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Are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: A systematic review and meta-analysis

Phosphodiesterase type 5 (PDE5) inhibitors are recommended for patients with erectile dysfunction by American Urological Association and European Association Urology guidelines. However, recent researches have shown that PDE5 inhibitors may lead to increased melanoma risk. Thus, we aimed to explore...

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Autores principales: Feng, Shijian, Zhou, Liang, Liu, Qinyu, He, Qing, Liao, Banghua, Wei, Xin, Li, Hong, Wang, Kunjie, Zhu, Yuchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779753/
https://www.ncbi.nlm.nih.gov/pubmed/29504984
http://dx.doi.org/10.1097/MD.0000000000009601
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author Feng, Shijian
Zhou, Liang
Liu, Qinyu
He, Qing
Liao, Banghua
Wei, Xin
Li, Hong
Wang, Kunjie
Zhu, Yuchun
author_facet Feng, Shijian
Zhou, Liang
Liu, Qinyu
He, Qing
Liao, Banghua
Wei, Xin
Li, Hong
Wang, Kunjie
Zhu, Yuchun
author_sort Feng, Shijian
collection PubMed
description Phosphodiesterase type 5 (PDE5) inhibitors are recommended for patients with erectile dysfunction by American Urological Association and European Association Urology guidelines. However, recent researches have shown that PDE5 inhibitors may lead to increased melanoma risk. Thus, we aimed to explore whether PDE5 inhibitors are associated with increased melanoma risk based on published literatures. We conducted a systematic online search on PubMed, EMBASE, Cochrane Library, Chinese Biochemical Literature, China National Knowledge Infrastructure, and Chinese Science and Technology Periodical databases to identify the related studies. Odds ratios (ORs), risk ratios, and hazard ratios with 95% confidence intervals (CIs) were extracted and calculated to assess the strength of associations between PDE5 inhibitors and melanoma risk. We also extracted the basal cell carcinoma (BCC) to validate the association in this study. We included 5 studies containing 100,932 participants in our systematic review and meta-analysis. The calculated results suggested positive results of PDE5 inhibitors on melanoma risk (OR: 1.13; 95%CI: 1.04–1.23). For localized and nonlocalized melanoma, the results were different (OR: 1.22; 95%CI: 1.04–1.43 for localized melanoma) (OR: 0.62; 95%CI: 0.39–0.98 for nonlocalized melanoma). It also showed that PDE5 inhibitors were associated with increased BCC risk (OR: 1.18; 95%CI: 1.11–1.27). The association between PDE5 inhibitors and melanoma might not be causal due to potential bias (patient selection, and so on) and limitations.
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spelling pubmed-57797532018-02-05 Are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: A systematic review and meta-analysis Feng, Shijian Zhou, Liang Liu, Qinyu He, Qing Liao, Banghua Wei, Xin Li, Hong Wang, Kunjie Zhu, Yuchun Medicine (Baltimore) 7300 Phosphodiesterase type 5 (PDE5) inhibitors are recommended for patients with erectile dysfunction by American Urological Association and European Association Urology guidelines. However, recent researches have shown that PDE5 inhibitors may lead to increased melanoma risk. Thus, we aimed to explore whether PDE5 inhibitors are associated with increased melanoma risk based on published literatures. We conducted a systematic online search on PubMed, EMBASE, Cochrane Library, Chinese Biochemical Literature, China National Knowledge Infrastructure, and Chinese Science and Technology Periodical databases to identify the related studies. Odds ratios (ORs), risk ratios, and hazard ratios with 95% confidence intervals (CIs) were extracted and calculated to assess the strength of associations between PDE5 inhibitors and melanoma risk. We also extracted the basal cell carcinoma (BCC) to validate the association in this study. We included 5 studies containing 100,932 participants in our systematic review and meta-analysis. The calculated results suggested positive results of PDE5 inhibitors on melanoma risk (OR: 1.13; 95%CI: 1.04–1.23). For localized and nonlocalized melanoma, the results were different (OR: 1.22; 95%CI: 1.04–1.43 for localized melanoma) (OR: 0.62; 95%CI: 0.39–0.98 for nonlocalized melanoma). It also showed that PDE5 inhibitors were associated with increased BCC risk (OR: 1.18; 95%CI: 1.11–1.27). The association between PDE5 inhibitors and melanoma might not be causal due to potential bias (patient selection, and so on) and limitations. Wolters Kluwer Health 2018-01-19 /pmc/articles/PMC5779753/ /pubmed/29504984 http://dx.doi.org/10.1097/MD.0000000000009601 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 7300
Feng, Shijian
Zhou, Liang
Liu, Qinyu
He, Qing
Liao, Banghua
Wei, Xin
Li, Hong
Wang, Kunjie
Zhu, Yuchun
Are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: A systematic review and meta-analysis
title Are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: A systematic review and meta-analysis
title_full Are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: A systematic review and meta-analysis
title_fullStr Are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: A systematic review and meta-analysis
title_full_unstemmed Are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: A systematic review and meta-analysis
title_short Are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: A systematic review and meta-analysis
title_sort are phosphodiesterase type 5 inhibitors associated with increased risk of melanoma?: a systematic review and meta-analysis
topic 7300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779753/
https://www.ncbi.nlm.nih.gov/pubmed/29504984
http://dx.doi.org/10.1097/MD.0000000000009601
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