A genome-wide association study of chronic lymphocytic leukaemia (CLL) suggested that common variants at 15q25.2 (rs783540) and 18q21.1 (rs1036935) influence CLL. To validate these associations and explore their relationship with CLL risk we genotyped case-control datasets from Poland, UK and Italy totalling 1428 cases and 1920 controls. Combined data from these and previously genotyped series (2503 cases and 5789 controls) provided evidence for an association between 15q25.2 and 18q21.1 loci and CLL risk (P(combined) = 1·10 × 10(-7) and 1·30 × 10(-5) respectively). These data provide further evidence for the involvement of common genetic variants in CLL risk and insight into the biological basis of disease development.
Crowther Swanepoel, D., Di Bernardo, M., Jamroziak, K., Karabon, L., Frydecka, I., Deaglio, S., D'Arena, G., Rossi, D., Gaidano, G., Olver, B., Lloyd, A., Broderick, P., Laurenti, L., Szemraj Rogucka, Z., Robak, T., Catovsky, D., Houlston, R., Common genetic variation at 15q25.2 impacts on chronic lymphocytic leukaemia risk, <<BRITISH JOURNAL OF HAEMATOLOGY>>, 2011; 154 (2): 229-233. [doi:10.1111/j.1365-2141.2011.08706.x] [http://hdl.handle.net/10807/4957]
Common genetic variation at 15q25.2 impacts on chronic lymphocytic leukaemia risk
Laurenti, Luca;
2011
Abstract
A genome-wide association study of chronic lymphocytic leukaemia (CLL) suggested that common variants at 15q25.2 (rs783540) and 18q21.1 (rs1036935) influence CLL. To validate these associations and explore their relationship with CLL risk we genotyped case-control datasets from Poland, UK and Italy totalling 1428 cases and 1920 controls. Combined data from these and previously genotyped series (2503 cases and 5789 controls) provided evidence for an association between 15q25.2 and 18q21.1 loci and CLL risk (P(combined) = 1·10 × 10(-7) and 1·30 × 10(-5) respectively). These data provide further evidence for the involvement of common genetic variants in CLL risk and insight into the biological basis of disease development.
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