共 41 条
Impact of impaired glucose tolerance on clopidogrel response in patients with coronary artery disease
被引:11
作者:

Ueno, Masafumi
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机构:
Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Fujita, Kosuke
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Yamamoto, Hiroyuki
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Ikeda, Tomoyuki
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Suga, Tatsuya
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Yamaji, Kenji
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Ikuta, Shinichiro
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Kobuke, Kazuhiro
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Iwanaga, Yoshitaka
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Angiolillo, Dominick J.
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Univ Florida, Coll Med Jacksonville, Jacksonville, FL USA Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan

Miyazaki, Shunichi
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Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan
机构:
[1] Kinki Univ, Fac Med, Dept Internal Med, Div Cardiol, Osakasayama, Osaka 5898511, Japan
[2] Univ Florida, Coll Med Jacksonville, Jacksonville, FL USA
关键词:
Impaired glucose tolerance;
Insulin resistance;
Clopidogrel;
Platelet function;
Coronary artery disease;
TYPE-2;
DIABETES-MELLITUS;
PLATELET REACTIVITY;
ANTIPLATELET THERAPY;
PPAR-GAMMA;
CARDIOVASCULAR OUTCOMES;
MYOCARDIAL-INFARCTION;
FASTING GLUCOSE;
INSULIN;
RISK;
PIOGLITAZONE;
D O I:
10.1007/s11239-015-1177-7
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Although patients with impaired glucose tolerance (IGT) are at increased atherothrombotic risk, it is unclear how antiplatelet drugs act in patients with IGT. The aim of this study was to investigate the pharmacodynamic response to clopidogrel in patients with IGT and insulin resistance (IR). A 75 g oral glucose tolerance test was performed in 65 coronary artery disease (CAD) patients on aspirin and clopidogrel therapy. Platelet function tests were assessed at 3 time-points by light transmittance aggregometry using ADP (5 and 20 mu mol/L) stimuli. 30 patients had IGT and 35 normal glucose tolerance (NGT). Among them, 13 patients showed IR. Following ADP stimuli, patients with IGT showed significantly higher maximal platelet aggregation at each time point than those with NGT patients. This resulted in greater high on-treatment platelet reactivity (HPR) rates at each time point in IGT patients (53.3-36.7 vs. 14.3-11.4 %, p < 0.05). A multivariable logistic regression analysis showed that IGT status was the strongest predictor of HPR (odds ratio 7.54, 95 % CI 1.95-29.1, p = 0.003). Following a glucose load, profiles of platelet reactivity varied according to IR status, with minimal changes over time in patients with IR, while there was a significant reduction in the non-IR patients. In aspirin and clopidogrel-treated patients with CAD, IGT is associated with enhanced platelet reactivity and increased rates of HPR compared with NGT patients. These findings suggest the presence of platelet dysfunction in patients with IGT, which may be attributed to the presence of IR.
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收藏
页码:174 / 181
页数:8
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Karolinska Inst, Dept Med, Cardiol Unit, Stockholm, Sweden Karolinska Inst, Dept Med, Cardiol Unit, Stockholm, Sweden

Wedel, Hans
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Nord Sch Publ Hlth, Gothenburg, Sweden Karolinska Inst, Dept Med, Cardiol Unit, Stockholm, Sweden

Ryden, Lars
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Karolinska Inst, Dept Med, Cardiol Unit, Stockholm, Sweden Karolinska Inst, Dept Med, Cardiol Unit, Stockholm, Sweden