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Endometriosis Is Associated with Rare Copy Number Variants

Endometriosis is a complex gynecological condition that affects 6–10% of women in their reproductive years and is defined by the presence of endometrial glands and stroma outside the uterus. Twin, family, and genome-wide association (GWA) studies have confirmed a genetic role, yet only a small part...

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Autores principales: Chettier, Rakesh, Ward, Kenneth, Albertsen, Hans M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118997/
https://www.ncbi.nlm.nih.gov/pubmed/25083881
http://dx.doi.org/10.1371/journal.pone.0103968
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author Chettier, Rakesh
Ward, Kenneth
Albertsen, Hans M.
author_facet Chettier, Rakesh
Ward, Kenneth
Albertsen, Hans M.
author_sort Chettier, Rakesh
collection PubMed
description Endometriosis is a complex gynecological condition that affects 6–10% of women in their reproductive years and is defined by the presence of endometrial glands and stroma outside the uterus. Twin, family, and genome-wide association (GWA) studies have confirmed a genetic role, yet only a small part of the genetic risk can be explained by SNP variation. Copy number variants (CNVs) account for a greater portion of human genetic variation than SNPs and include more recent mutations of large effect. CNVs, likely to be prominent in conditions with decreased reproductive fitness, have not previously been examined as a genetic contributor to endometriosis. Here we employ a high-density genotyping microarray in a genome-wide survey of CNVs in a case-control population that includes 2,126 surgically confirmed endometriosis cases and 17,974 population controls of European ancestry. We apply stringent quality filters to reduce the false positive rate common to many CNV-detection algorithms from 77.7% to 7.3% without noticeable reduction in the true positive rate. We detected no differences in the CNV landscape between cases and controls on the global level which showed an average of 1.92 CNVs per individual with an average size of 142.3 kb. On the local level we identify 22 CNV-regions at the nominal significance threshold (P<0.05), which is greater than the 8.15 CNV-regions expected based on permutation analysis (P<0.001). Three CNV's passed a genome-wide P-value threshold of 9.3×10(−4); a deletion at SGCZ on 8p22 (P = 7.3×10(−4), OR = 8.5, Cl = 2.3–31.7), a deletion in MALRD1 on 10p12.31 (P = 5.6×10(−4), OR = 14.1, Cl = 2.7–90.9), and a deletion at 11q14.1 (P = 5.7×10(−4), OR = 33.8, Cl = 3.3–1651). Two SNPs within the 22 CNVRs show significant genotypic association with endometriosis after adjusting for multiple testing; rs758316 in DPP6 on 7q36.2 (P = 0.0045) and rs4837864 in ASTN2 on 9q33.1 (P = 0.0002). Together, the CNV-loci are detected in 6.9% of affected women compared to 2.1% in the general population.
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spelling pubmed-41189972014-08-04 Endometriosis Is Associated with Rare Copy Number Variants Chettier, Rakesh Ward, Kenneth Albertsen, Hans M. PLoS One Research Article Endometriosis is a complex gynecological condition that affects 6–10% of women in their reproductive years and is defined by the presence of endometrial glands and stroma outside the uterus. Twin, family, and genome-wide association (GWA) studies have confirmed a genetic role, yet only a small part of the genetic risk can be explained by SNP variation. Copy number variants (CNVs) account for a greater portion of human genetic variation than SNPs and include more recent mutations of large effect. CNVs, likely to be prominent in conditions with decreased reproductive fitness, have not previously been examined as a genetic contributor to endometriosis. Here we employ a high-density genotyping microarray in a genome-wide survey of CNVs in a case-control population that includes 2,126 surgically confirmed endometriosis cases and 17,974 population controls of European ancestry. We apply stringent quality filters to reduce the false positive rate common to many CNV-detection algorithms from 77.7% to 7.3% without noticeable reduction in the true positive rate. We detected no differences in the CNV landscape between cases and controls on the global level which showed an average of 1.92 CNVs per individual with an average size of 142.3 kb. On the local level we identify 22 CNV-regions at the nominal significance threshold (P<0.05), which is greater than the 8.15 CNV-regions expected based on permutation analysis (P<0.001). Three CNV's passed a genome-wide P-value threshold of 9.3×10(−4); a deletion at SGCZ on 8p22 (P = 7.3×10(−4), OR = 8.5, Cl = 2.3–31.7), a deletion in MALRD1 on 10p12.31 (P = 5.6×10(−4), OR = 14.1, Cl = 2.7–90.9), and a deletion at 11q14.1 (P = 5.7×10(−4), OR = 33.8, Cl = 3.3–1651). Two SNPs within the 22 CNVRs show significant genotypic association with endometriosis after adjusting for multiple testing; rs758316 in DPP6 on 7q36.2 (P = 0.0045) and rs4837864 in ASTN2 on 9q33.1 (P = 0.0002). Together, the CNV-loci are detected in 6.9% of affected women compared to 2.1% in the general population. Public Library of Science 2014-08-01 /pmc/articles/PMC4118997/ /pubmed/25083881 http://dx.doi.org/10.1371/journal.pone.0103968 Text en © 2014 Chettier et al 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 author and source are properly credited.
spellingShingle Research Article
Chettier, Rakesh
Ward, Kenneth
Albertsen, Hans M.
Endometriosis Is Associated with Rare Copy Number Variants
title Endometriosis Is Associated with Rare Copy Number Variants
title_full Endometriosis Is Associated with Rare Copy Number Variants
title_fullStr Endometriosis Is Associated with Rare Copy Number Variants
title_full_unstemmed Endometriosis Is Associated with Rare Copy Number Variants
title_short Endometriosis Is Associated with Rare Copy Number Variants
title_sort endometriosis is associated with rare copy number variants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4118997/
https://www.ncbi.nlm.nih.gov/pubmed/25083881
http://dx.doi.org/10.1371/journal.pone.0103968
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