Liver Functions & Investigations Flashcards

1
Q

What is the Liver?

A
  • Located in the upper right quadrant of the abdomen
  • Largest Organ in the Body
  • Vital role in metabolism
  • Large capacity for regeneration
  • Large functional reserve capacity
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2
Q

What is the structure of the Liver?

A

Dual blood supply:

  • 2/3 from portal vein which drains from the gut
  • Everything from the gut comes straight to the liver
  • Remainder from the hepatic artery

Substances for excretion are secreted from hepatocytes into canaliculi

  • These lead to intrahepatic ducts
  • Finally reach the duodenum via the common bile duct
  • Bile canaliculus is a thin tube that collects bile secreted by hepatocytes. The bile canaliculi merge and form bile ductules, which eventually become the common hepatic duct.

Hepatocytes constitute 60% liver mass

  • Each hepatocyte is in contact with: Sinusoid, Bile canaliculus, Neighbouring hepatocyte
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3
Q

What are liver functions?

A
  • Carbohydrate metabolism: Gluconeogenesis, Glycogen synthesis and metabolism
  • Fat Metabolism: Fatty acid synthesis, Cholesterol synthesis and excretion, Lipoprotein synthesis, Bile Acid synthesis, Ketogenesis
  • Protein Metabolism: Synthesis of plasma proteins (not Igs), Urea synthesis and nitrogen removal
  • Hormone Metabolism: Metabolism of steroid hormones, 25-hydroxylation of vitamin D, Metabolism of polypeptide hormones
  • Storage: Glycogen, Vitamins A, Vitamin B12, Iron
  • Toxin/Drug: Metabolism and Excretion
  • Bilirubin: Metabolism and Excretion
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4
Q

What is the use of Liver Function Tests?

A
  • Screening for the presence of liver disease
  • Assessing prognosis
  • Measuring the efficacy of treatments for liver disease
  • Differential diagnosis: predominantly hepatic or cholestatic
  • Assessing severity, especially in patients with cirrhosis
  • Monitoring disease progression
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5
Q

What are clinical manisfestations of Liver Disease?

A
  • Ascites
  • Hepatic Encephalopathy
  • Hepatorenal syndrome
  • Jaundice
  • Disordered Haemostasis
  • Enzyme Release
  • Portal Hypertension
  • Palmar Erythema
  • Gynaecomastia
  • GI Varices
  • Spider Naevi
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6
Q

What is included in the Liver Profile test?

A

Usually includes:

  • Serum bilirubin
  • AST or ALT: Indicate hepatocellular damage
  • ALP: Indicate a cholestatic picture
  • Serum albumin: Determines synthetic function and Determines chronicity of disease

May also include:

  • PT or INR: Determines synthetic function and Helps identify severity of disease
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7
Q

What is hepatic and cholestasis?

A

Hepatocellular injury

  • Injury to hepatocytes causes intracellular contents to be released

Cholestasis

  • Reduction or absence of bile flow in the duodenum
  • Impairment of bile secretion at the level of bile ductules
  • Functional defect in bile formation at hepatocyte level
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8
Q

How Haem broken down?

A
  • Heme is converted to Bilverdin by Heme Oxygenase
  • Bilverdin is converted to Unconjugated Bilirubin by Bilverdin Reductase
  • Unconjugated Bilirubin is converted to Conjugated Bilirubin through addition of glucoronic acid by UDP-glucuronyltransferase (UGT) which can be readily excred in urine and faeces
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9
Q

How is Bilirubin transported?

A
  • Reversible addition of albumin allows unconjugated bilirubin to be transported in the blood yet kept in the vascular space
  • Free bilirubin can cause cerebral toxicity
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10
Q

How is Bilirubin metabolised?

A
  • In the intestinal tract bilirubin glucuronides are hydrolysed and reduced by bacteria to form colourless urobilinogens
  • These undergo enterohepatic circulation
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11
Q

What are bile acids and how are they produced?

A
  • Cholesterol homeostasis is largely maintained by the conversion of cholesterol to bile acids and their subsequent metabolism
  • Requires the terminal ileum to absorb bile acids for recirculation
  • Essential to normal digestion especially the absorption and metabolism of fats
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12
Q

What are characterisitics of Alanine Aminotransferase?

