While psychotic experiences are core symptoms of mental health disorders like schizophrenia, they are also reported by 5–10% of the population. Both smoking behaviour and genetic risk for psychiatric disorders have been associated with psychotic experiences, but the interplay between these factors remains poorly understood. We tested whether smoking status, maternal smoking around birth, and number of packs smoked/year were associated with lifetime occurrence of three psychotic experiences phenotypes: delusions (n = 2067), hallucinations (n = 6689), and any psychotic experience (delusions or hallucinations; n = 7803) in 157,366 UK Biobank participants. We next calculated polygenic risk scores for schizophrenia (PRSSCZ), bipolar disorder (PRSBP), major depression (PRSDEP) and attention deficit hyperactivity disorder (PRSADHD) in 144,818 UK Biobank participants of European ancestry to assess whether association between smoking and psychotic experiences was attenuated after adjustment of diagnosis of psychiatric disorders and the PRSs. Finally, we investigated whether smoking exacerbates the effects of genetic predisposition on the psychotic phenotypes in gene-environment interaction models. Smoking status, maternal smoking, and number of packs smoked/year were associated with psychotic experiences (p < 1.77 × 10−5). Except for packs smoked/year, effects were attenuated but remained significant after adjustment for diagnosis of psychiatric disorders and PRSs (p < 1.99 × 10−3). Gene-environment interaction models showed the effects of PRSDEP and PRSADHD (but not PRSSCZ or PRSBP) on delusions (but not hallucinations) were significantly greater in current smokers compared to never smokers (p < 0.002). There were no significant gene-environment interactions for maternal smoking nor for number of packs smoked/year. Our results suggest that both genetic risk of psychiatric disorders and smoking status may have independent and synergistic effects on specific types of psychotic experiences.
Psychotic experiences, such as hallucinations (unreal visual or auditory perceptions) and delusions (unreal beliefs or impressions, i.e. conspiracy against self, unreal communications or signs), are reported by 5–10% of the general population1. Psychotic experiences are core symptoms of severe mental disorders, such as schizophrenia, and therefore may be an indicator of risk for mental health problems even in apparently healthy individuals. Understanding their aetiology could help identify individual susceptibility for different mental health outcomes and develop tailored prevention and intervention strategies.
Genetic factors influence psychotic experiences, explaining between 30% and 50% of the variance in twin studies2,3 and common genetic variation explaining between 3% and 17% of the variance in molecular genetic studies4,5. Twin studies also suggest that the genetic component of psychotic experiences is shared with psychiatric disorders such as schizophrenia, bipolar disorder, depression and attention deficit hyperactivity disorder (ADHD)6. Large genome-wide studies of psychotic experiences in UK Biobank (UKB) confirm these findings: polygenic risk scores (PRS) of schizophrenia, bipolar disorder, depression, and ADHD explain 0.11%, 0.06%, 0.32% and 0.05% of the variance in psychotic experiences, respectively7. Linkage disequilibrium score regression (LDSC) indicates the genetic correlation estimates between psychotic experiences and schizophrenia, bipolar disorder, depression and ADHD are 0.21, 0.15, 0.46 and 0.247.
In addition to genetic influences, environmental factors explain between 50% and 70% of the variance in psychotic experiences3. Smoking is one of the best established environmental risk factors associated with the occurrence of psychotic experiences in case-control studies of schizophrenia and bipolar disorder, as well as in population-based samples. Longitudinal studies suggest that continued smoking is a causal factor for psychotic experiences among people with the first episode of psychosis8, schizophrenia, and bipolar disorder patients9. The observation of a dose-response effect in prospective studies10,11,12,13, together with recent Mendelian randomization studies14, further support a causal effect of smoking on the occurrence of psychotic experiences. In addition, the associations between lifetime tobacco use and subsequent psychotic experiences15,16 in the general population remained significant after adjusting for other psychiatric disorders16, suggesting that smoking may lead to psychotic experiences independently from mental health status.
Associations between other smoking phenotypes and psychotic experiences are less well-established. There is much less evidence for an increased risk of psychotic experiences in former smokers, leading some to suggest that the effects of smoking are reversible17,18. However, it is still unclear whether these findings are false positives resulting from a lack of power in relatively small samples. Maternal smoking during pregnancy is associated with psychotic experiences in offspring19. However within-family studies suggest that once familial factors are taken into account, maternal smoking during pregnancy has no effect on the risk of psychotic experiences20.
