Try it
Biochemistry · Ketone bodies: urine nitroprusside test in DKA
Sample itemA 16-year-old girl with type 1 diabetes is brought with vomiting, Kussmaul breathing, glucose 480 mg/dL and an anion gap acidosis. A urine dipstick using sodium nitroprusside shows only a trace to 1+ ketone reaction. What best explains this?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
D. Beta-hydroxybutyrate predominates because of a high NADH/NAD+ ratio, and the nitroprusside reaction does not detect it
In severe ketoacidosis the mitochondrial redox state is highly reduced, so acetoacetate is converted to beta-hydroxybutyrate, which can outnumber acetoacetate several fold. Nitroprusside reacts with acetoacetate (and weakly with acetone) but not with beta-hydroxybutyrate, so the test can underestimate ketosis. Serum beta-hydroxybutyrate measurement is more reliable.
Option by option
A. Acetoacetate is converted to glucose in the kidney, so very little is excreted
Acetoacetate is not converted to glucose by the kidney, and ketone bodies are excreted in urine.
B. The nitroprusside test detects only acetone, which is volatile and exhaled
Nitroprusside reacts mainly with acetoacetate, and acetone is only a weak reactant.
C. Ketone bodies are not produced in type 1 diabetes, so the acidosis is purely lactic
Insulin deficiency increases hepatic ketogenesis, so the acidosis is from ketoacids.
D. Beta-hydroxybutyrate predominates because of a high NADH/NAD+ ratio, and the nitroprusside reaction does not detect it (correct)
A reduced redox state favours beta-hydroxybutyrate, which the dipstick cannot detect.
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.
More Biochemistry questions
- Nucleotide metabolismA 4-year-old boy has intellectual disability, dystonia, self-mutilation and hyperuricaem…
- VitaminsA patient with megaloblastic anaemia and mild neurological signs has raised serum methyl…
- Amino acid metabolismA baby has a mousy odour, fair skin and developmental delay. Which enzyme is deficient?
- Glycogen storage diseasesA child has severe fasting hypoglycaemia, hepatomegaly, lactic acidosis and hyperuricaem…