Idiopathic macrocytic anaemia in the aged: molecular and cytogenetic findings

Br J Haematol. 1995 Aug;90(4):797-803. doi: 10.1111/j.1365-2141.1995.tb05198.x.

Abstract

Macrocytosis in the elderly is often caused by abnormalities of haematological stem cell differentiation. In this study, a group of elderly patients was analysed for four molecular and cell biological parameters. The aim of the study was to screen elderly patients with idiopathic macrocytic anaemia or MDS for a set of alterations which are related to haematological dysplasia. The analyses used were: DNA-methylation at the calcitonin A gene 5'-area, NRAS point mutations at codons 12 and 13, in vitro colony formation of peripheral blood progenitor cells and cytogenetics of bone marrow cells. The results show that a significant portion of elderly patients with idiopathic macrocytosis have one or more of the abnormalities analysed. Hypermethylation of the calcitonin A gene 5'-area at the chromosome 11 band p15 is relatively common (7/15). Chromosomal aberrations (3/12) and NRAS oncogene point mutations (0/15) were rare findings. In vitro culture of erythroid progenitor cells was relatively frequently abnormal (7/15). Eight of our nine macrocytic patients who did not fulfill the FAB criteria for MDS had at least one of the alterations studied; this suggests that these patients might represent early phases of a stem cell disorder.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Anemia, Macrocytic / genetics
  • Anemia, Macrocytic / pathology*
  • Calcitonin / genetics
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 11
  • DNA / metabolism
  • Female
  • Hematopoietic Stem Cells / pathology
  • Humans
  • Karyotyping
  • Male
  • Methylation
  • Myelodysplastic Syndromes / genetics
  • Myelodysplastic Syndromes / pathology*
  • Point Mutation

Substances

  • Calcitonin
  • DNA