403 research outputs found
Long-Term Effects of Autologous Bone Marrow Stem Cell Treatment in Acute Myocardial Infarction: Factors That May Influence Outcomes
- Author
- A Abdel-Latif
- A Halkin
- A Hirsch
- AA Quyyumi
- Anthony Mathur
- B Assmus
- B Jin
- C Fernandez-Pereira
- Carolyn Doree
- David M. Clifford
- DM Clifford
- E Martin-Rendon
- Enca Martin-Rendon
- F Cao
- FB Nogueira
- G Montalescot
- Giuseppe Biondi-Zoccai
- GP Meyer
- GW Stone
- H Arnesen
- J Higgins
- J Meluzin
- J Roncalli
- J Suarez de Lezo
- JH Traverse
- JH Traverse
- JJ McMurray
- JP Higgins
- JP Ioannidis
- K Lunde
- K Yao
- KA Robinson
- KC Wollert
- KC Wollert
- M Gnecchi
- M Penicka
- M Tendera
- MF Piepoli
- Mike J. Clarke
- MJ Lipinski
- ML Simoons
- NS Zhukova
- RS Karpov
- RS Velagaleti
- S Grajek
- S Hopewell
- S Hopewell
- S Janssens
- Sheila A. Fisher
- SJ Brunskill
- SL Chen
- SP Janssens
- Susan J. Brunskill
- Suzanne M. Watt
- TA Trikalinos
- V Schachinger
- V Schachinger
- ZQ Li
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
AIMS: To investigate whether there are important sources of heterogeneity between the findings of different clinical trials which administer autologous stem cell treatment for acute myocardial infarction (AMI) and to evaluate what factors may influence the long-term effects of this treatment. METHODS AND RESULTS: MEDLINE (1950-January 2011), EMBASE (1974-January 2011), CENTRAL (The Cochrane Library 2011, Issue 1), CINAHL (1982-January 2011), and ongoing trials registers were searched for randomised trials of bone marrow stem cells as treatment for AMI. Hand-searching was used to screen recent, relevant conference proceedings (2005-2010/11). Meta-analyses were conducted using random-effects models and heterogeneity between subgroups was assessed using chi-squared tests. Planned analyses included length of follow-up, timing of cell infusion and dose, patient selection, small trial size effect, methodological quality, loss of follow-up and date of publication. Thirty-three trials with a total of 1,765 participants were included. There was no evidence of bias due to publication or time-lag, methodological quality of included studies, participant drop-out, duration of follow-up or date of the first disclosure of results. However, in long-term follow-ups the treatment seemed more effective when administered at doses greater than 10(8) cells and to patients with more severe heart dysfunction. CONCLUSIONS: Evaluation of heterogeneity between trials has not identified significant sources of bias in this study. However, clinical differences between trials are likely to exist which should be considered when undertaking future trials
Increasing vegetable intakes: rationale and systematic review of published interventions
- Author
- A Agudo
- A Astrup
- A Fildes
- A Gibson
- A Knaapila
- A Koushik
- A Lakkakula
- A Maier
- A Nagao
- A Olsen
- AA Kiadaliri
- AAM Poelman
- AAM Poelman
- AAM Poelman
- AC Tsai
- AD Blatt
- AF Vinha
- AJ Cooper
- AJ Luo
- AL Macready
- AM Jiménez-Monreal
- Ann Bevan
- Ann Hemingway
- AR Vieira
- AS Anderson
- AS Maier
- AT McMahon
- B Franchini
- B Han
- B Li
- B Liu
- B Liu
- B Liu
- B Wansink
- B Yao
- BC Galobardes
- BC Tohill
- BJ Rolls
- BT Izumi
- C Barends
- C Barends
- C Bosetti
- C Glasson
- C Sandeno
- C Sweetman
- CA Gunn
- CA Johnston
- Caterina Dinnella
- CBM Kamphius
