%0 Meta-Analysis
%T Loci on chromosome 20 interact with rs16969968 to influence cigarettes per day in European ancestry individuals.
%A Romero Villela PN
%A Evans LM
%A Palviainen T
%A Border R
%A Kaprio J
%A Palmer RHC
%A Keller MC
%A Ehringer MA
%J Drug Alcohol Depend
%V 257
%N 0
%D 2024 Apr 1
%M 38387257
%F 4.852
%R 10.1016/j.drugalcdep.2024.111126
%X <B>BACKGROUND: </B>The understanding of the molecular genetic contributions to smoking is largely limited to the additive effects of individual single nucleotide polymorphisms (SNPs), but the underlying genetic risk is likely to also include dominance, epistatic, and gene-environment interactions.<BR><B>METHODS: </B>To begin to address this complexity, we attempted to identify genetic interactions between rs16969968, the most replicated SNP associated with smoking quantity, and all SNPs and genes across the genome.<BR><B>RESULTS: </B>Using the UK Biobank European subsample, we found one SNP, rs1892967, and two genes, PCNA and TMEM230, that showed a significant genome-wide interaction with rs16969968 for log10 CPD and raw CPD, respectively, in a sample of 116 442 individuals who self-reported currently or previously smoking. We extended these analyses to individuals of South Asian descent and meta-analyzed the combined sample of 117 212 individuals of European and South Asian ancestry. We replicated the gene findings in a meta-analysis of five Finnish samples (N=40 140): FinHealth, FINRISK, Finnish Twin Cohort, GeneRISK, and Health-2000-2011.<BR><B>CONCLUSIONS: </B>To our knowledge, this represents the first reliable epistatic association between single nucleotide polymorphisms for smoking behaviors and provides a novel direction for possible future functional studies related to this interaction. Furthermore, this work demonstrates the feasibility of these analyses by pooling multiple datasets across various ancestries, which may be applied to other top SNPs for smoking and/or other phenotypes.