The goal of this study is to identify the molecular regulatory mechanisms that result in loss of skeletal muscle in cirrhotic patients. Current strategies involve prolonged tracer infusion and multiple muscle biopsies. We will use an innovative approach to determine the rates of skeletal muscle protein synthesis and breakdown using multiple tracers administered at short intervals followed by a single muscle biopsy. These studies are likely to provide a conceptual advance in determining the cellular and molecular responses of the skeletal muscle in cirrhosis.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
The diagnosis of cirrhosis based on liver biopsy and/or clinical, biochemical, and imaging criteria.
Patients with Child Pugh score from A5- to B7
Control group: Subject in control group should have serum ALT and AST within normal range.
You may not be if
diabetes
cancer
kidney failure
pregnancy
recent surgery (bowel resection or Gastric bypass operation)
Advanced cardiac or pulmonary disease
patient with thyroid disease \& Coagulopathy ( INR \>1.4 and platelet count \<80,000/ml)
Clareo Health | Novel Tracer Methods to Evaluate Muscle Protein Metabolism in Cirrhosis
