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Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles

Endometriosis is a poorly understood common debilitating women's reproductive disorder resulting from proliferative and ectopic endometrial tissue associated with variable clinical symptoms including dysmenorrhea (painful menstrual periods), dyspareunia (pain on intercourse), female infertility...

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Autores principales: Kondova, Ivanela, Braskamp, Gerco, Heidt, Peter J., Collignon, Wim, Haaksma, Tom, de Groot, Nanine, Otting, Nel, Doxiadis, Gaby, Westmoreland, Susan V., Vallender, Eric J., Bontrop, Ronald E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Copernicus GmbH 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041536/
https://www.ncbi.nlm.nih.gov/pubmed/32110699
http://dx.doi.org/10.5194/pb-4-117-2017
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author Kondova, Ivanela
Braskamp, Gerco
Heidt, Peter J.
Collignon, Wim
Haaksma, Tom
de Groot, Nanine
Otting, Nel
Doxiadis, Gaby
Westmoreland, Susan V.
Vallender, Eric J.
Bontrop, Ronald E.
author_facet Kondova, Ivanela
Braskamp, Gerco
Heidt, Peter J.
Collignon, Wim
Haaksma, Tom
de Groot, Nanine
Otting, Nel
Doxiadis, Gaby
Westmoreland, Susan V.
Vallender, Eric J.
Bontrop, Ronald E.
author_sort Kondova, Ivanela
collection PubMed
description Endometriosis is a poorly understood common debilitating women's reproductive disorder resulting from proliferative and ectopic endometrial tissue associated with variable clinical symptoms including dysmenorrhea (painful menstrual periods), dyspareunia (pain on intercourse), female infertility, and an increased risk of malignant transformation. The rhesus macaque (Macaca mulatta) develops a spontaneous endometriosis that is very similar to that seen in women. We hypothesized that specific major histocompatibility complex (MHC) alleles may contribute to the pathogenesis of endometriosis. As part of a collaboration between the Biomedical Primate Research Centre (BPRC) in the Netherlands and the New England Primate Research Center (NEPRC) in the United States, we analyzed DNA sequences of MHC class I (Macaca mulatta, Mamu-A1) and class II (Mamu-DRB) alleles from rhesus macaques with endometriosis and compared the allele frequencies with those of age-matched healthy macaques. We demonstrate that two MHC class I alleles are overrepresented in diseased macaques compared to controls: Mamu-A1*001, 33.3 % in BPRC animals with endometriosis vs. 11.6 % in healthy macaques ([Formula: see text]  0.007), and Mamu-A1*007, 21.9 % NEPRC rhesus macaques vs. 6.7 %, ([Formula: see text]  0.003). We provide evidence that select MHC class I alleles are associated with endometriosis in rhesus macaques and suggest that the disease pathogenesis contribution of MHC class I warrants further research.
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spelling pubmed-70415362020-02-27 Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles Kondova, Ivanela Braskamp, Gerco Heidt, Peter J. Collignon, Wim Haaksma, Tom de Groot, Nanine Otting, Nel Doxiadis, Gaby Westmoreland, Susan V. Vallender, Eric J. Bontrop, Ronald E. Primate Biol Research Article Endometriosis is a poorly understood common debilitating women's reproductive disorder resulting from proliferative and ectopic endometrial tissue associated with variable clinical symptoms including dysmenorrhea (painful menstrual periods), dyspareunia (pain on intercourse), female infertility, and an increased risk of malignant transformation. The rhesus macaque (Macaca mulatta) develops a spontaneous endometriosis that is very similar to that seen in women. We hypothesized that specific major histocompatibility complex (MHC) alleles may contribute to the pathogenesis of endometriosis. As part of a collaboration between the Biomedical Primate Research Centre (BPRC) in the Netherlands and the New England Primate Research Center (NEPRC) in the United States, we analyzed DNA sequences of MHC class I (Macaca mulatta, Mamu-A1) and class II (Mamu-DRB) alleles from rhesus macaques with endometriosis and compared the allele frequencies with those of age-matched healthy macaques. We demonstrate that two MHC class I alleles are overrepresented in diseased macaques compared to controls: Mamu-A1*001, 33.3 % in BPRC animals with endometriosis vs. 11.6 % in healthy macaques ([Formula: see text]  0.007), and Mamu-A1*007, 21.9 % NEPRC rhesus macaques vs. 6.7 %, ([Formula: see text]  0.003). We provide evidence that select MHC class I alleles are associated with endometriosis in rhesus macaques and suggest that the disease pathogenesis contribution of MHC class I warrants further research. Copernicus GmbH 2017-06-22 /pmc/articles/PMC7041536/ /pubmed/32110699 http://dx.doi.org/10.5194/pb-4-117-2017 Text en Copyright: © 2017 Ivanela Kondova et al. This work is licensed under the Creative Commons Attribution 3.0 Unported License. To view a copy of this licence, visit https://creativecommons.org/licenses/by/3.0/
spellingShingle Research Article
Kondova, Ivanela
Braskamp, Gerco
Heidt, Peter J.
Collignon, Wim
Haaksma, Tom
de Groot, Nanine
Otting, Nel
Doxiadis, Gaby
Westmoreland, Susan V.
Vallender, Eric J.
Bontrop, Ronald E.
Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles
title Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles
title_full Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles
title_fullStr Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles
title_full_unstemmed Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles
title_short Spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific Mamu-A1 alleles
title_sort spontaneous endometriosis in rhesus macaques: evidence for a genetic association with specific mamu-a1 alleles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041536/
https://www.ncbi.nlm.nih.gov/pubmed/32110699
http://dx.doi.org/10.5194/pb-4-117-2017
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