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GWAS Study

Genetic determinants of apixaban plasma levels and their relationship to bleeding and thromboembolic events.

Attelind S, Hallberg P, Wadelius M et al.

36186466 PubMed ID
GWAS Study Type
1325 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AS
Attelind S
HP
Hallberg P
WM
Wadelius M
HA
Hamberg AK
SA
Siegbahn A
GC
Granger CB
LR
Lopes RD
AJ
Alexander JH
WL
Wallentin L
EN
Eriksson N
Chapter II

Abstract

Summary of the research findings

Apixaban is a direct oral anticoagulant, a factor Xa inhibitor, used for the prevention of ischemic stroke in patients with atrial fibrillation. Despite using recommended dosing a few patients might still experience bleeding or lack of efficacy that might be related to inappropriate drug exposure. We conducted a genome-wide association study using data from 1,325 participants in the pivotal phase three trial of apixaban with the aim to identify genetic factors affecting the pharmacokinetics of apixaban. A candidate gene analysis was also performed for pre-specified variants in ABCB1, ABCG2, CYP3A4, CYP3A5, and SULT1A1, with a subsequent analysis of all available polymorphisms within the candidate genes. Significant findings were further evaluated to assess a potential association with clinical outcome such as bleeding or thromboembolic events. No variant was consistently associated with an altered apixaban exposure on a genome-wide level. The candidate gene analyses showed a statistically significant association with a well-known variant in the drug transporter gene ABCG2 (c.421G > T, rs2231142). Patients carrying this variant had a higher exposure to apixaban [area under the curve (AUC), beta = 151 (95% CI 59-243), p = 0.001]. On average, heterozygotes displayed a 5% increase of AUC and homozygotes a 17% increase of AUC, compared with homozygotes for the wild-type allele. Bleeding or thromboembolic events were not significantly associated with ABCG2 rs2231142. This large genome-wide study demonstrates that genetic variation in the drug transporter gene ABCG2 is associated with the pharmacokinetics of apixaban. However, the influence of this finding on drug exposure was small, and further studies are needed to better understand whether it is of relevance for ischemic and bleeding events.

1,243 European ancestry individuals, 8 African American or Afro-Caribbean individuals, 71 Asian ancestry individuals, 3 unknown ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

1325
Total Participants
GWAS
Study Type
No
Replicated
European, African American or Afro-Caribbean, Asian unspecified
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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