- CE Holley
- CE Neville
- CL Perry
- CN Vihotogbe-Sossa
- D Aune
- D Burnier
- D Hu
- D Morizet
- David Morizet
- DC Correia
- DE Wall
- DJ Lamport
- DO McCall
- DR Just
- E Byrne
- E Koui
- E Mooney
- E Remy
- E Robinson
- E Trudeau
- EL Gibson
- EL Melbye
- Erminio Monteleone
- F. J. Armando Perez-Cueto
- FJ PĂ©rez-Cueto
- FM Stok
- G Masala
- G Roos
- GC Chen
- GG Zeinstra
- GG Zeinstra
- GG Zeinstra
- H Coulthard
- H Hausner
- Heather Hartwell
- HM Hendy
- HM Hendy
- J Brug
- J Brug
- J Golding
- J Jin
- J Polesel
- J SĆupski
- J Wardle
- J Wardle
- J Zhao
- JA Mennella
- JA Mennella
- JB Myhre
- JC Darian
- JK Ransley
- JL Brown
- JL Morris
- JL Slavin
- JL ValmĂłrbida
- JO Fisher
- JP Redden
- JS Meengs
- JS Savage
- JV Woodside
- JY Yeon
- K Giskes
- K Giskes
- K Glanz
- K Knecht
- K Peltzer
- Katherine M. Appleton
- KC Mathias
- KC Wroten
- KM Appleton
- KM Appleton
- KM Appleton
- KN Brown
- KW Cullen
- L Dauchet
- L Dauchet
- L Weatherly
- Laure Saulais
- Laurence Depezay
- LJ Cooke
- LS Snee
- M Bjelland
- M Draxten
- M Faber
- M Gholami
- M Li
- M Loef
- M Reicks
- MC Morris
- MJ Noradilah
- MK Spill
- MK Spill
- MK Spill
- ML OâConnell
- MM Hetherington
- MM Rahman
- MM Ratcliffe
- N Corsini
- NI Larson
- NM Gatto
- O Kushida
- O Oyebode
- O Tornwall
- P Carter
- P Clarke
- P Heath
- P Schreinemachers
- PA Carney
- PJ Morgan
- PR DomĂnguez
- Q Wang
- QJ Wu
- R AbuSabha
- R Bongoni
- R Villegas
- RC Curhan
- RC Havermans
- RG Tabak
- RH Liu
- RL Best
- RM Claro
- S Anzman-Frasca
- S Bouhlal
- S Bouhlal
- S Bouhlal
- S Imai
- S Mustonen
- S Pee de
- S Sharma
- SA Lanham New
- SA Tanumihardjo
- SC Dijkstra
- SE Middlestadt
- SF Shenoy
- SF Shenoy
- SH Kelder
- SJ Caton
- SL Fulton
- SM Ahern
- SM Droog de
- ST Yen
- T Bucher
- T Bucher
- T Kremer-Sadlik
- TA Ledoux
- TJ Key
- TM Dovey
- TM Leak
- TR Wenrich
- V Oskarsson
- V Savica
- VW Wild de
- VW Wild de
- W Wright
- WH Ahearn
- X Liu
- X Wang
- Y Bai
- Y Ogawa
- Y Takata
- Y Wu
- Y Yang
- YT Liu
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Purpose
While the health benefits of a high fruit and vegetable consumption are well known and considerable work has attempted to improve intakes, increasing evidence also recognises a distinction between fruit and vegetables, both in their impacts on health and in consumption patterns. Increasing work suggests health benefits from a high consumption specifically of vegetables, yet intakes remain low, and barriers to increasing intakes are prevalent making intervention difficult. A systematic review was undertaken to identify from the published literature all studies reporting an intervention to increase intakes of vegetables as a distinct food group.
Methods
DatabasesâPubMed, PsychInfo and Medlineâwere searched over all years of records until April 2015 using pre-specified terms.
Results
Our searches identified 77 studies, detailing 140 interventions, of which 133 (81 %) interventions were conducted in children. Interventions aimed to use or change hedonic factors, such as taste, liking and familiarity (n = 72), use or change environmental factors (n = 39), use or change cognitive factors (n = 19), or a combination of strategies (n = 10). Increased vegetable acceptance, selection and/or consumption were reported to some degree in 116 (83 %) interventions, but the majority of effects seem small and inconsistent.
