8 research outputs found
Neutralization Serotyping of BK Polyomavirus Infection in Kidney Transplant Recipients
- Author
- A Egli
- A Nakanishi
- A Roldao
- A Sener
- A Stolt
- AC Cheerva
- AP Sharma
- AS Dugan
- AY Leung
- BLZM Kasiske
- C Luo
- C Luo
- CB Buck
- CB Buck
- Christopher B. Buck
- Daniel C. Brennan
- DC Brennan
- DC Montefiori
- Diana V. Pastrana
- DL Bohl
- DL Bohl
- DL Bohl
- DV Pastrana
- DV Pastrana
- E Anzivino
- E Ramos
- F Ginevri
- FK Baksh
- G Shaw
- GJ Nabel
- Gregory A. Storch
- HH Hirsch
- HH Hirsch
- HK Singh
- HY Zheng
- J McMillen
- JA Low
- JH Harrison
- JM Smith
- JP Merrill
- JT Schiller
- K Sasnauskas
- Michael Imperiale
- N Guex
- Nicolas Çuburu
- P Randhawa
- P Randhawa
- Parmjeet S. Randhawa
- PM Day
- PS Randhawa
- R Boldorini
- R Boothpur
- R Purighalla
- Raphael P. Viscidi
- RL Garcea
- RM Schowalter
- RY Calne
- S Bodaghi
- S Tremolada
- S Zhong
- T Schachtner
- T Stehle
- TF Hogan
- TJ Kemp
- U Neu
- WA Knowles
- WA Knowles
- Y Matsuda
- Y Nishimoto
- Y Yogo
- Publication venue
- Public Library of Science
- Publication date
- 01/04/2012
- Field of study
BK polyomavirus (BKV or BKPyV) associated nephropathy affects up to 10% of kidney transplant recipients (KTRs). BKV isolates are categorized into four genotypes. It is currently unclear whether the four genotypes are also serotypes. To address this issue, we developed high-throughput serological assays based on antibody-mediated neutralization of BKV genotype I and IV reporter vectors (pseudoviruses). Neutralization-based testing of sera from mice immunized with BKV-I or BKV-IV virus-like particles (VLPs) or sera from naturally infected human subjects revealed that BKV-I specific serum antibodies are poorly neutralizing against BKV-IV and vice versa. The fact that BKV-I and BKV-IV are distinct serotypes was less evident in traditional VLP-based ELISAs. BKV-I and BKV-IV neutralization assays were used to examine BKV type-specific neutralizing antibody responses in KTRs at various time points after transplantation. At study entry, sera from 5% and 49% of KTRs showed no detectable neutralizing activity for BKV-I or BKV-IV neutralization, respectively. By one year after transplantation, all KTRs were neutralization seropositive for BKV-I, and 43% of the initially BKV-IV seronegative subjects showed evidence of acute seroconversion for BKV-IV neutralization. The results suggest a model in which BKV-IV-specific seroconversion reflects a de novo BKV-IV infection in KTRs who initially lack protective antibody responses capable of neutralizing genotype IV BKVs. If this model is correct, it suggests that pre-vaccinating prospective KTRs with a multivalent VLP-based vaccine against all BKV serotypes, or administration of BKV-neutralizing antibodies, might offer protection against graft loss or dysfunction due to BKV associated nephropathy
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
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- Avalos V
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- Youssef G
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- Zhang W
- Zhang Y
- Zhao R
- Zhou H
- Zidova M
- 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-1β, 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-1β 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.
