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 P<0.05) 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.
Smoking is a major risk factor for a variety of somatic diseases and strongly associates with several neuropsychiatric disorders,1, 2, 3 the most prominent comorbidity being alcohol use and dependence.4 One of the key factors driving persistent smoking is nicotine dependence (ND), manifested by development of tolerance, symptoms of craving and uncontrollable use due to the high addictive potential of nicotine.5 Abstaining from smoking results in nicotine withdrawal (NW) symptoms including, for example, irritability, depressed mood and restlessness,6 largely contributing to the high relapse rates among smokers trying to quit.7 Despite the availability of several smoking cessation pharmacotherapies including nicotine replacement therapy and medications such as varenicline, bupropion and cytisine, 6-month abstinence rates are at best only two- to threefold compared with pharmacologically unassisted quit attempts.8
Neuregulin signaling pathway (NSP) is involved in modulating neuronal migration and differentiation. The key functional components of this pathway are neuregulins (NRG1, NRG3) and their receptor (ERBB4), as well as beta secretase (BACE1) and the gamma-secretase complex (comprises PSEN1, PSEN2, APH1A, APH1B, PSENEN and NCSTN) (reviewed in ref. 9)). Deviation from an optimal level of NRG/ERBB signaling in the brain is shown to impair brain functions.10 Interestingly, several NSP genes have previously been implicated in schizophrenia (SCZ),9, 10, 11 a neurodevelopmental disorder with high comorbidity to smoking. Evidence is emerging for the involvement of the NSP in smoking behavior. Recently, we performed a genome-wide association study (GWAS) among smokers from the Finnish Twin Cohort (N=1104) and detected association between ND defined by Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM-IV)12 and ERBB4.13 Using a partly overlapping subset of families (N=505 twins and first degree relatives), we have previously identified linkage between smoking initiation (SI) and microsatellite markers at 2q33, overlapping the ERBB4 locus.14 Further, Nrg3 has recently been shown to associate with NW in a behavioral mouse model.15 Therefore, comprehensive scrutiny of the NSP may aid in identifying a common link for smoking behavior and comorbid disorders.16
GWAS has enabled discovery of genetic variants associated with disease traits. However, majority of the identified variants reside in non-coding regions. It is essential to identify the functionality/regulatory potential of the detected variants, for example, via mechanisms such as epigenetic regulation. Functional annotation of variants has boosted progress from genetic studies to biological understanding, aiding in development of therapeutic measures.17, 18, 19
In this study, we scrutinized association and linkage between common, low frequency and rare genetic variants in the 10 genes encoding the key functional components of the NSP in a Finnish twin family sample (N=1998 from 740 families). To comprehensively test whether NSP variants associate with nicotine use, we included nine smoking-related phenotypes in our analyses. In our secondary analyses, we included five alcohol-related phenotypes to evaluate (i) whether NSP variants associate with nicotine use specifically, or relate to general liability to addictions, and (ii) whether signals observed for smoking-related phenotypes are confounded by comorbid alcohol use. We detected statistically significant association with single-nucleotide polymorphisms (SNPs) and SI, DSM-IV ND and DSM-IV NW, in full agreement with previous studies of NSP in smoking behavior.13, 14, 15 Further, we performed comprehensive annotation of the detected associations, and revealed potential functions for majority of the associating SNPs.
Materials and methods
The NAG-FIN discovery sample has been previously described in detail.13, 14, 20 Briefly, the study sample was ascertained from the Finnish Twin Cohort consisting of 35 834 adult twins born in 1938–1957. On the basis of earlier data, the twin pairs concordant for ever-smoking were identified and recruited along with their family members (mainly siblings) for the Nicotine Addiction Genetics (NAG) Finland study (N=2265). Twin pairs concordant for heavy smoking were primarily targeted to increase the genetic load. Data collection took place in 2001–2005. The association and linkage study sample consisted of 1998 individuals from 740 families, including 980 dizygotic (DZ) twin individuals (both co-twins included), 139 monozygotic (MZ) twin individuals (one co-twin per twin pair was included), 46 individuals with unconfirmed zygosity (due to a lack of DNA sample from the co-twin) and 833 other family members (mostly siblings). The average number of individuals per family was 3 (range 1–10), and the data contained 185 families with at least 4 family members included in the study. Sample description is presented in Table 1. The study was approved by the ethics committee of the hospital district of Helsinki and Uusimaa, Finland in 2001 and 2016, and by the IRB of Washington University, St Louis, MO, USA. The participants have provided written informed consent.
