Table 1. Characteristics of the studies included for the gene–iron and gene–PD associations.
Data Source | n studies | Type of Study | Maximum Sample Size |
Gene–iron association | |||
GIS Consortiuma | 10 | GWA | 21,567 |
Gene–PD association | |||
PDGene database [13]–[21] | 9 | Candidate gene studies (HFE rs1800562 and HFE rs1799945) | 2,384 cases; 6,908 controls |
PD GWAS Consortium [22] | 5 | GWA | 4,238 cases; 4,239 controls |
23andMe [23] b | 1 | GWA | 4,127 cases; 62,037 controls |
IPDGC [24],[25] c | 4 | GWA | 4,258 cases; 10,152 controls |
IPDGC [24],[25] | 5 | Immunochip genotyping | 5,802 cases; 5,556 controls |
Unpublished data. The original sample size was 22,444, but genotype and phenotype data were available only for 21,567.
23andMe: slightly expanded version of the cohort used in [23].
IPDGC: USA-NIA and USA-dbGAP studies were not included in our analysis due to overlap with PD GWAS Consortium; the Icelandic dataset was not available for analysis.