10 research outputs found
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
- Author
- Abecasis G.
- Albert C.
- Armanios M.
- Arnett D.K.
- Arvanitis M.
- Ashley-Koch A.E.
- Aslibekyan S.
- Auer P.L.
- Aviv A.
- Barnes K.C.
- Barwick L.
- Battle A.
- Becker L.C.
- Bis J.C.
- Blackwell T.W.
- Blangero J.
- Bleecker E.R.
- Boerwinkle E.
- Bowden D.W.
- Brody J.A.
- Burchard E.G.
- Cade B.E.
- Celedón J.C.
- Chang Y.P.C.
- Chen Y.-D.I.
- Chen Z.
- Cho M.H.
- Conomos M.P.
- Correa A.
- Cox N.J.
- Cupples L.A.
- Curran J.E.
- Custer B.
- Darbar D.
- Daya M.
- de Andrade M.
- de las Fuentes L.
- Deka R.
- DeMeo D.L.
- Ellinor P.T.
- Eng C.
- Fingerlin T.E.
- Fornage M.
- Freedman B.I.
- Garrett M.E.
- Gelb B.D.
- Gilliland F.D.
- Gladwin M.T.
- Gogarten S.M.
- Gui H.
- Guo X.
- He J.
- Heavner B.
- Heckbert S.R.
- Hidalgo B.A.
- Hou L.
- Hwang S.-J.
- Irvin M.R.
- Islam T.
- Iyer K.R.
- Jain D.
- Johnsen J.M.
- Johnson W.C.
- Kaab S.
- Kaplan R.
- Kardia S.L.R.
- Keener R.
- Kelly S.
- Kenny E.E., The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States, Center for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, NY, United States
- Keramati A.
- Konkle B.A.
- Kooperberg C.
- Kumar R.
- Lane J.
- Lasky-Su J.
- Launer L.
- Laurie C.A.
- Laurie C.C.
- Lee J.
- Levin A.M.
- Levy D.
- Liu C.
- Liu S.
- Loos R.J.F.
- Mak A.C.Y.
- Mathias R.A.
- McGarvey S.T.
- McHugh C.P.
- Meyers D.A.
- Miller-Fleming T.W.
- Minster R.L.
- Mitchell B.D.
- Montgomery C.G.
- Moscati A.
- Naseri T.
- Nekhai S.
- NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
- Nickerson D.A.
- North K.E.
- Nouraie M.
- O'Connell J.
- Palmer N.D.
- Pankratz N.
- Peralta J.M.
- Perry J.A.
- Peyser P.A.
- Psaty B.M.
- Raby B.A.
- Rafaels N.
- Raffield L.M.
- Redline S.
- Reiner A.P.
- Reupena M.S.
- Rich S.S.
- Roden D.
- Rotter J.I.
- Ruczinski I.
- Sabino E.C.
- Schwartz D.A.
- Sciurba F.
- Seidman C.
- Sheu W.H.-H.
- Shoemaker M.B.
- Silverman E.K.
- Sinner M.F.
- Smith A.V.
- Smith J.A.
- Smith N.L.
- Taub M.A.
- Taylor J.G., VI
- Taylor K.D.
- Telen M.J.
- Thornton T.
- Tiwari H.K.
- TOPMed Hematology and Hemostasis Working Group
- TOPMed Structural Variation Working Group
- Tracy R.P.
- Vasan R.S.
- Weeks D.E.
- Weinstock J.S.
- Weiss S.T.
- Wen F.
- Wheeler M.M.
- White M.J.
- Wiggins K.L.
- Williams L.K.
- Wilson J.G.
- Yanek L.R.
- Yang I.V.
- Zhang Y.
- Zhao W.
