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Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization
Smoking is strongly associated with schizophrenia. Although it has been widely assumed that this reflects self-medication, recent studies suggest that smoking may be a risk factor for schizophrenia. We performed two-sample bi-directional Mendelian randomization using summary level genomewide associa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244403/ https://www.ncbi.nlm.nih.gov/pubmed/28102331 http://dx.doi.org/10.1038/srep40653 |
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author | Gage, Suzanne H. Jones, Hannah J. Taylor, Amy E. Burgess, Stephen Zammit, Stanley Munafò, Marcus R. |
author_facet | Gage, Suzanne H. Jones, Hannah J. Taylor, Amy E. Burgess, Stephen Zammit, Stanley Munafò, Marcus R. |
author_sort | Gage, Suzanne H. |
collection | PubMed |
description | Smoking is strongly associated with schizophrenia. Although it has been widely assumed that this reflects self-medication, recent studies suggest that smoking may be a risk factor for schizophrenia. We performed two-sample bi-directional Mendelian randomization using summary level genomewide association data from the Tobacco And Genetics Consortium and Psychiatric Genomics Consortium. Variants associated with smoking initiation and schizophrenia were combined using an inverse-variance weighted fixed-effects approach. We found evidence consistent with a causal effect of smoking initiation on schizophrenia risk (OR 1.73, 95% CI 1.30–2.25, p < 0.001). However, after relaxing the p-value threshold to include variants from more than one gene and minimize the potential impact of pleiotropy, the association was attenuated (OR 1.03, 95% CI 0.97–1.09, p = 0.32). There was little evidence in support of a causal effect of schizophrenia on smoking initiation (OR 1.01, 95% CI 0.98–1.04, p = 0.32). MR Egger regression sensitivity analysis indicated no evidence for pleiotropy in the effect of schizophrenia on smoking initiation (intercept OR 1.01, 95% CI 0.99–1.02, p = 0.49). Our findings provide little evidence of a causal association between smoking initiation and schizophrenia, in either direction. However, we cannot rule out a causal effect of smoking on schizophrenia related to heavier, lifetime exposure, rather than initiation. |
format | Online Article Text |
id | pubmed-5244403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52444032017-01-23 Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization Gage, Suzanne H. Jones, Hannah J. Taylor, Amy E. Burgess, Stephen Zammit, Stanley Munafò, Marcus R. Sci Rep Article Smoking is strongly associated with schizophrenia. Although it has been widely assumed that this reflects self-medication, recent studies suggest that smoking may be a risk factor for schizophrenia. We performed two-sample bi-directional Mendelian randomization using summary level genomewide association data from the Tobacco And Genetics Consortium and Psychiatric Genomics Consortium. Variants associated with smoking initiation and schizophrenia were combined using an inverse-variance weighted fixed-effects approach. We found evidence consistent with a causal effect of smoking initiation on schizophrenia risk (OR 1.73, 95% CI 1.30–2.25, p < 0.001). However, after relaxing the p-value threshold to include variants from more than one gene and minimize the potential impact of pleiotropy, the association was attenuated (OR 1.03, 95% CI 0.97–1.09, p = 0.32). There was little evidence in support of a causal effect of schizophrenia on smoking initiation (OR 1.01, 95% CI 0.98–1.04, p = 0.32). MR Egger regression sensitivity analysis indicated no evidence for pleiotropy in the effect of schizophrenia on smoking initiation (intercept OR 1.01, 95% CI 0.99–1.02, p = 0.49). Our findings provide little evidence of a causal association between smoking initiation and schizophrenia, in either direction. However, we cannot rule out a causal effect of smoking on schizophrenia related to heavier, lifetime exposure, rather than initiation. Nature Publishing Group 2017-01-19 /pmc/articles/PMC5244403/ /pubmed/28102331 http://dx.doi.org/10.1038/srep40653 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gage, Suzanne H. Jones, Hannah J. Taylor, Amy E. Burgess, Stephen Zammit, Stanley Munafò, Marcus R. Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization |
title | Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization |
title_full | Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization |
title_fullStr | Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization |
title_full_unstemmed | Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization |
title_short | Investigating causality in associations between smoking initiation and schizophrenia using Mendelian randomization |
title_sort | investigating causality in associations between smoking initiation and schizophrenia using mendelian randomization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244403/ https://www.ncbi.nlm.nih.gov/pubmed/28102331 http://dx.doi.org/10.1038/srep40653 |
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