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Get Free AccessUnlabelled Box Essentials • Risk of venous thrombosis (VT) related to common genetic variants in those aged 70+ is unknown. • We studied Factor V Leiden, prothrombin mutation, non‐O blood group and family history (FH) of VT. • Risk of VT was increased 2.2‐, 1.4‐, 1.3‐ and 2.1‐fold respectively. • FH is easy to obtain and can be implemented in clinical decision rules of VT risk in the elderly. Acknowledgements The authors wish to thank the directors of the anticoagulation clinics of Leiden (F. J. M. van der Meer) and Haarlem (E. van Meegen) who made the recruitment of patients in Leiden and Haarlem possible. We thank the directors of the Ultrasound Unit of the Radiology Department (N. Sturtevant) and the Vascular Laboratory (G. Steinthorsson) at Fletcher Allen Health Care, University of Vermont, and the study examiner and project coordinator, R. Abel. We thank all the individuals who participated in the AT‐AGE study. This study was supported by grants from the Netherlands Heart Foundation (grant no: 2009B50) and the Leducq Foundation, Paris, France, for the development of Transatlantic Networks of Excellence in Cardiovascular Research. Role of the Sponsor: The Netherlands Heart Foundation and the Fondation Leducq did not play a role in the: design and conduct of the study; collection, management, analysis and interpretation of the data; or preparation, review or approval of the manuscript. Netherlands Heart Foundation 2009B50 Leducq Foundation Click to hear Prof. Reitsma discuss genetic risk factors of arterial and venous thrombosis Summary: Background As the incidence of venous thrombosis (VT) increases steeply with age and the number of elderly people is on the rise, studies of VT in this age group are important. Objectives We aimed to study the associations of common genetic risk factors (i.e. the factor V Leiden and prothrombin G20210A mutations, non‐O blood group and family history of VT) with risk of a first VT in older age (> 70 years). Methods Four hundred and one consecutive cases with a first‐time thrombosis and 431 controls (all ≥ 70 years) were included in the AT‐AGE case–control study. Information on risk factors for VT, including family history of VT in first‐degree relatives, was obtained by interview. Unprovoked VT was defined as thrombosis not related to surgery, fracture, plaster cast or immobility within 3 months prior to VT. Results The risk of VT was 2.2‐fold increased in factor V Leiden carriers (95% confidence interval [CI], 1.2–3.9), 1.4‐fold increased in prothrombin mutation carriers (95% CI, 0.5–3.9), and 1.3‐fold increased in those with non‐O blood group (95% CI, 1.0–1.8). Positive family history of VT was associated with a 2.1‐fold increased risk of VT (95% CI, 1.5–3.1). The highest risk of VT was found in individuals who had both a positive family history and were carriers of one of the two prothrombotic mutations. Conclusions Genetic factors clearly related to VT in younger populations were also risk factors in older age and a positive family history was also important in this age group.
Zeki Karasu, M.J. Engbers, Mary Cushman, Frits R. Rosendaal, Astrid van Hylckama Vlieg (2016). Genetic risk factors for venous thrombosis in the elderly in a case–control study. Journal of Thrombosis and Haemostasis, 14(9), pp. 1759-1764, DOI: 10.1111/jth.13409.
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Type
Article
Year
2016
Authors
5
Datasets
0
Total Files
0
Language
English
Journal
Journal of Thrombosis and Haemostasis
DOI
10.1111/jth.13409
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