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Clustering of comorbid conditions among women who carry an FMR1 premutation

PURPOSE: Emerging evidence indicates that women who carry an FMR1 premutation can experience complex health profiles beyond the two well-established premutation-associated disorders: fragile X–associated primary ovarian insufficiency (FXPOI, affects ~20–30% carriers) and fragile X–associated tremor–...

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Autores principales: Allen, Emily Graves, Charen, Krista, Hipp, Heather S., Shubeck, Lisa, Amin, Ashima, He, Weiya, Hunter, Jessica Ezzell, Sherman, Stephanie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118023/
https://www.ncbi.nlm.nih.gov/pubmed/31896764
http://dx.doi.org/10.1038/s41436-019-0733-5
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author Allen, Emily Graves
Charen, Krista
Hipp, Heather S.
Shubeck, Lisa
Amin, Ashima
He, Weiya
Hunter, Jessica Ezzell
Sherman, Stephanie L.
author_facet Allen, Emily Graves
Charen, Krista
Hipp, Heather S.
Shubeck, Lisa
Amin, Ashima
He, Weiya
Hunter, Jessica Ezzell
Sherman, Stephanie L.
author_sort Allen, Emily Graves
collection PubMed
description PURPOSE: Emerging evidence indicates that women who carry an FMR1 premutation can experience complex health profiles beyond the two well-established premutation-associated disorders: fragile X–associated primary ovarian insufficiency (FXPOI, affects ~20–30% carriers) and fragile X–associated tremor–ataxia syndrome (FXTAS, affects ~6–15% carriers). METHODS: To better understand premutation-associated health profiles, we collected self-reported medical histories on 355 carrier women. RESULTS: Twenty-two health conditions were reported by at least 10% of women. Anxiety, depression, and headaches were reported by more than 30%. The number of comorbid conditions was significantly associated with body mass index (BMI) and history of smoking, but not age. Survival analysis indicated that women with FXPOI had an earlier age at onset for anxiety and osteoporosis than women without FXPOI. Cluster analysis identified eight clusters of women who reported similar patterns of comorbid conditions. The majority of carriers (63%) fell into three categories primarily defined by the presence of only a few conditions. Interestingly, a single cluster defined women with symptoms of FXTAS, and none of these women had FXPOI. CONCLUSION: Although some women with a premutation experience complex health outcomes, most carriers report only minimal comorbid conditions. Further, women with symptoms of FXTAS appear to be distinct from women with symptoms of FXPOI.
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spelling pubmed-71180232020-04-06 Clustering of comorbid conditions among women who carry an FMR1 premutation Allen, Emily Graves Charen, Krista Hipp, Heather S. Shubeck, Lisa Amin, Ashima He, Weiya Hunter, Jessica Ezzell Sherman, Stephanie L. Genet Med Article PURPOSE: Emerging evidence indicates that women who carry an FMR1 premutation can experience complex health profiles beyond the two well-established premutation-associated disorders: fragile X–associated primary ovarian insufficiency (FXPOI, affects ~20–30% carriers) and fragile X–associated tremor–ataxia syndrome (FXTAS, affects ~6–15% carriers). METHODS: To better understand premutation-associated health profiles, we collected self-reported medical histories on 355 carrier women. RESULTS: Twenty-two health conditions were reported by at least 10% of women. Anxiety, depression, and headaches were reported by more than 30%. The number of comorbid conditions was significantly associated with body mass index (BMI) and history of smoking, but not age. Survival analysis indicated that women with FXPOI had an earlier age at onset for anxiety and osteoporosis than women without FXPOI. Cluster analysis identified eight clusters of women who reported similar patterns of comorbid conditions. The majority of carriers (63%) fell into three categories primarily defined by the presence of only a few conditions. Interestingly, a single cluster defined women with symptoms of FXTAS, and none of these women had FXPOI. CONCLUSION: Although some women with a premutation experience complex health outcomes, most carriers report only minimal comorbid conditions. Further, women with symptoms of FXTAS appear to be distinct from women with symptoms of FXPOI. Nature Publishing Group US 2020-01-03 2020 /pmc/articles/PMC7118023/ /pubmed/31896764 http://dx.doi.org/10.1038/s41436-019-0733-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Allen, Emily Graves
Charen, Krista
Hipp, Heather S.
Shubeck, Lisa
Amin, Ashima
He, Weiya
Hunter, Jessica Ezzell
Sherman, Stephanie L.
Clustering of comorbid conditions among women who carry an FMR1 premutation
title Clustering of comorbid conditions among women who carry an FMR1 premutation
title_full Clustering of comorbid conditions among women who carry an FMR1 premutation
title_fullStr Clustering of comorbid conditions among women who carry an FMR1 premutation
title_full_unstemmed Clustering of comorbid conditions among women who carry an FMR1 premutation
title_short Clustering of comorbid conditions among women who carry an FMR1 premutation
title_sort clustering of comorbid conditions among women who carry an fmr1 premutation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118023/
https://www.ncbi.nlm.nih.gov/pubmed/31896764
http://dx.doi.org/10.1038/s41436-019-0733-5
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