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Association Between Nonalcoholic Fatty Liver Disease and Severe Male Reproductive Organ Impairment (Germinal Epithelial Loss): Study on a Mouse Model and on Human Patients
Metabolic syndrome (MS) has been associated with testicular damage. Nonalcoholic fatty liver disease (NAFLD) is a multisystemic disease that affects different organs, but its effect on the testes is unknown. A study analyzing germ cell involvement on BALB/c mice was carried out. A parallel comparati...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987961/ https://www.ncbi.nlm.nih.gov/pubmed/29577833 http://dx.doi.org/10.1177/1557988318763631 |
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author | López-Lemus, Uriel A. Garza-Guajardo, Raquel Barboza-Quintana, Oralia Rodríguez-Hernandez, Alejandrina García-Rivera, Alejandro Madrigal-Pérez, Violeta M. Guzmán-Esquivel, José García-Labastida, Laura E. Soriano-Hernández, Alejandro D. Martínez-Fierro, Margarita L. Rodríguez-Sánchez, Iram P. Sánchez-Duarte, Elizabeth Cabrera-Licona, Ariana Ceja-Espiritu, Gabriel Delgado-Enciso, Iván |
author_facet | López-Lemus, Uriel A. Garza-Guajardo, Raquel Barboza-Quintana, Oralia Rodríguez-Hernandez, Alejandrina García-Rivera, Alejandro Madrigal-Pérez, Violeta M. Guzmán-Esquivel, José García-Labastida, Laura E. Soriano-Hernández, Alejandro D. Martínez-Fierro, Margarita L. Rodríguez-Sánchez, Iram P. Sánchez-Duarte, Elizabeth Cabrera-Licona, Ariana Ceja-Espiritu, Gabriel Delgado-Enciso, Iván |
author_sort | López-Lemus, Uriel A. |
collection | PubMed |
description | Metabolic syndrome (MS) has been associated with testicular damage. Nonalcoholic fatty liver disease (NAFLD) is a multisystemic disease that affects different organs, but its effect on the testes is unknown. A study analyzing germ cell involvement on BALB/c mice was carried out. A parallel comparative study was conducted that investigated alterations in the germinal epithelium of male humans that died from an unrelated acute event. The complete medical histories and histologic samples of the thoracic aorta, liver tissue, and testicular tissue from the deceased subjects were collected. The degree of germinal epithelial loss (DGEL) was evaluated and the clinical and histologic data were compared between individuals with and without NAFLD. The only metabolic or morphologic variable that caused a significant difference in the DGEL, in both the animal model and humans, was the presence of liver steatosis. The percentage of steatosis was also correlated with the percentage of the DGEL. In humans, steatosis (greater than 20%) increased the risk 12-fold for presenting with a severe DGEL (OR: 12.5; 95% CI [1.2, 128.9]; p = .03). There was no association with age above 50 years or MS components. Steatosis grade was also correlated with atherosclerosis grade. NAFLD was a strongly associated factor implicated in severe DGEL, as well as the testis was identified as a probable target organ for damage caused by the disease. This finding could result in the search for new approach strategies in the management of men with fertility problems. Further studies are required to confirm these results. |
format | Online Article Text |
id | pubmed-5987961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-59879612018-06-07 Association Between Nonalcoholic Fatty Liver Disease and Severe Male Reproductive Organ Impairment (Germinal Epithelial Loss): Study on a Mouse Model and on Human Patients López-Lemus, Uriel A. Garza-Guajardo, Raquel Barboza-Quintana, Oralia Rodríguez-Hernandez, Alejandrina García-Rivera, Alejandro Madrigal-Pérez, Violeta M. Guzmán-Esquivel, José García-Labastida, Laura E. Soriano-Hernández, Alejandro D. Martínez-Fierro, Margarita L. Rodríguez-Sánchez, Iram P. Sánchez-Duarte, Elizabeth Cabrera-Licona, Ariana Ceja-Espiritu, Gabriel Delgado-Enciso, Iván Am J Mens Health Articles Metabolic syndrome (MS) has been associated with testicular damage. Nonalcoholic fatty liver disease (NAFLD) is a multisystemic disease that affects different organs, but its effect on the testes is unknown. A study analyzing germ cell involvement on BALB/c mice was carried out. A parallel comparative study was conducted that investigated alterations in the germinal epithelium of male humans that died from an unrelated acute event. The complete medical histories and histologic samples of the thoracic aorta, liver tissue, and testicular tissue from the deceased subjects were collected. The degree of germinal epithelial loss (DGEL) was evaluated and the clinical and histologic data were compared between individuals with and without NAFLD. The only metabolic or morphologic variable that caused a significant difference in the DGEL, in both the animal model and humans, was the presence of liver steatosis. The percentage of steatosis was also correlated with the percentage of the DGEL. In humans, steatosis (greater than 20%) increased the risk 12-fold for presenting with a severe DGEL (OR: 12.5; 95% CI [1.2, 128.9]; p = .03). There was no association with age above 50 years or MS components. Steatosis grade was also correlated with atherosclerosis grade. NAFLD was a strongly associated factor implicated in severe DGEL, as well as the testis was identified as a probable target organ for damage caused by the disease. This finding could result in the search for new approach strategies in the management of men with fertility problems. Further studies are required to confirm these results. SAGE Publications 2018-03-26 2018-05 /pmc/articles/PMC5987961/ /pubmed/29577833 http://dx.doi.org/10.1177/1557988318763631 Text en © The Author(s) 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Articles López-Lemus, Uriel A. Garza-Guajardo, Raquel Barboza-Quintana, Oralia Rodríguez-Hernandez, Alejandrina García-Rivera, Alejandro Madrigal-Pérez, Violeta M. Guzmán-Esquivel, José García-Labastida, Laura E. Soriano-Hernández, Alejandro D. Martínez-Fierro, Margarita L. Rodríguez-Sánchez, Iram P. Sánchez-Duarte, Elizabeth Cabrera-Licona, Ariana Ceja-Espiritu, Gabriel Delgado-Enciso, Iván Association Between Nonalcoholic Fatty Liver Disease and Severe Male Reproductive Organ Impairment (Germinal Epithelial Loss): Study on a Mouse Model and on Human Patients |
title | Association Between Nonalcoholic Fatty Liver Disease and Severe Male Reproductive Organ Impairment (Germinal Epithelial Loss): Study on a Mouse Model and on Human Patients |
title_full | Association Between Nonalcoholic Fatty Liver Disease and Severe Male Reproductive Organ Impairment (Germinal Epithelial Loss): Study on a Mouse Model and on Human Patients |
title_fullStr | Association Between Nonalcoholic Fatty Liver Disease and Severe Male Reproductive Organ Impairment (Germinal Epithelial Loss): Study on a Mouse Model and on Human Patients |
title_full_unstemmed | Association Between Nonalcoholic Fatty Liver Disease and Severe Male Reproductive Organ Impairment (Germinal Epithelial Loss): Study on a Mouse Model and on Human Patients |
title_short | Association Between Nonalcoholic Fatty Liver Disease and Severe Male Reproductive Organ Impairment (Germinal Epithelial Loss): Study on a Mouse Model and on Human Patients |
title_sort | association between nonalcoholic fatty liver disease and severe male reproductive organ impairment (germinal epithelial loss): study on a mouse model and on human patients |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987961/ https://www.ncbi.nlm.nih.gov/pubmed/29577833 http://dx.doi.org/10.1177/1557988318763631 |
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