Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1

Neuromuscular Disorders

Volumn 16, Issue 5, 2006, Pages 311-315

  Scott, Adrian Phillip ^a   Allcock, Richard James Nigel ^a   Mastaglia, Frank ^b   Nishino, Ichizo ^c   Nonaka, Ikuya ^c   Laing, Nigel ^d  

^a School of Surgery and Pathology   (Australia)

^b UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^c NATIONAL INSTITUTE OF MENTAL HEALTH   (Japan)

^d UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

Japanese; Major histocompatibility complex; MHC; sIBM; Sporadic inclusion body myositis

Indexed keywords

HLA A1 ANTIGEN; HLA B ANTIGEN; HLA B35 ANTIGEN; HLA B8 ANTIGEN; HLA DR ANTIGEN; HLA DR1 ANTIGEN; HLA DR3 ANTIGEN;

ADULT; AGED; ALLELE; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE PREDISPOSITION; ETHNOLOGY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HEREDITY; HUMAN; INCLUSION BODY MYOSITIS; JAPAN; MAJOR HISTOCOMPATIBILITY COMPLEX; MALE; PRIORITY JOURNAL;

AGED; ASIAN CONTINENTAL ANCESTRY GROUP; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HAPLOTYPES; HISTOCOMPATIBILITY ANTIGENS; HUMANS; INHERITANCE PATTERNS; MALE; MIDDLE AGED; MYOSITIS, INCLUSION BODY;

EID: 33646469854     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2006.02.002     Document Type: Article

References (29)

1. Phillips B.A., Zilko P.J., and Mastaglia F.L. Prevalence of sporadic inclusion body myositis in Western Australia. Muscle Nerve 23 (2000) 970-972
2. Badrising U.A., Maat-Schieman M., van Duinen S.G., et al. Epidemiology of inclusion body myositis in the Netherlands: a nationwide study. Neurology 55 (2000) 1385-1387
3. Yunis E.J., Larsen C.E., Fernandez-Vina M., et al. Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks. Tissue Antigens 62 (2003) 1-20
4. Dawkins R.L., Leelayuwat C., Gaudieri S., et al. Genomics of the major histocompatibility complex: haplotypes, duplication, retroviruses and disease. Immunol Rev 167 (1999) 275-304
5. Shiina T., Inoko H., and Kulski J.K. An update of the HLA genomic region, locus information and disease associations: 2004. Tissue Antigens 64 (2004) 631-649
6. Garlepp M.J., Laing B., Zilko P.J., Ollier W., and Mastaglia F.L. HLA associations with inclusion body myositis. Clin Exp Immunol 98 (1994) 40-45
7. Price P., Santoso L., Mastaglia F., et al. Two major histocompatibility complex haplotypes influence susceptibility to inclusion body myositis: critical evaluation of an association with HLA-DR3. Tissue Antigens 64 (2004) 575-580
8. Badrising U.A., Schreuder G.M.Th., Giphart M.J., et al. Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis. Neurology 63 (2004) 2396-2398
9. Lampe J.B., Gossrau G., Kempe A., et al. Analysis of HLA class I and II alleles in sporadic inclusion body myositis. J Neurol 250 (2003) 1313-1317
10. Koffman B.M., Sivakumar K., Simonis T., Stroncek D., and Dalakas M.C. HLA allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathies. Neuroimmunology 84 (1998) 139-142
11. Warabi Y., Matsubara S., Mizutani T., and Hayashi H. Inclusion body myositis after interferon-alpha treatment in a patient with HCV and HTLV-1 infection. Rinsho Shinkeigaku-Clin Neurol 44 (2004) 609-614
12. Tateyama M., Saito N., Fujihara K., et al. Familial inclusion body myositis: a report on two Japanese sisters. Intern Med 42 (2003) 928-929
13. Saito S., Ota S., Yamada E., Inoko H., and Ota M. Allele frequencies and haplotypic associations defined by allelic DNA typing at HLA class I and II loci in the Japanese population. Tissue Antigens 56 (2000) 522-529
14. Sayer D., Whidborne R., Brestovac B., Trimboli F., Witt C., and Christiansen F. HLA-DRB1 DNA sequencing based typing: an approach suitable for high throughput typing including unrelated bone marrow registry donors. Tissue Antigens 57 (2001) 46-54
15. Cattley S.K., Williamson J.F., Tay G.K., Martinez O.P., Gaudieri S., and Dawkins R.L. Further characterization of MHC haplotypes demonstrates conservation telomeric of HLA-A: update of the 4AOH and 10IHW cell panels. Eur J Immunogenet 27 (2000) 397-426
16. Kimura A., Kitamura H., Date Y., and Numano F. Comprehensive analysis of HLA genes in Takayasu arteritis in Japan. Int J Cardiol 54 (1996) S65-S73
17. Kitamura H., Kobayashi Y., Kimura A., and Numano F. Association of clinical manifestations with HLA-B alleles in Takayasu arteritis. Int J Cardiol 66 (1998) S121-S126
18. Dong R.P., Kimura A., Numano F., et al. HLA-DP antigen and Takayasu arteritis. Tissue Antigens 39 (1992) 106-110
19. Sugimura K., Asakura H., Mizuki N., et al. Analysis of genes within the HLA region affecting susceptibility to ulcerative colitis. Hum Immunol 32 (1993) 112-118
20. Sugimoto T., Sada M., Miyamoto T., and Yao H. Genetic analysis on HLA loci in Japanese patients with abdominal aortic aneurysm. Eur J Vasc Endovasc Surg 26 (2003) 215-218
21. Tomono N., Mori M., Nakajima S., et al. HLA-DRB1*15021 is the predominant allele in Japanese patients with juvenile dermatomyositis. J Rheumatol 31 (2004) 1847-1850
22. Awata T., and Kanazawa Y. Genetic markers for insulin-dependent diabetes mellitus in Japanese. Diabetes Res Clin Pract 24 (1994) S83-S87
23. Price P., Witt C.S., Allcock R., et al. The genetic basis for the association of the 8.1 ancestral haplotype (A1, B8, DR3) with multiple immunopathological diseases. Immunol Rev 167 (1999) 257-274
24. Ronningen K.S., Spurkland A., Tait B.D., et al. HLA class II associations in insulin-dependent diabetes mellitus among blacks, Caucasoids and Japanese. In: Tsuji K., Aizawa M., and Sasazuki T. (Eds). HLA 1991 (1991), Oxford University Press, New York
25. Reed A.M., Pachman L., and Ober C. Molecular genetic studies of major histocompatibility complex genes in children with juvenile dermatomyositis: Increased risk associated with HLA-DQA1*0501. Hum Immunol 32 (1991) 235-240
26. Friedman J.M., Pachman L.M., Matryjowski M.L., et al. Immunogenetic studies of juvenile dermatomyositis. Tissue Antigens 21 (1983) 45-49
27. Dalakas M.C., and Hohlfeld R. Polymyositis and dermatomyositis. Lancet 362 (2003) 971-982
28. Tawil R., and Griggs R.C. Inclusion body myositis. Curr Opin Rheumatol 14 (2002) 653-657
29. Askanas V., and Engel W.K. Proposed pathogenetic cascade of inclusion-body myositis: importance of amyloid-beta, misfolded proteins, predisposing genes, and aging. Curr Opin Rheumatol 15 (2003) 737-744