NAG-FIN genotype data
Genotyping for the NAG-FIN sample was performed with the Human670-QuadCustom Illumina BeadChip (Illumina, San Diego, CA, USA) (N=1097) at the Wellcome Trust Sanger Institute, UK, and with the Illumina Human Core Exome BeadChip (N=901) at the Wellcome Trust Sanger Institute, and at the Broad Institute of MIT and Harvard, USA. Quality controls (QC) for the genotype data have been previously described21 and are also presented in Supplementary Table 1. Pre-phasing of the data was done with SHAPEIT222 and imputation with IMPUTE223 using the 1000 Genomes Phase I integrated haplotypes reference panel.24 For analyses of the 10 NSP genes (NRG1, NRG3, ERBB4, BACE1, PSEN1, PSEN2, APH1A, APH1B, PSENEN and NCSTN), we extracted SNPs within the gene regions (according to the longest isoform reported at the UCSC Genome browser) with 50 kb flanking regions. Gene boundaries (according to GRCh37/hg19) are listed in Supplementary Table 1, along with the number of SNPs included for each gene. Only variants with minor allele frequency (MAF) <0.01 located in coding regions, splice sites, promoters or untranslated regions (UTRs) were included in the rare variant analysis. Altogether, 15 036 SNPs were analyzed in our discovery phase.
NAG-FIN phenotype data
To evaluate the role of genetic variants within the NSP genes in addictions, we initially tested nine phenotypes encompassing smoking behavior in our discovery sample (Supplementary Table 2 (I)). To test whether variants in NSP genes associate with nicotine use specifically, or relate to general liability to addictions, we also tested five alcohol use phenotypes (Supplementary Table 2 (II)). Data collection for the phenotypes has been previously described in detail.6, 20
For functional annotation of the associations detected in the discovery phase, we used the DILGOM 2007 (Dietary, Lifestyle and Genetic determinants of Obesity and Metabolic syndrome) study sample, which originates from the population-based national FINRISK 2007 study. The DILGOM study sample has been previously described in detail,25, 26 including a total of 631 unrelated Finnish individuals aged 25–74 years from the Helsinki area. For annotation analyses, we used 512 individuals with genome-wide genotype, gene expression and DNA methylation data available, all measured from peripheral blood leukocytes (46% males, mean age 52 years (s.d. 13.7)). DILGOM sample was used to perform population-specific expression (eQTL) and methylation quantitative trait loci (meQTL) analysis in blood tissue. We further analyzed differential transcriptome and methylome among smokers and never smokers in this data set. On the basis of self-reported smoking status the individuals in the sample can be categorized into current daily smokers (N=84), current occasional smokers (N=34), recent quitters (1–6 months of abstinence) (N=13), former smokers (>6 months of abstinence) (N=133), never smokers (N=245) and three with missing smoking status (as described in ref. 27). The DILGOM participants have provided written informed consent. The protocol was designed and performed according to the principles of the Helsinki Declaration and was approved by the coordinating ethics committee of the hospital district of Helsinki and Uusimaa, Finland.
DILGOM genotype data
Genotyping for the DILGOM sample was performed with the Illumina 610-Quad SNP array. Imputation was done with IMPUTE2 using the 1000 Genomes Phase I integrated haplotypes reference panel.23, 24 Stringent QC thresholds were applied to filter out low quality SNPs and samples as previously described.25 QCs and imputation for all Finnish GWAS data were done centrally at the Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Finland.
DILGOM gene-expression data
RNA protocols and data processing for the Illumina HT-12 expression array have been previously described.25 Briefly, peripheral blood was used as a source of RNA; all arrays were quantile normalized at the strip-level and technical replicates were combined via bead-count weighted average. Probes were removed if they mapped to a non-autosomal chromosome, erythrocyte globin components or more than one genomic position. A total of 19 probes mapped to the 10 NSP genes, of which 17 passed QC thresholds; none of the PSENEN probes passed QC. One probe per gene was selected based on highest interquartile range (IQR) representing highest variance for differential expression analysis.
