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Male fertility potential alteration in rheumatic diseases: a systematic review

BACKGROUND: Improved targeted therapies for rheumatic diseases were developed recently resulting in a better prognosis for affected patients. Nowadays, patients are living longer and with improved quality of life, including fertility potential. These patients are affected by impaired reproductive fu...

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Autores principales: Tiseo, Bruno Camargo, Cocuzza, Marcello, Bonfá, Eloisa, Srougi, Miguel, Clovis, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Urologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811221/
https://www.ncbi.nlm.nih.gov/pubmed/27120778
http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0595
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author Tiseo, Bruno Camargo
Cocuzza, Marcello
Bonfá, Eloisa
Srougi, Miguel
Clovis, A
author_facet Tiseo, Bruno Camargo
Cocuzza, Marcello
Bonfá, Eloisa
Srougi, Miguel
Clovis, A
author_sort Tiseo, Bruno Camargo
collection PubMed
description BACKGROUND: Improved targeted therapies for rheumatic diseases were developed recently resulting in a better prognosis for affected patients. Nowadays, patients are living longer and with improved quality of life, including fertility potential. These patients are affected by impaired reproductive function and the causes are often multifactorial related to particularities of each disease. This review highlights how rheumatic diseases and their management affect testicular function and male fertility. MATERIALS AND METHODS: A systematic review of literature of all published data after 1970 was conducted. Data was collected about fertility abnormalities in male patients with systemic lupus erythematosus, rheumatoid arthritis, dermatomyositis, ankylosing spondylitis, Behçet disease and gout. Two independent researchers carried out the search in online databases. RESULTS: A total of 19 articles were included addressing the following diseases: 7 systemic lupus erythematosus, 6 Behçet disease, 4 ankylosing spondylitis, 2 rheumatoid arthritis, 2 dermatomyositis and one gout. Systemic lupus erythematosus clearly affects gonadal function impairing spermatogenesis mainly due to antisperm antibodies and cyclophosphamide therapy. Behçet disease, gout and ankylosing spondylitis patients, including those under anti-TNF therapy in the latter disease, do not seem to have reduced fertility whereas in dermatomyositis, the fertility potential is hampered by disease activity and by alkylating agents. Data regarding rheumatoid arthritis is scarce, gonadal dysfunction observed as consequence of disease activity and antisperm antibodies. CONCLUSIONS: Reduced fertility potential is not uncommon. Its frequency and severity vary among the different rheumatic diseases. Permanent infertility is rare and often associated with alkylating agent therapy.
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spelling pubmed-48112212016-05-09 Male fertility potential alteration in rheumatic diseases: a systematic review Tiseo, Bruno Camargo Cocuzza, Marcello Bonfá, Eloisa Srougi, Miguel Clovis, A Int Braz J Urol Review Article BACKGROUND: Improved targeted therapies for rheumatic diseases were developed recently resulting in a better prognosis for affected patients. Nowadays, patients are living longer and with improved quality of life, including fertility potential. These patients are affected by impaired reproductive function and the causes are often multifactorial related to particularities of each disease. This review highlights how rheumatic diseases and their management affect testicular function and male fertility. MATERIALS AND METHODS: A systematic review of literature of all published data after 1970 was conducted. Data was collected about fertility abnormalities in male patients with systemic lupus erythematosus, rheumatoid arthritis, dermatomyositis, ankylosing spondylitis, Behçet disease and gout. Two independent researchers carried out the search in online databases. RESULTS: A total of 19 articles were included addressing the following diseases: 7 systemic lupus erythematosus, 6 Behçet disease, 4 ankylosing spondylitis, 2 rheumatoid arthritis, 2 dermatomyositis and one gout. Systemic lupus erythematosus clearly affects gonadal function impairing spermatogenesis mainly due to antisperm antibodies and cyclophosphamide therapy. Behçet disease, gout and ankylosing spondylitis patients, including those under anti-TNF therapy in the latter disease, do not seem to have reduced fertility whereas in dermatomyositis, the fertility potential is hampered by disease activity and by alkylating agents. Data regarding rheumatoid arthritis is scarce, gonadal dysfunction observed as consequence of disease activity and antisperm antibodies. CONCLUSIONS: Reduced fertility potential is not uncommon. Its frequency and severity vary among the different rheumatic diseases. Permanent infertility is rare and often associated with alkylating agent therapy. Sociedade Brasileira de Urologia 2016 /pmc/articles/PMC4811221/ /pubmed/27120778 http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0595 Text en 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 work is properly cited.
spellingShingle Review Article
Tiseo, Bruno Camargo
Cocuzza, Marcello
Bonfá, Eloisa
Srougi, Miguel
Clovis, A
Male fertility potential alteration in rheumatic diseases: a systematic review
title Male fertility potential alteration in rheumatic diseases: a systematic review
title_full Male fertility potential alteration in rheumatic diseases: a systematic review
title_fullStr Male fertility potential alteration in rheumatic diseases: a systematic review
title_full_unstemmed Male fertility potential alteration in rheumatic diseases: a systematic review
title_short Male fertility potential alteration in rheumatic diseases: a systematic review
title_sort male fertility potential alteration in rheumatic diseases: a systematic review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811221/
https://www.ncbi.nlm.nih.gov/pubmed/27120778
http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0595
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