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The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank
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 r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523004/ https://www.ncbi.nlm.nih.gov/pubmed/32989213 http://dx.doi.org/10.1038/s41398-020-01009-8 |
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author | García-González, Judit Ramírez, Julia Howard, David M. Brennan, Caroline H. Munroe, Patricia B. Keers, Robert |
author_facet | García-González, Judit Ramírez, Julia Howard, David M. Brennan, Caroline H. Munroe, Patricia B. Keers, Robert |
author_sort | García-González, Judit |
collection | PubMed |
description | 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 (PRS(SCZ)), bipolar disorder (PRS(BP)), major depression (PRS(DEP)) and attention deficit hyperactivity disorder (PRS(ADHD)) 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 PRS(DEP) and PRS(ADHD) (but not PRS(SCZ) or PRS(BP)) 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. |
format | Online Article Text |
id | pubmed-7523004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75230042020-10-19 The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank García-González, Judit Ramírez, Julia Howard, David M. Brennan, Caroline H. Munroe, Patricia B. Keers, Robert Transl Psychiatry Article 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 (PRS(SCZ)), bipolar disorder (PRS(BP)), major depression (PRS(DEP)) and attention deficit hyperactivity disorder (PRS(ADHD)) 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 PRS(DEP) and PRS(ADHD) (but not PRS(SCZ) or PRS(BP)) 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. Nature Publishing Group UK 2020-09-28 /pmc/articles/PMC7523004/ /pubmed/32989213 http://dx.doi.org/10.1038/s41398-020-01009-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article García-González, Judit Ramírez, Julia Howard, David M. Brennan, Caroline H. Munroe, Patricia B. Keers, Robert The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank |
title | The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank |
title_full | The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank |
title_fullStr | The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank |
title_full_unstemmed | The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank |
title_short | The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank |
title_sort | effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in uk biobank |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523004/ https://www.ncbi.nlm.nih.gov/pubmed/32989213 http://dx.doi.org/10.1038/s41398-020-01009-8 |
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