DILGOM DNA methylation data
DNA extracted from peripheral blood was bisulfite converted using EZ-96 DNA Methylation-Gold Kit (Zymo Research, Irvine, CA, USA) according to the manufacturer’s instructions. Illumina Infinium HumanMethylation450 BeadChip was used to measure the DNA methylation levels using the Infinium protocol for methylation workflow.28 DNA methylation data was pre-processed and normalized using the bioconductor R package ‘minfi’,29 with the Subset-quantile Within Array Normalization (SWAN) method. Probes with detection P-value >0.01 in any sample were discarded. Probes reported as cross-reactive (mapping to multiple genomic locations and known repeat regions) and probes with SNPs were also removed, as previously suggested.29 A total of 254 CpG probes mapped to the ten NSP genes, of which 226 passed QC thresholds. On average, there were 25 probes per gene (range 13–69).
In silico databases for replicating QTLs identified in blood
We utilized blood-derived gene expression and genotypic data available in the Genotype-Tissue Expression (GTEx) project database (gtexportal.org)30 to replicate detected eQTLs in the DILGOM sample. For replicating detected meQTLs in the DILGOM sample, we queried the mQTLdb database (mqtldb.org)31 containing blood-derived methylation and genotype data on mother–child pairs.
In silico databases for identifying QTLs in the brain
Given the neuropsychiatric nature of our phenotypes, we tested for eQTLs in different brain tissues using 13 brain tissues available in GTEx and in 10 brain regions available in the Brain eQTL Almanac (BRAINEAC; braineac.org) database.32 For meQTLs, we queried the epigenome-wide significant meQTLs reported by Hannon et al.33 in fetal brain samples (epigenetics.essex.ac.uk/mQTL).
Schizophrenia twin sample
In the expression analyses of the 10 NSP genes, we also utilized a SCZ twin sample, previously described in detail.34 The data consisted of 18 SCZ cases and 55 controls (including unaffected co-twins and additional unaffected twin pairs), with genome-wide gene-expression data generated with Illumina Human WG6 v3.0 Expression BeadChip, as previously described.34 One probe per gene was selected in accordance with the probe selection in DILGOM sample for expression analyses. Age and sex was available for all participants, whereas smoking status (defined as smoker versus non-smoker) was available for 13 SCZ cases and 41 controls.
In silico database for SCZ transcriptome analysis
We queried the database for Schizophrenia Genetic Research (SZDB; szdb.org)35 to identify differentially expressed NSP genes between SCZ cases and controls.
Altogether, 9924 common (MAF>0.05), 4106 low frequency (0.01⩽MAF⩽0.05) and 1006 rare (MAF<0.01) variants in the ten NSP genes were tested for association initially with nine smoking phenotypes and as secondary analyses with five alcohol-related phenotypes. We also examined common variants for linkage as well as joint linkage and linkage disequilibrium (LD). To account for multiple testing, we used the Benjamini and Hochberg method36 and considered false discovery rate (FDR) adjusted P-values below 0.05 as statistically significant. To visualize the gene regions showing significant associations in our discovery analyses, we used Locustrack37 and Haploview for defining LD blocks based on the ‘solid spine of LD’ option.38
Genetic association analysis of common and low frequency variants
Univariate linear mixed model (LMM) implemented in GEMMA (genome-wide efficient mixed-model association)39 was used to test association of SNPs with the quantitative traits. Genotype uncertainty was accounted for using allelic dosage data. Age and sex were used as covariates (fixed effects part of the model). Population stratification and genetic correlation within the sample was modeled with additional random effects using a standardized relatedness matrix calculated from genome-wide genotype data. P-values from Wald test were used to assess the association between each SNP and the phenotype.
Linkage and joint linkage and LD analysis of common variants
Two-point linkage analysis as well as joint linkage and LD analysis was performed for binary traits using the PSEUDOMARKER software,40 assuming a recessive mode of inheritance (identical to non-parametric affected sib-pair analysis (ASP), which is a special case of parametric linkage analysis).41, 42 PSEUDOMARKER has been evidenced as the most powerful family-based association analysis method for binary traits implementing the Elston–Stewart algorithm for full-likelihood analysis.43 Only common variants with MAF>0.05 were included in these analyses, to avoid analysis of monomorphic and uninformative markers in the sample. In our linkage analyses, we leveraged the extended twin family data, as our data contained 185 families with at least four family members included in the study.