- Publication venue
- Cell Press
- Publication date
- 01/01/2022
- Field of study
Genetic studies on telomere length are important for understanding age-related diseases. Prior GWASs for leukocyte TL have been limited to European and Asian populations. Here, we report the first sequencing-based association study for TL across ancestrally diverse individuals (European, African, Asian, and Hispanic/Latino) from the NHLBI Trans-Omics for Precision Medicine (TOPMed) program. We used whole-genome sequencing (WGS) of whole blood for variant genotype calling and the bioinformatic estimation of telomere length in n = 109,122 individuals. We identified 59 sentinel variants (p < 5 × 10−9) in 36 loci associated with telomere length, including 20 newly associated loci (13 were replicated in external datasets). There was little evidence of effect size heterogeneity across populations. Fine-mapping at OBFC1 indicated that the independent signals colocalized with cell-type-specific eQTLs for OBFC1 (STN1). Using a multi-variant gene-based approach, we identified two genes newly implicated in telomere length, DCLRE1B (SNM1B) and PARN. In PheWAS, we demonstrated that our TL polygenic trait scores (PTSs) were associated with an increased risk of cancer-related phenotypes
Metamorphosis of the mountain brook lamprey Ichthyomyzon greeleyi
- Author
- A.N. Poltorykhina
- B.J. Hill
- D.J. Bird
- D.J. Bird
- E.K. Balon
- E.K. Balon
- E.K. Balon
- E.K. Balon
- F.W.H. Beamish
- F.W.H. Beamish
- F.W.H. Beamish
- F.W.H. Beamishc
- F.W.H. Beamishc
- H.I. Battle
- I.C. Potter
- I.C. Potter
- J.E. Richards
- J.H. Youson
- J.H. Youson
- J.W. Moore
- M. W. Hardisty
- P.J. Manion
- R.W Hilliard
- T.E. Medland
- V.D. Vladykov
- W.E. Ricker
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Thermodynamics of surfaces and adsorption in the Fe-S, Fe-N, and Fe-S-N systems at 1823 K
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Individual Behavior Change
- Author
- A. Bandura
- A. Bandura
- A. Jain
- A. Kazdin
- A.E. Baughcum
- A.E. Baughcum
- A.L. Copeland
- A.N. Jeffery
- B.H. Marcus
- B.J. Rolls
- B.M. Beech
- B.S. Kanders
- C. Ferster
- C. Horwath
- C.B. Taylor
- C.B. Taylor
- C.D. Summerbell
- C.M. Doak
- Committee on Prevention of Obesity in Children and Youth
- D.A. Renjilian
- D.M. Matson-Koffman
- E.B. Kahn
- E.K. Battle
- E.M. Rogers
- G.D. Foster
- G.S. Goldfield
- H.A. Lando
- IOM
- J. Noia Di
- J. Pleas
- J.D. Latner
- J.O. Prochaska
- J.P. Foreyt
- J.W. Farquhar
- J.W. Farquhar
- J.W. Pearce
- K. Resnicow
- K.B. Horgen
- K.B. Horgen
- K.D. Brownell
- K.D. Brownell
- K.H. Littrell
- K.M. Gans
- L.G. Womble
- L.H. Epstein
- L.H. Epstein
- L.H. Epstein
- L.H. Epstein
- L.R. Simkin-Silverman
- M. Golan
- M. Golan
- M. Menza
- M.F. Jacobson
- M.G. Perri
- M.W. Verheijden
- R. Petty
- R. Stuart
- R.I. Berkowitz
- R.R Wing
- R.R. Wing
- R.W. Jeffery
- R.W. Jeffery
- S. Arenz
- S.A. French
- S.A. French
- S.A. French
- S.K. Kumanyika
- S.K. Kumanyika
- S.K. Kumanyika
- S.K. Kumanyika
- S.K. Kumanyika
- S.K. Kumanyika
- T.A. Wadden
- T.A. Wadden
- T.A. Wadden
- T.F. Heatherton
- T.N. Robinson
- T.N. Robinson
- T.N. Robinson
- U. Bronfenbrenner
- W. McNabb
- W. Rakowski
- W.D. Evans
- W.K. Bickel
- W.K. Bickel
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2007
- Field of study
Black LGB Health and Well-Being