Despite evidence showing associations between genetic risk for psychiatric disorders and psychotic experiences6,7, and a number of studies showing associations between smoking and psychotic experiences17,21,22,23, the interplay between smoking and genetic risk on psychotic experiences remains unknown. There are studies showing that PRSs for psychiatric disorders are associated with smoking24,25,26,27. This suggests that smoking may not be only a casual factor in the development of psychotic experiences, but that common genetic factors may affect both smoking and psychotic experiences. However, no studies have tested whether PRSs for psychiatric disorders and smoking make independent contributions to psychotic experiences. Significant gene-environment interactions (GxE) have been reported for several psychiatric traits including schizophrenia and depression28,29,30, but studies are yet to explore whether there is an interaction between smoking and PRSs for psychiatric disorders on psychotic experiences. That is, whether the effects of genetic risk are greater for individuals exposed to smoking.
Our first objective was to investigate whether smoking status (current, former or never smoker), number of packs smoked per year and maternal smoking around birth were associated with lifetime delusions or hallucinations or any psychotic experience (delusions or hallucinations) in the UKB cohort. We also tested whether the effects of smoking remained significant after adjustment for diagnosis of depression, ADHD and psychotic disorders (schizophrenia, mania, hypomania, bipolar or manic depression, and schizotypal or delusional disorders), as well as genetic risk for these disorders, captured by PRSs for depression (PRSDEP), ADHD (PRSADHD), schizophrenia (PRSSCZ) and bipolar disorder (PRSBP). Our second objective was to investigate whether the effects of smoking on psychotic experiences were exacerbated by genetic risk by testing additive and multiplicative GxE between these variables. We interrogated whether being a current, former or never a smoker; smoking more packs of cigarettes per year; or being exposed to maternal smoking around birth influenced the effects of PRSs on having hallucinations, delusions, or any of the two. When significant interactions between smoking and PRS were identified, we carried out sensitivity analyses excluding people with psychotic disorders. An overview of the study design is provided in Fig. 1.
UK Biobank sample
The sample was drawn from UKB, a population-based cohort from the United Kingdom with ~500,000 participants. From those, 157,366 participants completed an online mental health questionnaire. A detailed description of the mental health questionnaire has been provided elsewhere31. Ethical approval was provided by UKB (Application ID#42423) and all participants gave written consent.
Psychotic experiences were categorised based on the Composite International Diagnostic Interview included in the mental health questionnaire. Three outcomes were defined: delusions, hallucinations, and any psychotic experience. Delusions were ascertained as individuals reporting lifetime delusions of reference and/or persecutory delusions (Field IDs: 20474, 20468). Hallucinations were ascertained as individuals reporting lifetime visual and/or auditory hallucinations (Field IDs: 20471, 20463). Any lifetime psychotic experiences were ascertained as a positive response to any of the four symptom questions (Field IDs: 20474, 20468, 20471, 20463). Controls were defined as individuals that did not endorse lifetime psychotic experiences. A more detailed description of the outcome variables is provided in the Supplementary Tables 1–3.
Three smoking outcomes were defined using the UKB baseline questionnaire: smoking status (Field ID 20116), pack years of smoking (Field ID 20161) and maternal smoking around birth (Field ID 1787). The smoking status phenotype consisted of never smoker, former smokers and current smokers. Pack years of smoking were calculated for former and current smokers and it was defined as the number of cigarettes smoked per day, divided by twenty, multiplied by the number of years of smoking. Cases for maternal smoking were defined as individuals endorsing ‘Yes’ for the question ‘Did your mother smoke regularly around the time when you were born?’.
Other psychiatric disorders
Lifetime depression, ADHD, schizophrenia, mania, hypomania, bipolar or manic depression, and any other type of psychotic disorder were defined using both the UKB baseline and mental health questionnaires (Supplementary Tables 4 and 5).
UKB genetic dataset
The data release contained 488,377 individuals genotyped on either the UKB Axiom or the UK BiLEVE Axiom arrays. Genotype data were imputed centrally by UKB with IMPUTE2 using the Haplotype Reference Consortium panel32. UKB also provided metrics for quality control that were used to exclude individuals with poor genotype call rate (>5%) and discordance between the self-reported sex and the sex inferred from the genotypes. The first two principal components provided by UKB were used in a k-means clustering algorithm33 to identify a genetically homogeneous subsample. Related individuals were identified for each phenotype separately using the R package ‘ukbtools’34 and one individual from related pairs/trios were excluded (kinship coefficient > 0.0884). Details on the quality control (QC) of genetic data and sample sizes after QC exclusion are provided in Supplementary Table 6.
