Sex and age at diagnosis are correlated with the HLA-DR2, DQ6 haplotype in multiple sclerosis

被引:85
作者
Celius, EG [1 ]
Harbo, HF
Egeland, T
Vartdal, F
Vandvik, B
Spurkiand, A
机构
[1] Ullevaal Sykehus, Oslo City Hosp, Dept Neurol, Oslo, Norway
[2] Univ Oslo, Natl Hosp, Inst Immunol, Oslo, Norway
[3] Univ Oslo, Natl Hosp, Ctr Epidemiol, Oslo, Norway
关键词
multiple sclerosis; HLA class II association; age at diagnosis; gender; disease type; oligoclonal bands;
D O I
10.1016/S0022-510X(00)00389-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The KLA-DR2, DQ6 (i.e., HLA-DRB1*1501, DQA1*0102, DQB1*0602) haplotype contributes to the risk of developing multiple sclerosis (MS) in Caucasoids of Northern European heritage. A correlation between the clinical expression of MS and the presence of HLA-DR2, DQ6 has, however, not convincingly been shown. In this study conventional bivariate analysis and logistic regression analysis were used to study the relationship between HLA-DR2, DQ6 and four disease variables in a cohort of 286 Norwegian MS patients from the Oslo area. Logistic regression analysis showed that HLA-DR2, DQ6 was significantly more frequent among female than male patients (P=0.0251), and was negatively correlated with age at diagnosis regardless of sex (P=0.0254). No significant correlation was observed between KLA-DR2, DQ6 and type of disease (relapsing-remitting versus primary chronic progressive MS) or presence/absence of oligoclonal bands in the cerebrospinal fluid. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:132 / 135
页数:4
相关论文
共 28 条
[1]  
*BRIT DUTCH MULT S, 1988, J NEUROL NEUROSUR PS, V51, P412
[2]  
Compston A., 1998, MCALPINES MULTIPLE S, P283
[3]   HLA ANTIGENS AND PROGRESSION OF MULTIPLE-SCLEROSIS .2. [J].
DEJAEGHER, L ;
DEBRUYERE, M ;
KETELAER, P ;
CARTON, H .
JOURNAL OF NEUROLOGY, 1983, 229 (03) :167-174
[4]   HLA AND HETEROGENEITY OF MULTIPLE-SCLEROSIS [J].
ENGELL, T ;
RAUN, NE ;
THOMSEN, M ;
PLATZ, P .
NEUROLOGY, 1982, 32 (09) :1043-1046
[5]   Genetic predisposition to multiple sclerosis as revealed by immunoprinting [J].
Epplen, C ;
Jackel, S ;
Santos, EJM ;
DSouza, M ;
Poehlau, D ;
Dotzauer, B ;
Sindern, E ;
Haupts, M ;
Rude, KP ;
Weber, F ;
Stover, J ;
Poser, S ;
Gehler, W ;
Malin, JP ;
Przuntek, H ;
Epplen, JT .
ANNALS OF NEUROLOGY, 1997, 41 (03) :341-352
[6]   MULTIPLE-SCLEROSIS IN NORTHEAST SCOTLAND - AN ASSOCIATION WITH HLA-DQW1 [J].
FRANCIS, DA ;
BATCHELOR, JR ;
MCDONALD, WI ;
HING, SN ;
DODI, IA ;
FIELDER, AHL ;
HERN, JEC ;
DOWNIE, AW .
BRAIN, 1987, 110 :181-196
[7]   MULTIPLE-SCLEROSIS AND HLA - IS THE SUSCEPTIBILITY GENE REALLY HLA-DR OR -DQ [J].
FRANCIS, DA ;
THOMPSON, AJ ;
BROOKES, P ;
DAVEY, N ;
LECHLER, RI ;
MCDONALD, WI ;
BATCHELOR, JR .
HUMAN IMMUNOLOGY, 1991, 32 (02) :119-124
[8]   The significance of oligoclonal bands in multiple sclerosis in Japan: Relevance of immunogenetic backgrounds [J].
Fukazawa, T ;
Kikuchi, S ;
Sasaki, H ;
Hamada, K ;
Hamada, T ;
Miyasaka, K ;
Tashiro, K .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 158 (02) :209-214
[9]  
FUKAZAWA T, 1993, ACTA NEUROL SCAND, V88, P178
[10]   AN IMMUNOGENETIC HETEROGENEITY IN MULTIPLE-SCLEROSIS [J].
HILLERT, J ;
GRONNING, M ;
NYLAND, H ;
LINK, H ;
OLERUP, O .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1992, 55 (10) :887-890