- Author
- A. Bell
- A. Hacker
- A. Lorde
- A. Schultz
- A. Solarz
- A.V. Diez-Roux
- B. Greene
- B. Greene
- B. Major
- B. McEwen
- B.D.M. Wilson
- B.G. Link
- C. Caldwell
- C. Chan
- C. Kitzinger
- C. Lemert
- C. Miller
- C.A. Collins
- C.D. Ryff
- C.H. Cooley
- C.M. Steele
- C.P. Jones
- C.T. Pyant
- Council of Economic Advisers for the President’s Initiative on Race
- D. Binson
- D. Conley
- D. Lester
- D. Loiacano
- D.R. Williams
- D.R. Williams
- D.S. Strogatz
- E. Erikson
- E. Goffman
- E. Morales
- E. Pamuk
- E.K. Pavalko
- E.M. Dube
- G. Herek
- G. Herren
- G.H. Mead
- G.W. Allport
- H. Landrine
- H. Tajfel
- H.E. Burstin
- Hypertension Detection and Follow-Up Program Cooperative Group
- I. Crawford
- I.H. Meyer
- I.H. Meyer
- J. Battle
- J. Battle
- J. Cassel
- J. Crocker
- J. Crocker
- J. DeMarco
- J. DiPlacido
- J.A. Howard
- J.L. King
- J.L. White
- J.N. Shelton
- J.S. House
- J.S. Jackson
- J.S. Kaufman
- J.S. Phinney
- J.S. Phinney
- K. Boykin
- K. Jackson
- K. Lewin
- L. Icard
- L. Sigelman
- M. Akerlund
- M. Rosario
- M. Susser
- M.B. Munford
- M.J. Eliason
- M.L. Oliver
- M.T. Fullilove
- M.V.L. Badgett
- M.V.L. Badgett
- N. Adler
- N. Kreiger
- N. Krieger
- N. Krieger
- N. Krieger
- N. Krieger
- N. Krieger
- N. Pearce
- P.H. Collins
- R. Bass-Hass
- R. Clark
- R. Diaz
- R. Sapolsky
- R.C. Savin-Williams
- R.C. Savin-Williams
- R.G. Blaxton
- R.L. Sell
- R.L. Sell
- R.M. Fernquist
- R.M. Sellers
- R.M. Sellers
- R.M. Sellers
- R.M. Sellers
- R.M. Sellers
- R.R. Troiden
- R.R. Troiden
- R.S. Lazarus
- S. Bridgforth
- S. Stack
- S.A. James
- S.D. Cochran
- S.D. Cochran
- S.D. Cochran
- S.E. Gilman
- S.J. Rowley
- T. Asanti
- T. Asanti
- T. Asanti
- T. McKeown
- T.A. Forman
- T.A. Parham
- T.A. Parham
- V. Mays
- V.C. Cass
- V.M. Mays
- V.M. Mays
- V.M. Mays
- W. Darity
- W.A. Darity Jr.
- W.A. Darity Jr.
- W.A. Vega
- W.E. Cross
- W.E. Cross
- W.E. Cross
- W.E. Cross
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2007
- Field of study
Correction to: Potentially modifiable factors contributing to outcome from acute respiratory distress syndrome: the LUNG SAFE study
- Author
- Ã
- Ã
- A. Adolfsson
- A. Aneman
- A. Arizmendi
- A. Artigas
- A. Ascoli
- A. Barratt-Due
- A. Benslama
- A. Braschi
- A. Briquet
- A. Cani
- A. Ceniceros-Barros
- A. Chena
- A. Christiansen
- A. Combes
- A. Coppadoro
- A. Cortegiani
- A. Deicas
- A. Delsing
- A. Demoule
- A. Do Vale Fernandes
- A. Donnelly
- A. Ebeid
- A. Esteban
- A. Ferguson
- A. Follin
- A. Giarratano
- A. Hang
- A. Harrois
- A. Hirata
- A. Hunt
- A. Javeed
- A. Krstevski
- A. Kumar
- A. Larsson
- A. Lombardo
- A. Marcu
- A. Mattei
- A. Mcleod
- A. Mercat
- A. Molin
- A. Morin
- A. Morton
- A. Nichol
- A. Pronovost
- A. Protti
- A. Ramirez-Gutierrez
- A. Robine
- A. Rossi
- A. Schomer
- A. Seven
- A. Shenoy
- A. Siu-Ming
- A. Takaba
- A. Tinnirello
- A. Tulaimat
- A. Uchiyama
- A. Uppalapati
- A. Venti
- A. Vercueil
- A. Villagomez
- A. Youzhong
- A. Zazu
- A.A. Gazenkampf
- A.A. Saez
- A.A. Tallet Alfonso
- A.A. Zeggwagh
- A.A. Zeggwagh
- A.B. Guttormsen
- A.B. Schlichting
- A.B. Souissi
- A.C. Oâ
- A.C.P. Antã
- A.D. Frigyik
- A.G. Castro
- A.G. Franã
- A.G. Jimenez
- A.I. Gritsan
- A.J. Burtenshaw
- A.J. Villagomez
- A.J. Williams
- A.K. Baronia
- A.L. Ruiz-Aguilar
- A.M. Alvarez
- A.M. Araujo
- A.M. Dive
- A.M. Fernandez
