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: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 Biomarker disease BEFREE Angiotensin II type 1 receptor blockers (ARBs) are potentially useful in controlling the central blood pressure and arterial stiffness in mild to moderate essential hypertension, while the effects of ARBs in aged patients with essential hypertension are not entirely investigated. 30311805 2019
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 Biomarker disease BEFREE Angiotensin II type 1 receptor blocker losartan is potentially useful in controlling the central blood pressure and arterial stiffness in mild to moderate essential hypertension, while the effects of losartan in aged patients with essential hypertension are not entirely investigated. 30362602 2019
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Among individuals with essential hypertension certain relationships were documented between rs5182 and rs5186 polymorphisms of AGTR1 gene and rs1799998 polymorphism of CYP11B2 gene on one hand and the volume of carotid bodies on one other. 29627490 2018
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Hypomethylation of the Angiotensin II Type I Receptor (AGTR1) Gene Along with Environmental Factors Increases the Risk for Essential Hypertension. 28376480 2018
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE AC+CC genotype of AT1R and noise were the risky factors of EH. 28157766 2017
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 Biomarker disease GENOMICS_ENGLAND Molecular and clinical analysis of TRPC6 and AGTR1 genes in patients with pulmonary arterial hypertension. 25603901 2015
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Essential hypertension patients were genotyped for 11 polymorphisms of essential hypertension susceptibility genes including ADD1 (rs4961), GNB3 (rs5443, rs16932941), NOS3 (rs1799983, rs2070744), ACE (rs5186), AGTR1 (rs5186), AGT (rs699, rs4762), MR (rs5534), and TGFB1 (rs1800471). 26335431 2015
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE The present study suggests that CpG1 hypomethylation in the AGTR1 promoter is likely associated with the risk of EH in the population assessed. 26658476 2015
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE The aim of the present study is to assess the association between angiotensin II receptor type 1 polymorphisms and essential hypertension risk in Chinese Hani and Yi minorities. 25628312 2015
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE A significant association was found in the AT1R genotypes (AC+CC) with essential hypertension (χ2 = 22.48, p = 0.0001). 24992666 2014
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE The AT1-AAs, AGTR1 gene polymorphisms and haplotypes solely or jointly have influences on candesartan-based antihypertensive response in patients with primary hypertension. 24131669 2014
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE The purpose of this study was to investigate the association between angiotensin II type 1 receptor (AT1R) gene A(1166)C variants with essential hypertension and some related parameters in a sample of Jordanian hypertensive patients. 24047102 2014
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE To study the polymorphism of angiotensin-type 1 receptor (AT1R) gene A1166C in familial primary hypertension and its distribution in Han Yellow race of China. 24145933 2013
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Functional polymorphisms that predispose to increased basal GRK4 activity both decrease dopamine receptor activity and increase angiotensin II type 1 (AT1) receptor activity and are associated with essential hypertension in a number of different human cohorts. 22407378 2012
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Individuals carrying the mutated TT of AGT, DD of ACE and CC of AT1R genotypes had an 1.67 (P = 0.032), 3.09 (P < 0.001) and 3.45 (P < 0.001)-fold increased risk of HTA. 21779803 2012
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE The main aim of this study was to examine the association of A1166C polymorphism of angiotensin II type 1 receptor and telomere length with essential hypertension in Egyptian people. 21234654 2011
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Correlation between HLA-DRB1, HLA-DQB1 polymorphism and autoantibodies against angiotensin AT(1) receptors in Chinese patients with essential hypertension. 21557256 2011
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Angiotensin II type 1 receptor gene A1166C polymorphism and essential hypertension in Chinese: a meta-analysis. 20223791 2010
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 Biomarker disease BEFREE The aim of the study is to assess the association between the human AGTR1 gene and essential hypertension (EH) using a haplotype-based case-control study in Han Chinese subjects. 19833117 2010
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE The AGTR1 1166C allele when present in homozygous form may be associated with a form of essential hypertension characterized by high plasma aldosterone and low plasma renin levels, possibly due to increased AGTR1 mRNA levels and augmented angiotensin II action. 20027122 2010
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE The A1166C polymorphism of the AT1 receptor gene is not associated with reduction of blood pressure after treatment with ACEI in patients with essential hypertension. 18575418 2008
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Angiotensin II type 1 receptor (AGT1R) gene 1166A > C polymorphism has been shown to be associated with essential hypertension and aortic stiffness as measured by carotid femoral pulse wave velocity (PWV). 17227479 2007
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Although polymorphisms in renin-angiotensin-aldosterone (RAA) system genes for angiotensinogen (AGT M235T), angiotensin-converting enzyme (ACE I/D), angiotensin II type 1 receptor (AT1 A/C1166), and aldosterone synthase (CYP11B2-344T/C) have been major targets for genetic investigation in association with essential hypertension (EH), the influence of these genetic factors is still to be determined. 17190732 2007
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE These results suggest that the AGTR1 A1166C polymorphism is associated with essential hypertension and carotid atherosclerosis in a Chinese population. 16519598 2006
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.600 GeneticVariation disease BEFREE Associations of the angiotensin II type 1 receptor A1166C and the endothelial NO synthase G894T gene polymorphisms with silent subcortical white matter lesions in essential hypertension. 16109907 2005