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Statin and Aspirin Use and the Risk of Mood Disorders among Men

BACKGROUND: There is a growing understanding that depression is associated with systemic inflammation. Statins and aspirin have anti-inflammatory properties. Given these agents have been shown to reduce the risk of a number of diseases characterized by inflammation, we aimed to determine whether a s...

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Autores principales: Williams, Lana J., Pasco, Julie A., Mohebbi, Mohammadreza, Jacka, Felice N., Stuart, Amanda L., Venugopal, Kamalesh, O’Neil, Adrienne, Berk, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926800/
https://www.ncbi.nlm.nih.gov/pubmed/26839250
http://dx.doi.org/10.1093/ijnp/pyw008
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author Williams, Lana J.
Pasco, Julie A.
Mohebbi, Mohammadreza
Jacka, Felice N.
Stuart, Amanda L.
Venugopal, Kamalesh
O’Neil, Adrienne
Berk, Michael
author_facet Williams, Lana J.
Pasco, Julie A.
Mohebbi, Mohammadreza
Jacka, Felice N.
Stuart, Amanda L.
Venugopal, Kamalesh
O’Neil, Adrienne
Berk, Michael
author_sort Williams, Lana J.
collection PubMed
description BACKGROUND: There is a growing understanding that depression is associated with systemic inflammation. Statins and aspirin have anti-inflammatory properties. Given these agents have been shown to reduce the risk of a number of diseases characterized by inflammation, we aimed to determine whether a similar relationship exists for mood disorders (MD). METHODS: This study examined data collected from 961 men (24–98 years) participating in the Geelong Osteoporosis Study. MD were identified using a semistructured clinical interview (SCID-I/NP). Anthropometry was measured and information on medication use and lifestyle factors was obtained via questionnaire. Two study designs were utilized: a nested case-control and a retrospective cohort study. RESULTS: In the nested case-control study, exposure to statin and aspirin was documented for 9 of 142 (6.3%) cases and 234 of 795 (29.4%) controls (P < .001); after adjustment for age, exposure to these anti-inflammatory agents was associated with reduced likelihood of MD (OR 0.2, 95%CI 0.1–0.5). No effect modifiers or other confounders were identified. In the retrospective cohort study of 836 men, among the 210 exposed to statins or aspirin, 6 (2.9%) developed de novo MD during 1000 person-years of observation, whereas among 626 nonexposed, 34 (5.4%) developed de novo MD during 3071 person-years of observation. The hazard ratio for de novo MD associated with exposure to anti-inflammatory agents was 0.55 (95%CI 0.23–1.32). CONCLUSIONS: This study provides both cross-sectional and longitudinal evidence consistent with the hypothesis that statin and aspirin use is associated with a reduced risk of MD.
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spelling pubmed-49268002016-07-05 Statin and Aspirin Use and the Risk of Mood Disorders among Men Williams, Lana J. Pasco, Julie A. Mohebbi, Mohammadreza Jacka, Felice N. Stuart, Amanda L. Venugopal, Kamalesh O’Neil, Adrienne Berk, Michael Int J Neuropsychopharmacol Letter to Editor BACKGROUND: There is a growing understanding that depression is associated with systemic inflammation. Statins and aspirin have anti-inflammatory properties. Given these agents have been shown to reduce the risk of a number of diseases characterized by inflammation, we aimed to determine whether a similar relationship exists for mood disorders (MD). METHODS: This study examined data collected from 961 men (24–98 years) participating in the Geelong Osteoporosis Study. MD were identified using a semistructured clinical interview (SCID-I/NP). Anthropometry was measured and information on medication use and lifestyle factors was obtained via questionnaire. Two study designs were utilized: a nested case-control and a retrospective cohort study. RESULTS: In the nested case-control study, exposure to statin and aspirin was documented for 9 of 142 (6.3%) cases and 234 of 795 (29.4%) controls (P < .001); after adjustment for age, exposure to these anti-inflammatory agents was associated with reduced likelihood of MD (OR 0.2, 95%CI 0.1–0.5). No effect modifiers or other confounders were identified. In the retrospective cohort study of 836 men, among the 210 exposed to statins or aspirin, 6 (2.9%) developed de novo MD during 1000 person-years of observation, whereas among 626 nonexposed, 34 (5.4%) developed de novo MD during 3071 person-years of observation. The hazard ratio for de novo MD associated with exposure to anti-inflammatory agents was 0.55 (95%CI 0.23–1.32). CONCLUSIONS: This study provides both cross-sectional and longitudinal evidence consistent with the hypothesis that statin and aspirin use is associated with a reduced risk of MD. Oxford University Press 2016-02-02 /pmc/articles/PMC4926800/ /pubmed/26839250 http://dx.doi.org/10.1093/ijnp/pyw008 Text en © The Author 2016. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Letter to Editor
Williams, Lana J.
Pasco, Julie A.
Mohebbi, Mohammadreza
Jacka, Felice N.
Stuart, Amanda L.
Venugopal, Kamalesh
O’Neil, Adrienne
Berk, Michael
Statin and Aspirin Use and the Risk of Mood Disorders among Men
title Statin and Aspirin Use and the Risk of Mood Disorders among Men
title_full Statin and Aspirin Use and the Risk of Mood Disorders among Men
title_fullStr Statin and Aspirin Use and the Risk of Mood Disorders among Men
title_full_unstemmed Statin and Aspirin Use and the Risk of Mood Disorders among Men
title_short Statin and Aspirin Use and the Risk of Mood Disorders among Men
title_sort statin and aspirin use and the risk of mood disorders among men
topic Letter to Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926800/
https://www.ncbi.nlm.nih.gov/pubmed/26839250
http://dx.doi.org/10.1093/ijnp/pyw008
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