- A.M. Martinho
- A.M. Messias
- A.M. Pellicer
- A.M. Pesenti
- A.M. Rampinelli
- A.N. Cracchiolo
- A.O. Tibblin
- A.P. Hormis
- A.P. Nassar
- A.R. Bruhn
- A.S. Al Jabbary
- A.S. Raj
- A.S. Slutsky
- A.T. Dowling
- A.U. Alisasis
- A.W. Reske
- B. Brunettini
- B. Gelã
- B. Goubaux
- B. Holzgraefe
- B. Jovanovic
- B. Kennedy
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- B..T. Thompson
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- B.G. Villamagua
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- B.S. Oliveira
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- C. Daubin
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- C. Mellis
- C. Nutt
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- C. Reynolds
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- C. Serra
- C. Tainter
- C. Wang
- C. Whitehead
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- C.A. Ortiz
- C.A. Pellegrini
- C.A. Volta
- C.C. Macfie
- C.C. Rylander
- C.E. Battle
- C.G. Virgilio
- C.H. Gonã
- C.J. Scott
- C.K. Grissom
- C.M. Coxo
- C.M. Ramirez-Alfaro
- C.P. Perez
- C.Q. Grijalba
- C.R. Estrella
- C.S. Black
- C.S. Insaurralde
- C.S. Pereira
- D. Albiero
- D. Carpentier
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- D. Goldgran-Toledano
- D. Gomaa
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- D. Hadfield
- D. Ismail
- D. Matamis
- D. Mcauley
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- D. Niimi
- D. Nobrega
- D. Oâ
- D. Reuter
- D. Roux
- D. Sandesc
- D. Yu
- D.A. Fawkes
- D.A. Irvine
- D.C. Fontenele
- D.D. Llinares Moya
- D.E. Corneci
- D.F. Mcauley
- D.J. Hacking
- D.J. Yeatts
- D.M. Breen
- D.M. Combaux
- D.M. Dector
- D.M. Inskip
- D.M. Palma
- D.N. Vasquez
- D.O. Beraldo
- D.P. Marcos
- D.P. Toribio
- D.R. Crouch
- D.R. Crouch
- D.R. Gonzalez
- D.R. Tomescu
- D.V. Collins
- D.W. Wrathall
- E. Beck
- E. Cereijo
- E. Diaz-Rodriguez
- E. Erbabacan
- E. Estenssoro
- E. Fan
- E. Frati
- E. Grigoriev
- E. Kalaitzis
- E. Nishikawa
- E. Nuã
- E. Pecci
- E. Sã
- E. Tabhan
- E. Watanabe
- E.A. Meaney
- E.A. Piacentini
- E.B. Lopez
- E.C. Goligher
- E.E. Borotto
- E.E. Stamou
- E.E. Tabhan
- E.F. Labarca
- E.G. Curto
- E.H. Zogheib
- E.K. Bajwa
- E.K. Mouloudi
- E.L. Willett
- E.M. Osman
- E.O. Nagy
- E.P. Losada
- E.P. Sauvadet
- E.R. Vascotto
- E.S. Dunne
- E.V. Kiourtzieva
- E.V. Massa
- F. Abroug
- F. Amir
- F. Beloncle
- F. Berkelmans
- F. Daviaud
- F. Esteve
- F. Gordo
- F. Grelon
- F. Heidari
- F. Ito
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- F. Mojoli
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- F. Raponi
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- F. Roche-Campo
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- F. Zhang
- F. Zhou
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- F.A. Loiacono
- F.A. Montes Oscanoa
- F.D. Simonis
- F.G. Cazorla-Barranquero
- F.G. George
- F.H. Andersen
- F.J.F. Mejia
- F.L. Santoli
- F.M. Barros
- F.M. Kheir
- F.P. Huerta
- F.S. Lora
- F.T. Martinez
- G. Almekhlafi
- G. Bã
- G. Barberet
- G. Bellani
- G. Bugedo
- G. Buzancais
- G. Carteaux
- G. Cinnella
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- G. Curley
- G. Dã
- G. Dempsey
- G. Foti
- G. Frendl
- G. Henderson
- G. Kamel
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- G. Navarro
- G. Occhipinti