Polyomavirus-Associated Nephropathy in Renal Transplantation
- Author
- A. Chandraker
- A. Kazory
- A. Milstone
- A. Vats
- A.H. Jedai Al
- A.P. Limaye
- B. Celik
- B. Hurault de Ligny
- B.L. Padgett
- C.B. Drachenberg
- C.B. Drachenberg
- C.B. Drachenberg
- C.K. Buehrig
- D. Dadhania
- D.M. Hodur
- D.N. Howell
- E. Ramos
- E. Ramos
- E.F. Mackenzie
- E.R. Ramos
- F. Ginevri
- F. Ginevri
- F.K. Baksh
- H. Hausen zur
- H. Maiza
- H.H. Hirsch
- H.H. Hirsch
- H.H. Hirsch
- H.H. Hirsch
- H.H. Hirsch
- I. Agha
- I. Binet
- I.A. Atencio
- J. Trofe
- J. Trofe
- J. Trofe
- J.A. Fishman
- J.H. Helderman
- K.V. Shah
- M. Josephson
- M. Mayr
- M. Mengel
- M. Tognon
- M.C. Wen
- M.S. Sachdeva
- O. Pappo
- P. Boucek
- P. Comoli
- P. Randhawa
- P.S. Randhawa
- P.S. Randhawa
- P.S. Randhawa
- P.V. Kadambi
- R. Ding
- R. Purighalla
- R. Rahamimov
- R. Wali
- R.C. Drachenberg
- R.D. Poduval
- R.M. Li
- S. Rosen
- S.D. Gardner
- T Moriyama
- U. Moens
- U. Moens
- V. Nickeleit
- V. Nickeleit
- V. Nickeleit
- V. Nickeleit
- V.S. Mathur
- W.A. Knowles
- Y.M. Barri
- Y.N. Kang
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2006
- Field of study
BK Virus: A Clinical Review
- Author
- Altavilla G
- Andrews CA
- Arthur RR
- Bedi A
- Bogdanovic G
- Bogdanovic G
- Bogdanovic G
- Boldorini R
- Borgatti M
- Brooks BR
- Campioni D
- Chesters PM
- Coleman DV
- Coleman DV
- Coleman DV
- Corallini A
- Corallini A
- De Mattei M
- Degener AM
- Dolei A
- Dorries K
- Dyson N
- Flaegstad T
- Flaegstad T
- Garcia de Viedma D
- Gardner SD
- Gardner SD
- Goddard AG
- Goudsmit J
- Grinnell BW
- Grossi MP
- Grossi MP
- Hammarin AL
- Harris KF
- Harris KF
- Henson J
- Heritage J
- Hogan TF
- Hulette CM
- Kahan AV
- Kitamura T
- Koch S
- Major EO
- Mantyjarvi RA
- Markowitz R
- Mathur VS
- Moens U
- Moens U
- Moret H
- Nebuloni M
- Negrini M
- Negrini M
- Nelson JA
- Nickeleit V
- O'Reilly RJ
- Padgett BL
- Pagnani M
- Pappo O
- Portolani M
- Purighalla R
- Rekvig OP
- Rekvig OP
- Rosen S
- Rubinstein R
- Saitoh K
- Schneider EM
- Sekiguchi M
- Shah K
- Shah KV
- Smith RD
- Sugimoto C
- Sundsfjord A
- Sundsfjord A
- Sundsfjord A
- Taguchi F
- Takemoto KK
- Takemoto KK
- Telenti A
- Vago L
- Vago L
- Vallbracht A
- Van Der Noorda J
- Voltz R
- Watanabe S
- White FA III
- Publication venue
- 'University of Chicago Press'
- Publication date
- Field of study
Polyomaviruses and Human Diseases
- Author
- A. Beckmann
- A. Bedi
- A. Constantinescu
- A. Corallini
- A. Kazory
- A. Pahari
- A. Seber
- A. Sundsfjord
- A. Sundsfjord
- A. Sundsfjord
- A. Vallbracht
- A. Vats
- A.K. Kristoffersen
- A.P. Limaye
- A.Y. Leung
- B. Grinnell
- B. Padgett
- B.H. Sweet
- B.L. Padgett
- C. Chapman
- c. Cubitt
- C. Holmberg
- C. Tornatore
- C.A. Andrews
- C.A. Andrews
- C.B. Drachenberg
- C.H. Chen
- C.H. Rinaldo
- C.H. Rinaldo
- C.J. Horvath
- C.K. Liu
- D. Chang
- D. Chang
