Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:4.1.1.6 (
CAD
)
4,420
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Dual antiplatelet treatment with aspirin and clopidogrel is the standard therapy for patients undergoing percutaneous coronary intervention (PCI). However, a portion of patients suffer from clopidogrel resistance (CR) and consequently with recurrence of cardiovascular events. Genetic factors such as loss-of-function variants of
CYP2C19
contribute a lot to CR. Recently, the N-6-adenine-specific DNA methyltransferase 1 (
N6AMT1
) rs2254638 polymorphism is reported to be associated with clopidogrel response. To validate the association between
N6AMT1
rs2254638 polymorphism and clopidogrel response, 435 Chinese
CAD
patients receiving aspirin and clopidogrel were recruited.
N6AMT1
rs2254638 and
CYP2C19
*
2/
*
3
polymorphisms were genotyped. Platelet reaction index (PRI) was measured by VASP-phosphorylation assay after treated with a 300 mg loading dose (LD) clopidogrel or 75 mg daily maintenance dose (MD) clopidogrel for at least 5 days. There was a significant difference in PRI between LD cohort and MD cohort. Carriers of
CYP2C19
*
2
allele showed significantly increased PRI in the entire cohort and in respective of the MD and LD cohorts
(p
< 0.001,
p
= 0.003,
p
< 0.001, respectively). However, carriers of
CYP2C19
*
3
allele exhibited significantly higher PRI only in the entire cohort and LD cohort (
p
= 0.023,
p
= 0.023 respectively). PRI value was significantly higher in
CYP2C19
PM genotyped patients as compared with those carrying the IM genotypes and EM genotype (
p
< 0.001). Besides, carriers of the rs2254638 C allele showed significantly higher PRI in entire cohort and in the LD cohort
(p
= 0.023
, p
= 0.008, respectively). When the patients were grouped into clopidogrel resistance (CR) and non-clopidogrel resistance (non-CR) groups,
CYP2C19
*
2
was associated with increased risk of CR in the entire cohort, the LD cohort and the MD cohort
(p
< 0.001
, p
< 0.001, and
p
= 0.019, respectively). Carriers of the rs2254638 C allele also showed increased risk of CR in the entire cohort and the LD cohort
(p
= 0.024, and
p
= 0.028, respectively
)
.
N6AMT1
rs2254638 remained as a strong predictor for CR (TC vs. TT: OR = 1.880, 95% CI = 1.099-3.216,
p
= 0.021
;
CC vs. TT: OR = 1.930, 95% CI = 1.056-3.527,
p
= 0.032; TC + CC vs. TT: OR = 1.846, 95%CI = 1.126-3.026,
p
= 0.015) after adjustment for confounding factors. Our study confirmed the influence of
CYP2C19
*
2 and rs2254638 polymorphisms on clopidogrel resistance in Chinese
CAD
patients. Both
CYP2C19
*
2
and
N6AMT1
rs2254638 polymorphism may serve as independent biomarkers to predict CR.
...
PMID:Association of
N6AMT1
rs2254638 Polymorphism With Clopidogrel Response in Chinese Patients With Coronary Artery Disease. 3028 38
