Liver Function Tests Flashcards

1
Q

Explain how billirubin is metabolized and excreted both in a normal person and in a person with high levels of billirubin.

A

Billirubin is a breakdown product of heme. In the body, 85% of heme comes from the metabolism of old RBCs, but the remainder comes from recycling of myoglobin and enzymes that contain heme (cytochromes, catalases). The metabolism of heme to billirubin takes place in either macrophages or hepatocytes. Once billirubin is produced in these cells, it is secreted into the blood where it binds to albumin. Albumin carries it to the liver where the billirubin is actively uptaken into the hepatocyte and albumin is released back into the bloodstream. Once inside the liver cell, billirubin undergoes conjugation where it is made into glucuronide - billirubin by the enzyme UDP-glucuronide transferase. In a normal healthy person who does not have high levels of billirubin, conjugated billirubin is secreted from the liver in the bile and goes to the gallbladder. Once in the gallbladder, it is secreted as bile into the small intestine. In the GI tract, it is acted upon by bacteria in the colon which turn it into urobilogen. Urobilogen can be excreted in the feces (gives feces its brown color) or it can be absorbed into the blood and secreted in the urine. This is all normal.

When a person has high levels of billirubin in their blood, their liver is processing more billirubin than a normal person. As such, high levels of conjugated billirubin can accumulate in the liver and some of this can be secreted into the blood instead of the bile. Once in the blood, the conjugated billirubin is excreted in the urine, giving the urine a very dark yellow color. Additionally, when high billirubin is present in the blood, it’s possible that the person may not be able to uptake it all into the liver and you can see unconjugated billirubin in the blood. This cannot be excreted so it circulates and causes jaundice.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the risk factors for liver disease?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What liver pathology is seen here?

A

Cirrhosis that leads to obstruction of biliary secretion from liver so there is green nodules on liver due to build up of bile in liver

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What liver pathology is seen here?

A

Fatty liver (alcoholism, diabetes, metabolic syndrome, obesity)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What liver pathology is seen here?

A

Ascites

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the 3 classifications of jaundice?

A
  • Pre-hepatic / hemolytic –> drug induced, hemolytic anemia, etc –> results in build up of billirubin in blood that is unconjugated b/c liver can’t conjugate fast enogh
  • Hepatocellular –> damge to liver from toxins, infections, etc –> results in build up of both conjugated and unconjugated billirubin
  • Post-hepatic –> liver function is fine but there is an issue getting bile from liver to gallbladder (cirrhosis, tumor, gallstones) –> results in build up of conjugated billirubin
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

If unconjugated billirubin is found in the serum, it is most likely due to […]

A

Hemolytic disorder

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

If conjugated billirubin is found in the serum, it is most likely due to […]

A

Liver and/or billiary tract disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

If a person has unconjugated billirubin in serum, will you find billirubin in their urine?

A

No - can’t be excreted

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Billirubin found in the urine implies […]

A

That the billirubin is conjugated and the presence of hepatobilliary disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the possible causes of unconjugated hyperbillirubinemia?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
  • What is different about seeing unconjugated hyperbillirubinemia in a newborn vs. an adult?
  • What are the causes of this in a newborn?
  • What is the treatment if it is found to be pathologic?
  • What is the biggest consequence of untreated hyperbillirubinemia in a newborn?
A
  • It is sometimes not pathologic in newborn b/c their hepatobiliary system is immature so in some infants it clears on its own as the liver develops more
  • See slide for rest of questions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Why do we measure blood ammonia in relation to liver function?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

There are several liver enzymes that can be tested for tin the serum. What does increased enzyme activity tell you?

A

Only tells you about liver dysfunction, not liver function

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Let’s say a person has jaundice and you need to distinguish between the causes of jaundice. What 3 enzymes can be measured in serum to check for liver dysfunction that indicates hepatocellular damage?

A

AST

  • Non-specific to liver, also in RBCs so can be high with hemolytic jaundice also
  • Extramitochondrial and mitochondrial

ALT

  • Found primarily in liver, if this is high it indicates liver damage
  • Strictly extramitochondrial

LDH

  • Cytosolic enzyme, has several isozymes throughout body so it has poor diagnostic sensitivity and specificity for liver disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q
  • Let’s say that a person has elevated levels of AST and ALT. How do you distinguish between elevation that signals liver disease and elevation that may not be due to liver disease?
  • What does the ratio of AST:ALT tell you?
A
  • Normal range in serum is 10-20 Units/Liter
  • 20 U/L - 300 U/L is not specific to liver disease
  • > 1000 U/L indicates extensive liver damage due to drugs, virus, toxins
  • See image
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Let’s say a person has jaundice and you need to distinguish between the causes of jaundice. What 3 enzymes can be measured in serum to check for liver dysfunction that indicates cholestasis or post-hepatic jaundice?

