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Biochemistry · Amino acid metabolism: tryptophan load and vitamin B6
Sample itemAfter an oral tryptophan load, a patient on long-term isoniazid excretes large amounts of xanthurenic acid in urine. Deficiency of which vitamin is suggested by this test?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
D. Pyridoxine
Kynureninase, which converts kynurenine onward in tryptophan catabolism, needs pyridoxal phosphate. In deficiency, kynurenine is diverted to xanthurenic acid, which is excreted in excess after a tryptophan load. Isoniazid depletes pyridoxal phosphate, so supplementation is routine.
Option by option
A. Thiamine
Thiamine deficiency affects the pyruvate and alpha-ketoglutarate dehydrogenase complexes and not tryptophan catabolism.
B. Niacin
Niacin deficiency causes pellagra but does not block kynureninase.
C. Riboflavin
Riboflavin is needed for FAD-dependent enzymes and does not cause this metabolite pattern.
D. Pyridoxine (correct)
Correct. Kynureninase needs pyridoxal phosphate, so a block diverts kynurenine to xanthurenic acid.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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