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Associations between male infertility and ancestry in South Americans: a case control study

BACKGROUND: Infertility affects 15% of human couples, with men being responsible in approximately 50% of cases. Moreover, the aetiology of male factor infertility is poorly understood. The majority of male factor infertility remains idiopathic and potentially genetic in origin. The association of th...

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Autores principales: Skowronek, Maria Fernanda, Velazquez, Tatiana, Mut, Patricia, Figueiro, Gonzalo, Sans, Monica, Bertoni, Bernardo, Sapiro, Rossana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530489/
https://www.ncbi.nlm.nih.gov/pubmed/28747152
http://dx.doi.org/10.1186/s12881-017-0438-z
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author Skowronek, Maria Fernanda
Velazquez, Tatiana
Mut, Patricia
Figueiro, Gonzalo
Sans, Monica
Bertoni, Bernardo
Sapiro, Rossana
author_facet Skowronek, Maria Fernanda
Velazquez, Tatiana
Mut, Patricia
Figueiro, Gonzalo
Sans, Monica
Bertoni, Bernardo
Sapiro, Rossana
author_sort Skowronek, Maria Fernanda
collection PubMed
description BACKGROUND: Infertility affects 15% of human couples, with men being responsible in approximately 50% of cases. Moreover, the aetiology of male factor infertility is poorly understood. The majority of male factor infertility remains idiopathic and potentially genetic in origin. The association of the Y chromosome and mitochondrial haplogroups with male infertility has been previously reported. This association differs between studied populations and their geographical distributions. These effects have been only rarely analysed in mixed populations, such as South Americans. METHODS: In this study, we analysed the contributions of the Y chromosome and mitochondrial haplogroups to male infertility in a mixed population. A case control study was conducted. Regular PCR and high-resolution-melting-real-time PCR were performed to type haplogroups from fertile and infertile men. The sperm parameters from infertile men were compared in each haplogroup by logistic regression analysis and ANOVA. RESULTS: The genotyping confirmed the known admixture characteristic of the Uruguayan population. The European paternal contribution was higher than the maternal contribution in both fertile and infertile men. Neither maternal nor paternal ancestry presented differences between the cases and controls. Men belonging to the Y chromosome haplogroup F(xK) more frequently presented with an abnormal sperm morphology than men from other haplogroups. The sperm parameters were not associated with the mitochondrial haplogroups. CONCLUSIONS: The data presented in this study showed an association between male infertility and ancestry in the Uruguayan population. Specifically, abnormal sperm morphology was associated with the Y chromosome haplogroup F(xK). Since the Y chromosome lacks recombination, these data suggest that some genes that determine sperm morphology might be inherited in blocks with the region that determines specific haplogroups. However, the possible association between the Y chromosome haplogroup F(xK) and sperm morphology requires further confirmatory testing. Data linking infertility with ancestry are needed to establish the possible causes of infertility and define male populations susceptible to infertility. Whether the admixed characteristics of the Uruguayan population exert any pressure on male fertility potential must be further investigated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12881-017-0438-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-55304892017-08-02 Associations between male infertility and ancestry in South Americans: a case control study Skowronek, Maria Fernanda Velazquez, Tatiana Mut, Patricia Figueiro, Gonzalo Sans, Monica Bertoni, Bernardo Sapiro, Rossana BMC Med Genet Research Article BACKGROUND: Infertility affects 15% of human couples, with men being responsible in approximately 50% of cases. Moreover, the aetiology of male factor infertility is poorly understood. The majority of male factor infertility remains idiopathic and potentially genetic in origin. The association of the Y chromosome and mitochondrial haplogroups with male infertility has been previously reported. This association differs between studied populations and their geographical distributions. These effects have been only rarely analysed in mixed populations, such as South Americans. METHODS: In this study, we analysed the contributions of the Y chromosome and mitochondrial haplogroups to male infertility in a mixed population. A case control study was conducted. Regular PCR and high-resolution-melting-real-time PCR were performed to type haplogroups from fertile and infertile men. The sperm parameters from infertile men were compared in each haplogroup by logistic regression analysis and ANOVA. RESULTS: The genotyping confirmed the known admixture characteristic of the Uruguayan population. The European paternal contribution was higher than the maternal contribution in both fertile and infertile men. Neither maternal nor paternal ancestry presented differences between the cases and controls. Men belonging to the Y chromosome haplogroup F(xK) more frequently presented with an abnormal sperm morphology than men from other haplogroups. The sperm parameters were not associated with the mitochondrial haplogroups. CONCLUSIONS: The data presented in this study showed an association between male infertility and ancestry in the Uruguayan population. Specifically, abnormal sperm morphology was associated with the Y chromosome haplogroup F(xK). Since the Y chromosome lacks recombination, these data suggest that some genes that determine sperm morphology might be inherited in blocks with the region that determines specific haplogroups. However, the possible association between the Y chromosome haplogroup F(xK) and sperm morphology requires further confirmatory testing. Data linking infertility with ancestry are needed to establish the possible causes of infertility and define male populations susceptible to infertility. Whether the admixed characteristics of the Uruguayan population exert any pressure on male fertility potential must be further investigated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12881-017-0438-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-26 /pmc/articles/PMC5530489/ /pubmed/28747152 http://dx.doi.org/10.1186/s12881-017-0438-z Text en © The Author(s). 2017 Open AccessThis 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
Skowronek, Maria Fernanda
Velazquez, Tatiana
Mut, Patricia
Figueiro, Gonzalo
Sans, Monica
Bertoni, Bernardo
Sapiro, Rossana
Associations between male infertility and ancestry in South Americans: a case control study
title Associations between male infertility and ancestry in South Americans: a case control study
title_full Associations between male infertility and ancestry in South Americans: a case control study
title_fullStr Associations between male infertility and ancestry in South Americans: a case control study
title_full_unstemmed Associations between male infertility and ancestry in South Americans: a case control study
title_short Associations between male infertility and ancestry in South Americans: a case control study
title_sort associations between male infertility and ancestry in south americans: a case control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530489/
https://www.ncbi.nlm.nih.gov/pubmed/28747152
http://dx.doi.org/10.1186/s12881-017-0438-z
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