A

AlkPhos (ALP)

  • Has isozymes in other parts of body, but is found near biliary cannaliculi in liver
  • If elevated, and you don’t suspect other possible sources of elevation, it’s good indication of issue with biliary tract

Gamma glutamyl transpeptidase (GGT)

  • Helps in DiffDx when ALP is elevated but you may suspect another cause of elevated ALP (bone disease)

5’-nucleotidase (5’-NT)

  • Also found near bile cannalicular membrane, but not widely used clinically
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

In the image below, which liver enzymes would you expect to be elevated in the following types of jaundice?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Serum albumin is made exclusively by the liver. Is it a good measure of liver function?

A

It has a long half life (3 weeks) so if it is not normal it cannot detect acute disturbances to liver function. However, hypoalbuminemia is common in chronic liver disease like cirrhosis and reflects severe damage. However, you can also see hypoalbuminemia in other disorders. Important to measure other things too.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What does increased globulins in blood tell you?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Since albumin levels can’t detect acute liver damage, what other thing can you measure in the serum that can?

A

If you have cholestasis and can’t get bile into GI tract, you can’t absorb fat so you can’t absorb vitK which can lead to decreased clotting factors since many of these require vitK

22
Q

What other tests, aside from serum enzymes, albumin, globulin, and clotting factors, can be ordered to assess liver function?

A

Serology to look for virus

  • Hep A,B,C,D,E
  • Autoimmune Hep

Liver Biopsy

  • Look at histological differences

Imaging

  • Ultrasound, CT, MRI
23
Q

Compare the utility of LFTs with their limitations.

A
24
Q
A
25
Q

How is alcohol excreted?

A

Lungs, sweat, urine. Amount of excretion via these routes depends on how much is present in blood (i.e. at high blood alcohol see it excreted in breath, but not usually at low levels)

26
Q

What are the various ways in which alcohol is metabolized by the body?

A

Mostly liver, remainder occurs in brain, pancreas and stomach

Mechanisms of metabolism:

  • 80% via:
    • Ethanol –(alcohol dehydrogenase)–> Acetaldehyde –(aldehyde dehydrogenase)–>acetate
  • Remainder via:
    • Ethanol –(catalase)–>acetaldehyde –(aldehyde dehyrogenase)–> acetate
    • Ethanol –(CytP4502E1)–>acetaldehyde –(aldehyde dehyrogenase)–> acetate
27
Q

What is antabuse?

A

Antabuse uses drugs to treat alcoholism. These drugs cause a buildup of acetaldehyde in the blood from the rapid conversion of ethanol to aldehyde and slow conversion of aldehyde to acetate. This causes the person to feel terrible and not get any of the rewarding effects of drinking the alcohol.

28
Q

What is the Microsomal ethanol oxidizing system?

A
  • Rxn: Ethanol –(CytP4502E1)–> acetaldehyde –(aldehyde dehydrogenase)–> acetate
  • Inducible by chronic alcohol consumption
29
Q

All mechanisms of detoxifying alcohol result in a […] NADH:NAD+ ratio.

A

High –> the reactions result in the oxidation of the substrate so NAD+ is reduced to NADH as a result

30
Q

What compounds are produced as a result of alcohol metabolism?

A

ROS

31
Q

Why is GGT viewed as a possible marker for chronic alcohol abuse?

A

It is an inducible enzyme that is increased in the presence of chronic alcohol use (remember this detects cholestatic liver disease)

32
Q

Acetaldehyde is [short/long] lived in the body and is […] reactive. It causes acute [….] like effects.

A

Short

highly chemically

Antabuse

33
Q

What are the direct toxic effects of too much ethanol in the body?

A

Ethanol, if present in high enough quantities such that it cannot be detoxified quick enough, is able to integrate itself into biological membranes leading to increased membrane fluidity. This is particularly dangerous for the blood brain barrier, which needs to be kept as a very tight barrier.

34
Q

What are the metabolic consequences of alcohol detoxification resulting in a high NADH:NAD+ ratio?

