Premium
Genome‐wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway
Author(s) -
Hällfors Jenni,
Palviainen Teemu,
Surakka Ida,
Gupta Richa,
Buchwald Jadwiga,
Raevuori Anu,
Ripatti Samuli,
Korhonen Tellervo,
Jousilahti Pekka,
Madden Pamela A.F.,
Kaprio Jaakko,
Loukola Anu
Publication year - 2019
Publication title -
addiction biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.445
H-Index - 78
eISSN - 1369-1600
pISSN - 1355-6215
DOI - 10.1111/adb.12618
Subject(s) - nicotine , genome wide association study , single nucleotide polymorphism , genetic association , genetics , biology , snp , heritability , addiction , population , gene , bioinformatics , medicine , neuroscience , genotype , environmental health
Abstract The heritability of nicotine dependence based on family studies is substantial. Nevertheless, knowledge of the underlying genetic architecture remains meager. Our aim was to identify novel genetic variants responsible for interindividual differences in smoking behavior. We performed a genome‐wide association study on 1715 ever smokers ascertained from the population‐based Finnish Twin Cohort enriched for heavy smoking. Data imputation used the 1000 Genomes Phase I reference panel together with a whole genome sequence‐based Finnish reference panel. We analyzed three measures of nicotine addiction—smoking quantity, nicotine dependence and nicotine withdrawal. We annotated all genome‐wide significant SNPs for their functional potential. First, we detected genome‐wide significant association on 16p12 with smoking quantity ( P = 8.5 × 10 −9 ), near CLEC19A . The lead‐SNP stands 22 kb from a binding site for NF‐κB transcription factors, which play a role in the neurotrophin signaling pathway. However, the signal was not replicated in an independent Finnish population‐based sample, FINRISK ( n = 6763). Second, nicotine withdrawal showed association on 2q21 in an intron of TMEM163 ( P = 2.1 × 10 −9 ), and on 11p15 ( P = 6.6 × 10 −8 ) in an intron of AP2A2 , and P = 4.2 × 10 −7 for a missense variant in MUC6 , both involved in the neurotrophin signaling pathway). Third, association was detected on 3p22.3 for maximum number of cigarettes smoked per day ( P = 3.1 × 10 −8 ) near STAC. Associating CLEC19A and TMEM163 SNPs were annotated to influence gene expression or methylation. The neurotrophin signaling pathway has previously been associated with smoking behavior. Our findings further support the role in nicotine addiction.