Conclusions
Greater percent success is currently found from environmental, educational and multi-component interventions, but publication bias is likely, and long-term effects and cost-effectiveness are rarely considered. A focus on long-term benefits and sustained behaviour change is required. Certain population groups are also noticeably absent from the current list of tried interventions
Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets
- Author
- A Krohn
- A Parray
- Adam Butler
- Adam Lambert
- Alan Thompson
- Andrew Futreal
- Andrew G. Lynch
- Andrew Menzies
- Anne Y. Warren
- Anthony Ng
- AV Biankin
- Barbara Kremeyer
- Bissan Al-Lazikani
- BS Carver
- BS Taylor
- C Mitsopoulos
- C Pilati
- C Rudnicka
- C Seigne
- C Svensson
- Cancer Genome Atlas Research Network
- Cathy Corbishley
- CE Barbieri
- Charlie E. Massie
- Chris Sander
- Christopher Greenman
- Christopher Ogden
- Christopher S. Foster
- CJ Ryan
- Clare Verrill
- Colin S. Cooper
- CS Cooper
- CS Grasso
- Cyril Fisher
- D Chakravarty
- D Leongamornlert
- D Robinson
- Dan J. Woodcock
- Dan M. Berney
- Daniel Leongamornlert
- Daniel S. Brewer
- David C. Wedge
- David E. Neal
- David Jones
- David Nicol
- Declan Cahill
- DI Smith
- Douglas F. Easton
- E Castro
- E Lalonde
- EA Klein
- Edward Rowe
- Elizabeth Bancroft
- Erik Mayer
- FL Tarish
- Freddie C. Hamdy
- G Attard
- G Daniels
- G Gundem
- G Nilsen
- G. Steven Bova
- Gerhardt Attard
- Gunes Gundem
- H Li
- H Zhang
- Hayley Luxton
- Hayley Whitaker
- Hongwei Zhang
- Inigo Martincorena
- J Cuzick
- J Mateo
- J Weischenfeldt
- JC King
- JE Tym
- JF Goodwin
- JL Williams
- JM Mosquera
- Johann de Bono
- Jon Teague
- Jonathan Kay
- Jorge Zamora
- K Fischer
- K Keersmaecker De
- K Malinowska
- K Takayama
- K Ye
- Katalin Karaszi
- KC Bulusu
- Keiran Raine
- L Burkhardt
- LB Alexandrov
- LB Alexandrov
- LM FitzGerald
- LU Rodrigues
- Lucy Matthews
- Lucy Stebbings
- Ludmil B. Alexandrov
- Luke Marsden
- M Kluth
- M Kluth
- M Sasaki
- MA Collart
- Mahbubl Ahmed
- MF Berger
- Michael Fraser
- ML Nickerson
- MN Patel
- Mohammed Ghori
- N Bolli
- Naomi Livni
- ND James
- Nening Dennis
- Nicholas Van As
- Niedzica Camacho
- Nimish C. Shah
- P Heun
- P Loo Van
- P Workman
- Pardeep Kumar
- Paul C. Boutros
- Paul Workman
- PC Boutros
- Pelvender Gill
- Peter Van Loo
- PJ Boström
- R Malik
- Robert G. Bristow
- Rosalind A. Eeles
- S Jones
- S Kaikkonen
- S Nik-Zainal
- S Nik-Zainal
- S Orchard
- S Shin
- SA Forbes
- Sandra Edwards
- Sarah Thomas
- SC Baca
- Simon Tavaré
- Stefan Dentro
- Steve Hawkins
- Steven Hazell
- Stuart McLaren
- Sue Merson
- Tapio Visakorpi
- Thomas Mitchell
- Tim Dudderidge
- Tokhir Dadaev
- Ultan McDermott
- Valeria Bo
- Vincent Gnanapragasam
- Vincent Khoo
- W Liu
- W Liu
- W Yang
- W Zhao
- William Howat
- William Isaacs
- WR Polkinghorn
- X Mao
- Y Loriot
- YA Yang
- Yong-Jie Lu
- Yongwei Yu
- Z Chen
- Z Liu
- Zsofia Kote-Jarai
- Publication venue
- Publication date
- 13/04/2018
- Field of study
