Biochemical Investigations in Liver Disease. Dr Roshitha de Silva Department of Pathology Faculty of Medicine University of Kelaniya

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Transcription:

Biochemical Investigations in Liver Disease Dr Roshitha de Silva Department of Pathology Faculty of Medicine University of Kelaniya

Biochemical markers Albumin ALP ALT, AST Gamma-glutamyl transpeptidase (γgt) Serum bilirubin Urine bilirubin, urobilinogen Alpha feto protein

Serum albumin Albumin is the major protein in the human body Albumin is synthesized in the liver Decreased serum albumin levels are seen in chronic liver failure

Low Serum albumin Not specific for liver disease Low levels of albumin may be the result of Inadequate production Inadequate intake Protein malnutrition Excessive loss Nephrotic syndrome Protein losing enteropathies Burns

Alkaline Phosphatase Produced both from liver & bone Increased in any form of biliary tree obstruction Extrahepatic > intrahepatic obstruction (x 3)

Alkaline Phosphatase Cont. Billiary obstruction Iry/IIry hepatic cancer Infectious hepatitis Drugs Pregnancy (placental) Bone disorders- Paget disease, osteomalacia Transient ALP increase in children Benign 10 times the URL Liver/bone Slow removal

Alkaline Phosphatase Cont. Reference intervals ALP isoenzyme analysis

Transaminases Aspartate aminotransferase (AST or SGOT) Liver, skeletal muscle, cardiac muscle, kidneys, brain, etc. Alanine aminotransferase (ALT or SGPT) 1 in liver Sensitive indicators of liver cell injury Even very mild liver abnormalities can cause slightly elevated AST/ALT

Release of AST/ALT from Liver Cells during Acute Hepatocellular Injury ALT AST

Aminotranferases Convenient to measure Present in liver cells in large amounts quantitative assessment of ongoing hepatocyte necrosis Blood level roughly proportional to the number of hepatocytes that died recently (hours-days)

Problems with using transaminases to assess liver injury Only assess injury over the past 1-2 days Magnitude of elevation does not necessarily correlate with extent of liver function or dysfunction. AST and ALT = rate of destruction of hepatocytes Liver function = number of functional hepatocytes left

AST/ALT Ratio AST:ALT <1 Viral hepatitis Ischaemic necrosis Toxic hepatitis AST:ALT >1 Alcoholic steatosis Alcoholic hepatitis Alcoholic cirrhosis Low levels of cofactor pyridoxine-5-phosphate

Gamma-glutamyl transpeptidase Elevated in most subjects with liver disease regardless of the cause May be elevated with even minor, sub-clinical levels of liver dysfunction Most sensitive, but least specific of all LFTs Helpful in identifying the cause of an isolated elevation in ALP

Gamma-glutamyl transpeptidase Activity increased by alcohol. (upto 1 month) Isolated elevation can indicate alcohol abuse Can indicate excess alcohol consumption up to 3 or 4 weeks prior to the test. Is not specific to alcohol intoxication

Gamma-glutamyl transpeptidase Drugs can raise GGT levels barbiturates phenytoin Extrahepatic causes Pancreatitis Carcinoma of prostate Carcinoma of breast and lung Systemic lupus erythematosus

Serum bilirubin The byproduct of Hb breakdown Total bilirubin indirect bilirubin (when >80% of total bilirubin is unconjugated indirect hyperbilirubineamia) direct bilirubin

Hyperbilirubinemia Conjugated hyperbilirubinemia Cholestasis/biliary obstruction Hepatitis Rare disorders of canalicular secretion of conjugated bilirubin - DJ, Rotor Unconjugated hyperbilirubinemia Massive overproduction - acute hemolysis Impaired conjugation common: rare: Gilbert's syndrome (mild) Crigler-Najjar syndrome (severe)

Gilbert's syndrome Benign, familial disorder Present in 5% of the population Genetic origin-reduction in the glucuronidation activity of UGT Exacerbated by fasting, fasting, exertion, febrile illness Confirm unconjugated hyperbilirubinaemia Rule out haemolysis and underlying liver disease

Urine Bilirubin/Bile Not present in the urine of normal, healthy individuals Bilirubin leaks back into the blood stream and is excreted in urine in obstructive jaundice Hepatitis

Urine Urobilinogen Conjugated bilirubin is excreted via bile salts to intestine. Bacteria in the intestine break down bilirubin to urobilinogen for excretion in the feces Normally there are mere traces of urobilinogen in the urine. Detected by the Ehrlich s test

Condition Urine Bilirubin Result Urine Urobilinogen Result Hemolytic disease Negative Increased Hepatitic disease Positive or negative Increased Biliary obstruction Positive Negative

Cirrhosis Suspected Disorder Iry biliary cirrhosis Haemachromatosis Wilsons disease Alpha 1 antitrypsin deficiency Cystic fibrosis Confirmatory Investigations Antinuclear antibodies (ANAs) immunoglobulin levels (mainly IgM) Serum ferritin Transferrin saturation Caeruloplasmin Serum copper Alpha1 antitrypsin Sweat test

AFP Tumour marker for HC carcinoma Annual AFP and ultrasound screening in patients with cirrhosis Patients with cirrhosis or viral hepatitis may have slightly higher AFP values

Thank you