Key result
Insulin-treated diabetes is linked to higher platelet aggregation vs non-insulin treatment on steady DAPT.
Why the study?
The impact of insulin therapy on platelet dysfunction in patients with type 2 diabetes mellitus treated with P2Y12 antagonists was unknown.
Does insulin therapy affect platelet aggregation in patients with type 2 diabetes mellitus and coronary artery disease on dual antiplatelet therapy?
Observational (n=266)
Does insulin therapy affect platelet aggregation in patients with type 2 diabetes mellitus and coronary artery disease on dual antiplatelet therapy?
This study demonstrates that insulin-treated patients with type 2 diabetes on dual antiplatelet therapy have higher P2Y12-dependent platelet aggregation, which may explain their increased atherothrombotic risk.
OBJECTIVES This study sought to assess the influence of type 2 diabetes mellitus (T2DM) and the impact of hypoglycemic treatment (insulin vs. noninsulin) on platelet function profiles in patients treated with dual oral antiplatelet therapy. BACKGROUND Insulin inhibits platelet aggregation by suppressing the P2Y12 pathway. However, T2DM patients have a loss of responsiveness to insulin that leads to upregulation of the P2Y12 pathway, increased platelet reactivity, and reduced responsiveness to antiplatelet agents. Patients with insulin-treated diabetes mellitus (ITDM) have a more advanced disease status and higher atherothrombotic risk compared with non-ITDM (NITDM). However, the impact of insulin therapy on platelet dysfunction in patients treated with P2Y12 antagonists is unknown. METHODS A total of 201 T2DM and 65 nondiabetic patients with coronary artery disease in a steady phase of aspirin and clopidogrel treatment were studied. Platelet aggregation was assessed using agonists specific (6 and 20 microM adenosine diphosphate [ADP]) and nonspecific (6 microg/ml collagen and 20 microM epinephrine) for the P2Y12 pathway. High shear-induced platelet reactivity was assessed by means of the PFA-100 system (Dade-Behring International, Miami, Florida). RESULTS The T2DM patients had platelet aggregation and shear-induced platelet function significantly increased compared with nondiabetic patients using all assays. Platelet aggregation was increased in ITDM (n = 68) compared with NITDM (n = 133) patients after P2Y12-specific stimuli. Insulin treatment was the strongest predictor of ADP-induced aggregation. Platelet function profiles were similar between ITDM and NITDM using assays nonspecific to the P2Y12 pathway. Platelet dysfunction was independent of glycemic control and inflammatory status. CONCLUSIONS The P2Y12-dependent and -independent pathways of platelet reactivity are altered in T2DM compared with nondiabetic patients, and ITDM have greater ADP-induced platelet aggregation compared with NITDM.
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Angiolillo et al. (2006) conducted an observational in Type 2 diabetes mellitus and coronary artery disease (n=266). Insulin treatment vs. Non-insulin treatment or nondiabetic was evaluated on Platelet aggregation and shear-induced platelet function. Insulin-treated type 2 diabetes was associated with greater ADP-induced platelet aggregation compared with non-insulin treatment in patients on steady dual antiplatelet therapy.
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