We calculated PRSSCZ, PRSDEP, PRSADHD and PRSBP for each UKB participant using the software PRSice-235 and summary statistics from four recent genome-wide association studies GWAS of these disorders (Supplementary material)36,37,38,39. Logistic regression models were used to explore the association between PRSSCZ, PRSDEP, PRSADHD and PRSBP and psychotic experiences using PRSice-235. Analyses included the first ten principal components and genotyping batch as covariates.
Main effect analyses
Regression models were constructed to assess the association between maternal smoking, smoking status and number of packs smoked per year and psychotic experiences. To test whether the association between smoking and psychotic experiences was independent of diagnosis for psychiatric disorders and genetic predisposition, models were rerun adjusting for: diagnosis for psychotic disorders, depression, and ADHD, as well as the PRS with the highest predictive ability (p-value threshold = 0.2) on psychotic experiences.
Interaction effect analyses
We explored whether there were GxE between each of the PRSs and smoking on psychotic experiences (i.e. whether the effects of genetic risk differed among current, former or never smokers, among smokers that consumed more packs of cigarettes per year, and among individuals whose mothers smoked around time of participants’ birth). Interactions were tested on the multiplicative and additive scales using logistic and linear regressions, respectively. Interactions on the multiplicative scale assess whether the joint effect of the PRS and smoking is greater than the product of their individual effects. Interactions on the additive scale assess whether the joint effect of smoking and the PRS is greater than the sum of their individual effects. Modelling multiplicative and additive GxE using linear and logistic regressions has been described elsewhere29,30,40.
In the GxE regression models, we included individuals from UKB with genetic, smoking and psychotic experiences data (n = 143,320 for any psychotic experience, n = 143,043 for hallucinations, and n = 143,245 for delusions). Independent variables were the PRSDEP, PRSADHD, PRSSCZ or PRSBP for each individual, smoking phenotype, ten principal components and genotyping batch. Dependent variables were lifetime occurrence of hallucinations, delusions or any psychotic experience. Models also included the interaction of smoking and PRS with genotyping batch and the principal components, to control for the effect of these covariates on the interaction term41. To examine whether the GxE was significant after multiple testing correction (p < 0.0021 based on 24 models under additive and multiplicative models: 0.05/24 = 0.0021), we used the anova function from R package ‘car’. All models were constructed in R (3.5.1).
The inclusion of individuals with psychotic disorders (Supplementary Table 4) may inflate the variance explained by the PRSs and lead to false-positive GxE. Therefore, we repeated the significant interaction effect analysis after excluding individuals that met the criteria for psychotic disorders.
In all, 157,366 individuals completed the mental health questionnaire. From those, 2067 reported delusions, 6689 hallucinations and 7803 any psychotic experience. In all, 953 individuals had both lifetime delusions and hallucinations. Sample sizes for controls were 155,182, 150,336 and 149,289 for delusions, hallucinations, and any psychotic experience, respectively.
For the smoking variables derived from the full cohort, 273,542 individuals reported that they never smoked, 173,072 were former smokers and 52,979 were current smokers. The mean number of packs per year smoked was 23.4 (SD = 18.8). In all, 126,632 individuals reported that their mothers had smoked around the participant’s birth, whereas 306,266 reported the opposite. Table 1 includes demographic, psychiatric and behavioural characteristics of the sample before genetic data QC. Supplementary Table 7 shows the number of individuals with psychotic experiences stratified by smoking status, maternal smoking and mean number of packs smoked per year after genetic data QC.
Smoking and psychotic experiences
The odds of having delusions, hallucinations or any psychotic experience was significantly higher in current or former tobacco users when compared with non-users, and in participants whose mothers smoked around the time of birth (Table 2). There was a positive linear relationship between the number of packs of cigarettes and risk of psychotic experiences (Table 2). Associations between smoking and the likelihood of having psychotic experiences were strongest for continued tobacco smoking (current smoking vs never smoked). Associations were attenuated after adjustment for diagnosis of psychotic experiences, depression and ADHD but remained significant. Only packs smoked per year on occurrence of delusions did not pass the significance threshold after multiple testing correction (p < 0.0125) (Table 2).
