11 research outputs found
A922 Sequential measurement of 1 hour creatinine clearance (1-CRCL) in critically ill patients at risk of acute kidney injury (AKI)
- Author
- Abbott TE
- Abdallah RI
- Abdel-Aal IR
- Abdelmonem SA
- Abdo WF
- Abellan AN
- Abellán AN
- Abellán AN
- Abellán AN
- Abrams ST
- Ackerley C
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- Adhikari NK
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- Akalaev R
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- Akcan-Arikan A
- Akhlagh SH
- Akhtar N
- AKI Research Group
- Akiduki N
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- Ko JI
- Ko SB
- Kobayashi A
- Koco E
- Kodate A
- Kodate A
- Kodate A
- Kokkini S
- Kolnikova I
- Komuro T
- Kondili E
- Kongpolprom N
- Kooner G
- Kostalas M
- Kosuk ME
- Kotsopoulos A
- Kou PS
- Kouatchet A
- Kovacikova L
- Kox M
- Kraegpoeth A
- Krenn CG
- Krishna B
- Kristof J
- Kruger A
- Kruger A
- Krüger A
- Ku NS
- Ku NS
- Kubik M
- Kubota K
- Kuebler WM
- Kulaga EV
- Kulkarni AP
- Kumari BK
- Kumbamu A
- Kunze-Szikszay N
- Kurmukov IA
- Kurth T
- Kurtz P
- Kurtz P
- Kwon HM
- Kwon HM
- Kwon WY
- Kwon WY
- Kwon WY
- Kye YC
- Kyle UG
- Kyle UG
- Labaune MA
- Labra C
- Lacerda P
- Laerkner E
- Lafaurie M
- Lafuente E
- Lagonidis D
- Lagos R
- Lahmer T
- Lai CC
- Lai CH
- Lake K
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- Lapteva K
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- Latini R
- Latini R
- Latini R
- Latorre J
- Lattuada M
- Lattuada M
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- Laurent A
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- Le Brocque R
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- Lebiedz P
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- Lee EY
- Lee JH
- Lee S
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- Lee SJ
- Lee WY
- Lee YJ
- Lee YJ
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- Legrand M
- Legrand M
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- Leitao AL
- Leite RT
- Leonard H
- Leone M
- Leone M
- Lerma FA
- Lesmes SP
- Lesmes SP
- Lesmes SP
- Lesmes SP
- Lesmes SP
- Lesmes SP
- Letizia T
- Levrat Q
- Levy B
- León JL
- León JP
- León JP
- León JP
- Lheureux O
- Lheureux O
- Lheureux O
- Lheureux O
- Li R
- Li SH
- Liao X
- Lichtenstein D
- Lim TH
- Limuti R
- Lin KC
- Lin KC
- Lin KC
- Lin KC
- Lin KL
- Lin PH
- Lin SC
- Lin SC
- Lin SC
- Lin SC
- Lin WC
- Lin WC
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- Lischinsky A
- Lissonde F
- Lissonde F
- Litchfield K
- Liu CP
- Liu CP
- Liu CP
- Liu CP
- Liu D
- Llaurado-Serra M
- Llorente B
- Llorente MÁ
- Lobato MS
- Lobo-Civico A
- Loizou C
- Lombardo MD
- Londoño JG
- Longani N
- Longhi L
- Lopes JA
- Lopez GD
- Lopez R
- Lopez-Caler C
- Lopez-Gude MJ
- Lorini L
- Lortat-Jacob B
- Lortat-Jacob B
- Lotay R
- Loudet CI
- Louf-Durier A
- Louf-Durier A
- Louis B
- Lourido CM
- Lozano JA
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- Lucendo AP
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- Lucinio NM
- Luini M
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- Lukaszewicz AC
- Luna RR
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- Lusk J
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- Lázaro AS
- López AR
- López L
- López MA
- Macfarlane B
- MacKay A
- MacKay A
- Mackey G
- Mackey G
- MacPhee I
- Macrì M
- Madueño VP
- Maekawa K
- Maekawa K
- Maekawa K
- Maekawa K
- Maertens B
- Maggiorini M
- Maghsoudi B
- Magnanimi E
- Magnoni S
- Magret M
- Mainardi JL
- Maistry N
- Maitra S
- Makiko S
- Malagurski B
- Malek F
- Malo LR
- Maly M
- Malyshev A
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- Mancebo J
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- Mancino A
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- Marcos-Zambrano LJ
- Mariani M
- Mariman A
- Marin-Mateos H
- Marine-Vidal J
- Mariotte E
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- Marmanidou K
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- Martinez-Reyes L
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- Martínez F
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- Martínez-Carmona JF
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- Melo N
