Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathy

J Neurol Sci. 2007 Sep 15;260(1-2):124-31. doi: 10.1016/j.jns.2007.04.022. Epub 2007 Jun 1.

Abstract

The occurrence and nature of cytogenetic aberrations in polyneuropathy associated with IgM monoclonal gammopathy was determined. Therefore, interphase fluorescence in situ hybridization (FISH) was applied in 22 patients with polyneuropathy associated with IgM monoclonal gammopathy, multiplex ligation-dependent probe amplification (MLPA) assay in 18 of these patients and genome-wide-array-based comparative genomic hybridization (CGH) in eight of these 18 patients. Four patients had 10-20% and one patient had 30% B cells with IgH rearrangements; one patient had additional loss of 14qter; one patient had amplification of 6p and loss of 6q. Cytogenetic aberrations may be found in one third of the patients with neuropathy associated with IgM monoclonal gammopathy and are mainly associated with indolent Waldenstrom's Macroglobulinemia.

MeSH terms

  • Aged
  • B-Lymphocytes / immunology
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 14 / genetics*
  • DNA Mutational Analysis
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Genotype
  • Humans
  • Immunoglobulin M / genetics*
  • Immunoglobulin M / immunology
  • In Situ Hybridization, Fluorescence
  • Male
  • Middle Aged
  • Paraproteinemias / genetics*
  • Paraproteinemias / immunology
  • Paraproteinemias / physiopathology
  • Peripheral Nerves / immunology
  • Peripheral Nerves / physiopathology
  • Polyneuropathies / genetics*
  • Polyneuropathies / immunology
  • Polyneuropathies / physiopathology
  • Waldenstrom Macroglobulinemia / genetics
  • Waldenstrom Macroglobulinemia / immunology
  • Waldenstrom Macroglobulinemia / physiopathology

Substances

  • Immunoglobulin M