Human Molecular Genetics, Vol 7, 1235-1237, Copyright © 1998 by Oxford University Press
MG Marrosu, MR Murru, G Costa, R Murru, F Muntoni and F Cucca
Multiple sclerosis (MS) is a common neurological disease caused by genetic
and environmental factors. Previous genetic analyses have suggested that
theMHC/HLA region on chromosome 6p21 contains an MS- predisposing
component. Which of the many genes present in this region is primarily
responsible for disease susceptibility is still an open issue. In this
study, we evaluated, in a large cohort of MS families from the
Mediterranean island of Sardinia, the role of allelic variation at the
HLA-DRB1, DQA1 and DQB1 candidate loci in MS predisposition. Using the
transmission disequilibrium test (TDT), we found significant evidence of
association with MS in both the Sardinian- specific DRB1*0405(DR4)-
DQA1*0501-DQB1*0301 haplotype and the DRB1* 0301(DR3)-DQA1*0501-DQB1*0201
haplotype. Detailed comparative analysis of the DRB1-DQA1- DQB1 haplotypes
present in this data set did not identify an individual locus that could
explain MS susceptibility. The predisposing effect is haplotype specific,
in that it is confined to specific combinations of alleles at the DRB1,
DQA1 and DQB1 loci. Cross- ethnic comparison between the two HLA haplotypes
associated with MS in Sardinians and the DRB1*1501 (DR2)-DQA1*0102-DQB1*
0602 haplotype, associated with MS in other Caucasian populations, failed
to identify any shared epitopes in the DR and DQ molecules that segregated
with disease susceptibility. These results suggest that another MHC
gene(s), in linkage disequilibrium with specific HLA-DRB1, DQA1, DQB1
haploypes, might be primarily responsible for genetic susceptibility to MS.
Alternatively, the presence of complex interactions between different HLA
haplotypes, other non-HLA predisposing genes and environmental factors may
explain different associations in different populations.
ARTICLES
DRB1-DQA1-DQB1 loci and multiple sclerosis predisposition in the Sardinian population
Chair of Neurophysiopathology, University of Cagliari, 09124 Cagliari, Italy. gmarrosu@vaxca1.unica.it
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
S. Sawcer The complex genetics of multiple sclerosis: pitfalls and prospects Brain, December 1, 2008; 131(12): 3118 - 3131. [Abstract] [Full Text] [PDF] |
||||
![]() |
T Matsuoka, T Matsushita, M Osoegawa, Y Kawano, M Minohara, F Mihara, Y Nishimura, Y Ohyagi, and J Kira Association of the HLA-DRB1 alleles with characteristic MRI features of Asian multiple sclerosis Multiple Sclerosis, November 1, 2008; 14(9): 1181 - 1190. [Abstract] [PDF] |
||||
![]() |
S. J. Caillier, F. Briggs, B. A. C. Cree, S. E. Baranzini, M. Fernandez-Vina, P. P. Ramsay, O. Khan, W. Royal III, S. L. Hauser, L. F. Barcellos, et al. Uncoupling the Roles of HLA-DRB1 and HLA-DRB5 Genes in Multiple Sclerosis J. Immunol., October 15, 2008; 181(8): 5473 - 5480. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Fontaine and L. F. Barcellos Evidence for a complex interaction between HLA-DRB1 and environmental factors in MS Neurology, January 8, 2008; 70(2): 97 - 98. [Full Text] [PDF] |
||||
![]() |
G. Dean, T. W. Yeo, A. Goris, C. J. Taylor, R. S. Goodman, M. Elian, A. Galea-Debono, A. Aquilina, A. Felice, M. Vella, et al. HLA-DRB1 and multiple sclerosis in Malta Neurology, January 8, 2008; 70(2): 101 - 105. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Schmidt, D. Williamson, and A. Ashley-Koch HLA-DR15 Haplotype and Multiple Sclerosis: A HuGE Review Am. J. Epidemiol., May 15, 2007; 165(10): 1097 - 1109. [Abstract] [Full Text] [PDF] |
||||
![]() |
I A Hoppenbrouwers, L. P. Cortes, Y S Aulchenko, K Sintnicolaas, O Njajou, P J. Snijders, B A Oostra, C M van Duijn, and R Q Hintzen Familial clustering of multiple sclerosis in a Dutch genetic isolate Multiple Sclerosis, January 1, 2007; 13(1): 17 - 24. [Abstract] [PDF] |
||||
![]() |
N. M. Nielsen, T. Westergaard, M. Frisch, K. Rostgaard, J. Wohlfahrt, N. Koch-Henriksen, M. Melbye, and H. Hjalgrim Type 1 diabetes and multiple sclerosis: a danish population-based cohort study. Arch Neurol, July 1, 2006; 63(7): 1001 - 1004. [Abstract] [Full Text] [PDF] |
||||
![]() |
J M Greer and M P Pender The presence of glutamic acid at positions 71 or 74 in pocket 4 of the HLA-DR{beta}1 chain is associated with the clinical course of multiple sclerosis J. Neurol. Neurosurg. Psychiatry, May 1, 2005; 76(5): 656 - 662. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Khare, M. Rodriguez, and C. S. David HLA class II transgenic mice authenticate restriction of myelin oligodendrocyte glycoprotein-specific immune response implicated in multiple sclerosis pathogenesis Int. Immunol., April 1, 2003; 15(4): 535 - 546. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Karlsson, X. Zhao, I. Lonskaya, M. Neptin, R. Holmdahl, and A. Andersson Novel Quantitative Trait Loci Controlling Development of Experimental Autoimmune Encephalomyelitis and Proportion of Lymphocyte Subpopulations J. Immunol., January 15, 2003; 170(2): 1019 - 1026. [Abstract] [Full Text] [PDF] |
||||
![]() |
A E Hensiek, S J Sawcer, R Feakes, J Deans, A Mander, E Akesson, R Roxburgh, F Coraddu, S Smith, and D A S Compston HLA-DR 15 is associated with female sex and younger age at diagnosis in multiple sclerosis J. Neurol. Neurosurg. Psychiatry, February 1, 2002; 72(2): 184 - 187. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. G. Marrosu, M. Lai, E. Cocco, V. Loi, G. Spinicci, M. P. Pischedda, S. Massole, G. Marrosu, and P. Contu Genetic factors and the founder effect explain familial MS in Sardinia Neurology, January 22, 2002; 58(2): 283 - 288. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. G. Marrosu, R. Murru, M. R. Murru, G. Costa, P. Zavattari, M. Whalen, E. Cocco, C. Mancosu, L. Schirru, E. Solla, et al. Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia Hum. Mol. Genet., December 1, 2001; 10(25): 2907 - 2916. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. R. Merriman, H. J. Cordell, I. A. Eaves, P. A. Danoy, F. Coraddu, R. Barber, F. Cucca, S. Broadley, S. Sawcer, A. Compston, et al. Suggestive Evidence for Association of Human Chromosome 18q12-q21 and Its Orthologue on Rat and Mouse Chromosome 18 With Several Autoimmune Diseases Diabetes, January 1, 2001; 50(1): 184 - 194. [Abstract] [Full Text] |
||||
![]() |
J. H. Noseworthy, C. Lucchinetti, M. Rodriguez, and B. G. Weinshenker Multiple Sclerosis N. Engl. J. Med., September 28, 2000; 343(13): 938 - 952. [Full Text] [PDF] |
||||










