Subtle renal dysfunction and bleeding risk in atrial fibrillation : Symmetric dimethylarginine predicts HAS-BLED score
Procter, Nathan, Ball, Jocasta, Heresztyn, Tamila, Nooney, Vivek, Liu, Saifei, Chong, Cher-Rin, Ngo, Doan, Isenberg, Jeffrey, Chirkov, Yuliy, Stewart, Simon and Horowitz, John. (2015) Subtle renal dysfunction and bleeding risk in atrial fibrillation : Symmetric dimethylarginine predicts HAS-BLED score. American Journal of Cardiovascular Disease. 5(2), pp. 101 - 109.
|Authors||Procter, Nathan, Ball, Jocasta, Heresztyn, Tamila, Nooney, Vivek, Liu, Saifei, Chong, Cher-Rin, Ngo, Doan, Isenberg, Jeffrey, Chirkov, Yuliy, Stewart, Simon and Horowitz, John|
Background: Risk of substantial haemorrhage represents a critically important limitation to effective anti-thrombotic treatment in patients with atrial fibrillation (AF). While it is known that this risk is increased in anticoagulated patients either in the presence of anti-aggregatory drugs or concomitant renal insufficiency, there are currently few data on the potential interactions between endogenous platelet aggregability and bleeding risk. Objective: We therefore evaluated in a cohort of AF patients: (1), the putative relationship between platelet aggregability and HAS-BLED score; (2), the potential biochemical bases for such a relationship. Methods: Patients were included as part of SAFETY, a randomised controlled trial evaluating outpatient management of AF patients. Platelet response to ADP was evaluated via whole blood impedance aggregometry; clinical and biochemical correlates of platelet aggregation were sought via univariate and multivariate analysis. Results: Platelet aggregation correlated inversely (r=-0.220, p < 0.05) with HAS-BLED score. Univariate biochemical correlates of decreased platelet aggregation were plasma concentrations of symmetric dimethylarginine (SDMA) and asymmetric dimethylarginine (ADMA). On multivariate analyses, plasma SDMA concentration (β=-0.318, p < 0.01), platelet content of thioredoxin-interacting protein (Txnip, β=0.261, p < 0.05) and plasma thrombospondin-1 (TSP-1, β=0.249, p < 0.05) concentration were predictive of platelet ADP response. Consistent with previous reports, plasma SDMA concentrations were strongly and inversely correlated with estimated glomerular filtration rate (eGFR, r=-0.780, p < 0.001). Conclusions: These data therefore suggest that (1), physiologically impaired, like pharmacologically impaired, platelet aggregability may increase bleeding risk in anticoagulated AF patients; (2), the biochemical basis for this may include impaired effects of nitric oxide (via Txnip, TSP-1) but also concomitant renal dysfunction.
|Journal||American Journal of Cardiovascular Disease|
|Journal citation||5 (2), pp. 101 - 109|
|Web address (URL)||https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539096/|
|Page range||101 - 109|
|Research Group||Mary MacKillop Institute for Health Research|
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