Hyperhomocysteinemia and functional cobalamin deficiency due to granulocytosis-induced alterations in the cobalamin-binding protein

Haematologica. 2006 Mar;91(3):394-6.

Abstract

Serum cobalamin and homocysteine levels were studied in patients with chronic myelogenous leukemia (CML) and in stem cell donors treated with granulocyte-colony stimulating factor (G-CSF). Cytoreductive treatment in patients with CML resulted in a decrease of cobalamin and homocysteine levels. In stem cell donors cobalamin and homocysteine levels increased after G-CSF administration. The increase of homocysteine level was accompanied by a decrease in the serum levels of the cobalamin-binding protein transcobalamin. We hypothesize that the increased homocysteine levels in patients with CML and donors treated with G-CSF may be the result of a functional methylcobalamin deficiency due to decreased transcobalamin levels.

Publication types

  • Comparative Study

MeSH terms

  • Granulocyte Colony-Stimulating Factor / therapeutic use
  • Humans
  • Hyperhomocysteinemia / blood*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / blood
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy
  • Transcobalamins / metabolism*
  • Vitamin B 12 Deficiency / blood*
  • Vitamin B 12* / analogs & derivatives
  • Vitamin B 12* / blood

Substances

  • Transcobalamins
  • Granulocyte Colony-Stimulating Factor
  • mecobalamin
  • Vitamin B 12