The PRSSCZ, PRSDEP, PRSADHD and PRSBP were significantly associated with psychotic experiences (Fig. 2) and with smoking behaviour (Supplementary Fig. 1). The proportion of variance in psychotic experiences explained by PRSs was small, the highest was for PRSSCZ, which predicted 0.89% of the variance for lifetime delusions (Fig. 2a). Results were dependent on the type of psychotic experience: PRSSCZ and PRSBP explained almost double the percentage of the variance for delusions than for hallucinations (Fig. 2a, d), and p-values for PRSADHD passed multiple testing correction for hallucinations and any psychotic experience, but not for delusions (Fig. 2c).
Therefore, it is possible that genetic risk confounds the relationship between smoking and psychotic experiences. To test this hypothesis, we included PRSSCZ, PRSDEP, PRSADHD and PRSBP as covariates in the analyses. All the regression models (except packs smoked per year on delusions and hallucinations) remained significant after the inclusion of the PRSSCZ, PRSDEP, PRSADHD and PRSBP (Table 2).
Interaction between genetic risk of psychiatric disorders and smoking on psychotic experiences
We found significant additive interactions between PRSADHD and PRSDEP (but not PRSSCZ and PRSBP) and smoking status (current vs never smoker) on reporting lifetime delusions. That is, the combined effect of PRSADHD and smoking, or PRSDEP and smoking was significantly greater than the sum of their individual effects (Fig. 3 and Supplementary Table 8 for OR and β values). However, there were no significant interactions between PRSs and smoking status for hallucinations or any psychotic experiences (Fig. 3).
To ensure that the significant interaction for PRSADHD and PRSDEP was not entirely driven by participants with a diagnosis of bipolar disorder or schizophrenia, we excluded individuals meeting criteria for diagnosis of psychotic disorders (Supplementary Table 9) and repeated the GxE analyses. All the interaction terms remained significant (Supplementary Fig. 2 and Supplementary Table 10).
Our study investigated whether smoking is associated with the occurrence of psychotic experiences independently from diagnosis of psychotic disorders, depression or ADHD, or genetic predisposition for these disorders. We also tested whether the effects of smoking were modulated by the genetic risk in gene-environment interaction models. We found smoking status, maternal smoking and number of packs smoked per year were all significantly associated with increased risk of psychotic experiences. GxE modelling indicated the effects of two PRSs (DEP & ADHD) on delusions was significantly greater in current smokers compared to never smokers. These results suggest both genetic risk and smoking behaviour contribute to specific types of psychotic experiences.
A few previous studies have assessed PRS-environment interactions on psychotic experiences finding that higher genetic risk exacerbates environmental effects. However, these studies have focused exclusively on genetic risk of schizophrenia and environmental factors such as stress42 and birth weight43. Our study is the first one to explore PRS by environment interactions with smoking on psychotic experiences and the first to explore these effects in the context of genetic risk of depression, bipolar disorder and ADHD. Further, our study had greater power than previous ones because we used at least 30 times larger sample sizes, we calculated multiple PRSs at higher p-values that increased the predictive power of the genetic score, and we used the largest GWAS summary statistics available to date.
The interaction of smoking status with PRSDEP, but not with PRSSCZ or PRSBP, on predicting delusions is of particular interest. Delusions of reference and persecution are classified as some of the core symptoms of psychotic disorders (i.e. schizophrenia and bipolar disorder) but they are rarely part of the diagnostic criteria for depression44. Wooton et al.14 reported that genetic risk for depression increased smoking, but there was unclear evidence for genetic risk for schizophrenia increasing smoking. Our finding that PRSDEP (but not PRSSCZ or PRSBP) interacts with smoking on predicting psychotic experiences points at a stronger relationship between smoking and depression than between smoking and schizophrenia or between smoking and bipolar disorder. Our sensitivity analyses, where the interaction remained significant after excluding people with psychotic disorders, supports this hypothesis.