A
  • Other important metabolic reactions require NAD+ in order to function.
    • If there is insufficient NAD+, then pyruvate that is produced at the end of glycolysis will be preferentially converted to lactate to try and restore levels of NAD+ (pyruvate –> lactate consumes NADH and regenerates NAD+). This will prevent the pyruvate from being used in TCA and ETC, resulting in decreased cellular metabolism when in a fed state.
    • Additionally, when in a fasted state, gluconeogenesis will be inhibited as well because pyruvate is needed as a substrate so the body will be unable to make new glucose when fasted.
    • Fatty acid oxidation will also be inhibited because one of the steps in oxidizing the acetyl-coA to fatty-acyl coA requries NAD+.
    • NADH is used directly by the ETC to synthesize ATP. High NADH signals to the body that it’s in a high energy state, and slows glycolysis and, FA oxidation, and TCA cycle.
35
Q

What are the consequences of a build up of acetaldehyde from alcohol metabolism?

A
36
Q

What are the consequences of a build up of acetate from alcohol metabolism?

A

Acetate can be converted to acetyl-coA which is used to generate fatty acids leading to a fatty liver. The liver can attempt to deal with this excess fat by storing the fat in VLDL which is then secreted into the blood. This can result in increased peripheral vascular damage in the form of atherosclerosis due to hypertriglyceridemia. Additionally, if acetate is converted to acetyl-coA, then high acetyl-coA will shut off the TCA. As noted, some of this will be shuttled to fatty acid synthesis, but some will also be used to make ketone bodies leading to acidosis and ketosis.

37
Q

Why would you see hypoglycemia in a person who abuses alcohol?

A

They are likely to be malnourished. Since they’re not taking in enough glucose because they likely get most of their calories from alcohol, they also are likely to have depleted glycogen stores. This puts them in a position to rely heavily on gluconeogenesis for new glucose to feed the brain. However, gluconeogenesis will be inhibited because of insufficient NAD+ that is needed to convert TCA precursors to pyruvate and the fact that any pyruvate that is made will be converted to lactate. Thus, they are at risk for hypoglycemia.

38
Q

How does high NADH:NAD+ relate to ROS?

A

High NADH:NAD+ also makes the cells more susceptible to damage from ROS because there is not enough NAD+ to oxidize the ROS

39
Q

Why are patients who abuse alcohol likely to present with acidosis?

A

Build up of lactic acid and ketoacids

40
Q

What is alcoholic liver disease?

A

Liver injury attributed to alcohol abuse

41
Q

What is the threshold at which a person is at risk for damaging their liver from alcohol consumption?

A

About 4 drinks/day for men and 2 drinks/day for women for a sustained period of time (I think he said 12 months). Exceeding threshold amounts in some liver injury in all persons but less than 50% will develop serious liver disease.

42
Q

True or false: damge to the liver from alcohol consumption is always irreversible.

A

False - there is a point at which, once crossed, abstinance from alcohol use no longer allows for return to baseline. However, before this threshold is crossed, it is possible for the liver to recover.

43
Q

Why does cirrhosis lead to portal HTN?

A

Damage from alcohol –> fibrosis –> nodule formation and disruption of normal liver sinusoid architecture leading to narrowed / blocked sinusoids –> blood can’t flow through sinusoids normally –> increased resistance to flow –> portal HTN

44
Q

Why does portal HTN lead to varices and GI bleeding?

A

Blood can’t flow in portal system due to high resistance to flow –> is rerouted through the systemic circulation via anastamoses between portal system and systemic veins –> this distends systemic veins and increases pressure in these veins which can lead to visibly distended veins (particularly on front abdominal wall) –> high pressure distended veins can lead to increased potential for ruture and GI bleeding

45
Q

Where is it most common to see varices?

A

Esophagus, rectum, stomach, abdominal wall (places where there are anastamoses)

46
Q

Why does ascites develop with liver damage?

A

Ascites is when lymph fluid leaks across hepatic sinusoids and leads to swelling of the abdomen. Thsi happens during cirrhosis because the sinusoids have increased pressure which pushes lymph fluid out into abdomen.

47
Q

What is hepatic encephalopathy?

A
48
Q

Other than diseases of the liver, what else might be observed or might develop in patients who abuse alcohol?

A

Hepatocellular carcinoma

Esophageal Cancer

Acute and/or chronic pancreatitis (–> diabetes)

Stroke

Cardiac disease

Fetal Alcohol syndrome

49
Q

What do each of these lab tests tell you about this patient and their chronic alcoholism?

A
50
Q

What vitamin deficiencies would you expect in a person who is a chronic alcoholic?

A