NORCET 3 - 2022 (Shift-2)
Biochemistry & Nutrition
Medium

In obstructive liver disease, which one of the following tests of liver function likely remains normal?

Appeared in: NORCET 3 - 2022 (Shift-2)

Explanation

  • Albumin is a protein synthesized by the liver and is a key marker of its long-term synthetic (protein-making) function.
  • It has a long half-life of approximately 2 to 3 weeks.
  • In obstructive liver disease, the primary issue is the blockage of bile flow (cholestasis), which does not immediately impair the liver's ability to produce proteins.
  • Therefore, serum albumin levels typically remain within the normal range (3.5–5.5 g/dL) in the early or acute stages of obstruction.
  • A fall in albumin levels is more indicative of chronic liver disease (like cirrhosis) or severe malnutrition, where synthetic function has been compromised over time.

Why Other Options Were Wrong

  • Option A: AST and ALT are markers of hepatocellular injury. While their primary role is to signal damage to liver cells (as in hepatitis), they can become mildly to moderately elevated during acute biliary obstruction due to pressure and inflammation. They are not the most likely test to remain completely normal.
  • Option B: Alkaline phosphatase (ALP) is a primary marker for cholestasis. Its levels become markedly elevated in obstructive liver disease because its synthesis is increased and its excretion via bile is blocked. It is one of the key abnormal findings, not a normal one.
  • Option D: Like ALP, 5'-Nucleotidase and γ-Glutamyl transpeptidase (GGT) are enzymes that are significantly elevated in cholestatic conditions. A rise in these enzymes confirms that an elevated ALP is of hepatobiliary origin. They are expected to be high, not normal.

Related Visual

A comparative table showing the typical patterns of Liver Function Tests LFTs in Hepatocellular Injury versus Cholestatic Obstructive Injury. Columns should include Test AS...
Clinical Relevance
  • Nursing practice connection: Knowing Interpretation of Liver Function Tests (LFTs) in Cholestatic vs. Hepatocellular Injury helps nurses interpret findings accurately and avoid errors in routine assessment, medication administration, and patient teaching.
  • Recognizing a cholestatic LFT pattern (high ALP/GGT, normal albumin) alerts the nurse to a potential biliary obstruction. This guides patient monitoring for key complications.
  • Nursing priorities for a patient with obstructive jaundice include assessing for and managing pruritus (itching from bile salt deposition), monitoring for bleeding (due to malabsorption of fat-soluble Vitamin K), and observing for pale stools and dark urine.
  • The nurse plays a role in preparing the patient for diagnostic imaging like ultrasound or procedures such as Endoscopic Retrograde Cholangiopancreatography (ERCP) to identify and potentially relieve the obstruction.
How to Approach the Question
  • First, identify the core condition in the question stem: 'obstructive liver disease'.
  • Recall that this condition causes a 'cholestatic' pattern of liver injury, which is distinct from a 'hepatocellular' pattern.
  • Categorize the lab tests in the options based on what they measure: AST/ALT (hepatocellular injury), ALP/GGT/5'-NT (cholestasis), and Albumin (synthetic function).
  • Analyze how each marker behaves in cholestasis. ALP, GGT, and 5'-NT are expected to be high. AST/ALT may be slightly elevated but are not the main feature.
  • Consider the function and half-life of albumin. It reflects long-term protein synthesis and has a long half-life (2-3 weeks), so it is not affected by acute obstructive events.
  • Conclude that albumin is the test most likely to remain within the normal range.
Concept Tested & Keywords
  • Concept Tested: Interpretation of Liver Function Tests (LFTs) in Cholestatic vs. Hepatocellular Injury
  • Stem keywords: obstructive liver disease, liver function tests, normal
  • Lead-in keywords: which one
  • Negative lead-in flag: false

Question ID

QG_ObAU2YKu-_I_w7T6FTK

Reference Book

E6 Medicine Davidson Principles Practice 24e p. 872-874

E6 Medicine Harrison 22e Part 2 p. 539-541

E6 Pathology-Textbook of PATHOLOGYHarsh Mohan Part 3 (515-969) p. 86-88

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