Rare variant association analysis
The rare variant association (RVA) analysis was divided into single-variant and gene-based tests. An expected kinship matrix was calculated using the pedigree information and we incorporated age and sex as covariates. For single-variant RVA analysis of quantitative traits, we used the ‘lmekin’ function from the ‘coxme‘ R package.44 To analyze binary traits R package ’pedigreemm’ was employed.45 Earlier studies have shown that single-variant tests suffer from loss of statistical power.46 Consequently, gene-based tests using SNP-set (Sequence) Kernel Association Test (SKAT)47 for quantitative traits and Hierarchical Bayesian Multiple Regression model (HBMR)48 for both quantitative and binary traits were performed using R packages. In the gene-based tests, only one variant was selected whenever multiple variants were in full LD, and each variant included had to be at least a singleton (that is, having an imputed genotype>0.5 for at least one individual). HBMR outputs results as Bayes factors (BFs), and we declared a nominally significant finding when BF exceeded a threshold of 2.45 (corresponding to a P-value<0.05), as previously suggested.49, 50
All SNPs showing statistically significant association or linkage (FDR P<0.05) in the discovery analyses were annotated to infer potential functional consequences. For this, we used quantitative trait loci analysis in a population-based sample (blood-derived data), and considered FDR adjusted P-values below 0.05 as statistically significant. To replicate QTLs detected in blood, we used publicly available databases. Further, as our phenotypes are neuropsychiatric disorders, we wanted to explore the effect of associating SNPs using publicly available brain tissue data.
Expression quantitative trait loci analysis in the DILGOM sample
Expression quantitative trait loci (eQTL) analysis was performed in the DILGOM sample to test the effect of genotypes of the highlighted SNPs on expression levels of NSP genes. R package ‘MatrixEQTL’ was used with a linear model setting.51 Age, sex, body mass index (BMI) and smoking status were used as covariates to test cis-acting eQTLs. Normalized expression values were log2 transformed and tested against SNP genotypes coded as 0, 1 or 2 copies of the effect allele.
Methylation quantitative trait loci analysis in the DILGOM sample
Methylation quantitative trait loci (meQTL) analysis was performed in the DILGOM sample to test the effect of genotypes of the highlighted SNPs on methylation levels of NSP genes. We tested cis-acting meQTLs using the R package ‘MatrixEQTL’ with linear model setting. Age, sex, BMI, smoking status and white blood cell counts estimated using houseman algorithm52 were added as covariates, as previously suggested.31, 53 Normalized methylation β-values were tested against SNP genotypes coded as 0, 1 or 2 copies of the effect allele.
In silico expression quantitative trait loci analysis
To replicate our eQTLs detected in the DILGOM sample (blood), we utilized GTEx whole-blood data. To explore the effects of our highlighted SNPs in the brain, we tested the SNPs as cis-eQTLs in 13 brain tissues available in GTEx, and in 10 brain regions available in BRAINEAC. All GTEx analyses (blood and brain tissues) were performed with the ‘Test Your Own’ eQTLs option.
In silico methylation quantitative trait loci analysis
To replicate our meQTLs detected in the DILGOM sample (blood), we used the mQTLdb assessing cis-meQTLs. To test the effect of genotypes in the brain, we queried the fetal brain meQTLs reported by Hannon and colleagues.
Other functional annotations
Ensembl Variant Effect Predictor (VEP)54 was used to procure predicted functional annotations for the highlighted SNPs. HaploReg v4 was used to annotate the SNPs for regulatory regions (promoter and enhancer histone marks, DNase I hypersensitivity, protein binding and regulatory motifs).55 In addition, SPANR56 scores for splicing disruption potential were extracted for the highlighted SNPs.
Differential expression and methylation analyses
As we detected association between smoking behavior and several NSP genes, we wanted to explore whether NSP gene expression and methylation levels are affected by smoking status. We performed differential expression and methylation analysis between never (N=245) and current daily smokers (N=84) in the DILGOM sample. We also compared never smokers (N=245) against a pooled sample of current daily and occasional smokers (N=118). We employed linear models using the ‘lm’ function in R while adjusting for age, sex and BMI. When comparing methylation levels, we further adjusted for estimated white blood cell counts.52 We considered FDR adjusted P<0.05 as evidence for significant difference.
Owing to the high comorbidity between SCZ and smoking, we wanted to explore the effect of smoking on NSP gene expression in the SCZ twin sample. We first examined expression differences between SCZ cases (N=18) and controls (N=55), while accounting for relatedness and using age and sex as covariates. We then added smoking status as a covariate. In this sample, we could only classify the subjects into smokers and non-smokers, as there was no information on former smoking. Owing to the small sample size, no correction for multiple testing was applied.
