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A meta-analysis of allopurinol therapy and the risk of prostate cancer
OBJECTIVE: The aim of the study was to investigate the risk of prostate cancer among people with gout and/or hyperuricemia who used allopurinol and who did not use allopurinol. METHODS: We conducted a meta-analysis to identify the cohort and case-control studies by searching PubMed and Web of Scienc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684161/ https://www.ncbi.nlm.nih.gov/pubmed/35356907 http://dx.doi.org/10.1097/MD.0000000000028998 |
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author | Lai, Shih-Wei Hwang, Bing-Fang Kuo, Yu-Hung Liu, Chiu-Shong Liao, Kuan-Fu |
author_facet | Lai, Shih-Wei Hwang, Bing-Fang Kuo, Yu-Hung Liu, Chiu-Shong Liao, Kuan-Fu |
author_sort | Lai, Shih-Wei |
collection | PubMed |
description | OBJECTIVE: The aim of the study was to investigate the risk of prostate cancer among people with gout and/or hyperuricemia who used allopurinol and who did not use allopurinol. METHODS: We conducted a meta-analysis to identify the cohort and case-control studies by searching PubMed and Web of Science. We used the random-effects model to calculate the pooled risk ratio with 95% confidence interval for the risk of prostate cancer associated with allopurinol treatment. RESULTS: There were 5 cohort studies and 2 case-control studies included in the meta-analysis. All 7 eligible studies were published between 2012 and 2021. The study period ranged from 8 to 13years. The number of study subjects ranged from 25,770 to 1,623,550. The age of study subjects ranged from 20 to 99years. Overall, allopurinol treatment was not associated with the risk of prostate cancer (risk ratio = 1.13, 95% confidence interval = 0.96-1.34 and P = .13). The heterogeneity was high between studies (I(2) = 93%). CONCLUSIONS: Our meta-analysis reveals that no association can be found between allopurinol treatment and the risk of prostate cancer among people with gout and/or hyperuricemia. We propose that the inhibition of xanthine oxidase and the reduction of serum uric acid via allopurinol treatment do not affect the probability of developing prostate cancer. Further studies are needed to confirm our findings. KEY POINTS: No association can be found between allopurinol treatment and the risk of prostate cancer. The inhibition of xanthine oxidase and the reduction of serum uric acid via allopurinol treatment do not affect the probability of developing prostate cancer. |
format | Online Article Text |
id | pubmed-10684161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-106841612023-11-30 A meta-analysis of allopurinol therapy and the risk of prostate cancer Lai, Shih-Wei Hwang, Bing-Fang Kuo, Yu-Hung Liu, Chiu-Shong Liao, Kuan-Fu Medicine (Baltimore) Systematic Review and Meta-Analysis OBJECTIVE: The aim of the study was to investigate the risk of prostate cancer among people with gout and/or hyperuricemia who used allopurinol and who did not use allopurinol. METHODS: We conducted a meta-analysis to identify the cohort and case-control studies by searching PubMed and Web of Science. We used the random-effects model to calculate the pooled risk ratio with 95% confidence interval for the risk of prostate cancer associated with allopurinol treatment. RESULTS: There were 5 cohort studies and 2 case-control studies included in the meta-analysis. All 7 eligible studies were published between 2012 and 2021. The study period ranged from 8 to 13years. The number of study subjects ranged from 25,770 to 1,623,550. The age of study subjects ranged from 20 to 99years. Overall, allopurinol treatment was not associated with the risk of prostate cancer (risk ratio = 1.13, 95% confidence interval = 0.96-1.34 and P = .13). The heterogeneity was high between studies (I(2) = 93%). CONCLUSIONS: Our meta-analysis reveals that no association can be found between allopurinol treatment and the risk of prostate cancer among people with gout and/or hyperuricemia. We propose that the inhibition of xanthine oxidase and the reduction of serum uric acid via allopurinol treatment do not affect the probability of developing prostate cancer. Further studies are needed to confirm our findings. KEY POINTS: No association can be found between allopurinol treatment and the risk of prostate cancer. The inhibition of xanthine oxidase and the reduction of serum uric acid via allopurinol treatment do not affect the probability of developing prostate cancer. Lippincott Williams & Wilkins 2022-03-18 /pmc/articles/PMC10684161/ /pubmed/35356907 http://dx.doi.org/10.1097/MD.0000000000028998 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://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 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | Systematic Review and Meta-Analysis Lai, Shih-Wei Hwang, Bing-Fang Kuo, Yu-Hung Liu, Chiu-Shong Liao, Kuan-Fu A meta-analysis of allopurinol therapy and the risk of prostate cancer |
title | A meta-analysis of allopurinol therapy and the risk of prostate cancer |
title_full | A meta-analysis of allopurinol therapy and the risk of prostate cancer |
title_fullStr | A meta-analysis of allopurinol therapy and the risk of prostate cancer |
title_full_unstemmed | A meta-analysis of allopurinol therapy and the risk of prostate cancer |
title_short | A meta-analysis of allopurinol therapy and the risk of prostate cancer |
title_sort | meta-analysis of allopurinol therapy and the risk of prostate cancer |
topic | Systematic Review and Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684161/ https://www.ncbi.nlm.nih.gov/pubmed/35356907 http://dx.doi.org/10.1097/MD.0000000000028998 |
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