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Wyszukujesz frazę "Engstrom, Thomas" wg kryterium: Autor


Wyświetlanie 1-3 z 3
Tytuł:
Subsequent event risk in individuals with established coronary heart disease : design and rationale of the GENIUS-CHD consortium
Autorzy:
Sun, Yan
Delgado, Graciela
Carpeggiani, Clara
Pilbrow, Anna
Lee, Vei-Vei
Kofink, Daniel
Wallentin, Lars
Fox, Keith
Lang, Chim
Nikus, Kjell
Patel, Riyaz
Mahmoodi, B.
Simon, Tabassome
Gong, Yan
Pare, Guillaume
Al Ali, Lawien
Deloukas, Panos
Mons, Ute
James, Stefan
Laurikka, Jari
Szczeklik, Wojciech
ten Berg, Jurrien
Holmes, Michael
Kaminski, Karol
van der Graaf, Yolanda
Quyyumi, Arshed
Muehlschlegel, Jochen
Stender, Steen
Dube, Marie-Pierre
Stewart, Alexandre
Brenner, Hermann
Hartiala, Jaana
Hovingh, G.
Brugts, Jasper
Jukema, J.
Dudbridge, Frank
Richards, A.
Baranova, Ekaterina
Van de Werf, Frans
Scholz, Markus
Fitzpatrick, Natalie
Cresci, Sharon
Gijsberts, Crystel
Niemcunowicz-Janica, Anna
McPherson, Ruth
Lotufo, Paulo
Tang, W.H.
Drexel, Heinz
Alver, Maris
Danchin, Nicolas
Burkhardt, Ralph
Wilde, Arthur
Anderson, Jeffrey
McCubrey, Raymond
Marziliano, Nicola
Pereira, Alexandre
Pepine, Carl
Pilote, Louise
Saely, Christoph
Carlquist, John
Grobbee, Diederick
Kleber, Marcus
Direk, Kenan
Lindholm, Daniel
Martinelli, Nicola
Sandesara, Pratik
Ardissino, Diego
Girelli, Domenico
Leiherer, Andreas
Johnson, Julie
Bogaty, Peter
Lagerqvist, Bo
Lehtimaki, Terho
Arsenault, Benoit
Levin, Daniel
Bots, Michiel
Kaczor, Marcin
Doughty, Robert
Virani, Salim
Sinisalo, Juha
Siegbahn, Agneta
Boersma, Eric
Wauters, Els
Algra, Ale
Duarte, Nubia
Lokki, Marja-Liisa
Engert, James
Smith, J.
Schmidt, Amand
Trompet, Stella
Marz, Winfried
Kettner, Jiri
van Setten, Jessica
Hagstrom, Emil
Sanak, Marek
Boeckx, Bram
Lenzini, Petra
Klungel, Olaf
Cooper-DeHoff, Rhonda
Body, Simon
Kahonen, Mika
Hingorani, Aroon
Breitling, Lutz
van der Laan, Sander
Tragante, Vinicius
Pitha, Jan
Samman-Tahhan, Ayman
Szpakowicz, Anna
Nelson, Christopher
Tanck, Michael
Deanfield, John
Spertus, John
Held, Claes
Tfelt-Hansen, Jacob
Condorelli, Gianluigi
Horne, Benjamin
Ballantyne, Christie
Sattar, Naveed
Melander, Olle
Metspalu, Andres
Tardif, Jean-Claude
Visseren, Frank
Ford, Ian
Teren, Andrej
Allayee, Hooman
Waltenberger, Johannes
Foco, Luisa
Hoefer, Imo
Maitland-van der Zee, Anke
Jabbari, Reza
Muhlestein, Joseph
Akerblom, Axel
Kuukasjarvi, Pekka
Palmer, Colin
Stott, David
Engstrom, Thomas
Thanassoulis, George
Eriksson, Niclas
de Faire, Ulf
Hubacek, Jaroslav
Lambrechts, Diether
Hazen, Stanley
Boerwinkle, Eric
Glinge, Charlotte
Heydarpour, Mahyar
Pasterkamp, Gerard
Dufresne, Line
Bezzina, Connie
Newton-Cheh, Christopher
Behlouli, Hassan
Anselmi, Chiara
Casu, Gavino
Lyytikainen, Leo-Pekka
Leander, Karin
Vlachopoulou, Efthymia
Gigante, Bruna
Andreassi, Maria
Bergmeijer, Thomas
Cameron, Vicky
Asselbergs, Folkert
Kiliszek, Marek
Carruthers, Kathryn
Thiery, Joachim
Brophy, James
Braund, Peter
Fox, Kim
Almgren, Peter
Hemingway, Harry
Briguori, Carlo
Timmis, Adam
van der Harst, Pim
Opolski, Grzegorz
Samani, Nilesh
Vilmundarson, Ragnar
Howe, Laurence
Ploski, Rafal
Torp-Pedersen, Christian
Olivieri, Oliviero
Kotti, Salma
Opis:
BACKGROUND: The Genetics of Subsequent Coronary Heart Disease (GENIUS-CHD) consortium was established to facilitate discovery and validation of genetic variants and biomarkers for risk of subsequent CHD events, in individuals with established CHD. METHODS: The consortium currently includes 57 studies from 18 countries, recruiting 185 614 participants with either acute coronary syndrome, stable CHD, or a mixture of both at baseline. All studies collected biological samples and followed-up study participants prospectively for subsequent events. RESULTS: Enrollment into the individual studies took place between 1985 to present day with a duration of follow-up ranging from 9 months to 15 years. Within each study, participants with CHD are predominantly of self-reported European descent (38%-100%), mostly male (44%–91%) with mean ages at recruitment ranging from 40 to 75 years. Initial feasibility analyses, using a federated analysis approach, yielded expected associations between age (hazard ratio, 1.15; 95% CI, 1.14-1.16) per 5-year increase, male sex (hazard ratio, 1.17; 95% CI, 1.13-1.21) and smoking (hazard ratio, 1.43; 95% CI, 1.35-1.51) with risk of subsequent CHD death or myocardial infarction and differing associations with other individual and composite cardiovascular endpoints. CONCLUSIONS: GENIUS-CHD is a global collaboration seeking to elucidate genetic and nongenetic determinants of subsequent event risk in individuals with established CHD, to improve residual risk prediction and identify novel drug targets for secondary prevention. Initial analyses demonstrate the feasibility and reliability of a federated analysis approach. The consortium now plans to initiate and test novel hypotheses as well as supporting replication and validation analyses for other investigators.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Contribution of common genetic variants to risk of early-onset ischemic stroke
Autorzy:
Jimenez-Conde, Jordi
Ryan, Kathleen A.