A
  • In terms of tissue distribution, most specific marker for liver injury (with GGT)
  • Also found in Muscle and kidney
  • Half life is ~47 hours
  • Cytosolic enzyme and therefore released upon cellular injury
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13
Q

What are characterisitics of Aspartate Aminotransferase?

A
  • AST is found in the liver, cardiac muscle, skeletal muscle, kidneys, brain, pancreas, lungs, leukocytes, and erythrocytes
  • Less specific than ALT for liver disease
  • Half life is ~17 hours
  • Found in the cytosol and mitochondria
  • Immunologically distinct isoenzymes
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14
Q

What are characteristics of γ Glutamyl Transferase (GGT)?

A
  • Enzyme catalyses transfer of the gamma-glutamyl group from peptides such as glutathione to other peptides and to L-amino acids
  • Relatively specific marker for liver injury but also found in cell membrane of kidneys, pancreas, gall bladder, spleen, heart and brain
  • Membrane-bound glycoprotein enzyme
  • Found on canalicular membrane of hepatocytes
  • In neonates, serum GGT activity is 6 - 7 times that of adults
  • Levels decline to adult levels by 5 to 7 months
  • Enzyme induction by drugs such as barbiturates and phenytoin
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15
Q

What are characteristics of Alkaline Phosphatase (ALP)?

A
  • Found in a number of tissues, primarily reflects bone and liver
  • Also intestinal and placental ALP
  • Membrane-bound glycoprotein enzyme
  • Found on canalicular membrane of hepatocytes
  • Major value in diagnosis of cholestatic disease
  • ALP is elevated in children which correlates well with rate of bone growth and appears to be accounted for by the influx of enzymes from osteoid tissue
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16
Q

What does hypoalbuminemia reflect?

A

-Hypoalbuminemia does not always reflect the presence of hepatic synthetic dysfunction

  • Negative acute phase reactant
  • Decreased in systemic inflammation, the nephrotic syndrome and malnutrition
  • Patients with ascites who may become hypoalbuminemic despite good hepatic synthetic function because of the increase in plasma volume

-Relatively long half life of ~20 days

-Hypoalbuminemia is more common in chronic liver disorders such as cirrhosis

17
Q

How does the Liver fucntion affect PT and INR?

A
  • Severe liver damage causes decrease in concentration of short lived hepatic proteins
  • Liver is the major site of synthesis of 11 blood coagulation proteins
  • Clotting factor deficiency frequently occurs during the course of liver disease: Prolonged Prothrombin Time (PT)/INR
18
Q

Is the prolonged PT specific to Liver disease?

A
  • May result from various conditions causing consumption of clotting factors (e.g. DIC or severe GI bleeding) and certain drugs
  • May be caused by a deficiency of vitamin K, which may be induced by inadequate dietary intake, prolonged cholestasis, intestinal malabsorption, or the administration of antibiotics that alter the gut flora
19
Q

How does the liver function affect the immune functions?

A

Immunoglobulins - Polyclonal increase is a frequent finding of chronic liver disease and may cause an increase in plasma total protein

  • IgA is often increased in all types of cirrhosis
  • IgG is often increased in autoimmune hepatitis and cirrhosis
  • IgM is often increased in primary biliary cirrhosis
  • All are non specific changes

Autoantibodies give more specific information:

  • Anti-mitochondrial antibody is increased in nearly all cases of primary biliary cirrhosis
  • Anti-smooth muscle and ANA increased in many cases of autoimmune hepatitis
20
Q

How does liver function affect urea and ammonia?

A

Urea

  • Patients with end stage liver disease may have a low plasma concentration of urea, but increased concentrations of urea precursors ammonia & amino acids

Ammonia

  • Produced mainly by the action of bacterial proteases, ureases and amine oxidases acting on GI tract components meaning the ammonia concentration in the portal vein is typically 5 – 10 fold that of the systemic circulation.
  • Under normal conditions this is mainly made to urea by hepatocytes as part of the urea cycle.
  • Severe or chronic liver disease leads to significant impairment of normal ammonia metabolism
21
Q

What are the effect of the liver function of ceruloplasmin, A1AT and αfetoprotein?

