
- Yang Jingshan
- Yang Lingli
- Yang Zhiming
- Yawila Suree
- Yildirim Rifat
- Yilmaz Faruk
- Yilmaz Ozcan
- Yokota Naoto
- Yokoyama Yasuhiro
- Yoon Eunji
- Yoon Jung Han
- Yoshida Keiki
- Yoshida Tetsuro
- Yoshida Tomohiro
- Yoshida Tomoki
- Yoshimura Akira
- Yoshizawa Naoto
- Yu HyunJu
- Yu Ting
- Yusuf Huma
- Yuyang Tan
- Zaatout Eman
- Zaitsu Ryuji
- Zak Jan
- Zakutynska-Kowalczyk Karolina
- Zaluska Roman
- Zaman Kashif
- Zateyshchikov Dmitry
- Zauzig Heinz-Dieter
- Zdrowotnej Zespol Opieki
- Zecca Cinzia
- Zemlianskaia Oksana
- Zhai Hong
- Zhan Qiong
- Zhang Guoshan
- Zhang Huaiqin
- Zhang Ran
- Zhang Yi
- Zhao Yusheng
- Zhuravleva Evgeniya
- Zidek Milan
- Zidkova Eva
- Zika Jiri
- Zillo Mariana
- Zimmett Leon
- Zimny Hans-Hermann
- Zincke Stephanie
- Zinka Elzbieta
- Zinka Elzbieta
- Zotova Irina
- Zubeeva Galina
- Zuber Mathieu
- Zutz Stefan
- Zwenkau Schwarz
- Zyczynska Malgorzata
- Publication venue
- 'American Medical Association (AMA)'
- Publication date
- 01/06/2019
- Field of study
IMPORTANCE Congestive heart failure (CHF) is commonly associated with nonvalvular atrial fibrillation (AF), and their combination may affect treatment strategies and outcomes
Rivaroxaban with or without aspirin in stable cardiovascular disease
- Author
- Abat M.
- Abatello M.
- Abdul Hafidz M. I.
- Abdul Rahim A. A.
- Abdullah W. M.
- Abe H.
- Abe M.
- Abe S.
- Abe Y.
- Abelson M.
- Abergel H.
- Abib E.
- Abitbul A.
- Abola M.
- Aboyans V.
- Abrantes J.
- Absi F.
- Abu Hassan M. R.
- Abu Kassim Z.
- Accassat S.
- Accini Diaz A.
- Accini Mendoza A.
- Accini Mendoza J.
- Acimic C.
- Acosta G.
- Actis M.
- Adamkova V.
- Adamo M.
- Adams K.
- Adler F.
- Agardi I.
- Agudelo Ramos L.
- Aguirre M.
- Agullo A.
- Ahmad H.
- Ahmed A.
- Ahuad Calvelo A.
- Ahuad Calvelo J.
- Ahuad Guerrero R.
- Aizawa Y.
- Ajax K.
- Akatsuka T.
- Akatsuka Y.
- Akhavuz O.
- Akiyama R.
- Akiyoshi H.
- Ako J.
- Al-Khalili F.
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- Alagban C.
- Alarcon J.
- Alarcon V.
- Alarie P.
- Albertijn S.
- Albertsson P.
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- Allegrini E.
- Almagro S.
- Almendrales L.
- Almroth H.
- Aloisi A.
- Alvarez D'Amelio A.
- Alvarez Damelio A.
- Alvarez M.
- Alvarez Y.
- Alwi S. M.
- Alzate J.
- Aman S.
- Amemiya H.
- Amemiya Y.
- Amerena J.
- Amir M. A.
- Amiya R.
- Amonchot A.
- Amorin R. C.
- An S.
- Anand S. S.
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- Andersson T.
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- Andrade G.
- Andrea G.
- Andrei C.
- Andrew G.
- Andrioli V.
- Angel Escobar J.
- Anghel L.
- Angie Lorena A.
- Anonuevo J.
- Antohi L.
- Antropova O.
- Anuschek V.
- Anzules N.
- Aoki S.
- Aotsuka S.
- Apostoie A.
- Appel K.
- Appel S.
- Aquino M. R.
- Aradi D.
- Arai M.
- Araki Y.
- Arantes FBB.
- Araujo V. L.
- Arbis M. G.
- Arciniegas J.
- Arcos Palma E.
- Ardeleanu I.
- Arimie R.
- Aristizabal J.
- Ariz A.
- Armean P.
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- Arriagada G.
- Arseneault M. C.
- Arsenescu C.
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- Asahi T.
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- Asayama H.
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- Ashton H.
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- Attanasio C.
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- Ausheva A.
- Austin D.
- Averkov O.
- Avezum A.
- Aviles A.
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- Ayano S.
- Azeddine B.
- Azzara G.
- Babapulle M.
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- Badts G.
- Bae J.
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- Baello R.
- Baghilovici Cretu D.
- Bahamondes J.
- Baharuddin S.
- Bai X.
- Baierlein A.
- Bailey S.
- Baillot R.
- Bainey K.
- Bajnok L.
- Bakai J.
- Bakeen F.
- Balaguera Mendoza J.
- Baldin M. G.
- Baldini E.
- Balingit P.
- Baluta M.
- Bandiez J.
- Bando M.
- Banerjee P.
- Banerjee S.
- Bang L.
- Banga D. K.
- Bangdiwala S.
- Banno S.
- Barabas M.
- Barbarash O.
- Barber-Charmoux N.
- Barbieri A.
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- Barilati P.
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- Barreto D.
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- Bartol C.
- Bartolacci I.
- Barton J.
- Basile F.
- Baskett R.
- Basri N. A.
- Basso N.
- Basson M.
- Bastien A.
- Bastone R.
- Batista R. F.
- Battistelli E.
- Battistoni I.
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- Zoet-Nugteren S.
- Zorzo JAT.
- Zsary A.
- Zsoriova T.
- Zubova E.
- Zuker S.
- Zukermann R.
- Zuleta I.
- Zuleta M.
- Zushi R.
- Zvi R.
- Zvi Y.
- Zwinnen W.
- 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