The impact of non-additive genetic associations on age-related complex diseases.
Marta Guindo-MartíneziD, Ramon AmelaiD, Sílvia Bonàs‐GuarchiD, Montserrat PuiggròsiD, Cecilia SalvoroiD, Irene Miguel-EscaladaiD, Caitlin E. CareyiD, Joanne B. ColeiD, Sina RüegeriD, Elizabeth G. AtkinsoniD, Aaron LeongiD, Friman SáncheziD, Cristian Ramon-CortesiD, Jorge EjarqueiD, Duncan S. PalmeriD, Mitja KurkiiD, Krishna G. AragamiD, José C. FloreziD, Rosa M. BadiaiD, Josep Maria MercaderiD, David TorrentsiD
Abstract
Genome-wide association studies (GWAS) are not fully comprehensive as current strategies typically test only the additive model, exclude the X chromosome, and use only one reference panel for genotype imputation. We implemented an extensive GWAS strategy, GUIDANCE, which improves genotype imputation by using multiple reference panels, includes the analysis of the X chromosome and non-additive models to test for association. We applied this methodology to 62,281 subjects across 22 age-related diseases and identified 94 genome-wide associated loci, including 26 previously unreported. We observed that 27.6% of the 94 loci would be missed if we only used standard imputation strategies and only tested the additive model. Among the new findings, we identified three novel low-frequency recessive variants with odds ratios larger than 4, which would need at least a three-fold larger sample size to be detected under the additive model. This study highlights the benefits of applying innovative strategies to better uncover the genetic architecture of complex diseases.
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