Biochemistry · Amino Acid Metabolism and Urea Cycle (Disorders, Phenylketonuria)

Histidine is degraded to glutamate via formiminoglutamate (FIGLU). In severe folate deficiency, which laboratory finding follows from this pathway?

  • A Decreased urinary FIGLU after histidine loading
  • B Increased urinary FIGLU excretion, the basis of the FIGLU test
  • C Elevated serum methylmalonic acid with normal homocysteine
  • D Increased urinary orotic acid from impaired pyrimidine recycling
Correct answer: B. Increased urinary FIGLU excretion, the basis of the FIGLU test

Explanation

Formiminoglutamate transfers its formimino group to tetrahydrofolate during histidine catabolism. Without THF, FIGLU accumulates and spills into urine, so a histidine load produces excess urinary FIGLU, the classical FIGLU test for folate deficiency. Option C describes vitamin B12 deficiency, where methylmalonic acid rises but homocysteine also rises, so it does not match. Orotic acid reflects urea cycle or pyrimidine pathway blocks, unrelated to folate.

Reference: Harper's Illustrated Biochemistry, 32nd ed.

High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP

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