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: UMLS:C0151744 (
myocardial ischemia
)
31,282
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Cytochrome P450 2C9
(
CYP2C9
) enzymes metabolize warfarin and arachidonic acid. We hypothesized that the
CYP2C9
(*)2 (rs.1799853) and
CYP2C9
(*)3 (rs.1057910) polymorphisms with decreased enzyme activity affect risk of subclinical atherosclerosis (reduced ankle brachial index and increased C-reactive protein), ischemic vascular diseases (
ischemic heart disease
, myocardial infarction, ischemic cerebrovascular disease and ischemic stroke) and death after an
ischemic heart disease
diagnosis. We genotyped the Copenhagen City Heart Study, a prospective study including 10 398 participants with 30-32 years of follow-up; the Copenhagen General Population Study, a cross-sectional study including 21 629 participants; and the Copenhagen
Ischemic Heart Disease
Study, a case-control study including 5082 cases and 14 904 controls.
CYP2C9
carriers versus noncarriers did not associate with subclinical atherosclerosis. Furthermore, the odds/hazard ratios for ischemic vascular disease did not differ from 1.0 for
CYP2C9
carriers versus noncarriers. Finally, we found no altered risk of early death after a diagnosis of
ischemic heart disease
. For all end points, we could exclude even minor changes in risk of disease with 90% power. In conclusion, in three independent studies totaling more than 52 000 individuals, we found no association between
CYP2C9
(*)2 and
CYP2C9
(*)3 polymorphisms and risk of subclinical atherosclerosis, ischemic vascular disease or death after
ischemic heart disease
.
...
PMID:Common polymorphisms in CYP2C9, subclinical atherosclerosis and risk of ischemic vascular disease in 52,000 individuals. 1965 64