Master Fructose Intolerance with Picmonic for Medicine

Fructose-1-phosphate is degraded by aldolase B into dihydroxyacetone-phosphate (DHAP) and glyceraldehyde (GA). A deficiency of aldolase B results in the accumulation of fructose-1-phosphate in cells and phosphate trapping.

Fructose-1-phosphate is degraded by aldolase B into dihydroxyacetone-phosphate (DHAP) and glyceraldehyde (GA).

A deficiency of aldolase B results in the accumulation of fructose-1-phosphate in cells. This traps phosphate in an unusable form that does not return to the general phosphate pool, resulting in depletion of phosphate and ATP stores. This has downstream effects on gluconeogenesis and glycogenolysis and the regeneration of ATP.

Glycogenolysis is the breakdown of glycogen to glucose-1-phosphate and glucose. In hereditary fructose intolerance, the accumulation of fructose-1-phosphate in cells leads to trapping of phosphate which decreases the amount of ATP available to cells. Decreased ATP leads to inhibition of glycogenolysis and gluconeogenesis.

Gluconeogenesis is a metabolic pathway that results in the generation of glucose from substrates such as lactate, glycerol, and glucogenic amino acids. In hereditary fructose intolerance, the accumulation of fructose-1-phosphate in cells leads to the trapping of phosphate which decreases the amount of ATP available to cells. Decreased ATP leads to inhibition of glycogenolysis and gluconeogensis.

Due to inhibition of glycogenolysis and gluconeogenesis, individuals with hereditary fructose intolerance suffer from hypoglycemia.

Vomiting is a common nonspecific symptom in hereditary fructose intolerance. Vomiting can also be seen secondary to hypoglycemia in this disorder.

Jaundice is yellowing of the skin and conjunctival membranes caused by hyperbilirubinemia, and it is often caused by liver disease. Aldolase B is preferentially expressed in the liver and deficiency can cause liver damage with presentation of jaundice.

Cirrhosis is characterized by fibrosis and scarring of the liver, leading to loss of function. Because aldolase B is expressed in the liver, deficiency can cause liver damage and cirrhosis.

This disease is inherited in an autosomal-recessive fashion.