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- Mendonca AV
- Mendsaikhan N
- Menendez R
- Mengelle C
- Mercat A
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- Mergulhão PJ
- Merino-Vega D
- Messenger D
- Mezidi M
- Mezidi M
- Michel L
- Midwinter MJ
- Mignot T
- Miguelena PR
- Mihara Y
- Millar M
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- Mimoz O
- Min A
- Min HJ
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- Miranda F
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- Mistry M
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- Mitchell M
- Mitchell S
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- Mizugaki A
- Mizugaki A
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- Olaechea P
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- Philips BJ
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- Radu V
- Rai S
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- Rodríguez FG
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- Romero I
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- Spahn DR
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- Spijkstra JJ
- Spronk PE
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- Sprung CL
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- Stamm J
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- Stanić R
- Starczewska M
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- Stiphout C
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- Stocchetti N
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- Stretti F
- Struijs A
- Stubbs C
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- Stümpfle R
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- Su PL
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- Suchomel P
- Suh GJ
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- Suh JW
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- Sun WZ
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- Suzuki T
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- Sánchez B
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- Sánchez EC
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- Tabatabaei HR
- Tabei SH
- Taccone F
- Taccone FS
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- Taccone FS
- Taccone FS
- Taccone FS
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- Taggu A
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- Takaki S
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- Takeda M
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- Takei T
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- Tamura T
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- Tanaka S
- Tanaka S
- Tane N
- Tang KB
- Tang LK
- Tapia A
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- Tapponnier R
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- Temprano-Gómez I
- Tena SA
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- Terzi N
- Terzi N
- Terzi N
- Terzi N
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- Thabut G
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- Thompson E
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- Tirkkonen J
- Tirumala S
- Tjepkema-Cloostermans MC
- Tobar M
- Tofiño AL
- Toh CH
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- Tomas E
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- Tonetti T
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- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2016
- Field of study
Meeting abstrac
Implementation of integration strategies between primary care units and a regional general hospital in Brazil to update and connect health care professionals: a quasi-experimental study protocol
- Author
- AL Kitson
- Alexandre Hannud Abdo
- Aline Pacífico Rodrigues
- AM Mosadeghrad
- Ana Carolina Cintra Nunes Mafra
- Ana Violeta Ferreira de Almeida Delgado
- C Moore
- C Walraven van
- E Mendes
- EH Morrato
- F Lefevre
- Fernando Antonio Basile Colugnati
- G Sharma
- Glauber Alves dos Prazeres
- Ises Abrahamsohn
- J Damschroder
- J Frenk
- J Montero-Marín
- J Paim
- José Carlos Teixeira
- KL Gwet
- M Kelly
- M Steinman
- Marcello Dala Bernardina Dalla
- Marcelo Marcos Piva Demarzo
- Mario Maia Bracco
- MD Cabana
