[en] Chromosomes, Human, Pair 5 ; Cohort Studies ; Female ; Gene Frequency ; Genome-Wide Association Study ; Genotype ; Germany ; Humans ; Linkage Disequilibrium ; Male ; Middle Aged ; Odds Ratio ; Parkinson Disease/genetics ; Polymorphism, Single Nucleotide ; Sequence Analysis, DNA
[en] A recently published whole genome association study showed the involvement of 13 SNPs in the pathogenesis of Parkinson disease (PD). We performed a replication study to assess their involvement in our sporadic cohort consisting of 663 cases and 1002 controls ascertained from Germany. One of the previously reported SNP, rs7723605, showed evidence of association (p value 0.04) in our sample. We further refined the signal by genotyping additional 22 SNPs around SNP rs7723605. Our refinement analysis, however, did not provide evidence for association in our sample after adjusting for multiple testing by permutation procedure. In conclusion, our study did not lend support to the finding that the reported SNPs are directly influencing the susceptibility to sporadic form of PD at least in our population.
Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group)
[University of Luxembourg > Faculty of Science, Technology and Communication (FSTC) > Life Science Research Unit]