We tested 15 036 SNPs mapping to the 10 NSP genes (with 50 kb flanking regions) for linkage, joint linkage and LD, and association identifying altogether 66 SNPs showing statistically significant signal (FDR P<0.05) with SI, ND and NW phenotypes (Supplementary Table 3). On the basis of LD structures, the 66 SNPs represent 23 LD blocks (Supplementary Figure 1). A summary of the results from the discovery analyses is presented in Table 2.
We detected evidence of linkage for SI, ND diagnosis and NW diagnosis with multiple SNPs in ERRB4, with the strongest signal emerging in rs1836721 for SI (log of the odds (LOD)=3.32) and ND (LOD=1.94), and in rs147786642 for NW (LOD=1.12).
Joint linkage and LD tests performed with PSEUDOMARKER detected a signal for SI in seven of the ten NSP genes (APH1A, PSEN2, ERBB4, NRG1, NRG3, BACE1 and PSENEN; FDR P<0.05) (Supplementary Figure 2), and signal for ND diagnosis in ERBB4 (FDR P=0.002 for rs13385826) (Supplementary Figure 3).
Association tests performed with GEMMA identified a signal for NW symptom count in ERBB4 (FDR P=0.008, β=−0.517 for rs13001305, and for three highly correlated SNPs: rs73989053, rs13006797, rs17328083) (Figure 1), suggesting that each copy of the effect allele lowers number of NW symptoms by half a count on a scale of 0–8 counts. Similar results were obtained for NRG3 SNP rs11192578 (FDR P=0.008, β=−0.773) (Supplementary Table 3), suggesting that each copy of the effect allele lowers number of NW symptoms by 0.8 counts.
No significant signal was detected in single-variant RVA analyses after correcting for multiple testing (data not shown). In the gene-based RVA analysis, neither methods (SKAT or HBMR) detected significantly associated variants for ND or NW symptom counts. In contrast, HBMR identified association between SI and both NRG1 (BF=3.073, P<0.0360) and PSEN1 (BF=9.693, P<0.0078), and between NW diagnosis and ERBB4 (BF=3.799, P<0.0267).
To test whether the 66 SNPs highlighted in the discovery phase associated with gene expression or DNA methylation levels of the NSP genes, we performed cis eQTL and meQTL analyses in the DILGOM sample (blood-derived data). Out of the 66 SNPs, two SNPs in ERBB4 and 23 SNPs in NRG1 were identified as eQTLs (FDR P<0.05) (Supplementary Table 4). Further, 12 SNPs in ERBB4 (eight of those forming meQTLs with multiple CpG sites), one SNP in PSENEN, and one SNP in NRG3 (FDR P<0.05) were identified as altogether 22 meQTLs (Supplementary Table 5).
To replicate our eQTL findings, we tested the 66 highlighted SNPs for cis-eQTLs in whole-blood data available in GTEx. We observed 17 eQTLs in NRG1, overlapping the 23 NRG1 eQTLs identified in DILGOM sample, and additional eQTLs in BACE1 and PSENEN (FDR P<0.05) (Supplementary Table 6). We then tested all 66 SNPs for cis-eQTLs in RNA expression data from 13 brain regions available in the GTEx and 10 brain regions available in the BRAINEAC database. Altogether, five brain eQTLs were detected: one ERBB4 SNP (rs13385826) in spinal cord, one NRG3 SNP (rs12774918) in amygdala, one BACE1 SNP (rs1261780) in cerebellar hemisphere and two ERBB4 SNPs (rs192584214, rs112465988) in cerebellar cortex (FDR P<0.05) (Supplementary Table 7). Overlap between eQTLs detected in brain and blood (GTEx) was observed only for rs1261780 in BACE1.
To replicate our meQTLs findings, we tested the 66 highlighted SNPs for cis-meQTLs in mQTLdb. Twelve meQTLs identified in DILGOM sample overlapped with results from mQTLdb with additional meQTLs observed for rs807483 in PSENEN (Supplementary Table 8). In addition, among the epigenome-wide significant meQTLs reported in fetal brain by Hannon and colleagues, we found four of the ERBB4 SNPs (rs73989053, rs17328083, rs13001305 and rs75489550) (Supplementary Table 9), all overlapping with meQTLs in the DILGOM sample, and all showing association with NW in our discovery sample.
