FGL1 as a modulator of plasma D-dimer levels: exome-wide marker analysis of plasma tPA, PAI-1 and D-dimer
dc.rights.license | open | en_US |
dc.contributor.author | THIBORD, Florian | |
dc.contributor.author | SONG, Ci | |
dc.contributor.author | PATTEE, Jack | |
dc.contributor.author | RODRIGUEZ, Benjamin A. T. | |
dc.contributor.author | CHEN, Ming-Huei | |
dc.contributor.author | O'DONNELL, Christopher J. | |
dc.contributor.author | KLEBER, Marcus E. | |
dc.contributor.author | DELGADO, Graciela E. | |
dc.contributor.author | GUO, Xiuqing | |
dc.contributor.author | YAO, Jie | |
dc.contributor.author | TAYLOR, Kent D. | |
dc.contributor.author | OZEL, Ayse Bilge | |
dc.contributor.author | BRODY, Jennifer A. | |
dc.contributor.author | MCKNIGHT, Barbara | |
dc.contributor.author | GYORGY, Beata | |
dc.contributor.author | SIMONSICK, Eleanor | |
dc.contributor.author | LEONARD, Hampton L. | |
dc.contributor.author | CARRASQUILLA, German D. | |
dc.contributor.author | GUINDO-MARTINEZ, Marta | |
dc.contributor.author | SILVEIRA, Angela | |
dc.contributor.author | TEMPRANO-SAGRERA, Gerard | |
dc.contributor.author | YANEK, Lisa R. | |
dc.contributor.author | BECKER, Diane M. | |
dc.contributor.author | MATHIAS, Rasika A. | |
dc.contributor.author | BECKER, Lewis C. | |
dc.contributor.author | RAFFIELD, Laura M. | |
dc.contributor.author | KILPELAINEN, Tuomas O. | |
dc.contributor.author | GRARUP, Niels | |
dc.contributor.author | PEDERSEN, Oluf | |
dc.contributor.author | HANSEN, Torben | |
dc.contributor.author | LINNEBERG, Allan | |
dc.contributor.author | HAMSTEN, Anders | |
dc.contributor.author | WATKINS, Hugh | |
dc.contributor.author | SABATER-LLEAL, Maria | |
dc.contributor.author | NALLS, Mike A. | |
hal.structure.identifier | Bordeaux population health [BPH] | |
dc.contributor.author | TREGOUET, David-Alexandre | |
dc.contributor.author | MORANGE, Pierre-Emmanuel | |
dc.contributor.author | PSATY, Bruce M. | |
dc.contributor.author | TRACY, Russel P. | |
dc.contributor.author | SMITH, Nicholas L. | |
dc.contributor.author | DESCH, Karl C. | |
dc.contributor.author | CUSHMAN, Mary | |
dc.contributor.author | ROTTER, Jerome I. | |
dc.contributor.author | DE VRIES, Paul S. | |
dc.contributor.author | PANKRATZ, Nathan D. | |
dc.contributor.author | FOLSOM, Aaron R. | |
dc.contributor.author | MORRISON, Alanna C. | |
dc.contributor.author | MARZ, Winfried | |
dc.contributor.author | TANG, Weihong | |
dc.contributor.author | JOHNSON, Andrew D. | |
dc.date.accessioned | 2021-06-30T10:05:00Z | |
dc.date.available | 2021-06-30T10:05:00Z | |
dc.date.issued | 2021-04-20 | |
dc.identifier.issn | 1538-7836 (Electronic) 1538-7836 (Linking) | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/94937 | |
dc.description.abstractEn | BACKGROUND: Use of targeted exome-arrays with common, rare variants and functionally enriched variation has led to discovery of new genes contributing to population variation in risk factors. Plasminogen activator-inhibitor 1 (PAI-1), tissue plasminogen activator (tPA), and the plasma product D-dimer are important components of the fibrinolytic system. There have been few large-scale genome-wide or exome-wide studies of PAI-1, tPA and D-dimer. OBJECTIVES: We sought to discover new genetic loci contributing to variation in these traits using an exome-array approach. METHODS: Cohort level analyses and fixed effects meta-analyses of PAI-1 (n = 15,603), tPA (n = 6,876) and D-dimer (n = 19,306) from 12 cohorts of European ancestry with diverse study design were conducted, including single-variant analyses and gene-based burden testing. RESULTS: Five variants located in NME7, FGL1 and the fibrinogen locus, all associated with D-dimer levels, achieved genome-wide significance (P < 5 × 10(-8) ). Replication was sought for these 5 variants, as well as 45 well-imputed variants with P < 1 × 10(-4) in the discovery using an independent cohort. Replication was observed for 3 out of the 5 significant associations, including a novel and uncommon (0.013 allele frequency) coding variant p.Trp256Leu in FGL1 (Fibrinogen-Like-1) with increased plasma D-dimer levels. Additionally, a candidate-gene approach revealed a suggestive association for a coding variant (rs143202684-C) in SERPINB2, and suggestive associations with consistent effect in the replication analysis include an intronic variant (rs11057830-A) in SCARB1 associated with increased D-dimer levels. CONCLUSION: This work provides new evidence for a role of FGL1 in hemostasis. | |
dc.language.iso | EN | en_US |
dc.subject.en | Computational biology | |
dc.subject.en | Exome | |
dc.subject.en | Fibrinogen | |
dc.subject.en | Fibrinolysis | |
dc.subject.en | Genetic association study | |
dc.title.en | FGL1 as a modulator of plasma D-dimer levels: exome-wide marker analysis of plasma tPA, PAI-1 and D-dimer | |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.1111/jth.15345 | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Santé publique et épidémiologie | en_US |
dc.identifier.pubmed | 33876560 | en_US |
bordeaux.journal | Journal of Thrombosis and Haemostasis | en_US |
bordeaux.hal.laboratories | Bordeaux Population Health Research Center (BPH) - UMR 1219 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.institution | INSERM | en_US |
bordeaux.team | VINTAGE | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
hal.identifier | hal-03274625 | |
hal.version | 1 | |
hal.date.transferred | 2021-06-30T10:05:06Z | |
hal.export | true | |
bordeaux.COinS | ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Thrombosis%20and%20Haemostasis&rft.date=2021-04-20&rft.eissn=1538-7836%20(Electronic)%201538-7836%20(Linking)&rft.issn=1538-7836%20(Electronic)%201538-7836%20(Linking)&rft.au=THIBORD,%20Florian&SONG,%20Ci&PATTEE,%20Jack&RODRIGUEZ,%20Benjamin%20A.%20T.&CHEN,%20Ming-Huei&rft.genre=article |
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