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Trimethylamine-N-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis

BACKGROUND: Previous clinical studies have suggested that trimethylamine-N-oxide (TMAO) could contribute to the development of atherosclerosis cardiovascular disease. However, the synthetic analysis in coronary heart disease (CHD) was not yet performed. We aimed to clarify the relationship between e...

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Autores principales: Yao, Miao-En, Liao, Peng-Da, Zhao, Xu-Jie, Wang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953212/
https://www.ncbi.nlm.nih.gov/pubmed/31918665
http://dx.doi.org/10.1186/s12872-019-01310-5
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author Yao, Miao-En
Liao, Peng-Da
Zhao, Xu-Jie
Wang, Lei
author_facet Yao, Miao-En
Liao, Peng-Da
Zhao, Xu-Jie
Wang, Lei
author_sort Yao, Miao-En
collection PubMed
description BACKGROUND: Previous clinical studies have suggested that trimethylamine-N-oxide (TMAO) could contribute to the development of atherosclerosis cardiovascular disease. However, the synthetic analysis in coronary heart disease (CHD) was not yet performed. We aimed to clarify the relationship between elevated plasma concentrations of TMAO and the incidence of major adverse cardiovascular events (MACE) in CHD patients. METHODS: Meta-analysis and dose-response analysis of hazard ratio data from prospective observational studies reporting on the association between TMAO plasma concentrations and the incidence of MACE in patients with CHD were conducted. RESULTS: Of the 2369 published articles identified in the search, seven papers, with data from nine cohort studies (10,301 patients), were included in the meta-analysis. Combined data showed that elevated plasma TMAO concentrations could increase 58% higher risk of MACE in patients with CHD (hazard ratios [HR]: 1.58; 95% confidence interval [CI] = 1.35–1.84, P = 0.000). For follow-up ≥ 1 year, it was associated with 62% higher risk of MACE in patients with longer-term than shorter-term (HR for follow-up ≥ 4 years: 1.96; 95% CI = 1.52–2.52 vs one to 3 years: 1.34; 95% CI = 1.26–1.43, P = 0.004). The dose-response analysis revealed a ‘J’ shaped association between TMAO concentration and the incidence of MACE (P = 0.033), with the concentration above 5.1 μmol/L being associated with HR of > 1. CONCLUSIONS: Elevated levels of TMAO are associated with an increased incidence of MACE in patients with CHD. TMAO concentration of 5.1 μmol/L may be a cut-off value for prognosis.
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spelling pubmed-69532122020-01-14 Trimethylamine-N-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis Yao, Miao-En Liao, Peng-Da Zhao, Xu-Jie Wang, Lei BMC Cardiovasc Disord Research Article BACKGROUND: Previous clinical studies have suggested that trimethylamine-N-oxide (TMAO) could contribute to the development of atherosclerosis cardiovascular disease. However, the synthetic analysis in coronary heart disease (CHD) was not yet performed. We aimed to clarify the relationship between elevated plasma concentrations of TMAO and the incidence of major adverse cardiovascular events (MACE) in CHD patients. METHODS: Meta-analysis and dose-response analysis of hazard ratio data from prospective observational studies reporting on the association between TMAO plasma concentrations and the incidence of MACE in patients with CHD were conducted. RESULTS: Of the 2369 published articles identified in the search, seven papers, with data from nine cohort studies (10,301 patients), were included in the meta-analysis. Combined data showed that elevated plasma TMAO concentrations could increase 58% higher risk of MACE in patients with CHD (hazard ratios [HR]: 1.58; 95% confidence interval [CI] = 1.35–1.84, P = 0.000). For follow-up ≥ 1 year, it was associated with 62% higher risk of MACE in patients with longer-term than shorter-term (HR for follow-up ≥ 4 years: 1.96; 95% CI = 1.52–2.52 vs one to 3 years: 1.34; 95% CI = 1.26–1.43, P = 0.004). The dose-response analysis revealed a ‘J’ shaped association between TMAO concentration and the incidence of MACE (P = 0.033), with the concentration above 5.1 μmol/L being associated with HR of > 1. CONCLUSIONS: Elevated levels of TMAO are associated with an increased incidence of MACE in patients with CHD. TMAO concentration of 5.1 μmol/L may be a cut-off value for prognosis. BioMed Central 2020-01-09 /pmc/articles/PMC6953212/ /pubmed/31918665 http://dx.doi.org/10.1186/s12872-019-01310-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.
spellingShingle Research Article
Yao, Miao-En
Liao, Peng-Da
Zhao, Xu-Jie
Wang, Lei
Trimethylamine-N-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis
title Trimethylamine-N-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis
title_full Trimethylamine-N-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis
title_fullStr Trimethylamine-N-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis
title_full_unstemmed Trimethylamine-N-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis
title_short Trimethylamine-N-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis
title_sort trimethylamine-n-oxide has prognostic value in coronary heart disease: a meta-analysis and dose-response analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6953212/
https://www.ncbi.nlm.nih.gov/pubmed/31918665
http://dx.doi.org/10.1186/s12872-019-01310-5
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