Among the highlighted 66 SNPs, Ensembl Variant Effect Predictor (VEP) indicated a missense variant in NRG1 (rs113317778), promoter region variants in NRG1 (rs75673683) and ERBB4 (rs73989053), and two APH1A SNPs (rs183423866, rs187135585) that overlap with transcription factor binding sites (Supplementary Table 10). According to HaploReg, a significant portion of ERBB4 and NRG3 SNPs overlap with promoter and/or enhancers in brain tissue (Supplementary Table 11).
Most of the highlighted 66 SNPs were either too far from splice junctions or had no overlapping coding transcripts for splicing disruption analysis with SPANR. Only ERBB4 variant rs13385826 had a delta psi score of 0.09 indicating splicing disruption potential (absolute delta psi>0.05).
Differential expression and methylation analyses
When examining the expression of the ten genes, we observed higher expression levels of NRG1 and PSEN1 among current daily versus never smokers (FDR P<0.05) (Supplementary Table 12). When occasional smokers were pooled together with current daily smokers, the differences were no longer significant. Expression levels in occasional smokers resembled those seen in never smokers (Supplementary Figure 5). No significant difference in methylation levels between current daily versus never smokers were observed (Supplementary Table 13), including occasional smokers among current daily smokers did not affect this result.
In the SCZ twin sample, NRG1, NRG3 and APH1B showed a trend (P-value<0.1) for differential expression between SCZ cases and controls in analyses adjusted for age and sex (Supplementary Table 14). When smoking status was added to the model, the trend disappeared.
Smoking behavior and ND are complex traits with several genes and pathways having crucial roles. In addition to the well-established role of genetic variation in nicotinic receptor genes57, 58, 59 and nicotine metabolizing enzymes,60, 61, 62 the NSP is emerging as a contributor in smoking behavior. By using a Finnish twin family sample, we have previously identified linkage of SI at the ERBB4 locus,14 and association between ND and ERBB4.13 Turner et al.15 have recently shown the involvement of Nrg3 and Erbb4 in the anxiety effects of NW in a behavioral mouse model, and association between NRG3 SNPs with smoking cessation success in a clinical trial. In the current study, we included 14 phenotypes assessing smoking behavior and alcohol use in a Finnish twin family sample (N=1998 individuals from 740 families). We scrutinized altogether 15 036 common, low frequency and rare variants in 10 NSP genes, and identified 66 SNPs (representing 23 LD blocks) significantly associated with SI, ND and NW. We then comprehensively annotated the functional potential of the highlighted variants in an independent population-based sample of smokers and non-smokers.
On the basis of LD figures generated for the seven genes, we estimate that the 66 highlighted SNPs represent 23 LD blocks. For all but three genes (APH1A, PSEN2 and PSENEN), SNPs in multiple LD blocks were highlighted. We detected linkage for SI with multiple SNPs in ERBB4, strengthening our previous linkage findings.14 Our sample size increased between the original linkage study and the current study (N=505 versus N=1998), and the evidence for linkage increased correspondingly (max parametric LOD=2.56 versus max LOD=3.32), despite the fact that biallelic markers (that is, SNPs) used in the current study provide less linkage information individually compared to multiallelic markers (that is, microsatellite markers)63 used in the original linkage study.14 ERBB4 variants also showed linkage for ND diagnosis (LOD=1.94) and NW diagnosis (LOD=1.12), joint linkage and LD for SI and ND diagnosis, and association for NW symptom count. These findings further support our previous association results13 and provide substantive evidence for future studies to characterize the role of ERBB4 in addictions.
