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Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis

BACKGROUND: To evaluate the association between apolipoprotein B gene polymorphism and coronary heart disease in some populations at home and abroad by means of meta-analysis. METHODS: Using the strict exclusion criteria for primary screening of the literature and applying the Hardy-Weinberg equilib...

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Autores principales: Feng, Ya Yun, Chen, Lu Yang, Liu, Yang, Luo, Meng, Yang, Tian Tian, Hu, Yu Hao, Chang, Jing, Mao, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268333/
https://www.ncbi.nlm.nih.gov/pubmed/32493216
http://dx.doi.org/10.1186/s12872-020-01545-7
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author Feng, Ya Yun
Chen, Lu Yang
Liu, Yang
Luo, Meng
Yang, Tian Tian
Hu, Yu Hao
Chang, Jing
Mao, Min
author_facet Feng, Ya Yun
Chen, Lu Yang
Liu, Yang
Luo, Meng
Yang, Tian Tian
Hu, Yu Hao
Chang, Jing
Mao, Min
author_sort Feng, Ya Yun
collection PubMed
description BACKGROUND: To evaluate the association between apolipoprotein B gene polymorphism and coronary heart disease in some populations at home and abroad by means of meta-analysis. METHODS: Using the strict exclusion criteria for primary screening of the literature and applying the Hardy-Weinberg equilibrium to test the genetic balance of the selected literature. The corresponding models were selected according to the results of the heterogeneity test. The Begg’s test and Egger’s test were used to evaluate publication bias, and meta-analysis was performed using Stata 12.0. RESULTS: The study included twelve articles. In the literature, a total of 1596 patients with coronary heart disease and 1431 controls.Meta-analysis results showed no statistical value in the following three genetic models: allelic comparison (a vs A,P = 0.811,OR = 0.95, 95%CI = 0.62–1.46), recessive genetic models (aa vs Aa/AA, P = 0.86,OR = 0.94, 95%CI = 0.45–1.96), or dominant genetic models (aa/Aa vs AA, P = 0.73,OR = 0.92, 95%CI = 0.58–1.47). Subgroup analysis based on ethnicity showed allelic comparison (a vs A,P = 0.464,OR = 1.32, 95%CI = 0.63–2.78), recessive genetic models (aa vs Aa/AA, P = 0.422,OR = 1.52, 95%CI = 0.55–4.21), and dominant genetic models (aa/Aa vs AA, P = 0.551,OR = 1.26, 95%CI = 0.58–2.73) in Asians, allelic comparison (a vs A,P = 0.410,OR = 0.79, 95%CI = 0.45–1.39), recessive genetic models (aa vs Aa/AA, P = 0.041,OR = 0.75,95%CI = 0.57–0.99),dominant genetic models (aa/Aa vs AA, P = 0.385,OR = 0.75, 95%CI = 0.40–1.43) in Caucasian; CONCLUSION: The ApoB(apolipoprotein B) XbaI locus is not a risk factor when it comes to the development of coronary heart disease in the domestic and international populations included in this paper. In Caucasians, people carrying the aa genotype may be less susceptible to CHD (coronary heart disease). The results of recessive genetic models have to take the effect of heterogeneity and sample sizes into account. Further research may require a larger and more rigorous research design.
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spelling pubmed-72683332020-06-07 Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis Feng, Ya Yun Chen, Lu Yang Liu, Yang Luo, Meng Yang, Tian Tian Hu, Yu Hao Chang, Jing Mao, Min BMC Cardiovasc Disord Research Article BACKGROUND: To evaluate the association between apolipoprotein B gene polymorphism and coronary heart disease in some populations at home and abroad by means of meta-analysis. METHODS: Using the strict exclusion criteria for primary screening of the literature and applying the Hardy-Weinberg equilibrium to test the genetic balance of the selected literature. The corresponding models were selected according to the results of the heterogeneity test. The Begg’s test and Egger’s test were used to evaluate publication bias, and meta-analysis was performed using Stata 12.0. RESULTS: The study included twelve articles. In the literature, a total of 1596 patients with coronary heart disease and 1431 controls.Meta-analysis results showed no statistical value in the following three genetic models: allelic comparison (a vs A,P = 0.811,OR = 0.95, 95%CI = 0.62–1.46), recessive genetic models (aa vs Aa/AA, P = 0.86,OR = 0.94, 95%CI = 0.45–1.96), or dominant genetic models (aa/Aa vs AA, P = 0.73,OR = 0.92, 95%CI = 0.58–1.47). Subgroup analysis based on ethnicity showed allelic comparison (a vs A,P = 0.464,OR = 1.32, 95%CI = 0.63–2.78), recessive genetic models (aa vs Aa/AA, P = 0.422,OR = 1.52, 95%CI = 0.55–4.21), and dominant genetic models (aa/Aa vs AA, P = 0.551,OR = 1.26, 95%CI = 0.58–2.73) in Asians, allelic comparison (a vs A,P = 0.410,OR = 0.79, 95%CI = 0.45–1.39), recessive genetic models (aa vs Aa/AA, P = 0.041,OR = 0.75,95%CI = 0.57–0.99),dominant genetic models (aa/Aa vs AA, P = 0.385,OR = 0.75, 95%CI = 0.40–1.43) in Caucasian; CONCLUSION: The ApoB(apolipoprotein B) XbaI locus is not a risk factor when it comes to the development of coronary heart disease in the domestic and international populations included in this paper. In Caucasians, people carrying the aa genotype may be less susceptible to CHD (coronary heart disease). The results of recessive genetic models have to take the effect of heterogeneity and sample sizes into account. Further research may require a larger and more rigorous research design. BioMed Central 2020-06-03 /pmc/articles/PMC7268333/ /pubmed/32493216 http://dx.doi.org/10.1186/s12872-020-01545-7 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Feng, Ya Yun
Chen, Lu Yang
Liu, Yang
Luo, Meng
Yang, Tian Tian
Hu, Yu Hao
Chang, Jing
Mao, Min
Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis
title Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis
title_full Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis
title_fullStr Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis
title_full_unstemmed Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis
title_short Association between apolipoprotein B XbaI polymorphisms and coronary heart disease: A meta-analysis
title_sort association between apolipoprotein b xbai polymorphisms and coronary heart disease: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268333/
https://www.ncbi.nlm.nih.gov/pubmed/32493216
http://dx.doi.org/10.1186/s12872-020-01545-7
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