Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk : The Tromso Study

Journal article


Sejrup, Joakim K., Morelli, Vania M., Løchen, Maja-Lisa, Njølstad, Inger, Mathiesen, Ellisiv B., Wilsgaard, Tom, Hansen, John-Bjarne and Brækkan, Sigrid K.. (2020). Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk : The Tromso Study. Research and Practice in Thrombosis and Haemostasis. 4(2), pp. 247-254. https://doi.org/10.1002/rth2.12306
AuthorsSejrup, Joakim K., Morelli, Vania M., Løchen, Maja-Lisa, Njølstad, Inger, Mathiesen, Ellisiv B., Wilsgaard, Tom, Hansen, John-Bjarne and Brækkan, Sigrid K.
Abstract

Background
The risk of venous thromboembolism (VTE) is increased after a myocardial infarction (MI). Some prothrombotic genotypes associated with VTE have also been associated with risk of MI. Whether prothrombotic single‐nucleotide polymorphisms (SNPs) further increase the risk of VTE in MI patients is scarcely investigated.

Aim
To study the combined effect of MI and prothrombotic SNPs on the risk of VTE.

Methods
Cases with incident VTE (n = 641) and a randomly sampled subcohort weighted for age (n = 1761) were identified from the 4 to 6 surveys of the Tromsø Study (1994‐2012). DNA was genotyped for rs8176719 (ABO), rs6025 (F5), rs1799963 (F2), rs2066865 (FGG), and rs2036914 (F11). Hazard ratios (HRs) for VTE with 95% confidence intervals (CIs) were estimated by categories of risk alleles and MI status.

Results
Patients with MI had a 1.4‐fold increased risk of VTE, and adjustments for the 5 SNPs, either alone or in combination, did not affect this relationship (adjusted HR, 1.52; 95% CI, 1.12‐2.07). In subjects without MI, an increased risk of VTE was observed for each of the individual SNPs (≥1 vs. 0 risk alleles), and the risk increased linearly with increasing number of risk alleles in the 5‐SNP score. The combination of MI and prothrombotic genotypes, either as individual SNPs or in the 5‐SNP score, did not result in an excess risk of VTE.

Conclusion
The relationship between MI and VTE was not explained by these 5 prothrombotic genotypes. Prothrombotic genotypes did not yield an excess risk of VTE in patients with MI.

Keywordsepidemiology; genetics; myocardial infarction; pulmonary embolism; risk factors; thromboembolism; venous
Year2020
JournalResearch and Practice in Thrombosis and Haemostasis
Journal citation4 (2), pp. 247-254
PublisherWiley-Blackwell Publishing Ltd.
ISSN2475-0379
Digital Object Identifier (DOI)https://doi.org/10.1002/rth2.12306
Open accessPublished as ‘gold’ (paid) open access
Research or scholarlyResearch
Page range247-254
Publisher's version
License
File Access Level
Open
Output statusPublished
Publication dates
Online27 Jan 2020
Publication process dates
Accepted26 Dec 2019
Deposited30 Apr 2021
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