| Literature DB >> 12577057 |
Marcelo T Mira1, Alexandre Alcaïs, Nguyen Van Thuc, Vu Hong Thai, Nguyen Thu Huong, Nguyen Ngoc Ba, Andrei Verner, Thomas J Hudson, Laurent Abel, Erwin Schurr.
Abstract
Leprosy, a chronic infectious disease caused by Mycobacterium leprae, affects an estimated 700,000 persons each year. Clinically, leprosy can be categorized as paucibacillary or multibacillary disease. These clinical forms develop in persons that are intrinsically susceptible to leprosy per se, that is, leprosy independent of its specific clinical manifestation. 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 = 5 x 10(-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 = 6.7 x 10(-4) and P = 5.9 x 10(-5), respectively).Entities:
Mesh:
Year: 2003 PMID: 12577057 DOI: 10.1038/ng1096
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330