Key result
Single antiplatelet therapy after kidney transplantation linked to ~33% lower risk of MACE and mortality.
Why the study?
The study investigated the association of single antiplatelet therapy with the reduction of cardiovascular disease events in kidney transplant recipients.
Does single antiplatelet therapy reduce the composite of MACE and all-cause mortality in kidney transplant recipients?
Cohort (n=518)
No
Does single antiplatelet therapy reduce the composite of MACE and all-cause mortality in kidney transplant recipients?
Effect estimate: HR 0.67 (95% CI 0.45-0.99)
Absolute Event Rate: 24% vs 22%
p-value: p=0.046
Single antiplatelet therapy after kidney transplantation is associated with a lower risk of MACE and all-cause mortality in the overall cohort, but not in patients without known cardiovascular disease.
May warrant single antiplatelet therapy in kidney transplant recipients; hypothesis-generating and requires randomized confirmation.
Background:We investigated the association of single antiplatelet (AP) therapy with reduction of cardiovascular disease (CVD) events in kidney transplantation recipients (KTRs). Material/Methods:This retrospective single-center study included KTRs from our institution between 2015 and 2024.Patients receiving anticoagulation or dual AP therapy were excluded.Patients were divided into those receiving AP therapy after kidney transplantation (AP group) and those not receiving such therapy (NoAP group).A separate analysis was performed for patients without known CVD.The primary outcome was a composite of all-cause mortality and major adverse cardiovascular events (MACE).Major bleeding events were also recorded.Kaplan-Meier survival curves and Cox proportional hazards models were constructed. Results:Overall, 518 KTRs met the study criteria (175 AP, 343 NoAP).The AP group was significantly older and had higher prevalences of diabetes and coronary artery disease.Over a median follow-up of 52.5 months (interquartile range: 33.1-71.1),41 (24%) patients in the AP group and 76 (22%) patients in the NoAP group experienced the composite study outcome.After adjustment for confounders, AP therapy was independently associated with a lower risk of the outcome (hazard ratio 0.67, 95% confidence interval 0.45-0.99,P=0.046).AP therapy was not associated with major bleeding events.No significant association between AP therapy and outcomes was observed among patients without known CVD. Conclusions:AP therapy after kidney transplantation was associated with lower risk of the composite outcome (MACE and all-cause mortality) in the overall cohort.No significant association was observed among patients without known CVD.
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Christy et al. (2026) conducted a cohort in Kidney Transplantation (n=518). Single antiplatelet therapy vs. No antiplatelet therapy was evaluated on Composite of all-cause mortality and major adverse cardiovascular events (MACE) (HR 0.67, 95% CI 0.45-0.99, p=0.046). Single antiplatelet therapy after kidney transplantation was independently associated with a 33% lower risk of the composite outcome of MACE and all-cause mortality (HR 0.67).
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