- ME Alfradique
- Ministry of Health of Brazil
- Ministry of Health of Brazil
- MPA Fleck
- P Peduzzi
- R Clay-Williams
- RM Cervero
- S Keng
- S Kripalani
- SA Schweikhart
- SE Nissen
- Silvio Possa
- T Bendell
- T Greenhalgh
- T Ohno
- TF Babor
- W Miltenburg
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
FGFR1 and NTRK3 actionable alterations in “Wild-Type” gastrointestinal stromal tumors
- Author
- Adam M. Burgoyne
- AF Ghetu
- B Liegl-Atzwanger
- B Shiotani
- BG Wilson
- BP Rubin
- C Beadling
- C Grasso
- C-X Liu
- Chih-Min Tang
- Christopher L. Corless
- CL Corless
- D Singh
- D Singh
- David Hong
- Deborah Morosini
- DM Ornitz
- Eileen Shi
- F Colotta
- G Vasileiou
- GL Ma
- GM Frampton
- Gregory M. Heestand
- Guhyun Kang
- H Prazeres
- J Herz
- J Mao
- James D. Murphy
- Jason K. Sicklick
- Jeffrey S. Ross
- JK Sicklick
- JL Merchant
- Jonathan C. Trent
- Juliann Chmielecki
- Kai Wang
- Katherine E. Fero
- KD Huynh
- LC Cerchietti
- Lisa Madlensky
- M Brenca
- M Lek
- M Nannini
- M Taipale
- MA Pantaleo
- MA Pantaleo
- Martina De Siena
- Michael C. Heinrich
- NA Cohen
- NP Agaram
- Olivier Harismendy
- PA Cowin
- Paul T. Fanta
- PT Fanta
- Razelle Kurzrock
- S Ni
- S Rossi
- S Veeriah
- SA Boikos
- Siraj M. Ali
- SR Krig
- SR Walker
- Sujana Movva
- X Liu
- X Liu
- X Zhang
- Y Gong
- Y-M Wu
- ZC Zhang
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/12/2016
- Field of study
BACKGROUND: About 10–15% of adult, and most pediatric, gastrointestinal stromal tumors (GIST) lack mutations in KIT, PDGFRA, SDHx, or RAS pathway components (KRAS, BRAF, NF1). The identification of additional mutated genes in this rare subset of tumors can have important clinical benefit to identify altered biological pathways and select targeted therapies. METHODS: We performed comprehensive genomic profiling (CGP) for coding regions in more than 300 cancer-related genes of 186 GISTs to assess for their somatic alterations. RESULTS: We identified 24 GIST lacking alterations in the canonical KIT/PDGFRA/RAS pathways, including 12 without SDHx alterations. These 24 patients were mostly adults (96%). The tumors had a 46% rate of nodal metastases. These 24 GIST were more commonly mutated at 7 genes: ARID1B, ATR, FGFR1, LTK, SUFU, PARK2 and ZNF217. Two tumors harbored FGFR1 gene fusions (FGFR1–HOOK3, FGFR1–TACC1) and one harbored an ETV6–NTRK3 fusion that responded to TRK inhibition. In an independent sample set, we identified 5 GIST cases lacking alterations in the KIT/PDGFRA/SDHx/RAS pathways, including two additional cases with FGFR1–TACC1 and ETV6–NTRK3 fusions. CONCLUSIONS: Using patient demographics, tumor characteristics, and CGP, we show that GIST lacking alterations in canonical genes occur in younger patients, frequently metastasize to lymph nodes, and most contain deleterious genomic alterations, including gene fusions involving FGFR1 and NTRK3. If confirmed in larger series, routine testing for these translocations may be indicated for this subset of GIST. Moreover, these findings can be used to guide personalized treatments for patients with GIST. Trial registration NCT 02576431. Registered October 12, 2015 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-016-1075-6) contains supplementary material, which is available to authorized users
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- Aldwairji MA
- Ali MM
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- Amarapurkar DN
- Andersen LB
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- Van Schoor NM
- van Valkengoed IGM
- van Zutphen EM
- Vander Hoorn S
- Vanderschueren D
- Vanuzzo D
- Vasan SK
- Vega T
- Velasquez-Melendez G
- Verstraeten R
- Viet L
- Villalpando S
- Vioque J
- Virtanen JK
- Viswanathan B
- Voutilainen A
- Vrkic TZ
- Wade AN
- Wang C
- Wang N
- Wang Q
- Wang Y-W
- Wang YX
- Wannamethee SG
- Webster-Kerr K
- Wedderkopp N
- Wei W
- Westbury LD
- Whincup PH
- Widhalm K
- Widyahening IS
- Wiecek A
- Wilks RJ
- Willeit J
- Willeit P
- Wilsgaard T
- Wojtyniak B
- Wong A
- Wong EB
- Wong NI
- Woodward M
- Wu FC
- Xu H
- Xu L
- Yaacob NA
- Yan L
- Yan W
- Yoosefi M
- Yoshihara A
- Younger-Coleman NO
- Yu Y
- Yu Y-L
- Yusoff AF
- Yusoff MFM
- Zainuddin AA
- Zamani F
- Zambon S
- Zampelas A
