A Study of Biochemical and Hematological Markers in Alcoholic Liver Cirrhosis
Neelesh Deshpande, Sabitha Kandi, Manohar Muddeshwar, Rajkumar Das, Kota V. Ramana
Abstract
Neelesh Deshpande, Sabitha Kandi, Manohar Muddeshwar, Rajkumar Das, Kota V. Ramana
Abstract
Progressive fibrosis and cirrhosis, clinically presenting as end-stage liver disease are common outcomes in alcoholic Liver disease (ALD) patients. A variety of laboratory tests are available to assist in the progression and diagnosis of cirrhosis to end stage liver disease. The aim of this study is to identify potential novel biomarkers for progression of cirrhosis to end-stage liver cirrhosis. The biomarkers evaluated in this study included liver function indicators including serum ferritin, prothrombin time, albumin, total bilirubin, alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyltransferase (GGT), renal parameters (urea and creatinine) and red blood cell counts, hemoglobin and blood glucose. The study included two groups based on severity of cirrhosis of liver; categorized as compensated and decompensated liver cirrhotic patients based on child Pugh criteria. All decompensated cirrhotic patients in the study group had significantly elevated biomarkers levels (P<0.001) than those with compensated cirrhotic patients and control group who were not suffering from liver cirrhosis. Thus these results suggest that elevated and altered liver and hematological biomarkers are associated with pathogenesis and progression of liver cirrhosis.
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Progressive fibrosis and cirrhosis, clinically presenting as end-stage liver disease are common outcomes in alcoholic Liver disease (ALD) patients. A variety of laboratory tests are available to assist in the progression and diagnosis of cirrhosis to end stage liver disease. The aim of this study is to identify potential novel biomarkers for progression of cirrhosis to end-stage liver cirrhosis. The biomarkers evaluated in this study included liver function indicators including serum ferritin, prothrombin time, albumin, total bilirubin, alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyltransferase (GGT), renal parameters (urea and creatinine) and red blood cell counts, hemoglobin and blood glucose. The study included two groups based on severity of cirrhosis of liver; categorized as compensated and decompensated liver cirrhotic patients based on child Pugh criteria. All decompensated cirrhotic patients in the study group had significantly elevated biomarkers levels (P<0.001) than those with compensated cirrhotic patients and control group who were not suffering from liver cirrhosis. Thus these results suggest that elevated and altered liver and hematological biomarkers are associated with pathogenesis and progression of liver cirrhosis.
Key concepts: Cirrhosis, Medicine, Gastroenterology, Internal medicine, Alcoholic liver disease, Liver function tests, Liver disease, Liver function