Luke, Sothear
Gieger, Christian
Pera, Joanna
Thijs, Vincent
Smith, Jennifer A.
Mitchell, Braxton D.
Chong, Michael
Rexrode, Kathryn
Cruchaga, Carlos
Torres-Aguila, Nuria P.
Markus, Hugh S.
Heitsch, Laura
Walters, Robin G.
Li, Jiang
Rosand, Jonathan
Jaworek, Thomas
Kamatani, Yoichiro
Meschia, James F.
Holliday, Elizabeth
Mcardle, Patrick F.
Anderson, Christopher D.
Ilinca, Andreea
Bell, Steven
Cushman, Mary
Gaynor, Brady J.
Muller-Nurasyid, Martina
Putaala, Jukka
Cole, John W.
Engstrom, Gunnar
Grittner, Ulrike
Strbian, Daniel
Kardia, Sharon L.R.
Levi, Christopher R.
Hong, Charles C.
O'Donnell, Martin
Pare, Guillaume
Zand, Ramin
Tuladhar, Anil M.
Faul, Jessica D.
Havulinna, Aki S.
Sacco, Ralph L.
Mcdonough, Caitrin W.
Jern, Christina
Boncoraglio, Giorgio B.
Hu, Jie
Rothwell, Peter M.
Metso, Tiina
Lin, Kuang
Giese, Anne-Katrin
Fecteau, Natalie S.
Jackson, Rebecca D.
Johnson, Julie A.
Ribases, Marta
Attia, John
Veldink, Jan H.
de Leeuw, Frank-Erik
Lemmens, Robin
O'Connor, Timothy D.
Danesh, John
Irvin, Marguerite R.
Perry, James A.
Hochberg, Marc C.
Stine, O. Colin
Fernandez-Cadenas, Israel
Tomppo, Liisa
Abedi, Vida
Grewal, Raji P.
Li, Liming
Sanchez-Mora, Cristina
Lange, Leslie
Ross, Owen A.
Chen, Zhengming
Debette, Stephanie
Wassertheil-Smoller, Sylvia
Stanne, Tara M.
Jacob, Mina A.
Smith, Nicholas L.
Dichgans, Martin
Sudlow, Cathie L.M.
Kittner, Steven J.
Rannikmae, Kristiina
Peddareddygari, Leema R.
Lopez, Haley
Peters, Annette
Benavente, Oscar R.
Weir, David R.
Salomaa, Veikko
Enzinger, Chris
Lindgren, Arne G.
Tatlisumak, Turgut
Durda, Jon Peter
Ray, Debashree
Xu, Huichun
Lee, Jin-Moo
Worrall, Bradford B.
Butterworth, Adam
Słowik, Agnieszka
Soderholm, Martin
Woo, Daniel
Carcel-Marquez, Jara
Duggan, David J.
Maguire, Jane
Koido, Masaru
Sharma, Pankaj
Terao, Chikashi
Malik, Rainer
Schmidt, Reinhold
Amouyel, Philippe
Kubo, Michiaki
Rabionet, Raquel
Tregouet, David-Alexandre
Armstrong, Nicole D.
Rundek, Tatjana
Opis:
Background and Objectives:Current genome-wide association studies of ischemic stroke have focused primarily on late-onset disease. As a complement to these studies, we sought to identify the contribution of common genetic variants to risk of early-onset ischemic stroke: Methods: We performed a meta-analysis of genome-wide association studies of early-onset stroke (EOS), ages 18–59 years, using individual-level data or summary statistics in 16,730 cases and 599,237 nonstroke controls obtained across 48 different studies. We further compared effect sizes at associated loci between EOS and late-onset stroke (LOS) and compared polygenic risk scores (PRS) for venous thromboembolism (VTE) between EOS and LOS. Results: We observed genome-wide significant associations of EOS with 2 variants in ABO, a known stroke locus. These variants tag blood subgroups O1 and A1, and the effect sizes of both variants were significantly larger in EOS compared with LOS. The odds ratio (OR) for rs529565, tagging O1, was 0.88 (95% confidence interval [CI]: 0.85–0.91) in EOS vs 0.96 (95% CI: 0.92–1.00) in LOS, and the OR for rs635634, tagging A1, was 1.16 (1.11–1.21) for EOS vs 1.05 (0.99–1.11) in LOS; p-values for interaction = 0.001 and 0.005, respectively. Using PRSs, we observed that greater genetic risk for VTE, another prothrombotic condition, was more strongly associated with EOS compared with LOS (p = 0.008). Discussion: The ABO locus, genetically predicted blood group A, and higher genetic propensity for venous thrombosis are more strongly associated with EOS than with LOS, supporting a stronger role of prothrombotic factors in EOS.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
    Wyświetlanie 1-3 z 3

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