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Liver Function Tests (LFTs) PowerPoint Presentation

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Description : Check out this medical presentation on Alanine Aminotransferase (alanine transaminase), which is titled "Liver Function Tests (LFTs)", to know about the major metabolic functions of the liver and causes of liver dysfunction, and the markers of liver function tests such as liver enzymes, bilirubin, albumin and prothrombin time that can diagnose hepatic injury and assess hepatic function.

Tags : Alanine Aminotransferase, alanine transaminase, Liver Function Tests, LFTs, metabolic functions, liver dysfunction

Published on : Jul 05, 2021 | Views : 6670 | Downloads : 30

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Slide 1-

Liver Function Tests (LFTs) GIT/Hematology Block
Slide 2-

Objectives Upon completion of this lecture, the students should be able to: Understand the major metabolic functions of the liver and causes of liver dysfunction. Discuss markers of liver function tests such as liver enzymes, bilirubin, albumin and prothrombin time that can diagnose hepatic injury and assess hepatic function.
Slide 3-

Major Metabolic Functions of the Liver Synthetic Function Plasma proteins (albumin, globulins), cholesterol, triglycerides and lipoproteins Detoxification and excretion Ammonia to urea (urea cycle), bilirubin, cholesterol, drug metabolites Storage Function Vitamins A, D, E, K and B12 Production of bile salts Helps in digestion
Slide 4-

Some example of liver dysfunction Hepatocellular disease Cholestasis (obstruction of bile flow) Cirrhosis Hepatitis Jaundice Liver cancer Steatosis (fatty liver) Genetic Disorders Hemochromatosis (iron storage)
Slide 5-

Liver Function Tests (LFTs) Noninvasive methods for screening of liver dysfunction Help in identifying general types of disorder Assess severity and allow prediction of outcome Disease and treatment follow up
Slide 6-

Liver Function Tests (LFTs) Broadly classified as: Tests to detect hepatic injury: Mild or severe; acute or chronic Nature of liver injury (hepatocellular or cholestasis) Tests to assess hepatic function
Slide 7-

Classification of LFTs Group I: Markers of liver dysfunction Serum bilirubin: total and conjugated Urine: bile salts and urobilinogen Total protein, serum albumin and albumin/globulin ratio Prothrombin Time
Slide 8-

Classification of LFTs Group II: Markers of hepatocellular injury Alanine aminotransferase (ALT) Aspartate aminotransferase (AST)
Slide 9-

Classification of LFTs Group III: Markers of cholestasis Alkaline phosphatase (ALP) g-glutamyltransferase (GGT)
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Limitations of LFTs Normal LFT values do not always indicate absence of liver disease Liver a has very large reserve capacity Asymptomatic people may have abnormal LFT results Diagnosis should be based on clinical examination
Slide 11-

Common serum liver chemistry tests
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Bilirubin A byproduct of red blood cell breakdown It is the yellowish pigment observed in jaundice High bilirubin levels are observed in: Gallstones, acute and chronic hepatitis
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Serum bilirubin levels Normal 0.2 – 0.8 mg/dL Unconjugated (indirect): 0.2 – 0.7 mg/dL Conjugated (direct): 0.1 – 0.4 mg/dL Latent jaundice: Above 1 mg/dL Jaundice: Above 2 mg/dL
Slide 16-

Bilirubin levels and jaundice
Slide 17-

Urobilinogen (UBG) and bile salts Most UBG is metabolized in the large intestine but a fraction is excreted in urine (less than 4 mg/day) Normally bile salts are NOT present in urine Obstruction in the biliary passages causes: Leakage of bile salts into circulation Excretion in urine
Slide 18-

Serum Albumin The most abundant protein synthesized by the liver Normal serum levels: 3.5 – 5 g/dL Synthesis depends on the extent of functioning liver cell mass Longer half-life: 20 days Its levels decrease in all chronic liver diseases
Slide 19-

Serum Globulin Normal serum levels: 2.5 – 3.5g/dL a and b-globulins mainly synthesized by the liver They constitute immunoglobulins (antibodies) High serum g-globulins are observed in chronic hepatitis and cirrhosis: IgG in autoimmune hepatitis IgA in alcoholic liver disease
Slide 20-

Albumin to globulin (A/G) ratio Normal A/G ratio: 1.2/1 – 1.5/1 Globulin levels increase in hypoalbuminemia as a compensation
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Prothrombin Time (PT) Prothrombin: synthesized by the liver, a marker of liver function Half-life: 6 hrs. (indicates the present function of the liver) PT is prolonged only when liver loses more than 80% of its reserve capacity Vitamin K deficiency also causes prolonged PT Intake of vitamin K does not affect PT in liver disease
Slide 22-

Aspartate aminotransferase (AST) Normal range: 8 – 20 U/L A marker of hepatocellular damage High serum levels are observed in: Chronic hepatitis, cirrhosis and liver cancer
Slide 23-

Alanine aminotransferase (ALT) More liver-specific than AST Normal range (U/L): Male: 13-35 Female: 10-30 High serum levels in acute hepatitis (300-1000U/L) Moderate elevation in alcoholic hepatitis (100-300U/L) Minor elevation in cirrhosis, hepatitis C and non-alcoholic steatohepatitis (NASH) (50-100U/L)
Slide 24-

Alanine aminotransferase (ALT) Appears in plasma many days before clinical signs appear A normal value does not always indicate absence of liver damage Obese but otherwise normal individuals may have elevated ALT levels
Slide 25-

Alkaline phosphatase (ALP) A non-specific marker of liver disease Produced by bone osteoblasts (for bone calcification) Present on hepatocyte membrane Normal range: 40 – 125 U/L Modearte elevation observed in: Infective hepatitis, alcoholic hepatitis and hepatocellular carcinoma
Slide 26-

Alkaline phosphatase (ALP) High levels are observed in: Extrahepatic obstruction (obstructive jaundice) and intrahepatic cholestasis Very high levels are observed in: Bone diseases
Slide 27-

g-glutamyltransferase (GGT) Used for glutathione synthesis Normal range: 10 – 30U/L Moderate elevation observed in: Infective hepatitis and prostate cancers GGT is increased in alcoholics despite normal liver function tests Highly sensitive to detecting alcohol abuse
Slide 28-

Take Home Messages LFTs help detect liver injury and function. LFTs do have some limitations.
Slide 29-

References Lippincott’s Illustrated Reviews Biochemistry: 6th edition, Unit IV, Chapter 21, Pages 282 - 285. Lecture notes: Clinical Biochemistry: 9th edition, Chapter 13, Pages 174 - 187. Clinical Chemistry - Techniques, Principales and Correlations: 6th edition, Chapter 24, Pages 520 -521.