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- G.A. Plotnikow
- G.A. Zacharas
- G.C. Hanlon
- G.D. Rubenfeld
- G.M. Albaiceta
- G.M. Elisabet
- G.M. Francois
- G.M. Montanha
- G.M. Mustafa
- G.P. Sellors
- G.S.R.F. Service
- H. Aguirre-Bermeo
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- H. Dawson
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- H. Liu
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- H. Shao
- H. Sula
- H. Suzuki
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- J.E. Palo
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- U. Higashijima
- U. Strauch
- U.M. Theresa
- V. Bumbasierevic
- V. Bumbasirevic
- V. Cerny
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- V.A. Brito
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- V.J. Ramesh
- V.K. Bhardwaj
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- V.M. Sales
- V.P. Imma
- W. Altaf
- W. Maazouzi
- W. Stigler
- W. Wang
- W. Ya
- W.H. Zhu
- X. Luo
- X. Wittebole
- X. Yonghao
- X.B. Huang
- X.Y. Zhang
- X.Y. Zhao
- Y. Arabi
- Y. Gao
- Y. Haddad
- Y. Han
- Y. Kameyama
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- Y. Rongguo
- Y. Tao
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- Y.D. Jarquin-Badiola
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- Y.M. Arabi
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 14/11/2017
- Field of study
Correction to: Intensive Care Med (2016) 42:1865\u20131876 DOI 10.1007/s00134-016-4571-
Mechanical ventilation in patients with cardiogenic pulmonary edema : a sub-analysis of the LUNG SAFE study
- Author
- Abad R.D.
- Abe Toshikazu
- Abroug Fekri
- Adams J.C.
- Adamsson R.O.
- Adolfsson A.
- Aguilar R.Z.
- Aguirre J.S.
- Aguirre-Bermeo Hernan
- Aisa T.M.
- Aisiku Imoigele P.
- Ajetunmobi O.O.
- Aker M.
- Akyol O.O.
- Al Dorzi H.M.
- Albaiceta G.M.
- Albaiceta Guillermo M.
- Albarrak M.M.
- Albiero D.
- Alda R.S.
- Alejandro Risso V.
- Alexander P.
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- Aliaga Felipe A.
- Alisasis A.U.
- AlJabbary A.S.
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- Amado-Rodríguez Laura
- Amin Pravin
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- Andruszkiewicz P.
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- Sun Renhua
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- Trinidad O.A.
- Tulaimat A.
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- Uchiyama A.
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- Ueno K.
- Umbrello M.
- Universitat Autònoma de Barcelona
- Unnikrishnan R.
- Uppalapati A.
- Van Haren Frank
- Van Haren Frank
- Van Wezel H.M.
- Vargas M.P.
- Vascotto E.R.
- Vasquez Daniela N.
- Vega Luis D.
- Venti A.
- Vercueil A.
- Vermassen Joris
- Verstraete Rik
- Villagomez A.J.
- Villagomez Asisclo
- Villamagua B.G.
- Villar Veronica
- Vinzio Mauricio
- Virgilio C.G.
- Vitale M.N.
- Volta C.A.
- Wang C.
- Wang Hua X.
- Wang S.H.
- Wang Wei
- Warren J.
- Watanabe E.
- Watt P.
- Welters I.D.
- Wenham T.
- Wessbergh J.
- Whitehead Christina
- Willett E.L.
- Williams A.J.
- Williams K.E.
- Wittebole Xavier
- Wong Helen S.
- Woods Paul W.
- Wrathall D.W.
- Wrigge Hermann
- Wrigge Hermann
- Wu Ya Q.
- Xin-Hua Q.
- Xu Y.
- Yamaguchi O.
- Yamaji Y.
- Yao Q.
- Ye Zheng L.
- Yeatts D.J.
- Yu R.
- Yu Tao
- Yu Wenkui
- Yumha Jacob S.
- Yuste L.J.