Prostate cancer represents a substantial clinical challenge because it is difficult to predict outcome and advanced disease is often fatal. We sequenced the whole genomes of 112 primary and metastatic prostate cancer samples. From joint analysis of these cancers with those from previous studies (930 cancers in total), we found evidence for 22 previously unidentified putative driver genes harboring coding mutations, as well as evidence for NEAT1 and FOXA1 acting as drivers through noncoding mutations. Through the temporal dissection of aberrations, we identified driver mutations specifically associated with steps in the progression of prostate cancer, establishing, for example, loss of CHD1 and BRCA2 as early events in cancer development of ETS fusion-negative cancers. Computational chemogenomic (canSAR) analysis of prostate cancer mutations identified 11 targets of approved drugs, 7 targets of investigational drugs, and 62 targets of compounds that may be active and should be considered candidates for future clinical trials
Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
- Author
- A Abbate
- A Abhyankar
- A Adams
- A Agafina
- A Akyea-Djamson
- A Alan
- A Alfieri
- A Alfrey
- A Alvarisqueta
- A Amos
- A Anadiotis
- A Anneveldt
- A Antolick
- A Arthur
- A Aslam
- Abaci F
- Abdullakutty J
- Abhaichand R
- Abib E Jr
- Aboufakher R
- Abrantes J
- Abreu M
- Abulencia K
- Acampora D
- Acampora M
- Accini Mendoza Jl
- Aceto L
- Acevedo B
- Acevedo L
- Acheatel R
- Actis Mv
- Adams M
- Adjic Nc
- Affaki Gs
- Agarwal Dk
- Aggarwal Rk
- Agosta Gf
- Aguilar M
- Aguilar M
- Ahire N
- Ahmad I
- Ahmed Sh
- Ahn Y
- Aish B
- Aiub F
- Aiub J
- Ajax K
- Ajioka M
- Akai Y
- Akatova E
- Akrap B
- Al Joundi T
- Al-Khalili F
- Albisu J
- Alcalde Jm
- Alcide P
- Alfonso T
- Allen J
- Alllison Dc
- Almaliky T
- Amerena J
- Andersen K
- Andor M
- Angelova I
- Angiolillo D
- Anita S
- Anker Sd
- Antalik L
- Antonicelli R
- Aparicio Cv
- Apel T
- Apostolovic S
- Ara M
- Aragorn L
- Arango Jl
- Araujo Fonseca M
- Ardissino D
- Arenas Leon Jl
- Arevalo S
- Argiolas G
- Arif I
- Armas E
- Aron G
- Arora S
- Asafu-Adjaye N
- Ashcom T
- Ashford M
- Ashino K
- Asim Oktay Ao
- Assarsson E
- Ata B
- Ather N
- Atieh M
- Aull L
- Avalos V
- Avdonina N
- Awasthi Ak
- Axthelm C
- Ayala M
- Ayasse D
- Ayasse M
- Azizad M
- Azize Gm
- B Becker
- Baar M
- Babu R
- Backer T
- Badea C
- Baden M
- Baehl S
- Baek C
- Baeumer A
- Bagi Es
- Bai A
- Bailey K
- Bailey S
- Bair S
- Baker A
- Baker C
- Bakhai A
- Bakker H
- Baksi A
- Baldin Mg
- Bali Hk
- Ballantyne C
- Ballmajo M
- Balode A
- Balukova E
- Bang Sa
- Banker D
- Banker K
- Baquero A
- Barbarash Ol
- Barbato E
- Barbosa E
- Barnett S
- Baron S
- Barreto M
- Barroso A
- Barroso W
- Bartkowiak A
- Bartosh L
- Bartuseviciene S
- Bashir K
- Baszak J
- Bata Ir
- Bayram E
- Beall K
- Beaudry M
- Beauregard La
- Beckett L
- Belejchak P
- Belle Isle J
- Belohlavek J
- Bendelow T
- Bender D
- Benedetti G
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- Berger V
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- Bergholtz T
- Bergler-Klein J
- Berk M
- Berli Ma
- Bernstein M
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- Berulfsen A
- Bevilacqua Mt
