Albumin is a carbohydrate-free protein, representing 55 – 65% of the total plasma proteins. It is synthesized in the liver and is noted for its ability of con guration...
Albumin is a carbohydrate-free protein, representing 55 – 65% of the total plasma proteins. It is synthesized in the liver and is noted for its ability of con guration changes. It maintains the plasma colloidal osmotic pressure, transports and stores a wide variety of ligands and serves as a source of endogenous amino acids. Albumin binds and solubilizes a variety of compounds amongst which are bilirubin, calcium, and long-chain fatty acids. Albumin also binds toxic heavy metal ions and many drugs, which is why a decrease in albumin in the blood can have important pharmacokinetic consequences2.
Hyperalbuminemia is of little diagnostic significance except in dehydration. Hypoalbuminemia is very common in many diseases and stems from various factors: impaired synthesis, either primary as a result of liver disease or secondary due to diminished protein intake; increased catabolism because of tissue damage (severe burns) or inflammation; malabsorption of amino acids (Crohn’s disease); proteinuria due to nephrotic syndrome; protein loss by way of feces (neoplastic disease). In severe hypoalbuminemia plasma albumin levels are below 2.5 g/dl. The low plasma oncotic pressure allows water to move out of the blood capillaries into the tissues (edema). Albumin measurements also allow monitoring of the patient’s response to nutritional support and are a useful test of liver function3.
Albumin is a carbohydrate-free protein, representing 55 – 65% of the total plasma proteins. It is synthesized in the liver and is noted for its ability of con guration changes. It maintains the plasma colloidal osmotic pressure, transports and stores a wide variety of ligands and serves as a source of endogenous amino acids. Albumin binds and solubilizes a variety of compounds amongst which are bilirubin, calcium, and long-chain fatty acids. Albumin also binds toxic heavy metal ions and many drugs, which is why a decrease in albumin in the blood can have important pharmacokinetic consequences2.
Hyperalbuminemia is of little diagnostic significance except in dehydration. Hypoalbuminemia is very common in many diseases and stems from various factors: impaired synthesis, either primary as a result of liver disease or secondary due to diminished protein intake; increased catabolism because of tissue damage (severe burns) or inflammation; malabsorption of amino acids (Crohn’s disease); proteinuria due to nephrotic syndrome; protein loss by way of feces (neoplastic disease). In severe hypoalbuminemia plasma albumin levels are below 2.5 g/dl. The low plasma oncotic pressure allows water to move out of the blood capillaries into the tissues (edema). Albumin measurements also allow monitoring of the patient’s response to nutritional support and are a useful test of liver function3.
