Telomere length and heavy-chain mutation status in familial chronic lymphocytic leukemia

Leuk Res. 2002 Sep;26(9):791-4. doi: 10.1016/s0145-2126(02)00010-3.

Abstract

We examined whether telomere lengths of peripheral blood mononuclear cells are associated with immunoglobulin gene usage in 21 familial chronic lymphocytic leukemia (CLL) patients. Subjects with unmutated V genes tended to have shorter telomeres than those with somatic mutations, especially after adjusting for age. Unlike V(H) mutation status, telomere length was not predictive for survival. Our results suggest that telomere length is associated with V(H) gene mutation status and provides further evidence that the biological basis of familial B-CLL is similar to that of sporadic patients.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • DNA, Neoplasm / genetics
  • Female
  • Gene Rearrangement, B-Lymphocyte, Heavy Chain*
  • Genes, Immunoglobulin*
  • Humans
  • Immunoglobulin Heavy Chains / genetics*
  • Immunoglobulin Variable Region / genetics*
  • Leukemia, Lymphocytic, Chronic, B-Cell / classification
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics*
  • Leukemia, Lymphocytic, Chronic, B-Cell / mortality
  • Life Tables
  • Male
  • Middle Aged
  • Neoplastic Syndromes, Hereditary / genetics*
  • Neoplastic Syndromes, Hereditary / mortality
  • Prognosis
  • Somatic Hypermutation, Immunoglobulin*
  • Survival Analysis
  • Telomere / ultrastructure*

Substances

  • DNA, Neoplasm
  • Immunoglobulin Heavy Chains
  • Immunoglobulin Variable Region