Key result
DOACs and VKAs linked to lower stroke risk in diabetic NVAF, with DOACs reducing risk ~76%.
Why the study?
Does the use of anticoagulants, antiplatelet agents, and oral antidiabetic drugs reduce the risk of stroke in patients with Type 2 diabetes mellitus and nonvalvular atrial fibrillation?
Case-Control (n=838)
Does the use of anticoagulants, antiplatelet agents, and oral antidiabetic drugs reduce the risk of stroke in patients with Type 2 diabetes mellitus and nonvalvular atrial fibrillation?
Effect estimate: aOR 0.24 for DOACs, aOR 0.42 for VKAs (95% CI 0.15-0.40 for DOACs, 0.27-0.67 for VKAs)
In patients with T2DM and NVAF, DOACs and VKAs are associated with a significantly reduced risk of stroke, with DOACs showing no increased risk of hemorrhagic stroke compared to VKAs.
Supports anticoagulation consideration in T2DM-NVAF; leaves open prospective confirmation of stroke benefit.
Type 2 diabetes mellitus (T2DM) and atrial fibrillation are risk factors for stroke. The potential preventive effects of cardiovascular and antidiabetic treatments on stroke risk in patients with these diseases remain insufficiently documented. Sulfonylureas have also been reported to be associated with stroke. This study aimed to assess the risk of stroke according to the use of drugs (anticoagulants, antiplatelet agents, and oral antidiabetic drugs [OADs]) in patients with T2DM and nonvalvular atrial fibrillation (NVAF). Patients with a history of T2DM and NVAF were identified from two systematic registries: a registry of patients with stroke and a registry of patients with atrial fibrillation. Patients with stroke were randomly matched to patients without prior stroke events based on age, sex, body mass index, and index date. All treatments administered 12 months before the index date were documented. The associations between anticoagulants, antiplatelet agents, and OADs and stroke were assessed using multivariate conditional logistic models that yielded adjusted odds ratios (aORs) and 95 % confidence intervals, controlling for risk factors identified in the univariate comparison of cases and matched referents. Three-hundred and fifteen patients with stroke with both diabetes and NVAF were matched to 523 referents with both diabetes and NVAF but no history of stroke. The aORs for the use of drugs and stroke were 0.24 [0.15–0.40] for direct oral anticoagulants (DOACs), 0.42 [0.27–0.67] for vitamin K agonists (VKA), 0.80 [0.52–1.24] for antiplatelet agents, and 0.68 [0.45–1.02] for OADs. No significant associations were found between individual OAD use and stroke risk. Similar results were obtained for ischemic stroke. Only VKAs were significantly associated with hemorrhagic stroke (odds ratio = 4.25 [1.16–15.64]). Anticoagulant use was associated with a protective effect against the risk of stroke in patients with diabetes and NVAF, with no increase in the risk of hemorrhagic stroke for DOAC. No increased risk of stroke was observed because of any OAD, including sulfonylureas. • Unlike other oral antidiabetic drugs, an increased risk of stroke has been suggested for sulfonylureas • First study assessing stroke’ risk according to the use of anticoagulants, antiplatelet and oral antidiabetic drugs (OADs). • Anticoagulants and OADs were associated with a protective effect against stroke risk in patients with diabetes and NVAF. • Antiplatelet agents were associated with a favorable, but limited, trend for reduced risk of stroke • No increase in the risk of stroke was observed in the users of OADs, including sulfonylureas
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Grimaldi‐Bensouda et al. (2024) conducted a case-control in Type 2 diabetes mellitus and nonvalvular atrial fibrillation (n=838). Anticoagulants, antiplatelet agents, and oral antidiabetic drugs vs. Non-use was evaluated on Risk of stroke (aOR 0.24 for DOACs, aOR 0.42 for VKAs, 95% CI 0.15-0.40 for DOACs, 0.27-0.67 for VKAs). Direct oral anticoagulants (aOR 0.24; 95% CI 0.15-0.40) and vitamin K agonists (aOR 0.42; 95% CI 0.27-0.67) were associated with a reduced risk of stroke in patients with diabetes and NVAF.
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