- D. Coleman
- D. Coleman
- D.H. Barouch
- D.L. Walker
- D.L. Walker
- D.M. Cibrik
- E. Mylonakis
- E. Ramos
- E.A. Mortimer
- E.O. Major
- E.O. Major
- E.O. Major
- E.P. Richardson
- F. Ginevri
- F. Ginevri
- F. Martini
- F. Mayall
- F. Taguchi
- F.A. White III
- G. Bratt
- G. Loeber
- G.B. Fogazzi
- G.S. Ault
- H. David
- H.H. Hirsch
- H.H. Hirsch
- H.H. Hirsch
- H.H. Hirsch
- H.J. Giesen von
- I. Binet
- I. Rayment
- I.A. Agha
- I.J. Koralnik
- J. Goudsmit
- J. MacKenzie
- J. Marshall
- J. Resnick
- J. Trofe
- J.A. Fishman
- J.A. Fishman
- J.D. McGhee
- J.E. Knepper
- J.E. Knepper
- J.F. Apperly
- J.G. Assouline
- J.M. Lee
- J.R. Berger
- J.R. Berger
- J.R. Berger
- J.S. Butel
- J.T. Newman
- K. Andreassen
- K. Dorries
- K. Khalili
- K. Reiss
- K. Shah
- K. Shah
- K. Shah
- K.E. Christie
- K.K. Takemoto
- K.V. Shah
- K.V. Shah
- L. Jin
- L.S. Hair
- M. Bergallo
- M. Carbone
- M. Carbone
- M. Cottier-Fox
- M. Imagawa
- M. Kondo
- M. Schmitz
- M. Thiele
- M. Tognon
- M.A. Gorder
- M.C. Monaco
- M.D. Reploeg
- M.M. Pater
- M.V. Gheule
- N. Ahsan
- N. Aoki
- O. Bjorang
- O. Cubukcu-Dimopulo
- O.P. Rekvig
- O.P. Rekvig
- P. Randhawa
- P. Randhawa
- P. Randhawa
- P. Randhawa
- P.F. Foster
- P.I. Gibson
- P.L. Lin
- P.S. Randhawa
- P.S. Randhawa
- P.S. Randhawa
- P.S. Randhawa
- P.V. Kadambi
- R. Boldorini
- R. Boldorini
- R. Ding
- R. Johnson
- R. Mantyjarvi
- R. Purighalla
- R.A. Vilchez
- R.A. Vilchez
- R.A. Vilchez
- R.B. Markowitz
- R.C. Liddington
- R.D. Kornberg
- R.D. Kornberg
- R.D. Poduval
- R.D. Poduval
- R.J. Frisque
- R.M. Li
- R.M. Li
- R.R. Arthur
- R.R. Arthur
- R.R. Arthur
- R.R. Arthur
- R.T. Tsai
- S. Endo
- S. Kenney
- S. Nevo
- S. Rosen
- S.D. Gardner
- S.D. Gardner
- S.H. Cheesman
- T. Petrogiannis-Haliotis
- T. Weber
- T.A. Gluck
- T.K. Held
- U. Moens
- U. Moens
- U. Moens
- U. Moens
- V. Nickeleit
- V. Nickeleit
- V. Nickleit
- V. Nickleit
- V. Pietropaolo
- V. Scantlebury
- W. Feiden
- W. Lee
- W.A. Knowles
- W.A. Knowles
- W.A. Knowles
- W.A. Knowles
- W.C. Breau
- W.F. Marshall
- W.J. Atwood
- W.J. Atwood
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2006
- Field of study
Polyomaviruses: Progressive Multifocal Leukoencephalopathy and Other Diseases
- Author
- A Caputo
- A Chakera
- A Corallini
- A Dumoulin
- A Egli
- A Kassem
- A Kazory
- A Krumbholz
- A Krumbholz
- A Langer-Gould
- A Matos
- A Pavesi
- A Rencic
- A Stolt
- AA Sima
- AB Hill
- AJ Girardi
- AM Gaynor
- AS Dugan
- AY Leung
- B Eddy
- B Krynska
- BH Sweet
- BK Kleinschmidt-DeMasters
- BL Padgett
- BL Padgett
- BP Gomez
- BW Grinnell
- C Martel-Jantin
- C Ryschkewitsch
- C Skoczylas
- C Sugimoto
- CB Buck
- CB Drachenberg
- CG Eberhart
- CK Liu
- CL Haycox
- CL Hitchcock
- CS Tan
- D Ahuja
- D Capello
- D Das
- D Geetha
- DB Clifford
- DE Rollison
- DE Rollison
- DE Rollison
- DE Rollison
- DE Rollison
- DF Smith
- DJ Bergsagel
