Research Article Details
Article ID: | A23342 |
PMID: | 23858556 |
Source: | Hepatogastroenterology |
Title: | Blood urea nitrogen is elevated in patients with non-alcoholic fatty liver disease. |
Abstract: | BACKGROUND/AIMS: Non-alcoholic fatty liver disease (NAFLD) is strongly associated with many predictors of cardiovascular disease such as hypercholesterolemia, hypertriglyceridemia, insulin resistance, central obesity and the metabolic syndrome. Activation of renin-angiotensin-aldosterone system (RAAS) has been proved in patients with NAFLD. Blood urea nitrogen (BUN) elevation is a high risk factor and biomarker of RAAS activation of heart failure and coronary heart disease. The aim of the current study was to investigate BUN in patients with NAFLD. METHODOLOGY: BUN and creatinine (Cr) values of 85 patients with NAFLD and of 30 age- and gender-matched healthy individuals were compared prospectively. Liver/spleen ratios of computed tomography (CT) values were used to determine fatty liver and to evaluate fatty deposition. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were employed to estimate inflammation. We analyzed the correlation between BUN and fatty deposition or inflammation. RESULTS: NAFLD patients had significantly higher BUN compared to the control cases (5.0353±1.1271 vs. 4.1263±1.0095 mmol/L; t=3.898, p<0.001). However, there was no difference in Cr (84.0941±14.4062 vs. 79.4667±16.7120 μmol/L; t=1.45, p=0.15). BUN was negatively correlated with liver/spleen ratio of CT values (r=0.009, p=0.1974), ALT (r=-0.012, p=0.941) and AST (r=-0.009, p=0.592). CONCLUSIONS: We have shown for the first time in the literature, that patients with NAFLD have higher BUN. It may have prognostic value in NAFLD patients indicating a possible cardiovascular disease (CVD) risk increase. |
DOI: |

Strategy ID | Therapy Strategy | Synonyms | Therapy Targets | Therapy Drugs | |
---|---|---|---|---|---|
S01 | Improve insulin resistance | insulin sensitizer; insulin resistance; glucose tolerance | Biguanide: increases 5-AMP activated protein kinase signaling; SGLT-2 inhibitor; Thiazalidinedione: selective PPAR-γ agonists; GLP-1 agonist | Metformin; Empagliflozin; Canagliflozin; Rosiglitazone; Pioglitazone; Liraglutide | Details |
Target ID | Target Name | GENE | Action | Class | UniProtKB ID | Entry Name |
---|
Diseases ID | DO ID | Disease Name | Definition | Class | |
---|---|---|---|---|---|
I13 | 3146 | Lipid metabolism disorder | An inherited metabolic disorder that involves the creation and degradation of lipids. http://en.wikipedia.org/wiki/Lipid_metabolism | disease of metabolism/ inherited metabolic disorder | Details |
I05 | 9352 | Type 2 diabetes mellitus | A diabetes that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both. A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin. http://en.wikipedia.org/wiki/Diabetes, http://en.wikipedia.org/wiki/Diabetes_mellitus_type_2 | disease of metabolism/inherited metabolic disorder/ carbohydrate metabolic disorder/glucose metabolism disease/diabetes/ diabetes mellitus | Details |
I14 | 9970 | Obesity | An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness. https://en.wikipedia.org/wiki/Obesity | disease of metabolism/acquired metabolic disease/ nutrition disease/overnutrition | Details |
Drug ID | Drug Name | Type | DrugBank ID | Targets | Category | Latest Progress | |
---|---|---|---|---|---|---|---|
D316 | S-adenosyl-L-methionine | Chemical drug | DB00118 | GNMT cofactor | Antiviral | Under clinical trials | Details |
D182 | Insulin | Biological drug | DB00030 | INSR agonist; CPE modulator&product of | -- | Under clinical trials | Details |
D199 | L-alanine | Chemical drug | DB00160 | KYNU | -- | Failed in clinical trials | Details |