Multiple susceptibility loci for multiple sclerosis.

Journal Article (Journal Article)

Multiple sclerosis (MS) is a common and frequently disabling autoimmune disorder mediated by autoaggressive T cells and autoantibodies that target central nervous system myelin. While numerous studies have demonstrated a strong genetic component to MS, it has been difficult to identify the specific genes involved. Several genomic screens have been undertaken to locate such genes, but have not provided consistent gene localization, except for the MHC on chromosome 6p21 and a locus on chromosome 19q13. To determine which of the original genomic locations presented in the US genome screen could be replicated, a more detailed analysis of additional families was performed. The results, derived from a population of 266 affected individuals belonging to 98 multiplex families, continue to support linkage to chromosomes 6p21, 6q27, and 19q13 with LOD scores>3.0, and suggest that regions on chromosomes 12q23-24 and 16p13 may also harbor susceptibility loci for MS. Analysis taking into account the known HLA-DR2 association identified two additional potential linkage regions on chromosomes 7q21-22 and 13q33-34. These regions can now be targeted for detailed study to identify the underlying MS susceptibility genes.

Full Text

Duke Authors

Cited Authors

  • Haines, JL; Bradford, Y; Garcia, ME; Reed, AD; Neumeister, E; Pericak-Vance, MA; Rimmler, JB; Menold, MM; Martin, ER; Oksenberg, JR; Barcellos, LF; Lincoln, R; Hauser, SL; Multiple Sclerosis Genetics Group,

Published Date

  • September 15, 2002

Published In

Volume / Issue

  • 11 / 19

Start / End Page

  • 2251 - 2256

PubMed ID

  • 12217953

International Standard Serial Number (ISSN)

  • 0964-6906

Digital Object Identifier (DOI)

  • 10.1093/hmg/11.19.2251


  • eng

Conference Location

  • England