A

-αfetoprotein

  • A normal component of foetal blood which falls to adult concentrations by 1 year of age
  • Mild increases are seen in patients with acute and chronic hepatitis and indicate hepatocellular regeneration
  • Present at higher concentrations in hepatocellular carcinoma

-Caeruloplasmin

  • Protein decreased in Wilson’s, cirrhosis and many causes of chronic hepatitis but maybe increased in inflammation, cholestasis, haemochromatosis, pregnancy and oestrogen therapy masking the expected decrease in Wilson’s

-α1-Antitrypsin

  • Major serine protease inhibitor in plasma decreased in homozygous deficiency and cirrhosis and increased in acute inflammation
22
Q

What are other tests of liver function?

A
  • Other non biochemical investigations of hepatobiliary disease also exist including ultrasound, cholangiography, CT or MRI
  • Other liver tests include dynamic tests which give an indication of functional hepatic cell mass – these are infrequently used. These tests measure the liver’s ability to clear endogenous or exogenous substances from the circulation. Clearance tests such as bromsulphalein (BSP) and indocyanine green (ICG)
23
Q

What are patterns of LFT abnormalities?

A

Hepatocellular pattern

  • Disproportionate elevation in the ALT/AST compared with ALP
  • Serum bilirubin may be elevated
  • Tests of synthetic function may be abnormal

Cholestatic pattern

  • Disproportionate elevation in ALP compared with ALT/AST
  • Serum bilirubin may be elevated
  • Tests of synthetic function may be abnormal

Isolated hyperbilirubinaemia

  • As the name implies, patients with isolated hyperbilirubinemia have an elevated bilirubin level with normal ALT/AST and ALP
24
Q

How are LFTs interperated?

A
  • Serum aminotransferases are elevated in most liver diseases
  • Highest elevations occur in disorders associated with extensive hepatocellular injury e.g. acute viral hepatitis, ischemic hepatitis (shock liver) and acute toxin-induced liver injury
  • Extent of liver cell necrosis correlates poorly with the magnitude of serum aminotransferase elevation
  • In primarily cholestatic disease there may be secondary hepatocellular damage and increased plasma aminotransferases
  • In cirrhosis concentration of plasma proteins decreases, whilst immunoglobulin concentration increases
  • Many liver proteins have relatively long half lives e.g. Albumin ½ life is ~20 days
  • Sensitivity and specificity of protein concentrations for the diagnosis of liver disease are far from ideal
25
Q

What are other disease show abnormal LFTs?

A
  • Heart failure
  • Sepsis/Infection
  • Inflammation
26
Q

What does the ALT:AST ratio show?

A

ALT:AST <2

  • Cirrhosis
  • Metastatic liver disease
  • Alcoholic Liver disease

ALT:AST >2

  • Viral hepatitis
  • Drugs/Toxins
  • NASH
  • Intra/extrahepatic obstruction
27
Q

How is Bilirubin measured and classified?

A

Total Bilirubin → Unconjugated & conjugated bilirubin (& delta-bilirubin)

Direct → Conjugated bilirubin (& delta-bilirubin)

Indirect → Unconjugated bilirubin maybe calculated

28
Q

What does increased indirect bilirubin show?

A
  • Overproduction of bilirubin (usually caused by haemolysis)
  • Decreased hepatic uptake
  • Abnormalities in conjugation (primarily due to congenital defects involving UGT)
  • Severe liver injury e.g. end stage cirrhosis
29
Q

What does increased direct bilirubin indicate?

A
  • Mechanical or functional impairment of bilirubin excretion from the hepatocyte
  • Biliary obstruction
30
Q

What is Jaundice?

A
  • Often used interchangeably with hyperbilirubinemia
  • Yellow discolouration of tissues due to bilirubin deposition
  • Clinical jaundice may not be evident until plasma bilirubin is >2.5x the ULN i.e. > 50 μmol/l
  • The causes of hyperbilirubinemia presenting in the neonatal period are quite different from those presenting later in life
31
Q

What are causes of Jaundice?

A

Haemolysis (increased bilirubin production):

  • Acquired autoimmune haemolytic anaemia
  • Drug induced
  • Congenital spherocytosis

Hepatocellular Damage (impaired bilirubin metabolism):

  • Toxins
  • Infections

Cholestasis (decreased bilirubin excretion):

  • Cirrhosis
  • Tumour
  • Gallstones