Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151650
Disease: Renal fibrosis
Renal fibrosis
0.020 Biomarker disease BEFREE MicroRNA21 promotes interstitial fibrosis via targeting DDAH1: a potential role in renal fibrosis. 26455824 2016
CUI: C0151650
Disease: Renal fibrosis
Renal fibrosis
0.020 Biomarker disease BEFREE Innovation and Conclusion: Our results provide the first direct evidence that the DDAH1 has a marked effect on kidney fibrosis and oxidative stress induced by aging or diabetes. 28594240 2017
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
0.020 AlteredExpression disease BEFREE These results indicate that suppression of DDAH2 expression is a culprit for homocysteine-induced impairments of DDAH/ADMA/NOS/NO pathway in endothelial cells, and therapeutic manipulation of DDAH2 expression may be a promising strategy for preventing endothelial dysfunction and cardiovascular diseases associated with hyperhomocysteinemia. 23171931 2012
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
0.020 AlteredExpression disease BEFREE Overexpression of DDAH1 protects from hyperhomocysteinemia-induced alterations in cerebral arteriolar structure and vascular muscle function. 20019334 2010
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 Biomarker disease BEFREE This study represents the first evidence for therapeutic inhibition of DDAH1 by small molecules in breast cancer. 30611984 2019
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 AlteredExpression disease BEFREE Here, we identified over-expression of DDAH1 in aggressive MDA-MB-231, MDA-MB-453 and BT549 breast cancer cell lines when compared to normal mammary epithelial cells. 29070803 2017
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 GeneticVariation disease BEFREE DDAH1 rs997251 TC + CC genotypes were associated with 2.3-fold higher risk of CAD than TT genotype (p = 0.0063). 30284143 2018
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 GeneticVariation disease BEFREE A novel loss-of-function DDAH1 promoter polymorphism is associated with increased susceptibility to thrombosis stroke and coronary heart disease. 20167924 2010
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 AlteredExpression disease BEFREE Our findings suggest that strategies to increase DDAH1 activity in neuronal cells may be a novel approach to attenuating AD development. 25499850 2015
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
0.010 AlteredExpression disease BEFREE However, overexpression of dimethylarginine dimethylaminohydrolase 1 (DDAH1) to promote ADMA degradation significantly attenuated oxidative stress and secretion in APPsw cells. 25499850 2015
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 Biomarker disease BEFREE In human subjects (n = 89) the FoxO1/DDAH1/ADMA pathway marks unstable atherosclerosis. 26226438 2015
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 GeneticVariation disease BEFREE The results of our study give no evidence to suggest that increased ADMA levels in RA relate to DDAH genetic polymorphisms. 25194333 2014
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 Biomarker disease BEFREE In human subjects (n = 89) the FoxO1/DDAH1/ADMA pathway marks unstable atherosclerosis. 26226438 2015
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
0.010 GeneticVariation disease BEFREE The rs480414 SNP in DDAH1 may be protective against the development of PH in patients with BPD. 26663142 2016
CUI: C0007274
Disease: Carotid Artery Thrombosis
Carotid Artery Thrombosis
0.010 Biomarker disease BEFREE DDAH1 Tg mice also were protected from hypertrophy of cerebral arterioles (P<0.05) but not from accelerated carotid artery thrombosis induced by the HM/LF diet. 20019334 2010
Diabetes Mellitus, Insulin-Dependent
0.010 GeneticVariation disease BEFREE We found limited evidence that genetic polymorphisms in DDAH genes influence serum ADMA levels in individuals with T1DM. 22521321 2012
CUI: C0015695
Disease: Fatty Liver
Fatty Liver
0.010 Biomarker disease BEFREE In this study, we used Ddah1<sup>-/-</sup> mice to investigate the effects of the ADMA/DDAH1 pathway on high-fat diet (HFD)-induced hepatic steatosis. 27565538 2017
CUI: C0018801
Disease: Heart failure
Heart failure
0.010 Biomarker disease BEFREE Here, we examine mechanisms of abnormal NO production in heart failure, with particular focus on the role of ADMA and DDAH1. 26923818 2016
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 AlteredExpression disease BEFREE In this study, we found that downregulation of DDAH1 was frequently detected in GC tissues and strongly correlated with more aggressive phenotypes and poor prognosis. 28580735 2017
CUI: C0034069
Disease: Pulmonary Fibrosis
Pulmonary Fibrosis
0.010 Biomarker disease BEFREE However, DDAH1 knockout significantly aggravated monocrotaline-induced lung and RV oxidative stress, lung vascular remodeling and fibrosis, pulmonary hypertension and RV hypertrophy in rats. 31402164 2019
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 Biomarker disease BEFREE Inhibition of Dimethylarginine Dimethylaminohydrolase 1 Improves the Outcome of Sepsis in Pregnant Mice. 31821207 2019
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.010 AlteredExpression disease BEFREE In contrast, cDDAH1 KO mice exposed to TAC showed no increase in LV DDAH1 expression, slightly increased LV tissue ADMA levels, no increase in plasma ADMA, but significantly exacerbated LV hypertrophy, fibrosis, nitrotyrosine production, and LV dysfunction. 28819685 2017
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.010 Biomarker disease BEFREE Asymmetric dimethylarginine had and OR of 1.08 per SD (95% CI 0.99-1.19) for IHD based on 4 SNPs from DDAH1. 27914500 2016
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.010 Biomarker disease BEFREE Overall, our data revealed that long non-coding RNA H19 confers resistance to gefitinib via miR-148b/dimethylarginine dimethylaminohydrolase-1 axis in lung adenocarcinoma, which offers a new insight into the epidermal growth factor receptor tyrosine kinase inhibitors therapy resistance. 31503013 2020
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
0.010 Biomarker disease BEFREE Herein, we used an inducible cardiac-specific DDAH1 knockdown mouse (cardiac DDAH1<sup>-/-</sup>) to investigate the role of cardiomyocyte DDAH1 in left-ventricular (LV) remodeling after acute myocardial infarction (AMI). 29892894 2018