- Zaw KK
- Zdrojewski T
- Zeng Y
- Zhang Z-Y
- Zholdin B
- Zhou B
- Zimmet P
- Zitt E
- Zoghlami N
- Publication venue
- Nature Research
- Publication date
- 09/11/2023
- Field of study
Fasting plasma glucose (FPG) and hemoglobin A1c (HbA1c) are both used to diagnose diabetes, but these measurements can identify different people as having diabetes. We used data from 117 population-based studies and quantified, in different world regions, the prevalence of diagnosed diabetes, and whether those who were previously undiagnosed and detected as having diabetes in survey screening, had elevated FPG, HbA1c or both. We developed prediction equations for estimating the probability that a person without previously diagnosed diabetes, and at a specific level of FPG, had elevated HbA1c, and vice versa. The age-standardized proportion of diabetes that was previously undiagnosed and detected in survey screening ranged from 30% in the high-income western region to 66% in south Asia. Among those with screen-detected diabetes with either test, the age-standardized proportion who had elevated levels of both FPG and HbA1c was 29–39% across regions; the remainder had discordant elevation of FPG or HbA1c. In most low- and middle-income regions, isolated elevated HbA1c was more common than isolated elevated FPG. In these regions, the use of FPG alone may delay diabetes diagnosis and underestimate diabetes prevalence. Our prediction equations help allocate finite resources for measuring HbA1c to reduce the global shortfall in diabetes diagnosis and surveillance
Variation in sensitivity of large benthic Foraminifera to the combined effects of ocean warming and local impacts
- Author
- A Charmantier
- A McIntyre-Wressnig
- C Dettmering
- C Mora
- C Schmidt
- C Schmidt
- CA Belda-Baillie
- CDG Harley
- DE Williams
- DI Warton
- E Cockey
- E Sanford
- EJ Howells
- F Valladares
- HK Talge
- J Brodie
- J Hohenegger
- J Wiedenmann
- JJ Lee
- JL Dawson
- JM Pandolfi
- JM Pandolfi
- JM Pandolfi
- JM Sunday
- JN Harney
- K Fujita
- KE Fabricius
- KE Fabricius
- L Tonk
- LM Chevin
- M Ateweberhan
- M Prazeres
- M Prazeres
- M Prazeres
- MP Lesser
- MR Langer
- MS Roth
- NC Ban
- P Hallock
- P Hallock
- P Hallock
- P Hallock
- P Hallock
- P Hallock
- P Hallock
- PL Munday
- R Todd
- S Muko
- S Uthicke
- S Uthicke
- S Uthicke
- SA Wooldridge
- SE McMurray
- SJ Sawyer
- T Hosono
- YR Narayan
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Feasibility of Chlorella vulgaris to waste products removal from cheese whey
- Author
- A Audebert
- A Karimov
- A Richmond
- AP Abreu
- AR Prazeres
- B Lekshmi
- BG Ryu
- C Ma
- C Yang
- E Daneshvar
- E Sforza
- F Carvalho
- FC Bertoldi
- G Mujtaba
- H Yan
- H Zheng
- J Rivas
- J Seyfabadi
- L Delgadillo-Mirquez
- L Wang
- L Wang
- LS de Leite
- M Martínez
- MA Chia
- MM Montazer-Rahmati
- O Perezgarcia
- OH Lowry
- P Bohutskyi
- PS Hooda
- S Rangabhashiyam
- S Zhu
- SA Razzak
- SW Jeffrey
- T Cai
- WS da Borges
- YK Lee
- Z Li
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Development of RT-qPCR and semi-nested RT-PCR assays for molecular diagnosis of hantavirus pulmonary syndrome
- Author
- A MacNeil
- A Plyusnin
- A Plyusnin
- A Plyusnin
- A Saksida
- A Suzuki
- A Vaheri
- A. PLYUSNIN
- Adriana Freitas Moraes
- Alessandra da Conceição Miranda Santos
- Alice Louize Nunes Queiroz
- AM Johnson
- AM Johnson
- AM Machado
- AMQ King
- Ana Alice de Aquino
- AR Trombley
- AS Whale
- AS Whale
- B Hjelle
- BJ Hindson
- Bruno Tardelli Diniz Nunes
- C Firth
- C McCaughey
- C Sibold
- Carla Conceição Cardoso
- D Garin
- D Morisset
- D Safronetz
- Daniela Sueli Guerreiro Rodrigues
- Daniele Barbosa de Almeida Medeiros
- Darci Smith
- Darlene de Brito Simith
- DBA Medeiros
- E. NEGURA
- Elizabeth Salbé Travassos da Rosa
- ES Travassos da Rosa
- ES Travassos da Rosa
- ES Travassos da Rosa
- F Wei
- G Sabino-Santos
- H Galeno
- HM Hafez
- I Takayama
- IM Mackay
- Ivy Tsuya Essashika Prazeres
- J Araujo
- J de Araujo
- J Hoorfar
- J Kawada
- J Näslund
- JC Butler
- JF EISENBERG
- JS Kumar
- L Drago
- L Ninove
- Livia Carício Martins
- M Aitichou
- M Bharadwaj
- M Evander
- M Kramski
- M Kubista
- M Oldal
- M Terajima
- M Weidmann
- M. AYRES
- Maria Helena Rodrigues de Mendonça
