Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke
dc.rights.license | open | en_US |
dc.contributor.author | COLE, J. W. | |
dc.contributor.author | XU, H. | |
dc.contributor.author | RYAN, K. | |
dc.contributor.author | JAWOREK, T. | |
dc.contributor.author | DUEKER, N. | |
dc.contributor.author | MCARDLE, P. | |
dc.contributor.author | GAYNOR, B. | |
dc.contributor.author | CHENG, Y. C. | |
dc.contributor.author | O'CONNELL, J. | |
dc.contributor.author | BEVAN, S. | |
dc.contributor.author | MALIK, R. | |
dc.contributor.author | AHMED, N. U. | |
dc.contributor.author | AMOUYEL, Philippe | |
dc.contributor.author | ANJUM, S. | |
dc.contributor.author | BIS, J. C. | |
dc.contributor.author | CROSSLIN, D. | |
dc.contributor.author | DANESH, J. | |
dc.contributor.author | ENGELTER, S. T. | |
dc.contributor.author | FORNAGE, M. | |
dc.contributor.author | FROSSARD, P. | |
dc.contributor.author | GIEGER, C. | |
dc.contributor.author | GIESE, A. K. | |
dc.contributor.author | GROND-GINSBACH, C. | |
dc.contributor.author | HO, W. K. | |
dc.contributor.author | HOLLIDAY, E. | |
dc.contributor.author | HOPEWELL, J. | |
dc.contributor.author | HUSSAIN, M. | |
dc.contributor.author | IQBAL, W. | |
dc.contributor.author | JABEEN, S. | |
dc.contributor.author | JANNES, J. | |
dc.contributor.author | KAMAL, A. | |
dc.contributor.author | KAMATANI, Y. | |
dc.contributor.author | KANSE, S. | |
dc.contributor.author | KLOSS, M. | |
dc.contributor.author | LATHROP, M. | |
dc.contributor.author | LEYS, D. | |
dc.contributor.author | LINDGREN, A. | |
dc.contributor.author | LONGSTRETH, W. T., Jr. | |
dc.contributor.author | MAHMOOD, K. | |
dc.contributor.author | MEISINGER, C. | |
dc.contributor.author | METSO, T. M. | |
dc.contributor.author | MOSLEY, T., Jr. | |
dc.contributor.author | MULLER-NURASYID, M. | |
dc.contributor.author | NORRVING, B. | |
dc.contributor.author | PARATI, E. | |
dc.contributor.author | PETERS, A. | |
dc.contributor.author | PEZZINI, A. | |
dc.contributor.author | QUERESHI, I. | |
dc.contributor.author | RASHEED, A. | |
dc.contributor.author | RAUF, A. | |
dc.contributor.author | SALAM, T. | |
dc.contributor.author | SHEN, J. | |
dc.contributor.author | SLOWIK, A. | |
dc.contributor.author | STANNE, T. | |
dc.contributor.author | STRAUCH, K. | |
dc.contributor.author | TATLISUMAK, T. | |
dc.contributor.author | THIJS, V. N. | |
dc.contributor.author | TIEDT, S. | |
dc.contributor.author | TRAYLOR, M. | |
dc.contributor.author | WALDENBERGER, M. | |
dc.contributor.author | WALTERS, M. | |
dc.contributor.author | ZHAO, W. | |
dc.contributor.author | BONCORAGLIO, G. | |
hal.structure.identifier | Bordeaux population health [BPH] | |
dc.contributor.author | DEBETTE, Stephanie | |
dc.contributor.author | JERN, C. | |
dc.contributor.author | LEVI, C. | |
dc.contributor.author | MARKUS, H. | |
dc.contributor.author | MESCHIA, J. | |
dc.contributor.author | ROLFS, A. | |
dc.contributor.author | ROTHWELL, P. | |
dc.contributor.author | SALEHEEN, D. | |
dc.contributor.author | SESHADRI, Sudha | |
dc.contributor.author | SHARMA, P. | |
dc.contributor.author | SUDLOW, C. | |
dc.contributor.author | WORRALL, B. | |
dc.contributor.author | STINE, O. C. | |
dc.contributor.author | KITTNER, S. J. | |
dc.contributor.author | MITCHELL, B. D. | |
dc.date.accessioned | 2020-11-02T09:32:50Z | |
dc.date.available | 2020-11-02T09:32:50Z | |
dc.date.issued | 2018-11-02 | |