- Bhadade S
- Bilazarian S
- Bilodeau N
- Binder A
- Binns Y
- Birdane A
- Bisne V
- Bitzer V
- Blagdon M
- Blahey M
- Blankenberg S
- Blazsek Z
- Bloch S
- Blom Kb
- Bluemel J
- Blumberg C
- Blumenthal R
- Bocanera M
- Bodanese L
- Boffetti P
- Bohra P
- Bohula E
- Boivin Mc
- Bolduc H
- Boley K
- Bolognesi Mg
- Bolsmann C
- Boman K
- Bonner J
- Borrayo Na
- Boström PÄ
- Botelho R
- Botta C
- Boudreaux R
- Boulanger K
- Bourgeois S
- Bouvy C
- Bowen L
- Boyarkin M
- Bradley A
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- Bramlet D
- Brath H
- Braun P
- Bredlau C
- Brickman T
- Briggs S
- Briké C
- Brodmann M
- Brons S
- Brousalis L
- Brouwer M
- Brown C
- Brown N
- Brown S
- Buchannan C
- Budaj A
- Budassi N
- Budkova J
- Bugan V
- Buhlman S
- Bulashova O
- Bunschoten P
- Burke W
- Burley T
- Burova N
- Burris H
- Burton C
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- BĂžen Rh
- C Clavier-Firmin
- C Conradie
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- C Covert
- C Cuneo
- Caballero-Valiente B
- Cabau Jr
- Calabrese A
- Campanale Eg
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- Cantor W
- CANTOS Trial Group. Krum H
- Capova L
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- Carr K
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- Chhabra A
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- Choi Aj
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- Christensen L
- Christenson S
- Chung A
- Churina S
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- Ciglenecki N
- Cioffi A
- Cislowski D
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- Clocotan M
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- Coufalova Z
- Covell W
- Cox B
- Cox R
- Craig W
- Crandall L
- Crawford G
- Crea F
- Crepps K
- Crocamo A
- Cromer M
- Cruz H
- Cruz H
- Cruz M
- Csala L
- Cucher F
- Cuentas I
- Cuervo A
- Curiac D
- Cymerman K
- Cyprian R
- Czerski T
- D'Amours Dg
- D Dash
- D Dattani
- D Denham
- D Desai
- D Desalle
- D Digangi
- D Dunn
- Da Costa F
- Da Silva A
- Da Silva D Jr
- Da Silva O Jr
- Dahlen G
- Dalseg Am
- Damron M
- Danik J
- Davalos C
- Dave B
- Dave K
- Davidsson K
- Davies M
- Davies N
- Davis B
- Davis M
- Dawkins-Hughes S
- Dawood Sy
- Dayer M
- De Boer P
- De Caterina R
- De Jong C
- De Knijf K
- De Krumbach L
- De Los Milagros Had M
- De Los Rios M
- De Rosa S
- De Vos A
- De Wolf L
- Dean J
- Debnam S
- Decsi K
- Decsi Kl
- Dedek V
- Dedkova S
- Defosse C
- Degennaro N
- Dehning M
- Dela Llana A
- Delfonso F
- Delforge M
- Delgadillo T
- Dellasa M
- Dellborg M
- Dellorso M
- Demidova M
- Den Hartog F
- Denecke C
- Dengler T
- Dermitzakis A
- Deslongchamps F
- Dessalvi Cc
- Destro M
- Dettmer M
- Devasia T
- Deweerdt N
- Dhanak R
- Dhawan M
- Di Biase M
- Diago M
- Diaz M
- Dicken T
- Dickstein K
- Diederich C
- Diederich M
- Diehl R
- Diller P
- Dimattia M
- Dimitrov G
- Diodati J
- Dobariya H
- Dobilas V
- Dodds G
- Doesborg L
- Doggett J
- Dognini Gp
- Doi M
- Dokupilova A
- Dommerholt R
- Donahue K
- Donath M
- Donaubauer T
- Dong X
- Dormidontova G
- Dorogova I
- Dos Santos A
