Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population

被引:135
作者
Mira, MT
Alcaïs, A
Van Thuc, N
Thai, VH
Huong, NT
Ba, NN
Verner, A
Hudson, TJ
Abel, L
Schurr, E
机构
[1] McGill Univ, McGill Ctr Study Host Resistance, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Dept Human Genet, Montreal, PQ H3G 1A4, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3G 1A4, Canada
[4] McGill Univ, Dept Biochem, Montreal, PQ H3G 1A4, Canada
[5] Univ Paris 05, Inst Natl Sante & Rech Med, U550, Unite Human Genet Infect Dis,Necker Med Sch, Paris, France
[6] Hosp Dermato Venereol, Ho Chi Minh City, Vietnam
[7] McGill Univ, Montreal Genome Ctr, Ctr Hlth, Montreal, PQ H3G 1A4, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1038/ng1096
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Leprosy, a chronic infectious disease caused by Mycobacterium leprae, affects an estimated 700,000 persons each year(1). Clinically, leprosy can be categorized as paucibacillary or multibacillary disease(2). These clinical forms develop in persons that are intrinsically susceptible to leprosy per se, that is, leprosy independent of its specific clinical manifestation(3). We report here on a genome-wide search for loci controlling susceptibility to leprosy per se in a panel of 86 families including 205 siblings affected with leprosy from Southern Vietnam. Using model-free linkage analysis, we found significant evidence for a susceptibility gene on chromosome region 6q25 (maximum likelihood binomial (MLB) lod score 4.31; P=5x10(-6)). We confirmed this by family-based association analysis in an independent panel of 208 Vietnamese leprosy simplex families. Of seven microsatellite markers underlying the linkage peak, alleles of two markers (D6S1035 and D6S305) showed strong evidence for association with leprosy (P=6.7x10(-4) and P=5.9x10(-5), respectively).
引用
收藏
页码:412 / 415
页数:4
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