In line with previous studies, we found significant associations between the smoking phenotypes and psychotic experiences10,11,12,13,17, and between PRSSCZ, PRSDEP, PRSADHD and PRSBP and the smoking phenotypes and psychotic experiences25,36,45,46. These findings suggest that the relationship between the smoking variables and psychotic experiences may be confounded by shared genetic influences. However, the effects of smoking remained very similar after adjusting for PRSs, providing little evidence of genetic confounding by common genetic variation associated with schizophrenia, depression, ADHD and bipolar disorder. Previous studies have shown that the effects of smoking on psychotic experiences remain significant after adjustment for psychiatric disorders16. However, this is the first study to show these effects also remain significant after adjustment for genetic risk of specific psychiatric disorders.
The effects of maternal smoking after adjusting for the PRSs are also interesting. Previous within-family studies suggest that, once unmeasured familial factors are taken into account, maternal smoking has little effect on psychotic disorders20. In the current study, the effects of maternal smoking persisted following adjustment for PRSSCZ, PRSDEP PRSADHD and PRSBP. This tentatively suggests that genetic risk for these disorders does not confound the relationship between maternal smoking and psychotic experiences. Nevertheless, the PRSs tested only capture a small fraction of the genetic risk for psychiatric disorders. Replication of these effects using more powerful estimates of genetic risk will be required to test this hypothesis.
There are some limitations of this study: it is retrospective meaning it is subject to recalling biases, which occur when participants do not accurately remember past experiences, and this can lead to spurious results. We have relied on self-reported data, which might be affected by different conceptions of what it is a psychotic experience. There were 351 individuals that completed the UKB mental health questionnaire that may have also participated in the Psychiatric Genomic Consortium cohorts analysed by Wray et al.37. The sample overlap was minimal, with 0.079% for the discovery sample (351/446,238), and 0.242% for the target sample (351/144,818). The overlap was identified using a checksum-based approach as described in Howard et al.47 and the impact over this overlap is unknown. We reported an interaction between genetic risk and smoking, but the percentage of variance explained by the PRSs was very low (<1%), therefore further work is required to understand the remaining sources of phenotypic variance. There is also evidence of a ‘healthy volunteer’ bias in UKB48, especially among people who completed the mental health questionnaire31, which may make this study not fully representative of the general population. Finally, the present study was focused on individuals of European ancestry therefore these results might not be valid for other ancestries49.
Despite the limitations, we report for the first time that smoking is associated with occurrence of psychotic experiences after adjusting for genetic risk for mental health and that current smokers with higher genetic risk for depression and ADHD are more likely to experience delusions but not hallucinations. These results emphasise the importance of assessing environmental and genetic factors jointly and separately, and exploring particular types of psychotic experiences, as they can be differentially associated with smoking or other risk factors. This study also highlights the relationship between smoking and depression, and between smoking and ADHD on the occurrence of specific types of psychotic experiences in the general population, encouraging further studies to explore the effect of genetic risk for other psychiatric disorders on psychosis. Taken together, our results support the distinction of types of psychotic symptoms, the inclusion of environmental factors, and the study of cross-disorder genetic predictors to inform biological mechanisms underlying psychotic experiences.
Analytical code used to define outcomes and regression models for this project is available at https://github.com/juditperala/PRSxSmoking.
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This paper is dedicated to the memory of our dear friend and colleague Rob Keers, who sadly passed away while this paper was being peer-reviewed.
We thank the UK Biobank participants who donated their time, experiences and DNA to this research, and to the UK Biobank team for making the data available. J.G-G. would like to thank Dr. Jonathan Coleman, Dr. Christopher Hübel and Olakunle Oginni for valuable feedback on the analyses and the paper draft. J.G-G. acknowledges support from the Queen Mary Principal’s Research Studentship in the School of Biological and Chemical Sciences. D.M.H. is supported by a Sir Henry Wellcome Postdoctoral Fellowship (Reference 213674/Z/18/Z) and a 2018 NARSAD Young Investigator Grant from the Brain & Behavior Research Foundation (Ref: 27404). P.B.M. acknowledges support from the National Institutes of Health Research (NIHR) Cardiovascular Biomedical Centre at Barts and The London, Queen Mary University of London (QMUL). J.R. acknowledges support from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 786833. C.H.B. acknowledges support from NIH grant No UO1 DA04440001A1. C.H.B. is a member of the Royal Society Industry Fellows’ College. R.K. is supported by Wellcome Trust Grant 208881/Z/17/Z.
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García-González, J., Ramírez, J., Howard, D.M. et al. The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank. Transl Psychiatry 10, 330 (2020). https://doi.org/10.1038/s41398-020-01009-8
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