dc.identifier.issn | 1932-6203 (Electronic) 1932-6203 (Linking) | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/11564 | |
dc.description.abstractEn | BACKGROUND AND PURPOSE: Polymorphisms in coagulation genes have been associated with early-onset ischemic stroke. Here we pursue an a priori hypothesis that genetic variation in the endothelial-based receptors of the thrombomodulin-protein C system (THBD and PROCR) may similarly be associated with early-onset ischemic stroke. We explored this hypothesis utilizing a multi-stage design of discovery and replication. METHODS: Discovery was performed in the Genetics-of-Early-Onset Stroke (GEOS) Study, a biracial population-based case-control study of ischemic stroke among men and women aged 15-49 including 829 cases of first ischemic stroke (42.2% African-American) and 850 age-comparable stroke-free controls (38.1% African-American). Twenty-four single-nucleotide-polymorphisms (SNPs) in THBD and 22 SNPs in PROCR were evaluated. Following LD pruning (r2>/=0.8), we advanced uncorrelated SNPs forward for association analyses. Associated SNPs were evaluated for replication in an early-onset ischemic stroke population (onset-age<60 years) consisting of 3676 cases and 21118 non-stroke controls from 6 case-control studies. Lastly, we determined if the replicated SNPs also associated with older-onset ischemic stroke in the METASTROKE data-base. RESULTS: Among GEOS Caucasians, PROCR rs9574, which was in strong LD with 8 other SNPs, and one additional independent SNP rs2069951, were significantly associated with ischemic stroke (rs9574, OR = 1.33, p = 0.003; rs2069951, OR = 1.80, p = 0.006) using an additive-model adjusting for age, gender and population-structure. Adjusting for risk factors did not change the associations; however, associations were strengthened among those without risk factors. PROCR rs9574 also associated with early-onset ischemic stroke in the replication sample (OR = 1.08, p = 0.015), but not older-onset stroke. There were no PROCR associations in African-Americans, nor were there any THBD associations in either ethnicity. CONCLUSION: PROCR polymorphisms are associated with early-onset ischemic stroke in Caucasians. | |
dc.language.iso | EN | en_US |
dc.subject.en | VINTAGE | |
dc.title.en | Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke | |
dc.title.alternative | PLoS One | en_US |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.1371/journal.pone.0206554 | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Santé publique et épidémiologie | en_US |
dc.identifier.pubmed | 30383853 | en_US |
bordeaux.journal | PLoS ONE | en_US |
bordeaux.page | e0206554 | en_US |
bordeaux.volume | 13 | en_US |
bordeaux.hal.laboratories | Bordeaux Population Health Research Center (BPH) - UMR 1219 | en_US |
bordeaux.issue | 11 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
hal.identifier | hal-03164563 | |
hal.version | 1 | |
hal.date.transferred | 2021-03-10T08:16:21Z | |
hal.export | true | |
bordeaux.COinS | ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS%20ONE&rft.date=2018-11-02&rft.volume=13&rft.issue=11&rft.spage=e0206554&rft.epage=e0206554&rft.eissn=1932-6203%20(Electronic)%201932-6203%20(Linking)&rft.issn=1932-6203%20(Electronic)%201932-6203%20(Linking)&rft.au=COLE,%20J.%20W.&XU,%20H.&RYAN,%20K.&JAWOREK,%20T.&DUEKER,%20N.&rft.genre=article |
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