AGT, angiotensinogen, 183

N. diseases: 765; N. variants: 43
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 Biomarker disease BEFREE Association of angiotensin II type I and type II receptor genes polymorphisms with the presence of premature coronary disease and metabolic syndrome. 24385301 2014
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE The M235T single nucleotide polymorphism in the angiotensinogen gene is associated with coronary artery calcium in patients with a family history of coronary artery disease. 23137822 2013
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE The AGT M235T polymorphism associates with AMI risk and influences CAD severity. 20663844 2011
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE Angiotensin-converting enzyme and angiotensin II receptor 1 polymorphism in coronary disease and malignant ventricular arrhythmias. 10615414 1999
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 Biomarker disease BEFREE Comparative Effectiveness of Combination Therapy with Statins and Angiotensin-Converting Enzyme Inhibitors versus Angiotensin II Receptor Blockers in Patients with Coronary Heart Disease: A Nationwide Population-Based Cohort Study in Korea. 30225928 2018
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE The angiotensinogen M235T variant was analyzed in 871 consecutive patients with clinically suspected coronary artery disease submitted to coronary angiography study. 16045904 2005
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE The purpose of this study was to evaluate the association of common polymorphisms in endothelial nitric oxide synthesis (eNOS; G894T) and renin-angiotensin-aldosterone system (angiotensin converting enzyme [ACE]-I/D, angiotensinogen-T704C, and angiotensin II receptor type 1-A1166C) as risk factors in the pathogenesis of coronary artery disease (CAD) in Bulgarian patients. 26670794 2016
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 Biomarker disease BEFREE Coexistence effect of hypertension and angiotensin II on the risk of coronary heart disease: a population-based prospective cohort study among Inner Mongolians in China. 30917708 2019
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE Gene polymorphisms of components of the renin-angiotensin system, angiotensinogen, angiotensin I-converting enzyme (ACE) and angiotensin II type 1 receptor (AT-1), have been considered to contribute to inherited predisposition towards coronary artery disease (CAD). 15320825 2004
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 Biomarker disease BEFREE Angiotensin II receptor blockers versus angiotensin-converting enzyme inhibitors in patients with stable coronary artery disease: Prevalence, correlates, and prognostic impact (from the CORONOR study). 27283338 2017
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 Biomarker disease BEFREE We examined the association of polymorphisms of angiotensin-converting enzyme (ACE), angiotensinogen (AGT), and angiotensin II type 1 receptor (AT(1) receptor) with severe CAD in CABG patients. 20223792 2010
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 Biomarker disease BEFREE Therefore, we analyzed the angiotensinogen gene as a modifier gene for coronary heart disease risk in patients with familial hypercholesterolemia. 18300856 2008
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE The present study strengthens the hypothesis of an association of both angiotensinogen gene polymorphisms with the extent of coronary heart disease. 10488958 1999
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE Results indicate that the M235T and T174M variants of the angiotensinogen gene are not associated with CAD in Japanese men. 9313606 1997
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 Biomarker disease BEFREE These data are important to our understanding of the divergent role of angiotensin II acting at its receptor subtypes and coronary disease pathogenesis and for the development of future cardiovascular therapies. 12925562 2003
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE Our results indicate that the T/T genotype of AGT codon 174 may be a risk factor for CAD in Japanese individuals with low BMI, lesser CAD risk factors, or ACE I/I genotype. 9822117 1998
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE Association of angiotensinogen M235T and A(-6)G gene polymorphisms with coronary heart disease with independence of essential hypertension: the PROCAGENE study. Prospective Cardiac Gene. 11345362 2001
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE To assess the association of the angiotensin II type 2 (AT2) receptor (-1332 G/A) gene polymorphism with premature coronary artery disease (CAD) and investigate for a further role in both myocardial infarction and predominantly stenotic atherosclerosis requiring revascularisation. 17336987 2007
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE To determine the prognostic significance of a combination of three common polymorphisms of RAS genes (angiotensin converting enzyme - ACE Ins/Del, angiotensin receptor type 1 - AGT1R A1166C and angiotensinogen - ATG M235T) in patients with CAD. 21769789 2011
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE The significant relations observed between the AGT M235T variant, its protein product, and the cardiovascular disease phenotypes provide evidence for a possible role of elevated circulating AGT in the pathogenesis of coronary artery disease. 10097233 1999
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE Since there are no existing data for the Tunisian population, we investigated the association between these polymorphisms (angiotensin-converting enzyme [ACE] insertion/deletion [Ins/Del]; the angiotensinogen T174M and M235T; and the angiotensin II type 1 receptor A1166C polymorphisms) and CAD in Tunisians. 20854100 2010
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE This report focuses on the interactions between M235T polymorphism of AGT gene and traditional risk factors of CAD. 18409009 2008
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE In addition, most importantly, we found no interaction between angiotensin II type 1 receptor A1166C gene variation and angiotensin I-converting Insertion/Deletion polymorphism, either in connection with the risk of coronary artery disease or myocardial infarction. 9857918 1998
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.200 GeneticVariation disease BEFREE Female gender synergistically enhances (or male gender reverses) the effects of AGT gene haplotypes on the risk of CAD in the presence of hypertension. 18653189 2009