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Statin Use and Risk of Prostate Cancer: A Meta-Analysis of Observational Studies

BACKGROUND: Emerging evidence suggests that statins may decrease the risk of cancers. However, available evidence on prostate cancer (PCa) is conflicting. We therefore examined the association between statin use and risk of PCa by conducting a detailed meta-analysis of all observational studies publ...

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Autores principales: Bansal, Dipika, Undela, Krishna, D'Cruz, Sanjay, Schifano, Fabrizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462187/
https://www.ncbi.nlm.nih.gov/pubmed/23049713
http://dx.doi.org/10.1371/journal.pone.0046691
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author Bansal, Dipika
Undela, Krishna
D'Cruz, Sanjay
Schifano, Fabrizio
author_facet Bansal, Dipika
Undela, Krishna
D'Cruz, Sanjay
Schifano, Fabrizio
author_sort Bansal, Dipika
collection PubMed
description BACKGROUND: Emerging evidence suggests that statins may decrease the risk of cancers. However, available evidence on prostate cancer (PCa) is conflicting. We therefore examined the association between statin use and risk of PCa by conducting a detailed meta-analysis of all observational studies published regarding this subject. METHODS: Literature search in PubMed database was undertaken through February 2012 looking for observational studies evaluating the association between statin use and risk of PCa. Before meta-analysis, the studies were evaluated for publication bias and heterogeneity. Pooled relative risk (RR) estimates and 95% confidence intervals (CIs) were calculated using random-effects model (DerSimonian and Laird method). Subgroup analyses, sensitivity analysis and cumulative meta-analysis were also performed. RESULTS: A total of 27 (15 cohort and 12 case-control) studies contributed to the analysis. There was heterogeneity among the studies but no publication bias. Statin use significantly reduced the risk of both total PCa by 7% (RR 0.93, 95% CI 0.87–0.99, p = 0.03) and clinically important advanced PCa by 20% (RR 0.80, 95% CI 0.70–0.90, p<0.001). Long-term statin use did not significantly affect the risk of total PCa (RR 0.94, 95% CI 0.84–1.05, p = 0.31). Stratification by study design did not substantially influence the RR. Furthermore, sensitivity analysis confirmed the stability of results. Cumulative meta-analysis showed a change in trend of reporting risk from positive to negative in statin users between 1993 and 2011. CONCLUSIONS: Our meta-analysis provides evidence supporting the hypothesis that statins reduce the risk of both total PCa and clinically important advanced PCa. Further research is needed to confirm these findings and to identify the underlying biological mechanisms.
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spelling pubmed-34621872012-10-05 Statin Use and Risk of Prostate Cancer: A Meta-Analysis of Observational Studies Bansal, Dipika Undela, Krishna D'Cruz, Sanjay Schifano, Fabrizio PLoS One Research Article BACKGROUND: Emerging evidence suggests that statins may decrease the risk of cancers. However, available evidence on prostate cancer (PCa) is conflicting. We therefore examined the association between statin use and risk of PCa by conducting a detailed meta-analysis of all observational studies published regarding this subject. METHODS: Literature search in PubMed database was undertaken through February 2012 looking for observational studies evaluating the association between statin use and risk of PCa. Before meta-analysis, the studies were evaluated for publication bias and heterogeneity. Pooled relative risk (RR) estimates and 95% confidence intervals (CIs) were calculated using random-effects model (DerSimonian and Laird method). Subgroup analyses, sensitivity analysis and cumulative meta-analysis were also performed. RESULTS: A total of 27 (15 cohort and 12 case-control) studies contributed to the analysis. There was heterogeneity among the studies but no publication bias. Statin use significantly reduced the risk of both total PCa by 7% (RR 0.93, 95% CI 0.87–0.99, p = 0.03) and clinically important advanced PCa by 20% (RR 0.80, 95% CI 0.70–0.90, p<0.001). Long-term statin use did not significantly affect the risk of total PCa (RR 0.94, 95% CI 0.84–1.05, p = 0.31). Stratification by study design did not substantially influence the RR. Furthermore, sensitivity analysis confirmed the stability of results. Cumulative meta-analysis showed a change in trend of reporting risk from positive to negative in statin users between 1993 and 2011. CONCLUSIONS: Our meta-analysis provides evidence supporting the hypothesis that statins reduce the risk of both total PCa and clinically important advanced PCa. Further research is needed to confirm these findings and to identify the underlying biological mechanisms. Public Library of Science 2012-10-01 /pmc/articles/PMC3462187/ /pubmed/23049713 http://dx.doi.org/10.1371/journal.pone.0046691 Text en © 2012 Bansal et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bansal, Dipika
Undela, Krishna
D'Cruz, Sanjay
Schifano, Fabrizio
Statin Use and Risk of Prostate Cancer: A Meta-Analysis of Observational Studies
title Statin Use and Risk of Prostate Cancer: A Meta-Analysis of Observational Studies
title_full Statin Use and Risk of Prostate Cancer: A Meta-Analysis of Observational Studies
title_fullStr Statin Use and Risk of Prostate Cancer: A Meta-Analysis of Observational Studies
title_full_unstemmed Statin Use and Risk of Prostate Cancer: A Meta-Analysis of Observational Studies
title_short Statin Use and Risk of Prostate Cancer: A Meta-Analysis of Observational Studies
title_sort statin use and risk of prostate cancer: a meta-analysis of observational studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462187/
https://www.ncbi.nlm.nih.gov/pubmed/23049713
http://dx.doi.org/10.1371/journal.pone.0046691
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