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Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis
A cluster of three genes CELSR2, PSRC1, and SORT1 has been associated with cardiovascular diseases. Thus, the aim of this study was (i) to perform a systematic review and updated meta-analysis of the association of three polymorphisms (rs646776, rs599839, and rs464218) of this cluster with cardiovas...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056735/ https://www.ncbi.nlm.nih.gov/pubmed/36975855 http://dx.doi.org/10.3390/jcdd10030091 |
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author | Castillo-Avila, Rosa Giannina González-Castro, Thelma Beatriz Tovilla-Zárate, Carlos Alfonso Martínez-Magaña, José Jaime López-Narváez, María Lilia Juárez-Rojop, Isela Esther Arias-Vázquez, Pedro Iván Borgonio-Cuadra, Verónica Marusa Pérez-Hernández, Nonanzit Rodríguez-Pérez, José Manuel |
author_facet | Castillo-Avila, Rosa Giannina González-Castro, Thelma Beatriz Tovilla-Zárate, Carlos Alfonso Martínez-Magaña, José Jaime López-Narváez, María Lilia Juárez-Rojop, Isela Esther Arias-Vázquez, Pedro Iván Borgonio-Cuadra, Verónica Marusa Pérez-Hernández, Nonanzit Rodríguez-Pérez, José Manuel |
author_sort | Castillo-Avila, Rosa Giannina |
collection | PubMed |
description | A cluster of three genes CELSR2, PSRC1, and SORT1 has been associated with cardiovascular diseases. Thus, the aim of this study was (i) to perform a systematic review and updated meta-analysis of the association of three polymorphisms (rs646776, rs599839, and rs464218) of this cluster with cardiovascular diseases, and (ii) to explore by PheWAS signals of the three SNPs in cardiovascular diseases and to evaluate the effect of rs599839 with tissue expression by in silico tools. Three electronic databases were searched to identify eligible studies. The meta-analysis showed that the rs599839 (allelic OR 1.19, 95% CI 1.13–1.26, dominant OR 1.22, 95% CI 1.06–1.39, recessive OR 1.23, 95% CI 1.15–1.32), rs646776 (allelic OR 1.46, 95% CI 1.17–1.82) polymorphisms showed an increased risk for cardiovascular diseases. PheWas analysis showed associations with coronary artery disease and total cholesterol. Our results suggest a possible involvement of the CELSR2-PSRC1-SORT1 cluster variants in the risk association of cardiovascular diseases, particularly coronary artery disease. |
format | Online Article Text |
id | pubmed-10056735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100567352023-03-30 Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis Castillo-Avila, Rosa Giannina González-Castro, Thelma Beatriz Tovilla-Zárate, Carlos Alfonso Martínez-Magaña, José Jaime López-Narváez, María Lilia Juárez-Rojop, Isela Esther Arias-Vázquez, Pedro Iván Borgonio-Cuadra, Verónica Marusa Pérez-Hernández, Nonanzit Rodríguez-Pérez, José Manuel J Cardiovasc Dev Dis Systematic Review A cluster of three genes CELSR2, PSRC1, and SORT1 has been associated with cardiovascular diseases. Thus, the aim of this study was (i) to perform a systematic review and updated meta-analysis of the association of three polymorphisms (rs646776, rs599839, and rs464218) of this cluster with cardiovascular diseases, and (ii) to explore by PheWAS signals of the three SNPs in cardiovascular diseases and to evaluate the effect of rs599839 with tissue expression by in silico tools. Three electronic databases were searched to identify eligible studies. The meta-analysis showed that the rs599839 (allelic OR 1.19, 95% CI 1.13–1.26, dominant OR 1.22, 95% CI 1.06–1.39, recessive OR 1.23, 95% CI 1.15–1.32), rs646776 (allelic OR 1.46, 95% CI 1.17–1.82) polymorphisms showed an increased risk for cardiovascular diseases. PheWas analysis showed associations with coronary artery disease and total cholesterol. Our results suggest a possible involvement of the CELSR2-PSRC1-SORT1 cluster variants in the risk association of cardiovascular diseases, particularly coronary artery disease. MDPI 2023-02-21 /pmc/articles/PMC10056735/ /pubmed/36975855 http://dx.doi.org/10.3390/jcdd10030091 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Systematic Review Castillo-Avila, Rosa Giannina González-Castro, Thelma Beatriz Tovilla-Zárate, Carlos Alfonso Martínez-Magaña, José Jaime López-Narváez, María Lilia Juárez-Rojop, Isela Esther Arias-Vázquez, Pedro Iván Borgonio-Cuadra, Verónica Marusa Pérez-Hernández, Nonanzit Rodríguez-Pérez, José Manuel Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis |
title | Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis |
title_full | Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis |
title_fullStr | Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis |
title_full_unstemmed | Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis |
title_short | Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis |
title_sort | association between genetic variants of celsr2-psrc1-sort1 and cardiovascular diseases: a systematic review and meta-analysis |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056735/ https://www.ncbi.nlm.nih.gov/pubmed/36975855 http://dx.doi.org/10.3390/jcdd10030091 |
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