Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2

Nathan Pankratz, Gary W. Beecham, Anita L. Destefano, Ted M. Dawson, Kimberly F. Doheny, Stewart A. Factor, Taye H. Hamza, Albert Y. Hung, Bradley T. Hyman, Adrian J. Ivinson, Dmitri Krainc, Jeanne C. Latourelle, Lorraine N. Clark, Karen Marder, Eden R. Martin, Richard Mayeux, Owen A. Ross, Clemens R. Scherzer, David K. Simon, Caroline TannerJeffery M. Vance, Zbigniew K. Wszolek, Cyrus P. Zabetian, Richard H. Myers, Haydeh Payami, William K. Scott, Tatiana Foroud

Research output: Contribution to journalArticlepeer-review

181 Scopus citations


Objective: Genome-wide association (GWAS) methods have identified genes contributing to Parkinson's disease (PD); we sought to identify additional genes associated with PD susceptibility. Methods: A 2-stage design was used. First, individual level genotypic data from 5 recent PD GWAS (Discovery Sample: 4,238 PD cases and 4,239 controls) were combined. Following imputation, a logistic regression model was employed in each dataset to test for association with PD susceptibility and results from each dataset were meta-analyzed. Second, 768 single-nucleotide polymorphisms (SNPs) were genotyped in an independent Replication Sample (3,738 cases and 2,111 controls). Results: Genome-wide significance was reached for SNPs in SNCA (rs356165; G: odds ratio [OR] = 1.37; p = 9.3 × 10 -21), MAPT (rs242559; C: OR = 0.78; p = 1.5 × 10 -10), GAK/DGKQ (rs11248051; T: OR = 1.35; p = 8.2 × 10 -9/rs11248060; T: OR = 1.35; p = 2.0 × 10 -9), and the human leukocyte antigen (HLA) region (rs3129882; A: OR = 0.83; p = 1.2 × 10 -8), which were previously reported. The Replication Sample confirmed the associations with SNCA, MAPT, and the HLA region and also with GBA (E326K; OR = 1.71; p = 5 × 10 -8 Combined Sample) (N370; OR = 3.08; p = 7 × 10 -5 Replication sample). A novel PD susceptibility locus, RIT2, on chromosome 18 (rs12456492; p = 5 × 10 -5 Discovery Sample; p = 1.52 × 10 -7 Replication sample; p = 2 × 10 -10 Combined Sample) was replicated. Conditional analyses within each of the replicated regions identified distinct SNP associations within GBA and SNCA, suggesting that there may be multiple risk alleles within these genes. Interpretation: We identified a novel PD susceptibility locus, RIT2, replicated several previously identified loci, and identified more than 1 risk allele within SNCA and GBA.

Original languageEnglish (US)
Pages (from-to)370-384
Number of pages15
JournalAnnals of neurology
Issue number3
StatePublished - Mar 2012

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology


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