TY - JOUR KW - Asian Continental Ancestry Group KW - Chromosomes, Human KW - Chromosomes, Human, Pair 2 KW - Family KW - Female KW - Genetic Linkage KW - Genetic Predisposition to Disease KW - Genome-Wide Association Study KW - Humans KW - leprosy KW - Lod Score KW - Male KW - Pedigree KW - Polymorphism, Single Nucleotide AU - Yang Q AU - Liu H AU - Low H AU - Wang H AU - Yu Y AU - Fu X AU - Yu G AU - Chen M AU - Yan X AU - Chen S AU - Huang W AU - Liu J AU - Zhang F AB -

BACKGROUND: A genetic component to the etiology of leprosy is well recognized but the mechanism of inheritance and the genes involved are yet to be fully established.

METHODOLOGY: A genome-wide single nucleotide polymorphism (SNP) based linkage analysis was carried out using 23 pedigrees, each with 3 to 7 family members affected by leprosy. Multipoint parametric and non-parametric linkage analyses were performed using MERLIN 1.1.1.

PRINCIPAL FINDINGS: Genome-wide significant evidence for linkage was identified on chromosome 2p14 with a heterogeneity logarithm of odds (HLOD) score of 3.51 (rs1106577) under a recessive model of inheritance, while suggestive evidence was identified on chr.4q22 (HLOD 2.92, rs1349350, dominant model), chr. 8q24 (HLOD 2.74, rs1618523, recessive model) and chr.16q24 (HLOD 1.93, rs276990 dominant model). Our study also provided moderate evidence for a linkage locus on chromosome 6q24-26 by non-parametric linkage analysis (rs6570858, LOD 1.54, pā€Š=ā€Š0.004), overlapping a previously reported linkage region on chromosome 6q25-26.

CONCLUSION: A genome-wide linkage analysis has identified a new linkage locus on chromosome 2p14 for leprosy in Pedigrees from China.

BT - PloS one C1 - http://www.ncbi.nlm.nih.gov/pubmed/22238647?dopt=Abstract C2 - USA CY - San Francisco DA - 2012 DO - 10.1371/journal.pone.0029747 IS - 1 J2 - PLoS ONE LA - eng N2 -

BACKGROUND: A genetic component to the etiology of leprosy is well recognized but the mechanism of inheritance and the genes involved are yet to be fully established.

METHODOLOGY: A genome-wide single nucleotide polymorphism (SNP) based linkage analysis was carried out using 23 pedigrees, each with 3 to 7 family members affected by leprosy. Multipoint parametric and non-parametric linkage analyses were performed using MERLIN 1.1.1.

PRINCIPAL FINDINGS: Genome-wide significant evidence for linkage was identified on chromosome 2p14 with a heterogeneity logarithm of odds (HLOD) score of 3.51 (rs1106577) under a recessive model of inheritance, while suggestive evidence was identified on chr.4q22 (HLOD 2.92, rs1349350, dominant model), chr. 8q24 (HLOD 2.74, rs1618523, recessive model) and chr.16q24 (HLOD 1.93, rs276990 dominant model). Our study also provided moderate evidence for a linkage locus on chromosome 6q24-26 by non-parametric linkage analysis (rs6570858, LOD 1.54, pā€Š=ā€Š0.004), overlapping a previously reported linkage region on chromosome 6q25-26.

CONCLUSION: A genome-wide linkage analysis has identified a new linkage locus on chromosome 2p14 for leprosy in Pedigrees from China.

PB - Public Library of Science PP - San Francisco PY - 2012 EP - e29747 T2 - PloS one TI - Chromosome 2p14 is linked to susceptibility to leprosy. UR - http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253103/?tool=pubmed VL - 7 SN - 1932-6203 ER -