TY - JOUR
T1 - A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting
AU - Karason, Ari
AU - Gudjonsson, Johann E
AU - Upmanyu, Ruchi
AU - Antonsdottir, Arna A
AU - Hauksson, Valdimar B
AU - Runasdottir, E Hjaltey
AU - Jonsson, Hjortur H
AU - Gudbjartsson, Daniel F
AU - Frigge, Michael L
AU - Kong, Augustine
AU - Stefansson, Kari
AU - Valdimarsson, Helgi
AU - Gulcher, Jeffrey R
PY - 2003/1/1
Y1 - 2003/1/1
N2 - Several genetic loci have been reported for psoriasis, but none has been specifically linked to psoriatic arthritis (PsA), a condition that affects >10% of patients with psoriasis. A genetic component for PsA is suggested by segregation within families and high concordance among identical twins. We performed a linkage scan to map genes contributing to PsA. We identified 178 patients with PsA out of 906 patients who were included in our genetic study of psoriasis. Using a comprehensive genealogy database, we were able to connect 100 of these into 39 families. We genotyped the patients using a framework marker set of 1,000 microsatellite markers, with an average density of 3 cM, and performed multipoint, affected-only, allele-sharing linkage analysis using the Allegro program. On the basis of the initial results, we genotyped more markers for the most prominent loci. A linkage with a LOD score of 2.17 was observed on chromosome 16q. The linkage analysis, conditioned on paternal transmission to affected individuals, gave a LOD score of 4.19, whereas a LOD score of only 1.03 was observed when conditioned for maternal transmission. A suggestive locus on chromosome 16q has previously been implicated in psoriasis. Our data indicate that a gene at this locus may be involved in paternal transmission of PsA.
AB - Several genetic loci have been reported for psoriasis, but none has been specifically linked to psoriatic arthritis (PsA), a condition that affects >10% of patients with psoriasis. A genetic component for PsA is suggested by segregation within families and high concordance among identical twins. We performed a linkage scan to map genes contributing to PsA. We identified 178 patients with PsA out of 906 patients who were included in our genetic study of psoriasis. Using a comprehensive genealogy database, we were able to connect 100 of these into 39 families. We genotyped the patients using a framework marker set of 1,000 microsatellite markers, with an average density of 3 cM, and performed multipoint, affected-only, allele-sharing linkage analysis using the Allegro program. On the basis of the initial results, we genotyped more markers for the most prominent loci. A linkage with a LOD score of 2.17 was observed on chromosome 16q. The linkage analysis, conditioned on paternal transmission to affected individuals, gave a LOD score of 4.19, whereas a LOD score of only 1.03 was observed when conditioned for maternal transmission. A suggestive locus on chromosome 16q has previously been implicated in psoriasis. Our data indicate that a gene at this locus may be involved in paternal transmission of PsA.
KW - Alleles
KW - Arthritis, Psoriatic
KW - Chromosome Mapping
KW - Chromosomes, Human, Pair 16
KW - Female
KW - Genetic Predisposition to Disease
KW - Genomic Imprinting
KW - Humans
KW - Lod Score
KW - Male
KW - Microsatellite Repeats
KW - Alleles
KW - Arthritis, Psoriatic
KW - Chromosome Mapping
KW - Chromosomes, Human, Pair 16
KW - Female
KW - Genetic Predisposition to Disease
KW - Genomic Imprinting
KW - Humans
KW - Lod Score
KW - Male
KW - Microsatellite Repeats
U2 - 10.1086/345646
DO - 10.1086/345646
M3 - Article
C2 - 12474146
SN - 0002-9297
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
ER -