- Zacharas Giannis A
- Zacharowski Kai
- Zani G.
- Zantua C.K.S.
- Zazu Alan
- Zeggwagh Amine Ali
- Zein Salem Ould
- Zender Hervé O
- Zhai Zhe
- Zhang Fan
- Zhang X.Y.
- Zhao Huiying
- Zhao Jun
- Zhao X.Y.
- Zheng Ruiqiang
- Zhou Fa C.
- Zhou S.
- Zhu Bao H.
- Zhu W.H.
- Zogheib Elie
- Ñamendys-Silva S.A.
- Ünal N.
- Publication venue
- Publication date
- 01/01/2022
- Field of study
Patients with acute respiratory failure caused by cardiogenic pulmonary edema (CPE) may require mechanical ventilation that can cause further lung damage. Our aim was to determine the impact of ventilatory settings on CPE mortality. Patients from the LUNG SAFE cohort, a multicenter prospective cohort study of patients undergoing mechanical ventilation, were studied. Relationships between ventilatory parameters and outcomes (ICU discharge/hospital mortality) were assessed using latent mixture analysis and a marginal structural model. From 4499 patients, 391 meeting CPE criteria (median age 70 [interquartile range 59-78], 40% female) were included. ICU and hospital mortality were 34% and 40%, respectively. ICU survivors were younger (67 [57-77] vs 74 [64-80] years, p < 0.001) and had lower driving (12 [8-16] vs 15 [11-17] cmHO, p < 0.001), plateau (20 [15-23] vs 22 [19-26] cmHO, p < 0.001) and peak (21 [17-27] vs 26 [20-32] cmHO, p < 0.001) pressures. Latent mixture analysis of patients receiving invasive mechanical ventilation on ICU day 1 revealed a subgroup ventilated with high pressures with lower probability of being discharged alive from the ICU (hazard ratio [HR] 0.79 [95% confidence interval 0.60-1.05], p = 0.103) and increased hospital mortality (HR 1.65 [1.16-2.36], p = 0.005). In a marginal structural model, driving pressures in the first week (HR 1.12 [1.06-1.18], p < 0.001) and tidal volume after day 7 (HR 0.69 [0.52-0.93], p = 0.015) were related to survival. Higher airway pressures in invasively ventilated patients with CPE are related to mortality. These patients may be exposed to an increased risk of ventilator-induced lung injury. Trial registration Clinicaltrials.gov NCT02010073
Resolved versus confirmed ARDS after 24 h: insights from the LUNG SAFE study
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- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2018
- Field of study
Purpose: To evaluate patients with resolved versus confirmed ARDS, identify subgroups with substantial mortality risk, and to determine the utility of day 2 ARDS reclassification. Methods: Our primary objective, in this secondary LUNG SAFE analysis, was to compare outcome in patients with resolved versus confirmed ARDS after 24\ua0h. Secondary objectives included identifying factors associated with ARDS persistence and mortality, and the utility of day 2 ARDS reclassification. Results: Of 2377 patients fulfilling the ARDS definition on the first day of ARDS (day 1) and receiving invasive mechanical ventilation, 503 (24%) no longer fulfilled the ARDS definition the next day, 52% of whom initially had moderate or severe ARDS. Higher tidal volume on day 1 of ARDS was associated with confirmed ARDS [OR 1.07 (CI 1.01\u20131.13), P = 0.035]. Hospital mortality was 38% overall, ranging from 31% in resolved ARDS to 41% in confirmed ARDS, and 57% in confirmed severe ARDS at day 2. In both\ua0resolved and confirmed\ua0ARDS, age, non-respiratory SOFA score, lower PEEP and P/F ratio, higher peak pressure and respiratory rate were each\ua0associated with mortality. In confirmed ARDS, pH and the presence of immunosuppression or neoplasm were also associated\ua0with mortality. The increase in area under the receiver operating curve for ARDS reclassification on day 2 was marginal. Conclusions: ARDS, whether resolved or confirmed at day 2, has a high mortality rate. ARDS reclassification at day 2 has limited predictive value for mortality. The substantial mortality risk in severe confirmed ARDS suggests that complex interventions might best be tested in this population. Trial Registration: ClinicalTrials.gov NCT02010073. \ua9 2018, Springer-Verlag GmbH Germany, part of Springer Nature and ESICM
Death in hospital following ICU discharge : insights from the LUNG SAFE study
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- Ñamendys-Silva S.A.
