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Type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a Mendelian randomization study

BACKGROUND: Observational studies have reported an inverse association of type 2 diabetes (T2D) with thoracic aortic aneurysm (TAA). However, the causality of the association has not been established yet. The present study aims to clarify the causal relationship between T2D and TAA via a Mendelian r...

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Autores principales: Zhang, Yiran, Li, Yongxin, Dai, Xiaoyi, Lin, Haokai, Ma, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245418/
https://www.ncbi.nlm.nih.gov/pubmed/37280690
http://dx.doi.org/10.1186/s13098-023-01101-1
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author Zhang, Yiran
Li, Yongxin
Dai, Xiaoyi
Lin, Haokai
Ma, Liang
author_facet Zhang, Yiran
Li, Yongxin
Dai, Xiaoyi
Lin, Haokai
Ma, Liang
author_sort Zhang, Yiran
collection PubMed
description BACKGROUND: Observational studies have reported an inverse association of type 2 diabetes (T2D) with thoracic aortic aneurysm (TAA). However, the causality of the association has not been established yet. The present study aims to clarify the causal relationship between T2D and TAA via a Mendelian randomization (MR) approach. METHODS: Causality of associations were assessed using a two-sample MR framework. Genome-wide association study (GWAS) summary statistics were obtained for T2D, glycated hemoglobin (HbA1c), fasting glucose (FG) and fasting insulin (FI) as exposures, and TAA, ascending aortic diameter (AAoD) and descending aortic diameter (DAoD) as outcomes. Four different methods (inverse variance weighted [IVW], weight median, MR-Egger and MR-PRESSO) were used to calculate causal estimates. Heterogeneity and horizontal pleiotropy were assessed using Cochran Q test and MR-Egger regression intercept, respectively. RESULTS: Genetically predicted T2D was inversely associated with the risk of TAA (OR: 0.931, 95% CI 0.870 to 0.997, p = 0.040, IVW method) and AAoD (Beta: -0.065, 95%CI −0.099 to  − 0.031, p = 1.7e−04, IVW method), but not with DAoD (p > 0.05). Genetically predicted FG level was inversely associated with AAoD (Beta: −0.273, 95% CI −0.396 to –0.150, p = 1.41e−05, IVW method) and DAoD (Beta: −0.166, 95% CI −0.281 to −0.051, p = 0.005, IVW method), but not with TAA (p > 0.05). The effect of genetically predicted HbA1c and FI on TAA, AAoD and DAoD did not reach statistical significance (p > 0.05). CONCLUSIONS: Genetic predisposition to T2D decreases the risk of TAA. Genetically predicted T2D is inversely associated with AAoD, but not with DAoD. Genetically predicted FG level was inversely associated with AAoD and DAoD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-023-01101-1.
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spelling pubmed-102454182023-06-08 Type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a Mendelian randomization study Zhang, Yiran Li, Yongxin Dai, Xiaoyi Lin, Haokai Ma, Liang Diabetol Metab Syndr Research BACKGROUND: Observational studies have reported an inverse association of type 2 diabetes (T2D) with thoracic aortic aneurysm (TAA). However, the causality of the association has not been established yet. The present study aims to clarify the causal relationship between T2D and TAA via a Mendelian randomization (MR) approach. METHODS: Causality of associations were assessed using a two-sample MR framework. Genome-wide association study (GWAS) summary statistics were obtained for T2D, glycated hemoglobin (HbA1c), fasting glucose (FG) and fasting insulin (FI) as exposures, and TAA, ascending aortic diameter (AAoD) and descending aortic diameter (DAoD) as outcomes. Four different methods (inverse variance weighted [IVW], weight median, MR-Egger and MR-PRESSO) were used to calculate causal estimates. Heterogeneity and horizontal pleiotropy were assessed using Cochran Q test and MR-Egger regression intercept, respectively. RESULTS: Genetically predicted T2D was inversely associated with the risk of TAA (OR: 0.931, 95% CI 0.870 to 0.997, p = 0.040, IVW method) and AAoD (Beta: -0.065, 95%CI −0.099 to  − 0.031, p = 1.7e−04, IVW method), but not with DAoD (p > 0.05). Genetically predicted FG level was inversely associated with AAoD (Beta: −0.273, 95% CI −0.396 to –0.150, p = 1.41e−05, IVW method) and DAoD (Beta: −0.166, 95% CI −0.281 to −0.051, p = 0.005, IVW method), but not with TAA (p > 0.05). The effect of genetically predicted HbA1c and FI on TAA, AAoD and DAoD did not reach statistical significance (p > 0.05). CONCLUSIONS: Genetic predisposition to T2D decreases the risk of TAA. Genetically predicted T2D is inversely associated with AAoD, but not with DAoD. Genetically predicted FG level was inversely associated with AAoD and DAoD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-023-01101-1. BioMed Central 2023-06-07 /pmc/articles/PMC10245418/ /pubmed/37280690 http://dx.doi.org/10.1186/s13098-023-01101-1 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
Zhang, Yiran
Li, Yongxin
Dai, Xiaoyi
Lin, Haokai
Ma, Liang
Type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a Mendelian randomization study
title Type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a Mendelian randomization study
title_full Type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a Mendelian randomization study
title_fullStr Type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a Mendelian randomization study
title_full_unstemmed Type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a Mendelian randomization study
title_short Type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a Mendelian randomization study
title_sort type 2 diabetes has a protective causal association with thoracic aortic aneurysm: a mendelian randomization study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245418/
https://www.ncbi.nlm.nih.gov/pubmed/37280690
http://dx.doi.org/10.1186/s13098-023-01101-1
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