Cargando…

Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study

BACKGROUND: Metabolic disorders are increasing worldwide and are characterized by various risk factors such as abdominal obesity, insulin resistance, impaired glucose metabolism, and dyslipidemia. Observational studies suggested a bidirectional association between cardiovascular diseases and metabol...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Zhe, Chen, Jiawei, Zhu, Longyang, Jiao, Siqi, Chen, Yinong, Sun, Yihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617200/
https://www.ncbi.nlm.nih.gov/pubmed/37907844
http://dx.doi.org/10.1186/s12872-023-03567-3
_version_ 1785129556069318656
author Wang, Zhe
Chen, Jiawei
Zhu, Longyang
Jiao, Siqi
Chen, Yinong
Sun, Yihong
author_facet Wang, Zhe
Chen, Jiawei
Zhu, Longyang
Jiao, Siqi
Chen, Yinong
Sun, Yihong
author_sort Wang, Zhe
collection PubMed
description BACKGROUND: Metabolic disorders are increasing worldwide and are characterized by various risk factors such as abdominal obesity, insulin resistance, impaired glucose metabolism, and dyslipidemia. Observational studies suggested a bidirectional association between cardiovascular diseases and metabolic disorders and its components. However, the causal associations between them remained unclear. This study aims to investigate the causal relationship between metabolic disorders and cardiovascular disease through Mendelian randomization (MR) analysis. METHODS: A two-sample MR analysis based on publicly available genome-wide association studies were used to infer the causality. The single-nucleotide polymorphisms with potential pleiotropy were excluded by MR-PRESSO. The effect estimates were constructed using the random-effects inverse-variance-weighted method as the primary estimate. Furthermore, MR-Egger and weighted median were also performed to detect heterogeneity and pleiotropy. RESULTS: Genetically predicted metabolic disorders increased the risk for coronary heart disease (OR = 1.77, 95% CI: 1.55–2.03, p < 0.001), myocardial infarction (OR = 1.75, 95% CI: 1.52–2.03, p < 0.001), heart failure (OR = 1.26, 95% CI: 1.14–1.39, p < 0.001), hypertension (OR = 1.01, 95% CI: 1.00-1.02, p = 0.002), and stroke (OR = 1.19, 95% CI: 1.08–1.32, p < 0.001). The concordance of the results of various complementary sensitivity MR methods reinforces the causal relationship further. CONCLUSION: This study provides evidence of a causal relationship between metabolic disorders and increased risk of coronary heart disease, myocardial infarction, heart failure, hypertension, and stroke. Special attention should be paid to improving metabolic disorders to reduce the development of cardiovascular diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-023-03567-3.
format Online
Article
Text
id pubmed-10617200
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-106172002023-11-01 Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study Wang, Zhe Chen, Jiawei Zhu, Longyang Jiao, Siqi Chen, Yinong Sun, Yihong BMC Cardiovasc Disord Research BACKGROUND: Metabolic disorders are increasing worldwide and are characterized by various risk factors such as abdominal obesity, insulin resistance, impaired glucose metabolism, and dyslipidemia. Observational studies suggested a bidirectional association between cardiovascular diseases and metabolic disorders and its components. However, the causal associations between them remained unclear. This study aims to investigate the causal relationship between metabolic disorders and cardiovascular disease through Mendelian randomization (MR) analysis. METHODS: A two-sample MR analysis based on publicly available genome-wide association studies were used to infer the causality. The single-nucleotide polymorphisms with potential pleiotropy were excluded by MR-PRESSO. The effect estimates were constructed using the random-effects inverse-variance-weighted method as the primary estimate. Furthermore, MR-Egger and weighted median were also performed to detect heterogeneity and pleiotropy. RESULTS: Genetically predicted metabolic disorders increased the risk for coronary heart disease (OR = 1.77, 95% CI: 1.55–2.03, p < 0.001), myocardial infarction (OR = 1.75, 95% CI: 1.52–2.03, p < 0.001), heart failure (OR = 1.26, 95% CI: 1.14–1.39, p < 0.001), hypertension (OR = 1.01, 95% CI: 1.00-1.02, p = 0.002), and stroke (OR = 1.19, 95% CI: 1.08–1.32, p < 0.001). The concordance of the results of various complementary sensitivity MR methods reinforces the causal relationship further. CONCLUSION: This study provides evidence of a causal relationship between metabolic disorders and increased risk of coronary heart disease, myocardial infarction, heart failure, hypertension, and stroke. Special attention should be paid to improving metabolic disorders to reduce the development of cardiovascular diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-023-03567-3. BioMed Central 2023-10-31 /pmc/articles/PMC10617200/ /pubmed/37907844 http://dx.doi.org/10.1186/s12872-023-03567-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Wang, Zhe
Chen, Jiawei
Zhu, Longyang
Jiao, Siqi
Chen, Yinong
Sun, Yihong
Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study
title Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study
title_full Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study
title_fullStr Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study
title_full_unstemmed Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study
title_short Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study
title_sort metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617200/
https://www.ncbi.nlm.nih.gov/pubmed/37907844
http://dx.doi.org/10.1186/s12872-023-03567-3
work_keys_str_mv AT wangzhe metabolicdisordersandriskofcardiovasculardiseasesatwosamplemendelianrandomizationstudy
AT chenjiawei metabolicdisordersandriskofcardiovasculardiseasesatwosamplemendelianrandomizationstudy
AT zhulongyang metabolicdisordersandriskofcardiovasculardiseasesatwosamplemendelianrandomizationstudy
AT jiaosiqi metabolicdisordersandriskofcardiovasculardiseasesatwosamplemendelianrandomizationstudy
AT chenyinong metabolicdisordersandriskofcardiovasculardiseasesatwosamplemendelianrandomizationstudy
AT sunyihong metabolicdisordersandriskofcardiovasculardiseasesatwosamplemendelianrandomizationstudy