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DOI 10.5414/cp201784

Медицинская библиотека · International journal of clinical pharmacology and therapeutics · 2013

Factors that contribute to clopidogrel resistance in cardiovascular disease patients: environmental and genetic approach.

Al-Azzam Sayer I, Alzoubi Karem H, Khabour Omar F, Nusair Mohammad B, Al-Hadidi Hakam, Awidi Abdalla, Saleh Akram

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND AND

OBJECTIVE

Clopidogrel is a potent antiplatelet drug that reduces the risk of vascular events in patients with cardiovascular disease. However, several studies have shown that about a quarter of patients showed low or no response to clopidogrel therapy. In this study, factors that contribute to clopidogrel resistance were investigated in 270 cardiovascular disease patients from Jordan.

PATIENTS AND

METHODS

Clopidogrel resistance was determined through platelet aggregation analysis using the Multiplate analyzer®. Genetic factors (CYP2C19*2 and PON1 Q192R) were examined using polymerase chain reaction-restriction fragment length polymorphism analysis.

RESULTS

The incidence of clopidogrel resistance among Jordanians is about 32%. Significant association between clopidogrel resistance and female gender, concomitant use of calcium channel blockers, and low HDL was found (p < 0.05). In addition, presence of CYP2C19*2 allele is strongly related to clopidogrel resistance (p < 0.001). However, lack of contribution to clipidogrel resistance was found for PON1 Q192R polymorphism, age, diabetes, hypertension, smoking and aspirin use (p > 0.05).

CONCLUSION

Several factors might contribute to clopidogrel resistance including gender, concomitant use of calcium channel blockers, HDL and CYP2C19*2 polymorphism.

Для цитирования: Al-Azzam Sayer I, Alzoubi Karem H, Khabour Omar F, Nusair Mohammad B, Al-Hadidi Hakam, Awidi Abdalla, Saleh Akram. Factors that contribute to clopidogrel resistance in cardiovascular disease patients: environmental and genetic approach.. International journal of clinical pharmacology and therapeutics. 2013. DOI: 10.5414/cp201784.

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