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Liver Function Tests
DR. FARHANA ATIA
ASSOCIATE PROFESSOR
DEPARTMENT OF BIOCHEMISTRY
NILPHAMARI MEDICAL COLLEGE, NILPHAMARI
Liver Function Tests
LFT or liver panel are a
group of tests that help in
Diagnosis of liver disease,
monitor therapy &
assess prognosis of liver
disease
Functions of liver
Metabolic
Secretory- lipid, VLDL
Excretory- Bilirubin
Storage- Fat soluble vitamins, Vit-B12, Fe,
Carbohydrates
Detoxifying- Drug
Synthetic- Plasma protein, clotting factor
Liver Function Tests
Test Function assessed Utility
1. Serum bilirubin
(total &
conjugated)
Conjugation &
excretory function
D/D of jaundice
2. Total serum
protein & albumin
Biosynthetic function Indicator of severity of
chronic liver disease
3. Prothrombin
time
Biosynthetic function Indicator of severity of
acute liver disease
Liver Function Tests
Test Function assessed Utility
4. Serum
enzymes
 AST, ALT
 ALP, GGT
 Hepatocellular
integrity
 Biliary obstruction
• Early indicator of
damage
• Cholestasis
5. Blood
ammonia
Detoxification • ↑ in cirrhosis of liver
with portal
hypertension
• Disorder in urea cycle
Test for Synthetic Function
Total Plasma Protein- 6.0-8.3 g/dl 60-83 g/L
Serum albumin- 3.4-5.4 g/dl
Albumin is solely synthesized by liver
Half life is 3wks (20-25 days)
Low level indicates chronic liver disease, malnutrition
Immunoglobulin is not synthesized in liver. So A/G
ratio is altered in liver disease
Test for Synthetic Function
Half life of Prothrombin is 5-72 hours
In liver disease there are decreased of plasma clotting
factors
Assessed by lab by PT
PT is prolonged in liver damage (Acute LD, also in
chronic disease
Vitamin K (required for factor II, VII, IX, X) deficiency
should be ruled out by measuring prothrombin time
before & after vitamin K administration
Bilirubin Metabolism
 After ≈120 days in the circulation,
RBC are taken up and degraded by the
mononuclear phagocyte system (MPS), particularly in
the liver & spleen
Breakdown of heme to bilirubin in macrophages
Unconjugated bilirubin (complexed to albumin) is
transported through the blood to the liver
Bilirubin Metabolism
 Bilirubin is taken up
via facilitated diffusion
by the hepatocyte &
conjugated with
glucuronic acid to form
bilirubin diglucuronide
Bilirubin Metabolism
Conjugated bilirubin is
actively secreted into bile
and then the intestine
In the intestine,
glucuronic acid is removed
by bacteria. The resulting
bilirubin is converted to
urobilinogen
Bilirubin Metabolism
 Some of urobilinogen is reabsorbed
from the gut & enters the portal blood
A portion of urobilinogen participates
in the enterohepatic urobilinogen cycle
The reminder is transported by the
blood to the kidney, where it is
converted to yellow urobilin & excreted,
giving the urine its characteristic color
Urobilinogen
Bilirubin Metabolism
Urobilinogen is oxidized by
intestinal bacteria to brown
stercobilin
Plasma Bilirubin
Normal : 0.2–0.8 mg/dl
Unconjugated bilirubin: 0.2–0.6 mg/dl
Conjugated bilirubin: 0–0.2 mg/dl
Hyperbilirubinemia: >1mg/dl
Latent jaundice: 1 - 2 mg/dl
Clinical jaundice: > 2 mg/dl
Terminology
Jaundice: Refers to the yellowish discoloration of sclera, conjunctiva,
skin & mucous membrane due to deposition of bilirubin secondary to
hyperbilirubinemia
Icterus: Greek term for jaundice
Kernicterus: Bilirubin encephalopathy. It is a neurological syndrome
resulting from destruction of basal ganglia by deposition of bile pigment
in severe hemolytic anemia specially in premature infant whose BBB is
underdeveloped
Classification of Jaundice
Hemolytic
(prehepatic)
• Hemolysis/ abnormal
RBC
• Antibodies
• Drugs & toxins
• Thalassemia
• Hemoglobinopathies
Hepatocellular
(hepatic)
• Viral hepatitis
• Toxic hepatitis
• Intrahepatic
cholestasis
• Gilbert's syndrome
• Criglar-Najjar
syndrome
Obstructive
(posthepatic)
• Extrahepatic
cholestasis
• Gall stone
• Tumors of bile duct
• Carcinoma head of
the pancreas
• Carcinoma ampulla
of Vater
Jaundice Hemolytic
(prehepatic)
Hepatocellular
(hepatic)
Obstructive
(posthepatic)
Underlying
condition
Overproduction
of bilirubin
Decreased
conjugation of
bilirubin
Obstruction of
common bile duct
(extrahepatic
cholestasis
Total bilirubin Increased Increased Increased
Conjugated
bilirubin
Normal Increased Increased
Unconjugated
bilirubin
Increased Increased Normal
Jaundice Hemolytic
(prehepatic)
Hepatocellular
(hepatic)
Obstructive
(posthepatic)
Urobilinogen Increased Increased Absent
Urine color Normal Dark (urobilinogen
+ conjugated
bilirubin)
Dark (conjugated
bilirubin)
Stool color Normal Normal/ Pale Pale
Conjugated
bilirubin in urine
Not present Present Present
ALT/ AST Normal Increased Normal
ALP Normal Normal Increased
Thank You

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Liver Function Tests

