Biochemical markers for diagnosis and follow up of disease

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Presentation transcript:

Biochemical markers for diagnosis and follow up of disease Foundation Block

Biochemical markers What is a biomarker? Enzymatic diagnosis and prognosis of a disease Enzymes as markers of disease: Amylase, ALT, AST Plasma proteins as markers of disease: Albumin Tumor markers: a-fetoprotein, PSA

What is a biomarker? A biological molecule found in blood, other body fluids, or tissues that indicates a normal or abnormal process such as a disease or a condition A biomarker is measured to follow up a disease or treatment

Diagnosis and prognosis Identification of a disease from its signs and symptoms Prognosis: The future outcome of a disease

Enzymatic diagnosis and prognosis of disease Enzymes are used clinically in three ways: As indicators of enzyme activity or conc. in body fluids (serum, urine) in the diagnosis/prognosis of a disease As analytical reagents in measuring activity of other enzymes or compounds in body fluids As therapeutic agents

Most common body fluids: serum and plasma Enzymes are: Plasma-specific or Nonplasma-specific

Plasma-specific enzymes Normally present in plasma Perform their functions in blood High level of activity in plasma than in tissue cells Examples: blood clotting enzymes (thrombin), cholinesterase, etc.

Nonplasma-specific enzymes Present inside the cell Conc. is lower in plasma Released into the body fluids in high conc. due to: cell damage defective cell membrane

Intracellular enzymes are present only in their cells of origin Some are secretory enzymes that are secreted by salivary glands, gastric mucosa and pancreas In disease, plasma levels of secretory enzymes increase when their cells are damaged The diagnosis of organ disease is done by measurement of enzymes of that tissue

Factors affecting serum enzyme levels Cell damage Rate of enzyme synthesis and clearance Enzyme inhibitors Glucose deficiency Localized hypoxia (less oxygen) Ischemia (obstruction of blood vessels) Necrosis Tissue infarction due to ischemic necrosis Myocardial infarction

Enzymatic markers Amylase Alanine aminotransferase (ALT) Aspartate aminotransferase (AST)

Amylase in acute pancreatitis Acute pancreatitis is the inflammation of pancreas caused by: Obstruction of the pancreatic duct Gallstones Alcohol abuse

Abnormal release of pancreatic enzymes and their premature activation The main pancreatic enzyme is trypsinogen Trypsinogen is activated to trypsin Trypsin converts other enzymes to active form such as kallikrein, phospholipase A2, elastase, etc. Effects of abnormal release of enzymes: autodigestion of pancreas, vasodilation, respiratory failure, etc.

Enzymatic diagnosis Measurement of pancreatic enzymes: Amylase Lipase Trypsinogen

Amylase appears in the serum within 2-12 hours after abdominal pain Elevated serum amylase level is a diagnostic indicator of acute pancreatitis Amylase level greater than 10 times the upper limit indicates acute pancreatitis The test has low specificity because elevated serum amylase level is also present in other diseases Amylase appears in the serum within 2-12 hours after abdominal pain Free amylase (unbound form) is rapidly cleared by the kidneys

High ALT and AST in liver diseases Alcohol abuse Medication Chronic hepatitis B and C Steatosis and steatohepatitis Autoimmune hepatitis Wilson’s disease a1-antitrypsin deficiency Malignancy Poisons and infectious agents

Serum enzymes used in the assessment of liver function: Markers used in hepatocellular necrosis Alanine aminotransferases Aspartate aminotransferases Markers used in cholestasis Alkaline phosphatase 5’-nucleotidase g-glutamyl transferase

Alanine aminotransferase (ALT) Mostly present in liver Small amounts in heart More specific for liver disease than AST Major diagnosis: liver disease

Aspartate aminotransferase (AST) Widely distributed in heart, liver, skeletal muscle, kidney Small amounts in erythrocytes High serum activity of AST found in: Liver disease, heart disease, skeletal muscle disease, hemolysis Major diagnosis: myocardial infarction, liver and muscle diseases

Plasma proteins as markers (albumin) Functions Oncotic pressure (pressure exerted by plasma proteins that pulls water into the circulatory system)– 80% of plasma oncotic pressure is maintained by albumin Fluid distribution in and outside cell, maintains plasma volume Buffering – some buffering function Transport – lipid-soluble molecules, hormones, calcium, drugs, etc. in blood

Plasma proteins as markers Hypoalbuminemia – Causes Decreased albumin synthesis – failure of synthesis due to genetic reasons and malnutrition Increased volume of albumin distribution – in liver disease Increased losses of albumin – increased catabolism in infections, nephrotic syndrome, hemorrhage, severe burns, etc.

Plasma proteins as markers Hypoalbuminemia – Effects Edema due to low oncotic pressure Albumin level drops in liver disease causing low oncotic pressure Fluid moves into the interstitial spaces causing edema Reduced transport of Substances in plasma Drugs (free form – more active)

Plasma proteins as markers Hyperalbuminemia – causes Dehydration is a major cause of hyperalbuminemia

Tumor markers A molecule secreted by a tumor that is measured for diagnosis and management of a tumor a-fetoprotein Prostate specific antigen (PSA)

a-Fetoprotein In newborn babies a-fetoprotein levels are very low High conc. are observed in: hepatocellular carcinomas (hepatoma) testicular carcinomas GI tract carcinomas However, high serum levels are also found in benign (non-cancerous) conditions e.g. hepatitis High conc. are not always suggestive of a tumor

Prostate specific antigen (PSA) A serine protease enzyme also called kallikrein III, seminin Produced by prostate gland Liquefies ejaculate High serum PSA levels are observed in prostate cancer Less specific in diagnosis High serum levels are also observed in benign prostatic hypertrophy (enlarged prostate gland)