Whole-genome screening in ankylosing spondylitis: Evidence of non-MHC genetic-susceptibility loci
Laval, S. H., Timms, A., Edwards, S., Bradbury, L., Brophy, S., Milicic, A., Rubin, L., Siminovitch, K. A., Weeks, D. E., Calin, A., Wordsworth, B. P., & Brown, M. A. (2001) Whole-genome screening in ankylosing spondylitis: Evidence of non-MHC genetic-susceptibility loci. American Journal of Human Genetics, 68(4), pp. 918-926.
Ankylosing spondylitis (AS) is a common inflammatory arthritis predominantly affecting the axial skeleton. Susceptibility to the disease is thought to be oligogenic. To identify the genes involved, we have performed a genomewide scan in 185 families containing 255 affected sibling pairs. Two-point and multipoint nonparametric linkage analysis was performed. Regions were identified showing "suggestive" or stronger linkage with the disease on chromosomes 1p, 2q, 6p, 9q, 10q, 16q, and 19q. The MHC locus was identified as encoding the greatest component of susceptibility, with an overall LOD score of 15.6. The strongest non-MHC linkage lies on chromosome 16q (overall LOD score 4.7). These results strongly support the presence of non-MHC genetic-susceptibility factors in AS and point to their likely locations.
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|Item Type:||Journal Article|
|Additional Information:||No file attached.|
|Keywords:||ankylosing spondylitis, arthritis, article, chromosome 16q, controlled study, genetic linkage, genetic screening, genetic susceptibility, human, inflammatory disease, major histocompatibility complex, priority journal, Chromosome Mapping, Chromosomes, Human, Cohort Studies, Female, Genetic Predisposition to Disease, Genome, Human, Genotype, Humans, Lod Score, Male, Matched-Pair Analysis, Nuclear Family, Software, Spondylitis, Ankylosing, Statistics, Nonparametric|
|Deposited On:||24 Sep 2015 02:26|
|Last Modified:||24 Sep 2015 02:26|
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