  • 1. Liver Function Tests DR. FARHANA ATIA ASSOCIATE PROFESSOR DEPARTMENT OF BIOCHEMISTRY NILPHAMARI MEDICAL COLLEGE, NILPHAMARI
  • 2. Liver Function Tests LFT or liver panel are a group of tests that help in Diagnosis of liver disease, monitor therapy & assess prognosis of liver disease
  • 3. Functions of liver Metabolic Secretory- lipid, VLDL Excretory- Bilirubin Storage- Fat soluble vitamins, Vit-B12, Fe, Carbohydrates Detoxifying- Drug Synthetic- Plasma protein, clotting factor
  • 4. Liver Function Tests Test Function assessed Utility 1. Serum bilirubin (total & conjugated) Conjugation & excretory function D/D of jaundice 2. Total serum protein & albumin Biosynthetic function Indicator of severity of chronic liver disease 3. Prothrombin time Biosynthetic function Indicator of severity of acute liver disease
  • 5. Liver Function Tests Test Function assessed Utility 4. Serum enzymes  AST, ALT  ALP, GGT  Hepatocellular integrity  Biliary obstruction • Early indicator of damage • Cholestasis 5. Blood ammonia Detoxification • ↑ in cirrhosis of liver with portal hypertension • Disorder in urea cycle
  • 6. Test for Synthetic Function Total Plasma Protein- 6.0-8.3 g/dl 60-83 g/L Serum albumin- 3.4-5.4 g/dl Albumin is solely synthesized by liver Half life is 3wks (20-25 days) Low level indicates chronic liver disease, malnutrition Immunoglobulin is not synthesized in liver. So A/G ratio is altered in liver disease
  • 7. Test for Synthetic Function Half life of Prothrombin is 5-72 hours In liver disease there are decreased of plasma clotting factors Assessed by lab by PT PT is prolonged in liver damage (Acute LD, also in chronic disease Vitamin K (required for factor II, VII, IX, X) deficiency should be ruled out by measuring prothrombin time before & after vitamin K administration
  • 8. Bilirubin Metabolism  After ≈120 days in the circulation, RBC are taken up and degraded by the mononuclear phagocyte system (MPS), particularly in the liver & spleen Breakdown of heme to bilirubin in macrophages Unconjugated bilirubin (complexed to albumin) is transported through the blood to the liver
  • 9. Bilirubin Metabolism  Bilirubin is taken up via facilitated diffusion by the hepatocyte & conjugated with glucuronic acid to form bilirubin diglucuronide
  • 10. Bilirubin Metabolism Conjugated bilirubin is actively secreted into bile and then the intestine In the intestine, glucuronic acid is removed by bacteria. The resulting bilirubin is converted to urobilinogen
  • 11. Bilirubin Metabolism  Some of urobilinogen is reabsorbed from the gut & enters the portal blood A portion of urobilinogen participates in the enterohepatic urobilinogen cycle The reminder is transported by the blood to the kidney, where it is converted to yellow urobilin & excreted, giving the urine its characteristic color Urobilinogen
  • 12. Bilirubin Metabolism Urobilinogen is oxidized by intestinal bacteria to brown stercobilin
  • 13. Plasma Bilirubin Normal : 0.2–0.8 mg/dl Unconjugated bilirubin: 0.2–0.6 mg/dl Conjugated bilirubin: 0–0.2 mg/dl Hyperbilirubinemia: >1mg/dl Latent jaundice: 1 - 2 mg/dl Clinical jaundice: > 2 mg/dl
  • 14. Terminology Jaundice: Refers to the yellowish discoloration of sclera, conjunctiva, skin & mucous membrane due to deposition of bilirubin secondary to hyperbilirubinemia Icterus: Greek term for jaundice Kernicterus: Bilirubin encephalopathy. It is a neurological syndrome resulting from destruction of basal ganglia by deposition of bile pigment in severe hemolytic anemia specially in premature infant whose BBB is underdeveloped
  • 15. Classification of Jaundice Hemolytic (prehepatic) • Hemolysis/ abnormal RBC • Antibodies • Drugs & toxins • Thalassemia • Hemoglobinopathies Hepatocellular (hepatic) • Viral hepatitis • Toxic hepatitis • Intrahepatic cholestasis • Gilbert's syndrome • Criglar-Najjar syndrome Obstructive (posthepatic) • Extrahepatic cholestasis • Gall stone • Tumors of bile duct • Carcinoma head of the pancreas • Carcinoma ampulla of Vater
  • 16. Jaundice Hemolytic (prehepatic) Hepatocellular (hepatic) Obstructive (posthepatic) Underlying condition Overproduction of bilirubin Decreased conjugation of bilirubin Obstruction of common bile duct (extrahepatic cholestasis Total bilirubin Increased Increased Increased Conjugated bilirubin Normal Increased Increased Unconjugated bilirubin Increased Increased Normal
  • 17. Jaundice Hemolytic (prehepatic) Hepatocellular (hepatic) Obstructive (posthepatic) Urobilinogen Increased Increased Absent Urine color Normal Dark (urobilinogen + conjugated bilirubin) Dark (conjugated bilirubin) Stool color Normal Normal/ Pale Pale Conjugated bilirubin in urine Not present Present Present ALT/ AST Normal Increased Normal ALP Normal Normal Increased