- ML Milazzo
- ML Moreli
- MW Pfaffl
- N Lagerqvist
- N Mohamed
- N Rački
- ND Tischler
- Organización Panamericana de la Salud
- P Bastien
- P Corbisier
- P Johansson
- Pedro Fernando da Costa Vasconcelos
- PJ Padula
- R Xiao
- RC de Oliveira
- Regis Bruni Andriolo
- RM Elliott
- RT Hayden
- S Arai
- S Bhat
- S Garcia
- S Levis
- S Martin-Latil
- S Menting
- SA Bustin
- SM Raboni
- SM Raboni
- SR Zaki
- ST Nichol
- SY Xiao
- T Briese
- T Briese
- T Koma
- TF Tsai
- W Jiang
- W Wang
- W-P Guo
- WS Mendes
- X Zhao
- Z Pang
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- Field of study
Skeletal muscle fibrosis: an overview
- Author
- A Bodanovsky
- A Iwabu
- A Turrina
- A Uezumi
- A Uezumi
- A Uezumi
- A Urciuolo
- A Yu
- AL Serrano
- AL Serrano
- AL Serrano
- AM Czerwinska
- AP Valencia
- AR Gillies
- AS Brack
- BC Yaden
- BK Pedersen
- C Lieu
- C Vial
- CJ Mann
- DH You
- DR Lemos
- E Brandan
- E-M Riso
- F Liu
- F Trensz
- FM Faturi
- G Juban
- G Sun
- H Amthor
- H Gilson
- H Karvinen
- H Kawai
- H Kim
- H Lei
- H Yin
- HS Alameddine
- IA Darby
- IR Murray
- J Kim
- J Maltzahn von
- J Menetrey
- J Rosenbloom
- J Zhu
- J Zhu
- JG Tidball
- JG Tidball
- JG Tidball
- JH Hwang
- JW Chen
- JW McGreevy
- K Delaney
- K Fukushima
- K Garg
- K Garg
- K Speck
- KD Huebner
- KJ Morine
- KL Walton
- KM Gutpell
- KM Gutpell
- KM Stearns-Reider
- KP Campbell
- L Arnold
- L Forcina
- L Madaro
- L Wollin
- LA Perandini
- LE Gosselin
- LI Filippin
- LR Rodino-Klapac
- LR Smith
- M Cheng
- M Elbaz
- M Fanbin
- M Hirunsai
- M Karalaki
- M Kjaer
- M Nozaki
- M Pines
- M Rodrigues
- M Saclier
- M Thorley
- M Zimowska
- MA Chapman
- MA Mahdy
- MA Mahdy
- MA Mahdy
- MD Grounds
- ME Ogle
- MG Morales
- MG Morales
- MG Morales
- MH Parker
- MH Ross
- MM Murphy
- Mohamed A. A. Mahdy
- MR Rajasekaran
- N Arrighi
- N Osses
- N Yucel
- NI Chaudhary
- O Soehnlein
- OK Hwang
- P Cisternas
- P Cisternas
- P Munoz-Canoves
- P Pessina
- P Piñol-Jurado
- PB Kang
- PHDM Prazeres
- PP Purslow
- PP Purslow
- R Sambasivan
- R Takagi
- RJ McCormick
- RL Lieber
- RT Kendall
- S Biressi
- S Chen
- S Ciciliot
- S Fukada
- S McCroskery
- S Zanotti
- SA Živković
- SB Charge
- SG Velleman
- T Kobayashi
- T Laumonier
- T Turgeman
- TA Jarvinen
- TA Jarvinen
- TN Burks
- TT Braga
- U Akpulat
- V Ameen
- V Kovanen
- W Foster
- W Rezende Pinto de
- WD Coley
- X Chen
- X Wang
- X Wang
- Y Guo
- Y Li
- Y Li
- Y Mimura
- Y Zhou
- YS Chan
- Z Wang
- ZB Li
- ZB Li
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/03/2019
- Field of study
Extracellular matrix (ECM) is an essential component of skeletal muscle. It provides a framework structure that holds myofibers and blood capillaries and nerves supplying the muscle. In addition, it has a principal role in force transmission, maintenance and repair of muscle fibers. Excessive accumulation of ECM components, especially collagens, either due to excessive ECM production, alteration in ECM-degrading activities, or a combination of both is defined as fibrosis. Skeletal muscle fibrosis impairs muscle function, negatively affects muscle regeneration after injury and increases muscle susceptibility to re-injury, therefore, it is considered a major cause of muscle weakness. Fibrosis of skeletal muscle is a hallmark of muscular dystrophies, aging and severe muscle injuries. Thus, a better understanding of the mechanisms of muscle fibrosis will help to advance our knowledge of the events that occur in dystrophic muscle diseases and develop innovative anti-fibrotic therapies to reverse fibrosis in such pathologic conditions. This paper explores an overview of the process of muscle fibrosis, as well as different murine models for studying fibrosis in skeletal muscles. In addition, factors regulating fibrosis and strategies to inhibit muscle fibrosis are discussed.The author is supported by a Postdoctoral Fellowship from the University of Pretoria, South Africa.http://link.springer.com/journal/4412020-11-12hj2018Anatomy and Physiolog
Efficacy and safety of tenecteplase in combination with enoxaparin, abciximab, or unfractionated heparin: The ASSENT-3 randomised trial in acute myocardial infarction
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- Abdul-Karim A.