- E Gorczynska
- E Meijden van der
- E Meijden van der
- E Soeda
- E Willoughby
- EA Engels
- EA Engels
- EA Engels
- EA Siebrasse
- EJ Duncavage
- EJ Duncavage
- EO Major
- EP Richardson Jr
- ES Lim
- F Lopez-Rios
- F Martini
- F Neske
- F Trusch
- FA White III
- FF Shadan
- FN Engsig
- G Assche Van
- G Barbanti-Brodano
- G Bloomgren
- G D’Souza
- G Giraud
- G Loeber
- G Perez-Liz
- G Yu
- G Zurhein
- GF Elphick
- GL Stoner
- GM Van
- H Feng
- H Ikegaya
- H Rennert
- H Sihto
- HA Zur
- HC Laude
- HD Strickler
- HD Strickler
- HD Strickler
- HH Hirsch
- HH Hirsch
- HH Hirsch
- HH zur
- HY Zheng
- HY Zheng
- I Ayzenberg
- I Penn
- I Steiner
- IJ Koralnik
- IJ Koralnik
- IL Tan
- IW Fong
- J Bayliss
- J Kaae
- J Low
- J MacKenzie
- J Sabatier
- JA Meeuwissen
- JC Becker
- JE Knepper
- JF Buell
- JG Iyer
- JJ Carter
- JM Kean
- JR Abend
- JR Berger
- JR Berger
- JR Berger
- JS Lee
- JT Nicol
- K Bhatia
- K Shah
- K Shah
- K Subsai
- KE Astrom
- KG Paulson
- KG Paulson
- KL Christensen
- KR Carson
- KR Carson
- KV Shah
- KV Shah
- KV Shah
- L Brade
- L Feigenbaum
- L Laghi
- L Silverman
- LA De
- LC Sperling
- LK Jeffers
- LM Lee
- M Carbone
- M Carbone
- M Cottler-Fox
- M Heath
- M Johannessen
- M Loyo
- M Mattei de
- M Muller
- M Perez-Losada
- M Poulsen
- M Safak
- M Shuda
- M Shuda
- M Shuda
- M Smith
- M Suzuki
- MA d’Arminio
- MC Monaco
- MC Monaco
- MJ Imperiale
- MK Grabowski
- MK White
- ML Whiteman
- MT Pho
- N Babel
- N Khanna
- N Sacktor
- N Scuda
- N Shivapurkar
- NB Meland
- NC Hodgson
- NF Blair
- NG Hoffman
- NL Nguyen
- NM Broekema
- P Castaigne
- P Lesprit
- P Miralles
- P Randhawa
- P Sehr
- PE Gibson
- PN Jensen
- PS Randhawa
- PT Tai
- Q Chen
- Q Zeng
- R Boldorini
- R Boldorini
- R Boldorini
- R Caldarelli-Stefano
- R Houben
- R Houben
- R Johne
- R Phan-Ba
- R Purighalla
- R Voltz
- RA Pasquier Du
- RA Pasquier Du
- RA Pasquier Du
- RA Vilchez
- RC Holman
- RC Holman
- RC Liddington
- RL Wattier
- RM Schowalter
- RP Viscidi
- RP Viscidi
- RP Viscidi
- RP Viscidi
- RR Arthur
- RR Arthur
- S Bialasiewicz
- S Bialasiewicz
- S Bialasiewicz
- S Binggeli
- S Bofill-Mas
- S Bofill-Mas
- S Bofill-Mas
- S Bossolasco
- S Eash
- S Goh
- S Guindon
- S Korup
- S Miller
- S Rao
- S Sanjose de
- S Verma
- SD Gardner
- SE Prosser
- SM Dilworth
- SM Gillespie
- SN Leech
- SR Lopes da
- T Allander
- T Chen
- T Flaegstad
- T Kitamura
- T Plavina
- T Schachtner
- T Suzuki
- T Tadmor
- T Takasaka
- T Tilling
- T Tominaga
- T Weber
- TA Gluck
- TF Warner
- U Moens
- U Moens
- U Moens
- U Wieland
- V Bouvard
- V Foulongne
- V Foulongne
- V Foulongne
- V Koljonen
- V Koljonen
- V Ravichandran
- V Sauvage
- VL Del
- WA Knowles
- X Sastre-Garau
- Y Chen
- Y Murakami
- Y Nishimoto
- Y Okada
- Y Yogo
- Y Yogo
- Y Yogo
- Y Yogo
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Liraglutide and Renal Outcomes in Type 2 Diabetes.
