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Estrogen receptor α polymorphism is associated with dementia in a Brazilian cohort
The growth of the elderly population is a worldwide phenomenon and it is associated with chronic diseases, including dementia. In this scenario, the present study aimed to evaluate a possible association of estrogen receptor α polymorphisms with dementia in a Brazilian cohort. The subject sample was...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747857/ https://www.ncbi.nlm.nih.gov/pubmed/33400738 http://dx.doi.org/10.18632/oncotarget.27744 |
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author | Magnago, Rafaella Papalino Lopes Barauna, Valerio Garrone Brun, Bruna Ferro Lo Prete, Ana Cristina Alvarenga, Aline Morgan Gastalho Campos, Luciene C. Rochette, Neuza Felix Gomes Rangel, Letícia Batista Azevedo Faria, Rodrigo Alves Santos, Paulo Caleb Junior Lima Silva, Ian Victor |
author_facet | Magnago, Rafaella Papalino Lopes Barauna, Valerio Garrone Brun, Bruna Ferro Lo Prete, Ana Cristina Alvarenga, Aline Morgan Gastalho Campos, Luciene C. Rochette, Neuza Felix Gomes Rangel, Letícia Batista Azevedo Faria, Rodrigo Alves Santos, Paulo Caleb Junior Lima Silva, Ian Victor |
author_sort | Magnago, Rafaella Papalino Lopes |
collection | PubMed |
description | The growth of the elderly population is a worldwide phenomenon and it is associated with chronic diseases, including dementia. In this scenario, the present study aimed to evaluate a possible association of estrogen receptor α polymorphisms with dementia in a Brazilian cohort. The subject sample was divided into two groups, control (n = 105) and case (n = 73), according to analysis of two predictive dementia tests (MMSE and CDR). The genotyping for the ERα PvuII (c.454-397T>C, rs2234693) and XbaI (c.454-351A>G, rs9340799) polymorphisms were performed by polymerase chain reaction-restriction fragment length polymorphism. The ERα PvuII pp genotype was associated with higher odds ratio for dementia (OR = 3.42, 95% CI = 1.33–8.77, p = 0.01, in a model including covariates. A linear regression model identified significant associations of the ERα PvuII genotypes (independent variable) with CDR scale (dependent variable), β = 0.26 and p = 0.001. In conclusion, estrogen receptor α PvuII polymorphism is associated with dementia in a Brazilian cohort. This finding may be useful for the identification of a possible set of significant genetic and clinical biomarkers for better understanding pathophysiology, early diagnosis and management of dementia. |
format | Online Article Text |
id | pubmed-7747857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-77478572021-01-04 Estrogen receptor α polymorphism is associated with dementia in a Brazilian cohort Magnago, Rafaella Papalino Lopes Barauna, Valerio Garrone Brun, Bruna Ferro Lo Prete, Ana Cristina Alvarenga, Aline Morgan Gastalho Campos, Luciene C. Rochette, Neuza Felix Gomes Rangel, Letícia Batista Azevedo Faria, Rodrigo Alves Santos, Paulo Caleb Junior Lima Silva, Ian Victor Oncotarget Research Paper The growth of the elderly population is a worldwide phenomenon and it is associated with chronic diseases, including dementia. In this scenario, the present study aimed to evaluate a possible association of estrogen receptor α polymorphisms with dementia in a Brazilian cohort. The subject sample was divided into two groups, control (n = 105) and case (n = 73), according to analysis of two predictive dementia tests (MMSE and CDR). The genotyping for the ERα PvuII (c.454-397T>C, rs2234693) and XbaI (c.454-351A>G, rs9340799) polymorphisms were performed by polymerase chain reaction-restriction fragment length polymorphism. The ERα PvuII pp genotype was associated with higher odds ratio for dementia (OR = 3.42, 95% CI = 1.33–8.77, p = 0.01, in a model including covariates. A linear regression model identified significant associations of the ERα PvuII genotypes (independent variable) with CDR scale (dependent variable), β = 0.26 and p = 0.001. In conclusion, estrogen receptor α PvuII polymorphism is associated with dementia in a Brazilian cohort. This finding may be useful for the identification of a possible set of significant genetic and clinical biomarkers for better understanding pathophysiology, early diagnosis and management of dementia. Impact Journals LLC 2020-12-15 /pmc/articles/PMC7747857/ /pubmed/33400738 http://dx.doi.org/10.18632/oncotarget.27744 Text en Copyright: © 2020 Magnago et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Magnago, Rafaella Papalino Lopes Barauna, Valerio Garrone Brun, Bruna Ferro Lo Prete, Ana Cristina Alvarenga, Aline Morgan Gastalho Campos, Luciene C. Rochette, Neuza Felix Gomes Rangel, Letícia Batista Azevedo Faria, Rodrigo Alves Santos, Paulo Caleb Junior Lima Silva, Ian Victor Estrogen receptor α polymorphism is associated with dementia in a Brazilian cohort |
title | Estrogen receptor α polymorphism is associated with dementia in a Brazilian cohort |
title_full | Estrogen receptor α polymorphism is associated with dementia in a Brazilian cohort |
title_fullStr | Estrogen receptor α polymorphism is associated with dementia in a Brazilian cohort |
title_full_unstemmed | Estrogen receptor α polymorphism is associated with dementia in a Brazilian cohort |
title_short | Estrogen receptor α polymorphism is associated with dementia in a Brazilian cohort |
title_sort | estrogen receptor α polymorphism is associated with dementia in a brazilian cohort |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747857/ https://www.ncbi.nlm.nih.gov/pubmed/33400738 http://dx.doi.org/10.18632/oncotarget.27744 |
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