- Abdulali S.
- Abizanda Campos R.
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- Adler L.
- Agraou B.
- Ahlstrom P.
- Ahmad G.
- Ahonen J.
- Ahremark U.
- Ahuad Guerrero R.
- Albisu J. P.
- Alcocer L.
- Alexander D.
- Alexander J.
- Allam S.
- Alonso Garcia M. A.
- Altamura G.
- Amaro Cendon A.
- Ambrosio G.
- Amerena J.
- Apostolou T.
- Arboleda Sanchez J. A.
- Armstrong P. W.
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- Arunasalam S.
- Auteri A.
- Aveta P.
- Avington D.
- Aylward P.
- Azzarito M.
- Backenkohler U.
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- Bandh S.
- Baradat G.
- Barbiero M.
- Barletta C.
- Baron S.
- Bassani Arrieta C. A.
- Bata I. R.
- Battistella P.
- Bavastro P.
- Bayat J.
- Bazin P.
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- Beckmann-Hiss H.
- Beel T.
- Beernaert A.
- Behnke M.
- Bekaert I.
- Bellamy B.
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- Publication date
- 01/01/2001
- Field of study
Background: Current fibrinolytic therapies fail to achieve optimum reperfusion in many patients. Low-molecular-weight heparins and platelet glycoprotein IIb/IIIa inhibitors have shown the potential to improve pharmacological reperfusion therapy. We did a randomised, open-label trial to compare the efficacy and safety of tenecteplase plus enoxaparin or abciximab, with that of tenecteplase plus weight-adjusted unfractionated heparin in patients with acute myocardial infarction. Methods: 6095 patients with acute myocardial infarction of less than 6 h were randomly assigned one of three regimens: full-dose tenecteplase and enoxaparin for a maximum of 7 days (enoxaparin group; n=2040), half-dose tenecteplase with weight-adjusted low-dose unfractionated heparin and a 12-h infusion of abciximab (abciximab group; n=2017), or full-dose tenecteplase with weight-adjusted unfractionated heparin for 48 h (unfractionated heparin group; n=2038). The primary endpoints were the composites of 30-day mortality, in-hospital reinfarction, or in-hospital refractory ischaemia (efficacy endpoint), and the above endpoint plus in-hospital intracranial haemorrhage or in-hospital major bleeding complications (efficacy plus safety endpoint). Analysis was by intention to treat. Findings: There were significantly fewer efficacy endpoints in the enoxaparin and abciximab groups than in the unfractionated heparin group: 233/2037 (11.4%) versus 315/2038 (15.4%; relative risk 0.74 [95% CI 0.63-0.87], p=0.0002) for enoxaparin, and 223/2017 (11.1%) versus 315/2038 (15.4%; 0.72 [0.61-0.84], p<0.0001) for abciximab. The same was true for the efficacy plus safety endpoint: 280/2037 (13.7%) versus 347/2036 (17.0%; 0.81 [0.70-0.93], p=0.0037) for enoxaparin, and 287/2016 (14.2%) versus 347/2036 (17.0%; 0.84 [0.72-0.96], p=0.01416) for abciximab. Interpretation: The tenecteplase plus enoxaparin or abciximab regimens studied here reduce the frequency of ischaemic complications of an acute myocardial infarction. In light of its ease of administration, tenecteplase plus enoxaparin seems to be an attractive alternative reperfusion regimen that warrants further study
Liraglutide and Renal Outcomes in Type 2 Diabetes.
- Author
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- Zubair I.
- Zuradzka-Wajda D
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- Álvarez de Arcaya Vicente A
- 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 .)