In addition to highlighting ERBB4, our results provide evidence for the involvement of other NSP genes in smoking behavior. A SNP in NRG3 was associated with NW symptom count, in line with findings from animal models and association analyses reported by Turner et al.15 The effect sizes detected for ERBB4 and NRG3 SNPs showing association with NW symptom count are prominent, corresponding to a decrease of 0.5–0.8 counts on a scale of 0–8 counts, per each copy of the effect allele. Further, joint linkage and LD analysis detected a signal for SI in seven of the NSP genes (majority of the highlighted SNPs), likely due to our discovery sample being heavily enriched for smoking (83% having initiated smoking) providing ample statistical power in our family sample. In our rare variant gene-based analyses using HMBR, we observed significant association of ERBB4, NRG1 and PSEN1 with SI and NW diagnosis. Overall, we provide strong evidence implying the NSP in smoking behavior while highlighting novel associations in five genes (NRG1, BACE1, APH1A, PSEN2 and PSENEN) for smoking behavior. It is noteworthy that among the 14 tested phenotypes (nine assessing smoking behavior and five alcohol use), the signal consistently emerges for (i) moking initiation, supporting our previous linkage finding for smoking initiation on 2q33, overlapping the ERBB4 locus,14 (ii) DSM-IV ND, supporting our previously reported association between ERBB4 and DSM-IV ND13 and (iii) NW, supporting previous findings by Turner et al.15 No significant signal was detected for ND assessed by FTND or smoking quantity. Further, no signal was detected for alcohol use phenotypes, suggesting that the role of the NSP is specific to nicotine, rather than being broadly involved in addictions in general. Lack of signal for alcohol use phenotypes also suggests that signals observed for smoking-related phenotypes are not confounded by comorbid alcohol use. Future studies are needed to assess the involvement of the NSP in use and dependence of other substances besides nicotine and alcohol. In our discovery data set, cannabis or other illicit drug use is very rare.64
Altogether, 38 of the 66 highlighted SNPs were identified either as eQTLs or meQTLs in the DILGOM sample, suggesting that they may affect expression and methylation levels of the NSP genes. Also, five of the 66 SNPs were detected as eQTLs in different brain tissues (cerebellar cortex, cerebellar hemisphere, amygdala and spinal cord) and four as meQTLs in fetal brain, indicating that at least some of our highlighted SNPs may affect gene expression or methylation in the brain. Three brain regions (amygdala, cerebellar cortex and cerebellar hemisphere) showing eQTLs in our study have previously been implicated in addiction studies.65, 66, 67, 68 Although spinal cord, another tissue showing eQTLs in our study, has not been studied previously with respect to addictions, our findings from GTEx data suggest spinal cord should be considered in addiction studies.30
Smoking has a prominent effect on methylation,69 and alters gene expression.70 Unfortunately, most publicly available eQTL and meQTL databases do not currently provide information on smoking status. Nevertheless, we could replicate most eQTLs and meQTLs detected in the DILGOM sample in blood. For example, out of the 23 NRG1 eQTLs detected in the DILGOM sample (blood), 17 replicated in GTEx (blood) but none were observed in brain tissue (GTEx, BRAINEAC), however, among the 20 ERBB4 meQTLs detected in the DILGOM sample (blood), 17 replicated in mQTLdb data (blood) and 4 of were also observed in fetal brain. Such inconsistent overlap may stem from differences in gene expression and methylation levels across tissues. Additional factors contributing towards incomplete overlap of QTL results between blood-derived results in DILGOM versus public databases (GTEx and mQTLdb) may include population-specific genetic background and lack of detailed phenotypic information (like smoking status) available in the databases. Further, small sample sizes for tissues that are difficult to access, such as brain, reduce the power to identify signals. In addition, data made available from published studies often only contain (epi)genome-wide significant results thereby limiting the possibility of replicating results of targeted studies like ours. Nonetheless, epigenome-wide significant meQTLs reported for the highlighted 66 SNPs in fetal brain overlap with meQTLs observed in DILGOM sample (blood data), indicating very robust associations between SNPs and methylation levels of these genes. The four ERBB4 promoter region meQTLs detected in both blood and fetal brain showed association with NW. These meQTLs were not detected in adult brain tissues in the same study by Hannon et al.;33 as smoking was not accounted for in this study, gene-by-environment interactions induced by smoking exposure cannot be ruled out. If future studies reveal that methylation at these CpG sites react to smoking exposure, this locus could be a potential target for epigenetic therapy for NW.
Owing to the limited access and availability of brain tissue, the use of blood as a substitute for transcript level analyses has been evaluated, and a modest overlap of ~19% has been observed, emphasizing the value of tissues that are specific to the pathophysiology of the trait of interest.71, 72 However, blood can be used as surrogate for brain tissues, especially for genes that are co-expressed between the two tissues.73 According to GTEx, seven out of the ten NSP genes are co-expressed in brain and blood. However, the expression levels differ significantly for almost all the genes between brain and blood.
