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Updated: May 23, 2026

RNA-seq Analysis of Transcriptomes in Thrombin-treated and Control Human Pulmonary Microvascular Endothelial Cells
Published on: February 13, 2013
Gene expression integration and similarity score-based modeling improve risk stratification in idiopathic venous
Pol Ezquerra-Condeminas1, Angel Martinez-Perez2, Cedric Howald3
1Unit of Genomics of Complex Disease, Institut de Recerca Sant Pau (IR Sant Pau), Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain; B2SLab, Institut de Recerca i Innovació en Salut (IRIS), Universitat Politècnica de Catalunya, Barcelona, Spain.
Background:
Idiopathic venous thromboembolism (VTE) occurs in the absence of provoking factors, limiting the efficacy of current risk stratification. In parallel, the lack of integration between transcriptomic data and established risk factors prevents the identification of individuals with a high baseline predisposition.
Objectives:
We aimed to improve risk stratification of idiopathic VTE beyond traditional clinical models by developing a similarity-based risk score that integrates transcriptomic profiles with conventional risk factors.
Methods:
We analyzed 790 individuals from the Genetic Analysis of Idiopathic Thrombophilia 2 familial study, including 70 participants with prior idiopathic VTE. Whole-blood RNA sequencing, known genetic variants, and clinical variables were integrated using supervised machine learning models (Elastic Net and XGBoost). Predictive gene expression features were evaluated through enrichment analyses. A unified similarity score combining both models was developed to identify control individuals who shared transcriptomic and clinical profiles with VTE cases.
Results:
In both models, von Willebrand factor abundance was the strongest predictor of VTE, followed by clinical factors (body mass index, ABO alleles, and age) and expression of 494 genes, including STS, FAM13A, GPRIN1, FLVCR2, FAM177B, and several long noncoding RNAs not previously linked to thrombosis. Known thrombosis-associated genes such as UQCRC2 and PRKRA were also identified. Significant enrichment was observed for cardiomyopathic Kyoto Encyclopedia of Genes and Genomes pathways and renal Human Protein Atlas terms. Similarity-based risk score construction improved classification, with 74% of VTE cases and 23% of controls assigned to the risk zone.
Conclusion:
Multivariate integration via machine learning enhances VTE risk stratification, identifying novel transcriptomic signatures and lncRNA biomarkers that offer new strategies for VTE personalized prevention.
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