- Author
- Aamir S
- Ababa M
- Abbas S
- Abbink-Zandbergen E
- Abbott EC
- Abell S
- Aboo N
- Abraham P
- Abreu M
- Abu-Bakare A
- Acevedo Castañeda ES
- Acikgoz A
- Ackefelt-Frick E
- Adams D
- Adams P
- Adamson K
- Aden J
- Advani A
- Agrawal M
- Aguilar D
- Aguillon A
- Ahdi M
- Ahmed A
- Ahmed A
- Ahmed B
- Ahmed I
- Ahn HY
- Akalın S
- Akalin S
- Akhtar A
- Akin S
- Akinci B
- Akkurt A
- Akright B
- Akright L
- Akturk M
- Al-Maweri A
- Alanis RR
- Alawadi F
- Albarracin C
- Albert S
- Albertse HW
- Alcolea JO
- Aleksic S
- Alencar E
- Alencar R
- Alexander E
- Alfaraj A
- Alfredsson H
- Ali M
- Ali S
- Aliaga Verdugo A
- Aliuddin B
- Alkis N
- Allen S
- Allison R
- Almasmary A
- Almeida AC
- Altun I
- Altunbas HA
- Altuntas Y
- Alur VC
- Alvarado Ruíz R
- Alves B
- Alves E
- Alves G
- Alves J
- Alzohaili O
- Amador W
- Ambrish C
- Amine M
- Amini S
- Anderlová K
- Andersen PH
- Anderson L
- Anderson M
- Anderson R
- Andrews M
- Angel J
- Anteer W
- Antenore A
- Anthony V
- Antillon A
- Antkowiak-Piatyszek K
- Anzures P
- Appelt S
- Araujo L
- Araz M
- Arciszewska M
- Arcon-Rios S
- Arechavaleta R
- Aribas S
- Arkin D
- Arnone M
- Arodak B
- Aronne L
- Aronoff S
- Arreola G
- Arroyo S
- Arruda V
- Arslan E
- Arslan G
- Arslan M
- Arturi F
- Asirvatham A
- Asirvatham E
- Asnani S
- Astudillo-Tee G
- Ataoglu EH
- Atkin S
- Augusto GA
- Ault S
- Austin B
- Avila V
- Avitabile N
- Avram R
- Awasty V
- Ayan F
- Aydin K
- Aydogan BI
- Aye M
- Ayvaz G
- Azam M
- Azar M
- Aziz A
- Aziz AA
- Babkowski MC
- Badat A
- Baerwald H
- Baggentoss R
- Bahadir MA
- Bahrami P
- Baig M
- Bailey K
- Bailey T
- Bain S
- Bain S
- Bajkowska-Fiedziukiewicz A
- Baker M
- Bala NS
- Balaji M
- Balaji V
- Balbes-Reyes I
- Balci MK
- Baldwin D
- Baldwin E
- Balentine T
- Balestrassi L
- Ballard T
- Baloch K
- Banarer S
- Bandgar TR
- Baney C
- Banka A
- Bao Y
- Barbaro V
- Barber L
- Barber M
- Barbosa M
- Barcelos I
- Bardoloi N
- Barker T
- Barnes K
- Barnett AH
- Barnum O
- Barone M
- Barra J
- Bartkowiak A
- Baruah M
- Basaran MN
- Bashier A
- Baskal N
- Basson M
- Batens AH
- Baula G
- Bautista A
- Bawa E
- Bayliss R
- Beaman M
- Beatty K
- Becker J
- Bedolla L
- Begum G
- Beilin V
- Bejnariu C
- Bekur R
- Belejchak P
- Belem L
- Beling E
- Bell A
- Bellary S
- Beltran M
- Belucher C
- Benedek P
- Benhalima K
- Benis A
- Benroubi M
- Bensfield E
- Benton J
- Berard L
- Bergamo K
- Bergenstal M
- Bergman B
- Berry M
- Bester F
- Betti RT
- Bettino K
- Beyea M
- Bhansali A
- Bhargava A
- Bhatia S
- Bhattacharya A
- Bhonsley S
- Bhuyan S
- Bilas A
- Birkeland K
- Bischoff L
- Bishara P
- Bixler L
- Bizjack S
- Blank R
- Blankfield R
- Blignaut S
- Block L
- Bloodworth J