Alternative splicing of ERBB4 has been reported to result in functionally distinct isoforms that can alter downstream signaling.74 Interestingly, the ND-associated SNP rs13385826 in ERBB4 is predicted to be a splicing disruption variant according to SPANR, plausibly inducing alternative splicing of exon 21 encoding for part of the kinase domain of ERBB4, crucial for downstream signaling.75 Functional validation of the splicing product of rs13385826 is needed to confirm the specific ERBB4 isoform and its consequences to the properties of the protein. Downstream targets of the NSP are being evaluated as drug targets in SCZ.76, 77 Despite only one SNP being in the coding region, there appears to be regulatory potential in 56 of the highlighted 66 SNPs by means of eQTLs, meQTLs and other regulatory features (overlapping enhancer and/or promoter or transcription factor binding sites) (Figure 2). However, further validation studies are required to confirm the predicted function of these SNPs.
In our expression analyses, we observed differential expression of NRG1 and PSEN1 between current daily and never smokers in the DILGOM sample, suggesting that smoking influences the expression of at least some of the NSP genes. Interestingly, merging current daily and occasional smokers diluted the signal. Further, our data show that expression levels of occasional smokers resemble more never smokers compared with the daily smokers. Occasional smokers by definition smoke irregularly and hence alternate between exposure and non-exposure to tobacco and its chemicals. This underlies the importance of careful definition of smoking status in gene-expression studies.
Differential expression in NRG1, NRG3, PSEN1, PSEN2, PSENEN and APH1A (FDR P<0.05) has been reported between SCZ cases and controls in SZDB;35 strikingly, smoking status has not been accounted for in any of the studies included in this database. In the current study, we detected a trend for differential expression of NRG1, NRG3 and APH1B in our small SCZ twin sample (N=73). However, after adjusting for smoking status the trend disappeared. Given the high co-occurrence and shared genetic component of SCZ and smoking,78 and our findings, the results from SZDB may partly reflect smoking status rather than the disease status, advocating the importance of accounting for confounding effects of smoking.
We detected no significant differences in NSP gene methylation levels between current daily and never smokers in the DILGOM sample. This suggests that the microarray used in this study may not have covered relevant CpG sites, or that other regulatory mechanisms besides methylation account for the detected differences in expression levels. Pooling occasional smokers together with current daily smokers had no effect, suggesting that methylation of NSP genes does not change rapidly in response to abstinence.
In our analyses, we utilized a Finnish twin family sample, heavily enriched for smoking. As the participants were on average 56 years old at the time of enrollment, we were not able to recruit parents but rather took advantage of the large number of affected sib-ships. We applied diligent quality controls to exclude low quality SNPs. Although the widely used threshold of imputation info score of >0.4 was applied, the average info score of the 66 highlighted SNPs was 0.89 (median 0.93), and only two SNPs had an info score <0.7. NRG3 SNP rs11192578 showed mild LD with neighboring SNPs plausibly explained by suggestive evidence of positive selection (iHS score 1.7 obtained from Haplotter (haplotter.uchicago.edu)79 and low minor allele frequency (MAF=0.04) in our sample. ERBB4 SNP rs13385826 (showing association with ND diagnosis) appears to be an orphan signal with no support from surrounding SNPs despite having several SNPs in high LD.
In conclusion, our twin family sample provided further evidence for the involvement of the NSP in smoking behavior but not in alcohol use and abuse phenotypes. Our differential expression analyses highlighted the importance of carefully defining the smoking status in gene-expression studies. Our results underlined the involvement of ERBB4 in SI, ND and NW. Further, we highlighted NRG3 for SI and NW, and additional five NSP genes for SI. By using both in-house data and publicly available databases we depicted potential function for an exceptionally high proportion (56/66) of the associated SNPs, suggesting the potential of these variants as future drug targets.
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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.
Dr Kaprio and Dr Korhonen have provided consultation to Pfizer on nicotine dependence and its treatment. Dr Cannon is a consultant to the Los Angeles County Department of Mental Health and to Boehringer Ingelheim Pharmaceuticals. The remaining authors declare no conflict of interest.
Supplementary Information accompanies the paper on the Translational Psychiatry website
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Gupta, R., Qaiser, B., He, L. et al. Neuregulin signaling pathway in smoking behavior. Transl Psychiatry 7, e1212 (2017). https://doi.org/10.1038/tp.2017.183
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