- Dos Santos F
- Dos Santos P
- Doughty A
- Doughty L
- Dovgalevskiy Y
- Dovgolis S
- Dragutksy B
- Dreese M
- Drost I
- Drouin K
- Duchesne L
- Duckert A
- Duda N
- Dudarev M
- Dudhatra N
- Duff J
- Duhan S
- Dunhurst F
- Dussan Ma
- Dutka C
- Dwenger E
- Dzupina A
- DĂ©kĂĄny Jn
- E Eleuteri
- E Englmann
- Earl J
- East C
- Eaton C
- Eaves W
- Ebeling K
- Ebrahim I
- Eccleston D
- Echeverria L
- Eder F
- Edgerton L
- Edillo C
- Edwards J
- Edwards T
- Eichinger G
- Einhorn D
- Eki Y
- El Hachem M
- El Hafi S
- Ellenbroek D
- Ellis M
- Emil B
- Endo T
- Engelen W
- Erhard M
- Erickson B
- Ervin W
- Eskridge L
- Espinosa V
- Everett Bm
- F Fedele
- F Fonseca
- F Fucci
- Facello A
- Facello M
- Faghih M
- Fail P
- Falcon D
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- Farias E
- Fattal P
- Fawson A
- Feitosa G
- Felario Junior Ga
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- Feng Y
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- Ferdinand K
- Ferkl R
- Fernandez Aa
- Ferrari V
- Ferrario M
- Ferraz R
- Ferreira Dos Santos T
- Ferreira-Jardim A
- Fien E
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- Filho P
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- Fisher J
- Fitilev S
- Fitz-Patrick D
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- Flaksa I
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- Flezar M
- Fliesser-Goerzer E
- Flores E
- Flores E
- Flores Gs
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- Floro T
- Foerster A
- Folkeringa Rj
- Fonseca A
- Fontaine S
- Forgon T
- Forgosh L
- Forker A
- Forster T
- Foster M
- Foucauld J
- Fowler V
- Fox B
- Franco M
- Francoeur L
- Frandsen B
- Frandsen B
- Frankenstein L
- Fratczak M
- Freitas E
- French J
- Frivold G
- Fruchter G
- Fu G
- Fucak E
- Fuchs R
- Fucili A
- Fukuike C
- Fullerton D
- Fulop P
- Fulop T
- Fulwani M
- Furch G
- Furuseth B
- G Gacioch
- G Gosselin
- Gabito A
- Gabor M
- Gabriel J
- Gabrielli D
- Gaeb-Strasas B
- Gamba C
- Ganau A
- Gapon L
- Garas S
- Garcia Duran R
- Garcia Pinna J
- Garcia Rinaldi R
- Garcia F
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- Garcia-Fragoso V
- Garcia-Portela M
- Garner K
- Gazizianova V
- Gelb R
- Genest J
- Genova D
- George F
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- Gersh B
- Gervais B
- Ghali J
- Ghondale N
- Ghosh N
- Ghosh S
- Giese C
- Gilbert J
- Gilley J
- Gits F
- Glancy R
- Glenny J
- Glover J
- Glynn Rj
- Godoy Sanchez M
- Goette A
- Goff R
- Goffinet C
- Gohel P
- Goldberg N
- Gomez Sanchez J
- Gonsorcik J
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- Gonzales V
- Gonzalez E
- Gordeev I
- Gorges R
- Gospodinov K
- Gotcheva N
- Goudev A
- Gould R
- Govindaraj D
- Goyal B
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- Zielinski M
- Zieve F
- Zineldine A.
- Zirlik A
- Zucchetti C
- Publication venue
- 'Massachusetts Medical Society'
- Publication date
- 01/01/2017
- Field of study
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1ÎČ, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1ÎČ innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.
