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Updated: Jun 13, 2025

The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Direct oral anticoagulants do not affect miR-27a-3p expression, a regulator of coagulation cascade, in atrial
Georgia Ragia1,2,3, Myria Pallikarou4,5, Chrysoula Michou4
1Laboratory of Pharmacology, Medical School, Democritus University of Thrace, Dragana Campus, Alexandroupolis, 68100, Greece. gragia@pharm.auth.gr.
Abstract:
miR-27a-3p targets several proteins on the coagulation cascade. The potential effect of direct oral anticoagulants (DOACs) treatment on miR-27a-3p expression and their broader regulative effect on anticoagulation is unknown. Fifty-nine atrial fibrillation patients treated with rivaroxaban (n = 19), apixaban (n = 27) or dabigatran (n = 13), were included in the study. miR-27a-3p expression was analyzed at baseline and after 7 days of DOAC therapy by using a predesigned TaqMan assay. Relative quantitation of miR-27a-3p expression was calculated and compared in pooled population and in different sample groups. DOAC therapy did not alter miR-27a-3p expression (0.80 fold-change, p = 0.486, pooled population; 0.839 fold-change, p = 0.706, rivaroxaban; 0.921 fold-change, p = 0.800, apixaban; 0.733 fold-change, p = 0.540, dabigatran). miR-27a-3p expression did not differ between controls and bleeding cases (0.833 fold-change, p = 0.588, baseline). Female patients had a trend towards increased baseline expression (1.564 fold-change, p = 0.177) and reduced expression after DOAC treatment (0.683 fold-change, p = 0.243) compared to male patients. Despite the regulatory role of miR-27a-3p on coagulation cascade, treatment with DOACs did not alter its expression. However, additional studies in different ethnic groups are necessary to fully elucidate the effect, if any, of DOACs on miR-27a-3p expression.
Insights
Direct oral anticoagulants (DOACs) did not change miR-27a-3p expression in atrial fibrillation patients. This microRNA plays a role in the coagulation cascade, but DOACs did not affect its levels in this study.
Area of Science:
- Biochemistry
- Genetics
- Pharmacology
Background:
- MicroRNA-27a-3p (miR-27a-3p) is known to target proteins involved in the coagulation cascade.
- The impact of direct oral anticoagulants (DOACs) on miR-27a-3p expression and its subsequent effect on anticoagulation remains largely unexplored.
Purpose of the Study:
- To investigate the effect of DOAC therapy on miR-27a-3p expression in patients with atrial fibrillation.
- To explore potential correlations between miR-27a-3p expression and anticoagulation status or bleeding events.
Main Methods:
- Fifty-nine atrial fibrillation patients receiving rivaroxaban, apixaban, or dabigatran were enrolled.
- miR-27a-3p expression was quantified using TaqMan assays at baseline and after 7 days of DOAC treatment.
- Expression levels were compared between treatment groups, sexes, and bleeding cases versus controls.
Main Results:
- DOAC therapy did not significantly alter miR-27a-3p expression in the pooled patient population or in individual treatment groups.
- No significant difference in miR-27a-3p expression was observed between patients who experienced bleeding events and controls.
- A trend towards higher baseline miR-27a-3p expression in females was noted, with a subsequent decrease after DOAC treatment compared to males.
Conclusions:
- Treatment with common DOACs does not appear to affect miR-27a-3p expression in atrial fibrillation patients.
- Further research, including diverse ethnic groups, is warranted to fully understand the relationship between DOACs and miR-27a-3p.
- The role of miR-27a-3p in anticoagulation and its modulation by DOACs requires additional investigation.
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