AGTR1, angiotensin II receptor type 1, 185

N. diseases: 440; N. variants: 33
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE We have now investigated the role of a common polymorphism of the AT1 receptor gene (an A-->C transversion at position 1166 of AGT1R) and looked for an interaction between ACE and AGT1R gene polymorphisms on the risk of myocardial infarction. 7934345 1994
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE The relation of the ACE and AT1R gene polymorphisms to coronary heart disease and the severity of coronary artery stenosis has now been investigated in 133 patients with myocardial infarction (MI) or angina pectoris who underwent coronary angiography and in 258 control subjects. 8842348 1996
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE A DNA polymorphism at the angiotensin II type 1 receptor (AT1R) locus and myocardial infarction. 9298740 1997
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 Biomarker disease RGD Alterations in sarcoplasmic reticulum and angiotensin II type 1 receptor gene expression after myocardial infarction in rats. 9652322 1998
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 AlteredExpression disease BEFREE Myocardial AT1 receptor density increases in association with ACE expression, and AT1 receptor activation is related to collagen formation following myocardial infarction in rats. 9796075 1998
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE However, the present study suggests that AT1R-810 T/A, or other polymorphisms which are in complete association with it, might be associated with the risk of myocardial infarction. 9814614 1998
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE We analysed the relationship, on the risk of ischaemic heart disease, of angiotensin II type 1 receptor A1166C gene variation, not only to myocardial infarction but also to coronary artery disease, and its potential interaction with angiotensin I-converting enzyme Insertion/Deletion gene polymorphism. 9857918 1998
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE I/D polymorphism and angiotensin II type 1 receptor genotypes did not relate individually to risk of myocardial infarction or atheroma in univariate or multivariate analysis. 10435047 1999
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE We analyzed the evolution with age of the frequencies of the I/D polymorphism of the angiotensin I-converting enzyme (ACE), a1166c of the angiotensin II AT1 receptor (AT1R), M235T of the angiotensinogen (AGT) and A225V of their methylenetetrahydrofolate reductase (MTHFR) gene in a healthy (H) population and the subsequent comparison to age- and sex-matched groups of myocardial infarction (MI) subjects. 10488956 1999
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Subjects carrying the ACE DD genotype and AT1R C allele showed a stronger association with myocardial infarction (OR=4.02, P<0.0001). 10731400 2000
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE The genotype distribution of AT1R polymorphism was significantly different between controls and patients, the prevalence of the C allele carriers being higher in patients with MI after the age of 45 than in control individuals (61 vs 45%, p <0.01), leading to an odds ratio (OR) of 2 (CI: 1.2-3.4). 10739375 2000
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 Biomarker disease BEFREE Among men and women the odds ratio for MI for AT1R (CC vs. AC + AA) was 1.02 (0.71, 1.47). 11122322 2000
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE A synergistic interaction between the insertion/deletion (I/D) polymorphism within the angiotensin-converting enzyme (ACE) gene and an A/C transversion at nucleotide position 1166 within the angiotensin II sub-type 1 receptor (AT1R) gene on risk of myocardial infarction has been reported. 11137090 2001
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE An interactive effect on MI risk was found between ACE-DD and AGT1R-AA genotypes (odds ratio [OR]=2, 95% CI= 1-3.9), between ACE-DD and angiotensinogen-TT genotypes (OR = 2.7, 95% CI = 1-7.3), as well as among ACE-DD, angiotensinogen-TT, and AGT1R-AA genotypes (OR=4.8, 95% CI = 1-22.8). 11330506 2001
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Molecular variants of the angiotensinogen (AGT) and the angiotensin II type 1 receptor (ATR) genes have been associated with the risk of coronary artery disease (CAD) and myocardial infarction (MI), but data so far available are conflicting. 11393670 2001
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 AlteredExpression disease BEFREE AT1R blockade is beneficial only when the AT1R was overexpressed, both in reducing the reperfusion-induced arrhythmias and mortality early after MI. 11904535 2002
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE The angiotensin II type 1 receptor A1166C polymorphism has been associated with increased risks of hypertension and myocardial infarction in several small studies. 12460700 2002
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Our study suggests that common genetic variations in the AGTR1 gene may affect the risk of MI in Chinese males, and that there might be several functional variants in AGTR1 gene and the combined effect of these variants seemed to have a larger effect on the risk of MI in Chinese males. 15454732 2004
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE The effect of angiotensin II type-1 receptor gene polymorphisms on doppler blood flow parameters of carotid and brachial arteries in patients with myocardial infarction. 16911325 2006
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 Biomarker disease LHGDN Angiotensin receptor blockers may increase risk of myocardial infarction: unraveling the ARB-MI paradox. 16923768 2006
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Although there have been several association studies of angiotensin II type 1 receptor (AT1R, A/C1166) gene polymorphism in clinical endpoints such as myocardial infarction (MI), hypertension, aortic stiffness, and left ventricular mass, the relationship between AT1R polymorphism and biventricular function in acute anterior MI has not been studied before. 16998258 2006
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE AGTR1 polymorphism has been reported to associate with hypertension, myocardial infarction (MI), and metabolic traits. 17211857 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE In a meta-analysis of 27 studies addressing the association of the angiotensin type 1 receptor (AT1R)+1166A/C polymorphism with MI (10,180 cases, 17,129 controls), the *C allele conferred an increase in MI risk (odds ratio = 1.13 per allele, p = 0.005). 17293603 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease LHGDN In a meta-analysis of 27 studies addressing the association of the angiotensin type 1 receptor (AT1R)+1166A/C polymorphism with MI (10,180 cases, 17,129 controls), the *C allele conferred an increase in MI risk (odds ratio = 1.13 per allele, p = 0.005). 17293603 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE The authors conducted a population-based, case-control study at Group Health (Seattle, Washington) between 1995 and 1999 to determine whether common haplotypes in the angiotensinogen gene (AGT), the renin gene, the angiotensin-converting enzyme gene, and the angiotensin II receptor type 1 and receptor type 2 genes were associated with the risk of myocardial infarction and stroke among pharmacologically treated hypertensive patients. 17522061 2007