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Genetic characterization and fine mapping of susceptibility loci for sarcoidosis in African Americans on chromosome 5
Authors:Courtney Gray-McGuire  Ritwik Sinha  Sudha Iyengar  Christopher Millard  Benjamin A Rybicki  Robert C Elston  Michael C Iannuzzi
Institution:(1) Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH, USA;(2) Department of Biostatistics and Research Epidemiology, Henry Ford Health System, Detroit, MI, USA;(3) Division of Pulmonary, Critical Care, and Sleep Medicine, Mt. Sinai School of Medicine, 1 Gustave Levy Place, Box 1232, New York, NY 10029, USA
Abstract:Sarcoidosis, a systemic granulomatous disease, likely results from both environmental agents and genetic susceptibility. Sarcoidosis is more prevalent in women and, in the United States, African Americans are both more commonly and more severely affected than Caucasians. We report a follow up of the first genome scan for sarcoidosis susceptibility genes in African Americans. Both the genome scan and the present study comprise 229 African American nuclear families ascertained through two or more sibs with sarcoidosis. Regions studied included those which reached a significance in the genome scan of 0.01 (2p25, 5q11, 5q35, 9q34, 11p15 and 20q13), 0.05 (3p25 and 5p15–13) or which replicated previous findings (3p14–11). We performed genotyping with additional markers in the same families used in the genome scan. We examined multi-locus models for epistasis and performed model-based linkage analysis on subsets of the most linked families to characterize the underlying genetic model. The strongest signal was at marker D5S407 (P=0.005) on 5q11.2, using both full and half sibling pairs. Our results support, in an African American population, a sarcoidosis susceptibility gene on chromosome 5q11.2, and a gene protective for sarcoidosis on 5p15.2. These fine mapping results further prioritize the importance of candidate regions on chromosomes 2p25, 3p25, 5q35, 9q34, 11p15 and 20q13 for African Americans. Additionally, our results suggest joint action of the effects of putative genes on chromosome 3p14–11 and 5p15.2. We conclude that multiple susceptibility loci for sarcoidosis exist in African Americans and that some may have interdependent effects on disease pathogenesis.
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