Integrated GWAS and Gene Expression Suggest ORM1 as a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk

Author:

Lopez Sonia1ORCID,Martinez-Perez Angel1ORCID,Rodriguez-Rius Alba1,Viñuela Ana2,Brown Andrew A.3,Martin-Fernandez Laura1456,Vilalta Noelia7,Arús Marc7,Panousis Nikolaos I.89,Buil Alfonso10,Sabater-Lleal Maria111,Souto Juan Carlos7,Dermitzakis Emmanouil T.9,Soria Jose Manuel1

Affiliation:

1. Genomics of Complex Diseases Unit, Research Institute Hospital de la Santa Creu i Sant Pau, IIB Sant Pau, Barcelona, Spain

2. Biosciences Institute, Faculty of Medicine, Newcastle University, Newcastle Upon Tyne, United Kingdom

3. Population Health and Genomics, University of Dundee, Dundee, Scotland, United Kingdom

4. Fundación Española de Trombosis y Hemostasia (FETH), Madrid, Spain

5. Congenital Coagulopathies Laboratory, Banc de Sang i Teixits, Barcelona, Spain

6. Transfusional Medicine, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona (VHIR-UAB), Barcelona, Spain

7. Haemostasis and Thrombosis Unit, Department of Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

8. Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, South Cambridgeshire, United Kingdom

9. Department of Genetic Medicine and Development, University of Geneva, Geneva, Switzerland

10. Institute of Biological Psychiatry, Mental Health Sct. Hans Hospital, Roskilde, Denmark

11. Cardiovascular Medicine Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden

Abstract

Plasma cell-free DNA (cfDNA) is a surrogate marker of neutrophil extracellular traps (NETs) that contribute to immunothrombosis. There is growing interest about the mechanisms underlying NET formation and elevated cfDNA, but little is known about the factors involved. We aimed to identify genes involved in the regulation of cfDNA levels using data from the Genetic Analysis of Idiopathic Thrombophilia (GAIT-2) Project.Imputed genotypes, whole blood RNA-Seq data, and plasma cfDNA quantification were available for 935 of the GAIT-2 participants from 35 families with idiopathic thrombophilia. We performed heritability and GWAS analysis for cfDNA. The heritability of cfDNA was 0.26 (p = 3.7 × 10−6), while the GWAS identified a significant association (rs1687391, p = 3.55 × 10−10) near the ORM1 gene, on chromosome 9. An eQTL (expression quantitative trait loci) analysis revealed a significant association between the lead GWAS variant and the expression of ORM1 in whole blood (p = 6.14 × 10−9). Additionally, ORM1 expression correlated with levels of cfDNA (p = 4.38 × 10−4). Finally, genetic correlation analysis between cfDNA and thrombosis identified a suggestive association (ρ g = 0.43, p = 0.089).All in all, we show evidence of the role of ORM1 in regulating cfDNA levels in plasma, which might contribute to the susceptibility to thrombosis through mechanisms of immunothrombosis.

Funder

Instituto de Salud Carlos III and Fondo de Investigación Sanitaria

Grupo Consolidado Generalitat de Catalunya

CERCA Programme/Generalitat de Catalunya

Fundación Española de Trombosis y Hemostasia

Activa'TT por la Salud

Agència de Gestió d'ajuts Universitaris i de Recerca

Miguel Servet contract from the ISCIII

European Social Fund

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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