It is a longstanding puzzle why non-coding variants in the complement factor H (CFH) gene are more strongly associated with age-related macular degeneration (AMD) than functional coding variants that directly influence the alternative complement pathway. The situation is complicated by tight genetic associations across the region, including the adjacentCFH-related genes CFHR3 and CFHR1, which may themselves influence the alternativecomplementpathwayandare contained within acommondeletion (CNP147) which is associated with protection against AMD. It is unclear whether this association ismediated through a protective effect of low plasma CFHR1 concentrations, high plasma CFH or both. We examined the triangular relationships of CFH/CFHR3/ CFHR1 genotype, plasma CFH or CFHR1 concentrations and AMD susceptibility in combined case-control (1256 cases, 1020 controls) and cross-sectional population (n 5 1004) studies and carried out genome-wide association studies of plasma CFH and CFHR1 concentrations. A non-coding CFH SNP (rs6677604) and the CNP147deletion were strongly correlated both with each otherandwith plasmaCFHandCFHR1concentrations. The plasma CFH-raising rs6677604 allele and raised plasma CFH concentration were each associated withAMD protection. In contrast, the protective association of the CNP147 deletion with AMD was not mediated by low plasma CFHR1, since AMD-free controls showed increased plasma CFHR1 compared with cases, but it maybe mediated by the association of CNP147 with raised plasma CFH concentration. The results are most consistent with a regulatory locus within a 32 kb region of the CFH gene, with amajor effect on plasma CFH concentration and AMD susceptibility.

doi.org/10.1093/hmg/ddt336, hdl.handle.net/1765/58512
Human Molecular Genetics
Department of Clinical Genetics

Ansari, M., Mckeigue, P., Skerka, C., Hayward, C., Rudan, I., Vitart, V., … Wright, A. (2013). Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration. Human Molecular Genetics, 22(23), 4857–4869. doi:10.1093/hmg/ddt336