PMID- 24152567 OWN - NLM STAT- MEDLINE DCOM- 20140701 LR - 20181202 IS - 1473-5830 (Electronic) IS - 0954-6928 (Linking) VI - 24 IP - 8 DP - 2013 Dec TI - Effect of cilostazol addition or clopidogrel doubling on platelet function profiles in diabetic patients undergoing a percutaneous coronary intervention. PG - 690-7 LID - 10.1097/MCA.0000000000000026 [doi] AB - BACKGROUND: We investigated the pharmacodynamic effect of cilostazol addition (100 mg twice, Triple) or clopidogrel doubling (150 mg daily, Double) on standard dual antiplatelet therapy in type 2 diabetes mellitus (T2DM) patients with clopidogrel resistance undergoing a percutaneous coronary intervention. METHODS AND RESULTS: This was a prospective, randomized, cross-over platelet function study. Percent inhibition less than 20% was used as the cutoff value of clopidogrel resistance. After percutaneous coronary intervention, a total of 50 T2DM patients with clopidogrel resistance were assigned to receive cilostazol 100 mg twice daily or clopidogrel 150 mg daily for 28 days; afterwards, they received cross-over treatment for another 28 days. Eight patients were excluded because of side effects and follow-up loss. The platelet function test using VerifyNow was performed at three time points: at baseline (T0), 28 days after randomization (T1), and 28 days after cross-over treatment (T2).A total of 42 T2DM patients completed the study protocol. The clopidogrel resistance improved significantly following cilostazol addition or clopidogrel doubling treatment compared with baseline (52.9+/-27.0 in Triple, 45.4+/-16.8% in Double, P<0.001 in both). This effect continued after cross-over treatment (58.1+/-26.1 and 41.0+/-20.0%, respectively, both P<0.05). A head-to-head comparison between two groups showed a lower P2Y12 reaction unit (PRU) and higher percentage of platelet inhibition in the Triple than those in the Double group (PRU, 138.7+/-88.2 vs. 198.8+/-19.5, P=0.049; %platelet inhibition, 58.1+/-26.1 vs. 40.97+/-20.0, P=0.048). CONCLUSION: Adjunctive treatment with cilostazol in T2DM patients on standard dual antiplatelet therapy might be a more effective strategy for overcoming clopidogrel resistance than clopidogrel doubling treatment. FAU - Ha, Sang Jin AU - Ha SJ AD - aDepartment of Internal Medicine, School of Medicine, Division of Cardiology, Kyung Hee University bCardiovascular Center, Kyung Sang University, Seoul, Korea. FAU - Kim, Soo-Joong AU - Kim SJ FAU - Hwang, Seok-Jae AU - Hwang SJ FAU - Woo, Jong Shin AU - Woo JS FAU - Kim, Weon AU - Kim W FAU - Kim, Woo-Shik AU - Kim WS FAU - Kim, Kwon Sam AU - Kim KS FAU - Kim, Myeong Kon AU - Kim MK LA - eng PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - England TA - Coron Artery Dis JT - Coronary artery disease JID - 9011445 RN - 0 (Platelet Aggregation Inhibitors) RN - 0 (Tetrazoles) RN - A74586SNO7 (Clopidogrel) RN - N7Z035406B (Cilostazol) RN - OM90ZUW7M1 (Ticlopidine) SB - IM MH - Blood Platelets/*drug effects MH - Cilostazol MH - Clopidogrel MH - Coronary Angiography MH - Coronary Artery Disease/blood/complications/diagnosis/*therapy MH - Cross-Over Studies MH - Diabetes Mellitus, Type 2/blood/*complications/diagnosis MH - Drug Resistance MH - Drug Therapy, Combination MH - Humans MH - *Percutaneous Coronary Intervention/adverse effects MH - Platelet Aggregation Inhibitors/*administration & dosage/adverse effects MH - Platelet Function Tests MH - Prospective Studies MH - Republic of Korea MH - Tetrazoles/*administration & dosage/adverse effects MH - Ticlopidine/administration & dosage/adverse effects/*analogs & derivatives MH - Time Factors MH - Treatment Outcome EDAT- 2013/10/25 06:00 MHDA- 2014/07/02 06:00 CRDT- 2013/10/25 06:00 PHST- 2013/10/25 06:00 [entrez] PHST- 2013/10/25 06:00 [pubmed] PHST- 2014/07/02 06:00 [medline] AID - 10.1097/MCA.0000000000000026 [doi] PST - ppublish SO - Coron Artery Dis. 2013 Dec;24(8):690-7. doi: 10.1097/MCA.0000000000000026.