- Bloomberg K
- Bloomberg R
- Blustin J
- Boban I
- Boesgaard T
- Bogdanski P
- Bolden A
- Bona R
- Boncu O
- Bookless P
- Booysen S
- Borah B
- Bosch FJ
- Bosco A
- Bowering CK
- Braicu MD
- Branda J
- Brassie C
- Braun D
- Brautigam D
- Bressler P
- Brewster R
- Bright N
- Brix J
- Bronstein M
- Brown C
- Brown C
- Brown D
- Brown F
- Brown-Frandsen K
- Brožová J
- Bruskewitz M
- Bryant D
- Buchanan C
- Buchanan N
- Buck G
- Buckley S
- Bueno J
- Bueno T
- Bugra MZ
- Bugter A
- Bulatovic A
- Bulcão T
- Burgess L
- Buric B
- Burke D
- Burton K
- Buscemi C
- Buscemi S
- Busch AK
- Buse JB
- Buske S
- Buzzetti R
- Buño MM
- Byars W
- Bye R
- Cahn A
- Cai X
- Caiado F
- Calan M
- Caldwell R
- Calle Pascual A
- Calvin K
- Camacho R
- Camazzola F
- Cambréa MF
- Campbell E
- Campos Hurtado S
- Campos Moreno OV
- Campos S
- Campos S
- Canani L
- Cannon D
- Cantrell J
- Caplan J
- Cardenas C
- Cardona Muñóz EG
- Carlan L
- Carlone A
- Carlton J
- Carpio G
- Carra MK
- Carreira Arias JN
- Carrol A
- Cartwright L
- Caruso S
- Caruso V
- Carvalho N
- Casadidio I
- Casanova G
- Casillo A
- Cassimjee S
- Castaneda L
- Castle M
- Castro D
- Castro L
- Catangay J
- Catrinoiu D
- Cavalcanti T
- Cavazos Oliveros FJ
- Cavdar U
- Cavichioli V
- Cederberg H
- Celik S
- Cepero García D
- Cercato C
- Cerrelli F
- Cetin F
- Chacra A
- Chaidarun S
- Chakrabarti AK
- Challela W
- Chambers J
- Chambliss T
- Chandra L
- Chang A
- Chang S
- Chapa Grimaldo JB
- Chappel C
- Chappel J
- Chappell T
- Charchar HS
- Charles C
- Chaudhury T
- Chaves C
- Chavira A
- Chaykin L
- Check E
- Chee L
- Cheifetz A
- Chellan G
- Chen J
- Chen J
- Chen JY
- Chen K
- Chen M
- Chen X
- Chen Y
- Chen YC
- Cheng A
- Cherry A
- Chestnut A
- Chiang CY
- Chiarot J
- Chin SO
- Chiniwala N
- Chionh K
- Choe J
- Choi SH
- Chon S
- Chou CW
- Choudhury S
- Chouinard S
- Chrisman C
- Chrisman C
- Christensen S
- Christiansen M
- Chrzanowski S
- Chuang E
- Chuck L
- Ciavarella A
- Cinar N
- Ciomos D
- Ciorba A
- Cipolloni L
- Clayton D
- Clever HU
- Clyatt J
- Coetzee K
- Cohan B
- Cohen O
- Cohen R
- Colbay M
- Colella A
- Colotto M
- Comi R
- Comlekci A
- Comulada-Rivera A
- Conner K
- Connor G
- Consoli A
- Contreras R
- Contreras Sandoval AY
- Conway J
- Cook K
- Cook R
- Cook R
- Cooper J
- Corder C
- Cornejo B Sr
- Cornette L
- Correia-Deur J
- Cortes G
- Cortez L
- Cosma NV
- Costa da Penha P
- Costa M
- Costi B
- Coutinho P
- Coutinho W
- Coves Figueras MJ
- Cox C
- Cox G
- Craig W
- Cramer B
- Creton C
- Crippa VG
- Crisby M
- Cromer C
- Cromer M
- Cuccuru I
- Cuddihy R
- Cufone S
- Cukierman-Yaffe T
- Culmer D
- Cunha MR
- Curran H
- Curran M
- Cvijovic G
- Cypryk K
- Czubek U
- Czupryniak L
- D'albuquerque Silva L
