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Volume 158, Issue 5, Pages 784.e1-784.e6 (November 2009)


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The relation between platelet reactivity and glycemic control in diabetic patients with cardiovascular disease on maintenance aspirin and clopidogrel therapy

Anand Singla, MD, Mark J. Antonino, BS, Kevin P. Bliden, BS, Udaya S. Tantry, PhD, Paul A. Gurbel, MDCorresponding Author Informationemail address

Received 15 June 2009; accepted 14 August 2009.

Background

High platelet reactivity (HPR) during aspirin and clopidogrel therapy in patients with diabetes has been reported and may affect outcomes. However, the relation of platelet reactivity to glycemic control is less studied in patients on dual antiplatelet therapy.

Methods

Platelet aggregation (PA) in response to 5 and 20 μmol/L adenosine diphosphate (ADP) was compared in type 2 diabetic (n = 36) and nondiabetic patients (n = 35) undergoing elective stenting on aspirin and clopidogrel maintenance therapy. The relation of glycosylated hemoglobin (HbA1c) <7 g/dL (n = 16) and HbA1c ≥7 g/dL (n = 20) on PA was examined. High platelet reactivity was defined as >46% for 5 μmol/L ADP-induced and >59% for 20 μmol/L ADP-induced PA.

Results

Diabetic patients had higher 5 and 20 μmol/L ADP-induced PA than nondiabetic patients (45 ± 17 vs 33 ± 12, P = .009 and 52 ± 19 vs 40 ± 12, P = .004, respectively). Diabetic patients with HbA1c ≥7.0 g/dL had significantly higher 5 and 20 μmol/L ADP-induced PA versus patients with diabetes with HbA1c <7.0 g/dL (54 ± 15 vs 34 ± 14, P < .001 and 62 ± 14 vs 40 ± 17, P < .001, respectively). Among diabetic patients with HbA1c ≥7 g/dL, the prevalence of HPR was 65% and 60%; and among diabetic patients with HbA1c <7 g/dL, the prevalence of HPR was 19% and 13% as measured by 5 and 20 μmol/L ADP-induced PA, respectively. A correlation was present between 5 and 20 μmol/L ADP-induced PA and HbA1c (r = 0.60 and 0.62, P = .0001, respectively).

Conclusion

An important relation exists between glycemic control and platelet reactivity in patients with type 2 diabetes mellitus treated with dual antiplatelet therapy. Poorly controlled patients with diabetes have the greatest platelet reactivity and may require alternative antiplatelet strategies, and further clinical investigations are warranted.

Sinai Center for Thrombosis Research, Baltimore, MD

Corresponding Author InformationReprint requests: Paul A. Gurbel, MD, Sinai Center for Thrombosis Research 2401 W. Belvedere Ave, Baltimore, MD 21215.

PII: S0002-8703(09)00640-1

doi:10.1016/j.ahj.2009.08.013


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