Combination of searches for heavy spin-1 resonances using 139 fbâ1 of proton-proton collision data at s = 13 TeV with the ATLAS detector
- Author
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- Aakvaag E
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- Zhemchugov A
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- Zimine NI
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- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- Springer Nature
- Publication date
- 19/04/2024
- Field of study
A combination of searches for new heavy spin-1 resonances decaying into different pairings of W, Z, or Higgs bosons, as well as directly into leptons or quarks, is presented. The data sample used corresponds to 139 fbâ1 of proton-proton collisions at
= 13 TeV collected during 2015â2018 with the ATLAS detector at the CERN Large Hadron Collider. Analyses selecting quark pairs (qq, bb,
, and tb) or third-generation leptons (ÏÎœ and ÏÏ) are included in this kind of combination for the first time. A simplified model predicting a spin-1 heavy vector-boson triplet is used. Cross-section limits are set at the 95% confidence level and are compared with predictions for the benchmark model. These limits are also expressed in terms of constraints on couplings of the heavy vector-boson triplet to quarks, leptons, and the Higgs boson. The complementarity of the various analyses increases the sensitivity to new physics, and the resulting constraints are stronger than those from any individual analysis considered. The data exclude a heavy vector-boson triplet with mass below 5.8 TeV in a weakly coupled scenario, below 4.4 TeV in a strongly coupled scenario, and up to 1.5 TeV in the case of production via vector-boson fusion
Measurement and interpretation of same-sign W boson pair production in association with two jets in pp collisions at s = 13 TeV with the ATLAS detector
- Author
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- Abbott B
- Abeling K
- Abicht NJ
- Abidi SH
- Aboulhorma A
- Abramowicz H
- Abreu H
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- Abusleme Hoffman AC
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- Zhemchugov A
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- Zhulanov V
- Zimine NI
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- Zoccoli A
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- Zorbas TG
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- Zwalinski L
- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- Springer Nature
- Publication date
- 01/04/2024
- Field of study
This paper presents the measurement of fducial and diferential cross sections for both the inclusive and electroweak production of a same-sign W-boson pair in association with two jets (W±W±jj) using 139 fbâ1 of proton-proton collision data recorded at a centre-of-mass energy of âs = 13 TeV by the ATLAS detector at the Large Hadron Collider. The analysis is performed by selecting two same-charge leptons, electron or muon, and at least two jets with large invariant mass and a large rapidity diference. The measured fducial cross sections for electroweak and inclusive W±W±jj production are 2.92 ± 0.22 (stat.) ± 0.19 (syst.)fb and 3.38±0.22 (stat.)±0.19 (syst.)fb, respectively, in agreement with Standard Model predictions. The measurements are used to constrain anomalous quartic gauge couplings by extracting 95% confdence level intervals on dimension-8 operators. A search for doubly charged Higgs bosons H±± that are produced in vector-boson fusion processes and decay into a same-sign W boson pair is performed. The largest deviation from the Standard Model occurs for an H±± mass near 450 GeV, with a global signifcance of 2.5 standard deviations
Measurement of the ttÂŻttÂŻ production cross section in pp collisions at âs=13 TeV with the ATLAS detector
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- Zhemchugov A
- Zheng Z
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- Zhukov K
- Zhulanov V
- Zieminska D
- Zimine NI
- Zimmermann S
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- Zoccoli A
- Zoch K
- Zorbas TG
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- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 16/11/2021
- Field of study
A measurement of four-top-quark production using proton-proton collision data at a centre-of-mass energy of 13 TeV collected by the ATLAS detector at the Large Hadron Collider corresponding to an integrated luminosity of 139 fbâ1 is presented. Events are selected if they contain a single lepton (electron or muon) or an opposite-sign lepton pair, in association with multiple jets. The events are categorised according to the number of jets and how likely these are to contain b-hadrons. A multivariate technique is then used to discriminate between signal and background events. The measured four-top-quark production cross section is found to be 26+17â15 fb, with a corresponding observed (expected) significance of 1.9 (1.0) standard deviations over the background-only hypothesis. The result is combined with the previous measurement performed by the ATLAS Collaboration in the multilepton final state. The combined four-top-quark production cross section is measured to be 24+7â6 fb, with a corresponding observed (expected) signal significance of 4.7 (2.6) standard deviations over the background-only predictions. It is consistent within 2.0 standard deviations with the Standard Model expectation of 12.0 ± 2.4 fb