- D'Alessio D
- D'Amours M
- D'Emden M
- D'Ignazio G
- da Costa A Jr
- Da Ros S
- da Silva Santos M
- Dabrowska M
- Dabrowski J
- Dadis C
- Dagdelen S
- Dagogo-Jack S
- Daher J Jr
- Dairywala I
- Damberg G
- Damci T
- Dang A
- Daniel K
- Daniels G
- Daoud D
- Darawsha M
- Das Gupta R
- Das M
- Dashe JF
- Davenport C
- Davidson M
- Davini E
- Davis T
- Davis T
- Davutoglu V
- de Bem A
- De Block C
- de Jesús Beltran Jaramillo T
- de Jesús Rodríguez Berrones DA
- de la Cuesta Mayor C
- de Tugwell B
- Dean J
- DeBold R
- Degtyareva E
- Deitz P
- Del M
- del Rosario Arechavaleta-Granell M
- Delaney D
- Delgado E
- DeMicco M
- Demir M
- Demir T
- Democh D Jr
- DeMuro MA
- DeSalle D
- Desideri C
- Desouza C
- Deuse U
- Devireddy K
- DeVries B
- Deyneli O
- DeYoung P
- Dezube M
- Dharmalingam M
- Dhatariya K
- Di Biagio R
- Di Carlo A
- Di Fulvio P
- Diab I
- Diakoumopoulou E
- Dias C
- Dicker D
- Diesburg-Stanwood A
- Dilliard J
- Dilling J
- Dillinger J
- Dincer I
- Diner J
- Ding SA
- Dishongh K
- Dodis R
- Dogan B
- Doing C
- Doll W
- Donoho A
- Donovan D
- Doremus N
- Dorfman S
- Dorkhan M
- Doshi P
- Dostou J
- Douglas D
- Douglas D
- Douglass S
- Dowell M
- Drazich E
- Drescik T
- Driver E
- Du Bois J
- Du H
- Dube F
- DuBose R III
- Dubova V
- Duclos M
- Dunn K
- Dunnam T
- Durham N
- Durán García S
- Dutta P
- Dvoryashina I
- Dye L
- Dziedzic S
- Dziewit T
- Eagerton D
- Eaton M
- Ebenibo S
- Edeoga C
- Eder M
- Edwards G
- Eeg-Olofsson K
- Eisma G
- Ekoe JM
- Ekwensi J
- El Asmar I
- El Sayad N
- Eliaschewitz F
- Eliasson B
- Eliasson K
- Eliopoulos C
- Elkosseifi M
- Elmer R
- Elmore M
- Elson D
- ElZein L
- Emmert L
- Engelbrecht J
- Engin I
- English P
- Eraydin A
- Erbas T
- Erbe L
- Erdogan MF
- Erdtsieck R
- Eriksson M
- Ernest P
- Ersoy C
- Erugu A
- Eschenbrücher K
- Esmanhoto Facin G
- Esser M
- Estes S
- Estrada A
- Estrada L
- Eveleigh T
- Everhart B
- Ewing J
- Faas F
- Fagan S
- Faircloth C
- Faligowska M
- Fallarino M
- Fardelin P
- Farias F
- Farmer M
- Febo F
- Feder A
- Fedor-Plenkowska G
- Fehr K
- Felício J
- Ferguson T
- Feria-Carot MD
- Fernandes J
- Fernandes V
- Ferree K
- Ferreiro Gómez M
- Ferrington B
- Figueiredo de Medeiros F
- Filetti S
- Filho CS
- Filho FF
- Filho M
- Filho RM
- Finegan K
- Fitzgibbons S
- Fitzhugh M
- Fitzsimmons R
- Flanders D
- Flores E
- Flores J
- Flores M
- Flores-Moreno CA
- Florida C
- Flynn J
- Flyvbjerg A
- Foffi C
- Folmar P
- Fonseca V
- Fontan D
- Fontenele AP
- Forbes R
- Ford I
- Ford W
- Forde H
- Formoso G
- Forti A
- Fouckova A
- Fowler M
- Frade Fernández AM
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- Ángeles Tapia Herrero M
- Ítalo Mota J
- Ørsted DD
- Žourek M