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2021
- Field of study
Altres ajuts: Italian Ministry of University and Research (MIUR)-Department of Excellence project PREMIA (PREcision MedIcine Approach: bringing biomarker research to clinic); Science Foundation Ireland Future Research Leaders Award; European Society of Intensive Care Medicine (ESICM), Brussels; St Michael's Hospital, Toronto; University of Milan-Bicocca, Monza, Italy.Background: To determine the frequency of, and factors associated with, death in hospital following ICU discharge to the ward. Methods: The Large observational study to UNderstand the Global impact of Severe Acute respiratory FailurE study was an international, multicenter, prospective cohort study of patients with severe respiratory failure, conducted across 459 ICUs from 50 countries globally. This study aimed to understand the frequency and factors associated with death in hospital in patients who survived their ICU stay. We examined outcomes in the subpopulation discharged with no limitations of life sustaining treatments ('treatment limitations'), and the subpopulations with treatment limitations. Results: 2186 (94%) patients with no treatment limitations discharged from ICU survived, while 142 (6%) died in hospital. 118 (61%) of patients with treatment limitations survived while 77 (39%) patients died in hospital. Patients without treatment limitations that died in hospital after ICU discharge were older, more likely to have COPD, immunocompromise or chronic renal failure, less likely to have trauma as a risk factor for ARDS. Patients that died post ICU discharge were less likely to receive neuromuscular blockade, or to receive any adjunctive measure, and had a higher pre- ICU discharge non-pulmonary SOFA score. A similar pattern was seen in patients with treatment limitations that died in hospital following ICU discharge. Conclusions: A significant proportion of patients die in hospital following discharge from ICU, with higher mortality in patients with limitations of life-sustaining treatments in place. Non-survivors had higher systemic illness severity scores at ICU discharge than survivors. Trial Registration: ClinicalTrials.gov NCT02010073
Whole-genome sequencing reveals host factors underlying critical COVID-19
- Author
- Abd Elghafar Mohamed S.
- Abdel-Aziz Mahmoud
- Abdelrazik Marwa
- Abdollahi Hamed
- Abdullah T.
- Abecasis Goncalo
- Abedalthagafi M.
- Abel Lynn
- Abernathy C.
- Abraheem Azmeralde
- Abul-Husn Noura S.
- Acquilini D.
- Adams C.
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- Adamsara Alireza
- Adanini Olurenke
- Adeleye O.
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- Afilalo M.
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- Afrasiabi Z.
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- Ahmadi Saeideh
- Ahmed A.
- Ahmed Cecilia
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- Akhtar M.N.
- Akinkugbe O.
- Aksentijevich Alexandra
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- Al-Awdah L.
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- Åsvold Bjørn Olav
- Publication venue
- Publication date
- 01/01/2022
- Field of study
Altres ajuts: Department of Health and Social Care (DHSC); Illumina; LifeArc; Medical Research Council (MRC); UKRI; Sepsis Research (the Fiona Elizabeth Agnew Trust); the Intensive Care Society, Wellcome Trust Senior Research Fellowship (223164/Z/21/Z); BBSRC Institute Program Support Grant to the Roslin Institute (BBS/E/D/20002172, BBS/E/D/10002070, BBS/E/D/30002275); UKRI grants (MC_PC_20004, MC_PC_19025, MC_PC_1905, MRNO2995X/1); UK Research and Innovation (MC_PC_20029); the Wellcome PhD training fellowship for clinicians (204979/Z/16/Z); the Edinburgh Clinical Academic Track (ECAT) programme; the National Institute for Health Research, the Wellcome Trust; the MRC; Cancer Research UK; the DHSC; NHS England; the Smilow family; the National Center for Advancing Translational Sciences of the National Institutes of Health (CTSA award number UL1TR001878); the Perelman School of Medicine at the University of Pennsylvania; National Institute on Aging (NIA U01AG009740); the National Institute on Aging (RC2 AG036495, RC4 AG039029); the Common Fund of the Office of the Director of the National Institutes of Health; NCI; NHGRI; NHLBI; NIDA; NIMH; NINDS.Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care or hospitalization after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes-including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)-in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease