Abstract | OBJECTIVE: RESEARCH DESIGN AND METHODS: T2DM patients were treated with TRIPLE (n = 41) or DOUBLE (n = 39) after percutaneous coronary intervention. Conventional aggregometry and VerifyNow were performed at baseline and at 30 days. The primary end point was absolute change in 20-μM ADP-induced maximal platelet aggregation (ΔMPA(20)) between baseline and switching values. RESULTS: TRIPLE versus DOUBLE showed greater ΔMPA(20) (22.9 ± 11.6 vs.12.7 ± 15.5%; difference, 10.2% [95% CI 4.2-16.3]; P < 0.001). Carriage of one (β coefficient, -5.4%; P = 0.162) and two CYP2C19 loss-of-function allele(s) (-8.3%; P = 0.007) were associated with lower ΔMPA(20) in DOUBLE-treated patients, but not in TRIPLE-treated patients. CONCLUSIONS: Among T2DM patients, adding cilostazol achieves greater platelet inhibition compared with clopidogrel (150 mg/d), which is not influenced by genetic polymorphisms.
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Authors | Young-Hoon Jeong, Udaya S Tantry, Yongwhi Park, Tae Jung Kwon, Jeong Rang Park, Seok-Jae Hwang, Kevin P Bliden, Eun-Ha Koh, Choong Hwan Kwak, Jin-Yong Hwang, Sunjoo Kim, Paul A Gurbel |
Journal | Diabetes care
(Diabetes Care)
Vol. 35
Issue 11
Pg. 2194-7
(Nov 2012)
ISSN: 1935-5548 [Electronic] United States |
PMID | 22837373
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Platelet Aggregation Inhibitors
- Tetrazoles
- Clopidogrel
- Cilostazol
- Ticlopidine
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Topics |
- Cilostazol
- Clopidogrel
- Diabetes Mellitus, Type 2
(drug therapy, genetics, metabolism)
- Female
- Humans
- Male
- Percutaneous Coronary Intervention
(methods)
- Platelet Aggregation
(drug effects)
- Platelet Aggregation Inhibitors
(administration & dosage, therapeutic use)
- Polymorphism, Genetic
(genetics)
- Tetrazoles
(administration & dosage, therapeutic use)
- Ticlopidine
(administration & dosage, analogs & derivatives, therapeutic use)
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