- Publication venue
- Publication date
- 01/01/2017
- Field of study
BACKGROUND:
In a randomized, controlled trial that compared liraglutide, a glucagon-like peptide 1 analogue, with placebo in patients with type 2 diabetes and high cardiovascular risk who were receiving usual care, we found that liraglutide resulted in lower risks of the primary end point (nonfatal myocardial infarction, nonfatal stroke, or death from cardiovascular causes) and death. However, the long-term effects of liraglutide on renal outcomes in patients with type 2 diabetes are unknown.
METHODS:
We report the prespecified secondary renal outcomes of that randomized, controlled trial in which patients were assigned to receive liraglutide or placebo. The secondary renal outcome was a composite of new-onset persistent macroalbuminuria, persistent doubling of the serum creatinine level, end-stage renal disease, or death due to renal disease. The risk of renal outcomes was determined with the use of time-to-event analyses with an intention-to-treat approach. Changes in the estimated glomerular filtration rate and albuminuria were also analyzed.
RESULTS:
A total of 9340 patients underwent randomization, and the median follow-up of the patients was 3.84 years. The renal outcome occurred in fewer participants in the liraglutide group than in the placebo group (268 of 4668 patients vs. 337 of 4672; hazard ratio, 0.78; 95% confidence interval [CI], 0.67 to 0.92; P=0.003). This result was driven primarily by the new onset of persistent macroalbuminuria, which occurred in fewer participants in the liraglutide group than in the placebo group (161 vs. 215 patients; hazard ratio, 0.74; 95% CI, 0.60 to 0.91; P=0.004). The rates of renal adverse events were similar in the liraglutide group and the placebo group (15.1 events and 16.5 events per 1000 patient-years), including the rate of acute kidney injury (7.1 and 6.2 events per 1000 patient-years, respectively).
CONCLUSIONS:
This prespecified secondary analysis shows that, when added to usual care, liraglutide resulted in lower rates of the development and progression of diabetic kidney disease than placebo. (Funded by Novo Nordisk and the National Institutes of Health; LEADER ClinicalTrials.gov number, NCT01179048 .)
Antiinflammatory therapy with canakinumab for atherosclerotic disease
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- Publication venue
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- Publication date
- 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-1β, 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-1β 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. Copyright © 2017 Massachusetts Medical Society