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Use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma

BACKGROUND: Phosphodiesterase 5A inhibitors (PDEIs), a common treatment for erectile dysfunction, were recently linked to an increased risk of melanoma. METHODS: We conducted two parallel case–control studies, using the Danish Nationwide Health Registries (DNHR) and the Kaiser Permanente Northern Ca...

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Autores principales: Pottegård, Anton, Schmidt, Sigrún Alba Johannesdottir, Olesen, Anne Braae, Achacoso, Ninah, Van Den Eeden, Stephen K, Hallas, Jesper, Sørensen, Henrik Toft, Friis, Søren, Habel, Laurel A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046205/
https://www.ncbi.nlm.nih.gov/pubmed/27529513
http://dx.doi.org/10.1038/bjc.2016.248
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author Pottegård, Anton
Schmidt, Sigrún Alba Johannesdottir
Olesen, Anne Braae
Achacoso, Ninah
Van Den Eeden, Stephen K
Hallas, Jesper
Sørensen, Henrik Toft
Friis, Søren
Habel, Laurel A
author_facet Pottegård, Anton
Schmidt, Sigrún Alba Johannesdottir
Olesen, Anne Braae
Achacoso, Ninah
Van Den Eeden, Stephen K
Hallas, Jesper
Sørensen, Henrik Toft
Friis, Søren
Habel, Laurel A
author_sort Pottegård, Anton
collection PubMed
description BACKGROUND: Phosphodiesterase 5A inhibitors (PDEIs), a common treatment for erectile dysfunction, were recently linked to an increased risk of melanoma. METHODS: We conducted two parallel case–control studies, using the Danish Nationwide Health Registries (DNHR) and the Kaiser Permanente Northern California (KPNC) electronic health records. Identifying men with histologically verified melanoma (cases) matched on birth year to 10 cancer-free controls, we estimated odds ratios (OR) for melanoma associated with high use of PDEIs (⩾100 tablets filled), adjusting for available confounders. RESULTS: We identified 7045 DNHR and 2972 KPNC cases with invasive melanoma. The adjusted OR for invasive melanoma associated with high PDEI use was 1.22 (95% confidence interval (CI), 0.99–1.49) in DNHR and 0.95 (95% CI, 0.78–1.14) in KPNC. Odds ratios were highest for localised invasive melanoma in DNHR (OR, 1.21) and melanoma in situ in KPNC (OR, 1.15), and lowest for non-localised disease in both populations (ORs 0.75 and 0.61, respectively). The increased ORs were slightly attenuated upon adjustment for markers of health-care utilisation. CONCLUSIONS: We found little evidence for a causal association between PDEI use and risk of melanoma. The marginally increased risk of early stage disease likely resulted from more frequent health-care contacts among PDEI users.
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spelling pubmed-50462052016-10-17 Use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma Pottegård, Anton Schmidt, Sigrún Alba Johannesdottir Olesen, Anne Braae Achacoso, Ninah Van Den Eeden, Stephen K Hallas, Jesper Sørensen, Henrik Toft Friis, Søren Habel, Laurel A Br J Cancer Epidemiology BACKGROUND: Phosphodiesterase 5A inhibitors (PDEIs), a common treatment for erectile dysfunction, were recently linked to an increased risk of melanoma. METHODS: We conducted two parallel case–control studies, using the Danish Nationwide Health Registries (DNHR) and the Kaiser Permanente Northern California (KPNC) electronic health records. Identifying men with histologically verified melanoma (cases) matched on birth year to 10 cancer-free controls, we estimated odds ratios (OR) for melanoma associated with high use of PDEIs (⩾100 tablets filled), adjusting for available confounders. RESULTS: We identified 7045 DNHR and 2972 KPNC cases with invasive melanoma. The adjusted OR for invasive melanoma associated with high PDEI use was 1.22 (95% confidence interval (CI), 0.99–1.49) in DNHR and 0.95 (95% CI, 0.78–1.14) in KPNC. Odds ratios were highest for localised invasive melanoma in DNHR (OR, 1.21) and melanoma in situ in KPNC (OR, 1.15), and lowest for non-localised disease in both populations (ORs 0.75 and 0.61, respectively). The increased ORs were slightly attenuated upon adjustment for markers of health-care utilisation. CONCLUSIONS: We found little evidence for a causal association between PDEI use and risk of melanoma. The marginally increased risk of early stage disease likely resulted from more frequent health-care contacts among PDEI users. Nature Publishing Group 2016-09-27 2016-08-16 /pmc/articles/PMC5046205/ /pubmed/27529513 http://dx.doi.org/10.1038/bjc.2016.248 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Epidemiology
Pottegård, Anton
Schmidt, Sigrún Alba Johannesdottir
Olesen, Anne Braae
Achacoso, Ninah
Van Den Eeden, Stephen K
Hallas, Jesper
Sørensen, Henrik Toft
Friis, Søren
Habel, Laurel A
Use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma
title Use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma
title_full Use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma
title_fullStr Use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma
title_full_unstemmed Use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma
title_short Use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma
title_sort use of sildenafil or other phosphodiesterase inhibitors and risk of melanoma
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046205/
https://www.ncbi.nlm.nih.gov/pubmed/27529513
http://dx.doi.org/10.1038/bjc.2016.248
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