Search for pair production of squarks or gluinos decaying via sleptons or weak bosons in final states with two same-sign or three leptons with the ATLAS detector
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- Yeo BK
- Yexley MR
- Yin P
- Yorita K
- Younas S
- Young C
- Young CJS
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- Zaazoua M
- Zabinski B
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- Zhemchugov A
- Zheng K
- Zheng X
- Zheng Z
- Zhong D
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- Zhulanov V
- Zimine NI
- Zinsser J
- Ziolkowski M
- Zoccoli A
- Zoch K
- Zorbas TG
- Zormpa O
- Zou W
- Zwalinski L
- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 15/02/2024
- Field of study
A search for pair production of squarks or gluinos decaying via sleptons or weak bosons is reported. The search targets a final state with exactly two leptons with same-sign electric charge or at least three leptons without any charge requirement. The analysed data set corresponds to an integrated luminosity of 139 fbâ1 of proton-proton collisions collected at a centre-of-mass energy of 13 TeV with the ATLAS detector at the LHC. Multiple signal regions are defined, targeting several SUSY simplified models yielding the desired final states. A single control region is used to constrain the normalisation of the WZ + jets background. No significant excess of events over the Standard Model expectation is observed. The results are interpreted in the context of several supersymmetric models featuring R-parity conservation or R-parity violation, yielding exclusion limits surpassing those from previous searches. In models considering gluino (squark) pair production, gluino (squark) masses up to 2.2 (1.7) TeV are excluded at 95% confidence level
Measurements of sensor radiation damage in the ATLAS inner detector using leakage currents
- Author
- Aad G
- Abbott B
- Abbott DC
- Abeling K
- Abhayasinghe DK
- Abidi SH
- AbouZeid OS
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- Zoch K
- Zorbas TG
- Zou R
- Zou W
- Zwalinski L
- Publication venue
- IOP
- Publication date
- 01/01/2021
- Field of study
Non-ionizing energy loss causes bulk damage to the silicon sensors of the ATLAS pixel and strip detectors. This damage has important implications for data-taking operations, charged-particle track reconstruction, detector simulations, and physics analysis. This paper presents simulations and measurements of the leakage current in the ATLAS pixel detector and semiconductor tracker as a function of location in the detector and time, using data collected in Run 1 (2010â2012) and Run 2 (2015â2018) of the Large Hadron Collider. The extracted fluence shows a much stronger |z|-dependence in the innermost layers than is seen in simulation. Furthermore, the overall fluence on the second innermost layer is significantly higher than in simulation, with better agreement in layers at higher radii. These measurements are important for validating the simulation models and can be used in part to justify safety factors for future detector designs and interventions.publishedVersio
Measurements of Higgs bosons decaying to bottom quarks from vector boson fusion production with the ATLAS experiment at â=13TeV
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- Ă kesson TPA
- Ăncel ĂO
- ĆœeniĆĄ T
- ĆœivkoviÄ L
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 23/06/2021
- Field of study
The paper presents a measurement of the Standard Model Higgs Boson decaying to b-quark pairs in the vector boson fusion (VBF) production mode. A sample corresponding to 126 fbâ1 of sâ=13TeV protonâproton collision data, collected with the ATLAS experiment at the Large Hadron Collider, is analyzed utilizing an adversarial neural network for event classification. The signal strength, defined as the ratio of the measured signal yield to that predicted by the Standard Model for VBF Higgs production, is measured to be 0.95+0.38â0.36 , corresponding to an observed (expected) significance of 2.6 (2.8) standard deviations from the background only hypothesis. The results are additionally combined with an analysis of Higgs bosons decaying to b-quarks, produced via VBF in association with a photon
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