Alopecia areata in families: Association with the HLA locus

被引:62
作者
de Andrade, M
Jackow, CM
Dahm, N
Hordinsky, M
Reveille, JD
Duvic, M
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dermatol Sect, Houston, TX 77030 USA
[2] Univ Texas, Sch Med, Dept Dermatol, Houston, TX USA
[3] Univ Texas, Sch Med, Dept Internal Med, Div Rheumatol, Houston, TX USA
[4] Univ Minnesota, Dept Dermatol, Minneapolis, MN 55455 USA
[5] Univ Texas, MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
关键词
autoimmune disease; baldness; hair; HLA disease association; linkage;
D O I
10.1038/sj.jidsp.5640215
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Alopecia areata (AA) is a T cell mediated disease directed against hair follicles that results in bald patches. It can range in severity from patchy (AA), to total scalp hair loss (alopecia totalis; AT) or body hair loss (alopecia universalis; AU). We have previously shown that HLA-DR4 and DR11 as well as HLA-DQ*03 alleles are increased in unrelated AA patients compared with controls. To study whether class II HLA alleles are linked to AA, we investigated 81 extended families that included 192 AA patients, including 89 with AT or AU. We also performed the transmission disequilibrium test (TDT) in 143 nuclear families. Results showed an association between alleles of HLA-DQB (p=0.014) and HLA-DR (p=0.010). We also performed linkage analysis in 75 families whose members' genomic DNA were available for HLA typing. Results from this analysis support linkage between AA and class II loci with a maximal LOD score of 2.42 to HLA-DQB at 5% recombination, and with a maximal LOD score of 2.34 to HLA-DR at 0% recombination. There was an increased incidence of atopic dermatitis and autoimmune thyroiditis in families. AA appears to be a class II HLA restricted organ specific immune response to die hair follicle.
引用
收藏
页码:220 / 223
页数:4
相关论文
共 50 条
[1]  
AVERBAKH EV, 1986, VESTN DERMATOL VENER, P24
[2]   ALOPECIA UNIVERSALIS IN IDENTICAL-TWINS [J].
COLE, GW ;
HERZLINGER, D .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1984, 23 (04) :283-283
[3]  
COLOMBE BW, 1995, J AM ACAD DERMATOL, V33, P757
[4]   ALOPECIA AREATA, THYROID DISEASE AND AUTOIMMUNITY [J].
CUNLIFFE, WJ ;
HALL, R ;
STEVENSO.CJ ;
WEIGHTMA.D .
BRITISH JOURNAL OF DERMATOLOGY, 1969, 81 (12) :877-&
[5]   A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES [J].
DAVIES, JL ;
KAWAGUCHI, Y ;
BENNETT, ST ;
COPEMAN, JB ;
CORDELL, HJ ;
PRITCHARD, LE ;
REED, PW ;
GOUGH, SCL ;
JENKINS, SC ;
PALMER, SM ;
BALFOUR, KM ;
ROWE, BR ;
FARRALL, M ;
BARNETT, AH ;
BAIN, SC ;
TODD, JA .
NATURE, 1994, 371 (6493) :130-136
[6]   ALOPECIA-AREATA - A CLINICAL-STUDY [J].
DEWEERT, J ;
TEMMERMAN, L ;
KINT, A .
DERMATOLOGICA, 1984, 168 (05) :224-229
[7]  
DUVIC M, 1995, J INVEST DERMATOL, V104, P581
[8]   HLA-D LOCUS ASSOCIATIONS IN ALOPECIA-AREATA - DRW52A MAY CONFER DISEASE RESISTANCE [J].
DUVIC, M ;
HORDINSKY, MK ;
FIEDLER, VC ;
OBRIEN, WR ;
YOUNG, R ;
REVEILLE, JD .
ARCHIVES OF DERMATOLOGY, 1991, 127 (01) :64-68
[9]  
EWENS WJ, 1995, AM J HUM GENET, V57, P455
[10]   HLA-DR4 IN ALOPECIA-AREATA [J].
FRENTZ, G ;
THOMSEN, K ;
JAKOBSEN, BK ;
SVEJGAARD, A .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1986, 14 (01) :129-129