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The male contribution to recurrent pregnancy loss

There are several known causes of recurrent pregnancy loss (RPL) in a couple, which include endocrine abnormalities, immunologic abnormalities, structural uterine abnormalities and karyotype abnormalities. The evaluation largely focuses on the female. The male contribution to RPL remains understudie...

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Detalles Bibliográficos
Autores principales: Ibrahim, Yetunde, Johnstone, Erica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6087842/
https://www.ncbi.nlm.nih.gov/pubmed/30159238
http://dx.doi.org/10.21037/tau.2018.05.14
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author Ibrahim, Yetunde
Johnstone, Erica
author_facet Ibrahim, Yetunde
Johnstone, Erica
author_sort Ibrahim, Yetunde
collection PubMed
description There are several known causes of recurrent pregnancy loss (RPL) in a couple, which include endocrine abnormalities, immunologic abnormalities, structural uterine abnormalities and karyotype abnormalities. The evaluation largely focuses on the female. The male contribution to RPL remains understudied. With the exception of the karyotype analysis, there is currently no other recommended testing for the male partner of a woman who has suffered multiple pregnancy losses. Chromosomal abnormalities are well defined causes of pregnancy losses in the literature. However, despite the fact that abnormal DNA fragmentation has been implicated in the pathogenesis of unexplained RPL, it is not routinely checked during the evaluation of RPL. This is likely due to the fact that abnormal DNA fragmentation is the end result of multiple different mechanisms including environmental exposures, varicoceles, gene alteration and epigenetic changes resulting in an inherent susceptibility to DNA damage? We are just beginning to scratch the surface of our understanding of the male contribution to RPL and more studies especially focusing on epigenetic modifications and gene alterations are needed.
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spelling pubmed-60878422018-08-29 The male contribution to recurrent pregnancy loss Ibrahim, Yetunde Johnstone, Erica Transl Androl Urol Review Article There are several known causes of recurrent pregnancy loss (RPL) in a couple, which include endocrine abnormalities, immunologic abnormalities, structural uterine abnormalities and karyotype abnormalities. The evaluation largely focuses on the female. The male contribution to RPL remains understudied. With the exception of the karyotype analysis, there is currently no other recommended testing for the male partner of a woman who has suffered multiple pregnancy losses. Chromosomal abnormalities are well defined causes of pregnancy losses in the literature. However, despite the fact that abnormal DNA fragmentation has been implicated in the pathogenesis of unexplained RPL, it is not routinely checked during the evaluation of RPL. This is likely due to the fact that abnormal DNA fragmentation is the end result of multiple different mechanisms including environmental exposures, varicoceles, gene alteration and epigenetic changes resulting in an inherent susceptibility to DNA damage? We are just beginning to scratch the surface of our understanding of the male contribution to RPL and more studies especially focusing on epigenetic modifications and gene alterations are needed. AME Publishing Company 2018-07 /pmc/articles/PMC6087842/ /pubmed/30159238 http://dx.doi.org/10.21037/tau.2018.05.14 Text en 2018 Translational Andrology and Urology. All rights reserved.
spellingShingle Review Article
Ibrahim, Yetunde
Johnstone, Erica
The male contribution to recurrent pregnancy loss
title The male contribution to recurrent pregnancy loss
title_full The male contribution to recurrent pregnancy loss
title_fullStr The male contribution to recurrent pregnancy loss
title_full_unstemmed The male contribution to recurrent pregnancy loss
title_short The male contribution to recurrent pregnancy loss
title_sort male contribution to recurrent pregnancy loss
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6087842/
https://www.ncbi.nlm.nih.gov/pubmed/30159238
http://dx.doi.org/10.21037/tau.2018.05.14
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