TY - JOUR
T1 - Neuregulin signaling pathway in smoking behavior
AU - Gupta, R.
AU - Qaiser, B.
AU - He, L.
AU - Hiekkalinna, T. S.
AU - Zheutlin, A. B.
AU - Therman, S.
AU - Ollikainen, M.
AU - Ripatti, S.
AU - Perola, M.
AU - Salomaa, V.
AU - Milani, L.
AU - Cannon, T. D.
AU - Madden, P. A.F.
AU - Korhonen, T.
AU - Kaprio, J.
AU - Loukola, A.
N1 - Funding Information:
We warmly thank the participating twin pairs and their family members, as well as the participants of the DILGOM study for their contribution. Data collection of the Finnish twin cohort samples has been supported by the Academy of Finland Center of Excellence in Complex Disease Genetics (Grants 213506 and 129680), the Academy of Finland (Grants 265240 and 263278 to JK), NIH Grant DA12854 (to PAFM), Sigrid Juselius Foundation (to JK), Global Research Award for Nicotine Dependence, Pfizer (to JK), the Wellcome Trust Sanger Institute, UK and the Broad Institute of MIT and Harvard, USA. The DILGOM study has been supported by the Academy of Finland Research (Grants 255935 to MP) for DNA methylation data and Sigrid Jusélius Foundation and Yrjö Jahnsson Foundation for gene-expression data. DNA methylation data for the DILGOM sample was generated at the Estonian Genome Center, University of Tartu, under the supervision of Prof Andres Metspalu.
Publisher Copyright:
© 2017, Springer Nature. All rights reserved.
PY - 2017
Y1 - 2017
N2 - Understanding molecular processes that link comorbid traits such as addictions and mental disorders can provide novel therapeutic targets. Neuregulin signaling pathway (NSP) has previously been implicated in schizophrenia, a neurodevelopmental disorder with high comorbidity to smoking. Using a Finnish twin family sample, we have previously detected association between nicotine dependence and ERBB4 (a neuregulin receptor), and linkage for smoking initiation at the ERBB4 locus on 2q33. Further, Neuregulin3 has recently been shown to associate with nicotine withdrawal in a behavioral mouse model. In this study, we scrutinized association and linkage between 15 036 common, low frequency and rare genetic variants in 10 NSP genes and phenotypes encompassing smoking and alcohol use. Using the Finnish twin family sample (N = 1998 from 740 families), we detected 66 variants (representing 23 LD blocks) significantly associated (false discovery rate Po0.05) with smoking initiation, nicotine dependence and nicotine withdrawal. We comprehensively annotated the associated variants using expression (eQTL) and methylation quantitative trait loci (meQTL) analyses in a Finnish population sample. Among the 66 variants, we identified 25 eQTLs (in NRG1 and ERBB4), 22 meQTLs (in NRG3, ERBB4 and PSENEN), a missense variant in NRG1 (rs113317778) and a splicing disruption variant in ERBB4 (rs13385826). Majority of the QTLs in blood were replicated in silico using publicly available databases, with additional QTLs observed in brain. In conclusion, our results support the involvement of NSP in smoking behavior but not in alcohol use and abuse, and disclose functional potential for 56 of the 66 associated single-nucleotide polymorphism.
AB - Understanding molecular processes that link comorbid traits such as addictions and mental disorders can provide novel therapeutic targets. Neuregulin signaling pathway (NSP) has previously been implicated in schizophrenia, a neurodevelopmental disorder with high comorbidity to smoking. Using a Finnish twin family sample, we have previously detected association between nicotine dependence and ERBB4 (a neuregulin receptor), and linkage for smoking initiation at the ERBB4 locus on 2q33. Further, Neuregulin3 has recently been shown to associate with nicotine withdrawal in a behavioral mouse model. In this study, we scrutinized association and linkage between 15 036 common, low frequency and rare genetic variants in 10 NSP genes and phenotypes encompassing smoking and alcohol use. Using the Finnish twin family sample (N = 1998 from 740 families), we detected 66 variants (representing 23 LD blocks) significantly associated (false discovery rate Po0.05) with smoking initiation, nicotine dependence and nicotine withdrawal. We comprehensively annotated the associated variants using expression (eQTL) and methylation quantitative trait loci (meQTL) analyses in a Finnish population sample. Among the 66 variants, we identified 25 eQTLs (in NRG1 and ERBB4), 22 meQTLs (in NRG3, ERBB4 and PSENEN), a missense variant in NRG1 (rs113317778) and a splicing disruption variant in ERBB4 (rs13385826). Majority of the QTLs in blood were replicated in silico using publicly available databases, with additional QTLs observed in brain. In conclusion, our results support the involvement of NSP in smoking behavior but not in alcohol use and abuse, and disclose functional potential for 56 of the 66 associated single-nucleotide polymorphism.
UR - http://www.scopus.com/inward/record.url?scp=85046843570&partnerID=8YFLogxK
U2 - 10.1038/tp.2017.183
DO - 10.1038/tp.2017.183
M3 - Article
C2 - 28892072
AN - SCOPUS:85046843570
SN - 2158-3188
VL - 7
JO - Translational Psychiatry
JF - Translational Psychiatry
M1 - e1212
ER -