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Erectile function in men with end-stage liver disease improves after living donor liver transplantation
BACKGROUND: Impaired liver function in men can result in erectile dysfunction or hypogonadism or both. We investigated whether living donor liver transplantation (LDLT) results in improvement in male sexual function. METHODS: A total of 58 patients with end-stage liver disease (ESLD) were included i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535392/ https://www.ncbi.nlm.nih.gov/pubmed/26268947 http://dx.doi.org/10.1186/s12894-015-0078-6 |
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author | Chien, You-Chiuan Chiang, Heng-Chieh Lin, Ping-Yi Chen, Yao-Li |
author_facet | Chien, You-Chiuan Chiang, Heng-Chieh Lin, Ping-Yi Chen, Yao-Li |
author_sort | Chien, You-Chiuan |
collection | PubMed |
description | BACKGROUND: Impaired liver function in men can result in erectile dysfunction or hypogonadism or both. We investigated whether living donor liver transplantation (LDLT) results in improvement in male sexual function. METHODS: A total of 58 patients with end-stage liver disease (ESLD) were included in this prospective, cross-sectional study. Erectile function was measured before and after LDLT using a five-item modified version of the International Index of Erectile Function scale (IIEF-5) and hypogonadism was evaluated before and after LDLT using the Androgen Deficiency in the Aging Male (ADAM) questionnaire. Differences in mean values from the questionnaires before and after the operation were than evaluated to determine whether there is an association between LDLT and improvement in sexual function. RESULTS: We found that mean IIEF-5 scores significantly increased after LDLT (from 11.7 ± 7.7 before LDLT to 14.7 ± 7.5 after LDLT, p <0.01), indicating that the operation played a role in improving erectile function. In addition, the prevalence of hypogonadism among the patients with ESLD decreased markedly after liver transplantation (hypogonadism before LDLT, n = 41 versus hypogonadism after LDLT, n = 31, p = 0.03). Patients with hypogonadism reported a higher prevalence of erectile dysfunction after LDLT than patients without hypogonadism (p <0.01). CONCLUSIONS: LDLT results in improvement in erectile function. In addition, improvement in erectile function is associated with self-reported absence of hypogonadism. |
format | Online Article Text |
id | pubmed-4535392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45353922015-08-14 Erectile function in men with end-stage liver disease improves after living donor liver transplantation Chien, You-Chiuan Chiang, Heng-Chieh Lin, Ping-Yi Chen, Yao-Li BMC Urol Research Article BACKGROUND: Impaired liver function in men can result in erectile dysfunction or hypogonadism or both. We investigated whether living donor liver transplantation (LDLT) results in improvement in male sexual function. METHODS: A total of 58 patients with end-stage liver disease (ESLD) were included in this prospective, cross-sectional study. Erectile function was measured before and after LDLT using a five-item modified version of the International Index of Erectile Function scale (IIEF-5) and hypogonadism was evaluated before and after LDLT using the Androgen Deficiency in the Aging Male (ADAM) questionnaire. Differences in mean values from the questionnaires before and after the operation were than evaluated to determine whether there is an association between LDLT and improvement in sexual function. RESULTS: We found that mean IIEF-5 scores significantly increased after LDLT (from 11.7 ± 7.7 before LDLT to 14.7 ± 7.5 after LDLT, p <0.01), indicating that the operation played a role in improving erectile function. In addition, the prevalence of hypogonadism among the patients with ESLD decreased markedly after liver transplantation (hypogonadism before LDLT, n = 41 versus hypogonadism after LDLT, n = 31, p = 0.03). Patients with hypogonadism reported a higher prevalence of erectile dysfunction after LDLT than patients without hypogonadism (p <0.01). CONCLUSIONS: LDLT results in improvement in erectile function. In addition, improvement in erectile function is associated with self-reported absence of hypogonadism. BioMed Central 2015-08-13 /pmc/articles/PMC4535392/ /pubmed/26268947 http://dx.doi.org/10.1186/s12894-015-0078-6 Text en © Chien et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Chien, You-Chiuan Chiang, Heng-Chieh Lin, Ping-Yi Chen, Yao-Li Erectile function in men with end-stage liver disease improves after living donor liver transplantation |
title | Erectile function in men with end-stage liver disease improves after living donor liver transplantation |
title_full | Erectile function in men with end-stage liver disease improves after living donor liver transplantation |
title_fullStr | Erectile function in men with end-stage liver disease improves after living donor liver transplantation |
title_full_unstemmed | Erectile function in men with end-stage liver disease improves after living donor liver transplantation |
title_short | Erectile function in men with end-stage liver disease improves after living donor liver transplantation |
title_sort | erectile function in men with end-stage liver disease improves after living donor liver transplantation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535392/ https://www.ncbi.nlm.nih.gov/pubmed/26268947 http://dx.doi.org/10.1186/s12894-015-0078-6 |
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